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[1] What Is Molecular Biology? Key Concepts, Techniques ... - Excedr — Gene therapy is another discipline in molecular biology that has been developed to modify, enhance, or suppress certain genes in an organism in order to treat or prevent disease, rather than relying on drugs to support immune responses and the nervous system. Molecular biology is a relatively recent field in science that came to prominence in the mid-1900’s due to important scientific discoveries that allowed scientists to visualize the structures of biological macromolecules and better understand molecular mechanisms and processes. Since its initial introduction and development, many different techniques have been created to further understand the processes of how DNA and proteins interact and function in cells, and studies including biochemistry and cell biology continue to increase our understanding of cell function on a microscopic and molecular level.
[2] Molecular biology - Wikipedia — The term 'molecular biology' was first used in 1945 by the English physicist William Astbury, who described it as an approach focused on discerning the underpinnings of biological phenomena—i.e. uncovering the physical and chemical structures and properties of biological molecules, as well as their interactions with other molecules and how these interactions explain observations of so-called classical biology, which instead studies biological processes at larger scales and higher levels of organization. In 1953, Francis Crick, James Watson, Rosalind Franklin, and their colleagues at the Medical Research Council Unit, Cavendish Laboratory, were the first to describe the double helix model for the chemical structure of deoxyribonucleic acid (DNA), which is often considered a landmark event for the nascent field because it provided a physico-chemical basis by which to understand the previously nebulous idea of nucleic acids as the primary substance of biological inheritance.
[3] Molecular Biology - an overview | ScienceDirect Topics — For example, the observation that certain proteins are made at various times in a cell’s replication cycle led to the discovery of operator sequences in DNAs and to the identification of specific proteins such as repressors which can bind them and upregulate or downregulate gene expression.28,29 This led to the complete chemical characterization of the sequence and structures of many such repressor molecules, and even to the rational design of altered DNA-binding proteins with new amino acid sequences.30,31 The field called structural biology, which can be considered a subset of molecular biology, strives further to identify the three-dimensional structures of such large purified molecules, usually by X-ray crystallographic methods or by solution-phase NMR spectroscopy.
[4] Understanding the Concept of Molecular Biology (With Diagram) — The basic concept of molecular biology is to investigate the activities of an organism's makeup at a sub-cellular level. The focus is on the sequence of the DNA (the genes), the rate and timing of the expression of those genes, the mechanisms involved in expressing those genes, and the effect that they have on the whole cell and ultimately the whole organism.
[7] Ethical and Social Issues in Gene Therapy — The biology of human gene therapy is very complex, and there are many techniques that still need to be developed and diseases that need to be understood more fully before gene therapy can be used appropriately. In addition, because gene therapy involves making changes to the body's genetic setup, it raises many unique ethical concerns.
[8] Ethics of Gene Therapy: Balancing Progress and Morality — Adhering to these principles helps navigate the complex ethical landscape of gene manipulation and therapy, facilitating progress while upholding moral values and ensuring responsible advancements in genetic treatment. The ethical implications surrounding gene therapy and genetic manipulation require careful consideration to strike a balance between the potential for progress and the preservation of moral standards. This section aims to critically evaluate the morality of gene manipulation by considering societal values, ethical principles, and the potential consequences of genetic editing. The public’s perspective on the moral and ethical considerations surrounding genetic manipulation and treatment is a critical aspect to consider as we navigate the advancements in gene editing and therapy.
[9] Ethical Challenges and Controversies in the Practice and Advancement of ... — Among the two gene therapy approaches, germline gene therapy is considered to have raised controversial arguments including off-target effects, mosaic mutation, informed consent, and eugenics. Although bioethical concerns may sound morally and socially legitimate to proponents, the public and even scientists, they are not conclusive enough to
[13] DNA vs. RNA Comparison: Structural and Functional Facts — Despite their shared importance and structural similarities, DNA and RNA differ significantly in their structure, chemical composition, and functions. 1. Chemical Structure of DNA and RNA RNA acts as a mediator between DNA and proteins. Messenger RNA (mRNA): Transcribes genetic information from DNA and carries it to ribosomes. This stability allows DNA to function as a long-term storage molecule for genetic information. This distribution enables RNA to mediate the flow of genetic information from DNA to ribosomes. 7.2 Transition from RNA to DNA | Feature | DNA | RNA | DNA’s stable, double-stranded structure makes it the ideal repository for genetic information, while RNA’s versatile, single-stranded structure equips it to play active roles in protein synthesis and gene regulation.
[14] DNA vs RNA - Introduction and Differences between DNA and RNA - BYJU'S — But at the molecular level, all life is fundamentally made up of the same building blocks - DNA and RNA. One of the primary differences between DNA and RNA is that DNA is double-stranded while RNA is single-stranded. Table of Contents. Difference; DNA. Structure; Types; RNA. RNA Types; Proteins; Frequently Asked Questions
[15] Nmr Spectroscopy - Biology Simple — NMR Spectroscopy works by applying a magnetic field to a sample and measuring the resonance frequencies of nuclei. It analyzes the magnetic properties of atomic nuclei.” } } , { “@type”: “Question”, “name”: “How does NMR Spectroscopy work?”, “acceptedAnswer”: { “@type”: “Answer”, “text”: “NMR Spectroscopy works by applying a magnetic field to a sample and measuring the resonance frequencies of nuclei.” } } , { “@type”: “Question”, “name”: “What are the applications of NMR Spectroscopy?”, “acceptedAnswer”: { “@type”: “Answer”, “text”: “NMR Spectroscopy is used in chemistry, biology, and medicine. It helps in studying molecular structures and dynamics.” } } , { “@type”: “Question”, “name”: “Why is NMR Spectroscopy important?”, “acceptedAnswer”: { “@type”: “Answer”, “text”: “NMR Spectroscopy provides detailed information about the structure, dynamics, and interactions of molecules.
[17] An Introduction to Biological NMR Spectroscopy - PMC — We then introduce the NMR spectral parameters used in structural biology, namely the chemical shift, the J-coupling, nuclear Overhauser effects, and residual dipolar couplings. The credibility of NMR as structural tool for proteins was strengthened over the years as its performance increased: 3D NMR was introduced first on unlabeled proteins followed quickly by a new set of triple resonance experiments (11) using 15N and 13C labeled samples. NMR 21, 75–76 [DOI] [PubMed] [Google Scholar] J. (1996) Protein NMR Spectroscopy: Principles and practice; Academic Press: San Diego, CA [Google Scholar] P. (2009) The structural analysis of protein-protein interactions by NMR spectroscopy. W. (2004) Validation of protein structures derived by NMR spectroscopy. J. Biomol .NMR 54, 267–283 [DOI] [PMC free article] [PubMed] [Google Scholar]
[42] History of molecular biology | PPT - SlideShare — The document provides a history of molecular biology, describing how it emerged from the union of biochemistry, genetics, microbiology, and virology in the 1930s. It summarizes several major discoveries and events, including identifying DNA as the genetic material in 1944, determining the double helix structure of DNA in 1953, cracking the
[44] Molecular biology - Wikipedia — The term 'molecular biology' was first used in 1945 by the English physicist William Astbury, who described it as an approach focused on discerning the underpinnings of biological phenomena—i.e. uncovering the physical and chemical structures and properties of biological molecules, as well as their interactions with other molecules and how these interactions explain observations of so-called classical biology, which instead studies biological processes at larger scales and higher levels of organization. In 1953, Francis Crick, James Watson, Rosalind Franklin, and their colleagues at the Medical Research Council Unit, Cavendish Laboratory, were the first to describe the double helix model for the chemical structure of deoxyribonucleic acid (DNA), which is often considered a landmark event for the nascent field because it provided a physico-chemical basis by which to understand the previously nebulous idea of nucleic acids as the primary substance of biological inheritance.
[47] The History of Molecular Biology: Pioneers and Discoveries — Friedrich Miescher’s groundbreaking discovery of DNA in 1869 laid the foundational stones for modern molecular biology, marking a significant turning point in the field of genetics. Miescher’s early encounter with DNA underscores a pivotal moment in the shift from classical Mendelian genetics to a more comprehensive molecular understanding of heredity, which continues to influence biological research and our comprehension of life itself in profound ways. Such milestones underscore the profound implications of molecular genetics on contemporary research and technology, highlighting how discoveries in this field have led to innovations in medicine, agriculture, and even forensic science, thereby changing our approach to various challenges and enhancing our ability to manipulate biological systems for future advancements.
[49] Milestones of Molecular Biology - 2016 - Wiley Analytical Science — In 1955, Arthur Kornberg isolated the first DNA polymerase. These enzymes play a key role in DNA replication. For this discovery, he received the Nobel Prize in Physiology or Medicine together with Severo Ochoa in 1959. In 1958, Francis Crick formulated the "sequence hypothesis" and the "central dogma" of molecular biology.
[50] History of Molecular Biology - Bitesize Bio — This chronology really gets at the basic science underpinning molecular biology as a field of study. At it's core is the so-called Central Dogma of Molecular Biology, where genetic material is transcribed into RNA and then translated into protein, despite being an oversimplified picture of molecular biology, still provides a good starting point for understanding the field.
[51] Key Discoveries in Molecular Biology Since the Double Helix - Bioradiations — The discovery of the double-helix structure of DNA 60 years ago led to a revolution in biological science, opening the floodgates for myriad subsequent discoveries and spawning new fields of research. Edwin Southern developed the eponymous DNA blotting technique, which enabled researchers to identify, locate, and quantitate specific DNA sequences in a sample of genomic DNA, for example, to detect a genetically modified organism or to clone a native gene. For the past 60 years, Bio-Rad has retained the entrepreneurial spirit of its early days while following its charter to accelerate scientific discovery processes by providing products and tools for life science researchers.
[52] The History of Molecular Biology: Pioneers and Discoveries — Friedrich Miescher’s groundbreaking discovery of DNA in 1869 laid the foundational stones for modern molecular biology, marking a significant turning point in the field of genetics. Miescher’s early encounter with DNA underscores a pivotal moment in the shift from classical Mendelian genetics to a more comprehensive molecular understanding of heredity, which continues to influence biological research and our comprehension of life itself in profound ways. Such milestones underscore the profound implications of molecular genetics on contemporary research and technology, highlighting how discoveries in this field have led to innovations in medicine, agriculture, and even forensic science, thereby changing our approach to various challenges and enhancing our ability to manipulate biological systems for future advancements.
[53] Friedrich Miescher and the discovery of DNA - ScienceDirect — While most of these discoveries and concepts were met with great interest by the scientific community at the time, the discovery of DNA was generally underappreciated. Although uncovering the molecular basis of cellular life had become one of the most fundamental problems of the time, no one grasped the real significance of Miescher's findings to answer this problem until the middle of the
[54] Who First Identified Nucleic Acids, and Where Were They Found? — Miescher's approach involved separating cell nuclei from the cytoplasm and isolating nuclein, laying the groundwork for future researchers. Following Miescher's discovery, the exploration of nucleic acids expanded as researchers experimented with different tissues to understand their role across biological systems.
[55] The Structure and Function of DNA - Molecular Biology of the Cell ... — DNA was known to be a long polymer composed of only four types of subunits, which resemble one another chemically. The observation that DNA was double-stranded was of crucial significance and provided one of the major clues that led to the Watson-Crick structure of DNA. In this section we examine the structure of the DNA molecule and explain in general terms how it is able to store hereditary information. A DNA Molecule Consists of Two Complementary Chains of Nucleotides A DNA molecule consists of two long polynucleotide chains composed of four types of nucleotide subunits. The discovery of the structure of the DNA double helix was a landmark in twentieth-century biology because it immediately suggested answers to both questions, thereby resolving at the molecular level the problem of heredity.
[56] DNA Double-Helix Structure Discovery: History, Controversies, and ... — The discovery of the DNA double-helix structure transformed molecular biology, driving breakthroughs in genetics, biotechnology, and medical research. Genetic Code Understanding. The double-helix model clarified how genetic information gets stored and transmitted.
[62] Methods in molecular biology and genetics: looking to the future — In addition, the resolution of the DNA structure paved the way for the invention of the Polymerase Chain Reaction (PCR) (by Kary Mullis), nucleotide synthesis and the Sanger sequencing method which revolutionized the field of genetics and led to the development of several sub-disciplines, including cytogenetics, biotechnology, bioprocess technology, and molecular biology. In this current Collection, we are calling for articles showcasing novel methods from molecular biology and genetics, written by scientists from around the world. He has worked with multiple methods of molecular biology and genetics and is an author of more than 100 articles in international journals, has been peer reviewer for more than 115 international scientific journals, in addition to being part of editorial boards of several international journals.
[81] Advancements in Molecular Techniques for Cutting-Edge Research — Explore the latest molecular techniques driving innovation in research, from gene editing to advanced sequencing technologies. The landscape of DNA sequencing technologies has evolved dramatically, offering researchers tools to decode the genetic blueprint of organisms with speed and accuracy. CRISPR-Cas9 has emerged as a transformative tool in genetic engineering, offering a precise method to modify DNA sequences in living organisms. Polymerase Chain Reaction (PCR) has long been a staple technique in molecular biology, renowned for its ability to amplify DNA sequences. This process has been harnessed in research and therapeutic settings, providing a versatile tool for studying gene function and developing treatments for diseases. Single-cell RNA sequencing (scRNA-seq) has emerged as a groundbreaking technique, offering insights into cellular diversity and function.
[83] Molecular Health Innovations: Redefining Personalized Care — Explore how molecular health innovations are enhancing personalized care through genetic, epigenetic, and biochemical insights for more precise health strategies. By analyzing biological markers at the genetic, epigenetic, proteomic, and metabolomic levels, researchers are developing more precise diagnostic tools and therapies. Differences in gene expression, protein interactions, and metabolism affect disease development and treatment response. Genetic differences influence disease development, environmental responses, and drug metabolism. Variants in key genes can alter biological pathways, increasing susceptibility to conditions like cardiovascular disease, cancer, and neurodegenerative disorders. By integrating metabolomic data, personalized nutritional plans optimize metabolic health, enhance weight management, and lower disease risk. Biomarkers—measurable biological indicators like proteins, metabolites, or genetic signatures—have revolutionized early disease detection, shifting healthcare from reactive treatment to proactive management.
[84] The Impact of Genetics and Genomics: Exploring their Applications and ... — The review examines real-world applications of genetics and genomics in clinical settings. It covers how genetic testing and genomic profiling are used to guide diagnosis, prognosis, and treatment decisions across a spectrum of diseases, including cancer, cardiovascular disorders, and rare genetic conditions.
[88] PDF — Next-generation sequencing technologies, by enabling vast data generation, will provide a comprehensive picture of normal human genome variation in the next few years. This will set the baseline by which genome variation in a genetic disease cohort can be evaluated. Efforts to couple the discovered variations to the disease
[89] CRISPR-CAS 9 In Gene Editing: Innovations, Applications and Ethical ... — The discovery of CRISPR-Cas9 as a tool for gene editing was made possible by the realization that its mechanism could be adapted to cut DNA at precise locations in any organism’s genome . The ability of Cas9 to target specific genetic sequences is what makes CRISPR-Cas9 a powerful tool for gene editing. The precision of CRISPR-Cas9 lies in the ability of the guide RNA to match the target DNA sequence, ensuring that only the intended gene is edited. CRISPR-Cas9 gene editing for sickle cell disease and ?-thalassemia. CRISPR-Cas9 gene editing for sickle cell disease and ?-thalassemia. Vaishnavi Bhad, Gaurav Bhalerao, Rani Deokar, CRISPR-CAS 9 In Gene Editing: Innovations, Applications and Ethical Challenges, Int. J.
[91] Advances in CRISPR-Cas technology and its applications: revolutionising ... — | Blood | Hemophilia B | F9 | Corrected F9 gene in iPSCs using CRISPR-Cas9; restored F9 expression in hepatocyte-like cells | Morishige et al. One prominent application of CRISPR-Cas9 technology is its application in engineering T-cells express CARs. CAR-T cell therapy is a genetically modified T-cell that expresses CARs, targeting tumour-associated antigens (TAAs) or tumour-specific antigens (TSAs) with high specificity, thereby targeting and eliminating cancer cells (Jogalekar et al., 2022). CRISPR-Cas9 technology has enhanced CAR-T therapy by enabling precise genetic edits that improve T cell functionality, persistence, and specificity (Dimitri et al., 2022). CRISPR-Cas gene editing is utilised to introduce oncolytic viruses with therapeutic genes, enhancing their cancer tissue selectivity and suppressing antiviral protective mechanisms employed by malignant cells (Wang et al., 2022b).
[92] CRISPR and Gene Editing: The Future of Personalized Medicine — CRISPR technology is at the forefront of this transformation, enabling the development of customized treatments based on a patient's unique genetic makeup. CRISPR in Genetic Disorders. One of the most promising applications of CRISPR in personalized medicine is in the treatment of genetic disorders.
[93] CRISPR in 3D: Innovations in Disease Modelling and Personalized Medicine — The CRISPR-Cas system of genetic engineering has had a significant impact on science and society since its advent in 2013. CRISPR integration with 3D culture systems such as organ-on-a-chips, as well as fast emerging commercial technologies, has encouraged translation of more complex pathophysiological modelling and personalized medicine.
[94] Applications and challenges of CRISPR-Cas gene-editing to disease ... — A variety of studies have applied CRISPR-Cas systems for effectively targeting different genes and have managed to prove the potential treatment ability for initiation or progression of lung cancer,64 breast cancer,65,66 and many other types of cancers.67–69 Meanwhile, the CRISPR-Cas system has been harnessed to serve as a powerful tool with the ability of unbiased screening of precision medicine including identification of new drug targets, biomarkers, and elucidation of mechanisms leading to drug resistance.70–72 In short, there are tremendous potential applications for CRISPR-Cas and their derivative systems (i.e. dCas9) due to the ability to accurately determine the underlying disease causes, genetic mutation variants, immunological regulatory factors, cell signaling mediators, and drug targets as well as drug molecules and therapeutics.
[95] Advances in CRISPR-Cas technology and its applications: revolutionising ... — | Blood | Hemophilia B | F9 | Corrected F9 gene in iPSCs using CRISPR-Cas9; restored F9 expression in hepatocyte-like cells | Morishige et al. One prominent application of CRISPR-Cas9 technology is its application in engineering T-cells express CARs. CAR-T cell therapy is a genetically modified T-cell that expresses CARs, targeting tumour-associated antigens (TAAs) or tumour-specific antigens (TSAs) with high specificity, thereby targeting and eliminating cancer cells (Jogalekar et al., 2022). CRISPR-Cas9 technology has enhanced CAR-T therapy by enabling precise genetic edits that improve T cell functionality, persistence, and specificity (Dimitri et al., 2022). CRISPR-Cas gene editing is utilised to introduce oncolytic viruses with therapeutic genes, enhancing their cancer tissue selectivity and suppressing antiviral protective mechanisms employed by malignant cells (Wang et al., 2022b).
[96] Ethical Implications of Gene Editing in Agriculture — Gene editing in agriculture presents a myriad of ethical questions that require ongoing deliberation, dialogue, and responsible action. While the promise of this technology to address food security, sustainability, and nutritional challenges is compelling, it must be accompanied by robust ethical frameworks and governance mechanisms.
[98] Addressing challenges in the clinical applications associated with ... — Here, we discuss the current and potential applications of CRISPR/Cas9 technology and its limitations in clinical applications, as well as ethical and legal considerations in the treatment, disease prevention or disability in somatic cells or human embryo via gene editing. This was first carried out in 2015 when Liang et al., demonstrated how these methods could be applied to human embryos by using CRISPR/Cas9 to cleave the endogenous beta-globing gene (HBB) off human tripronuclear zygotes, aiming to analyse the practicability and effectiveness of editing their genome to bring about therapeutic effects (Tang et al., 2017; Liang et al., 2015; Kang et al., 2016).
[99] CRISPR/Cas9 gene-editing: Research technologies, clinical applications ... — The repurposing of CRISPR/Cas9, an ancient bacterial immune defense system, into a gene-editing technology has armed researchers with a revolutionary tool for gene therapy. However, as the breadth of research and clinical applications of this technology continues to expand, outstanding technical challenges and ethical considerations will need to be addressed before clinical applications become commonplace. Here, we review CRISPR/Cas9 technology and discuss its benefits and limitations in research and the clinical context, as well as ethical considerations surrounding the use of CRISPR gene editing.
[114] Techniques used in Molecular Biology - Biology Discussion — ADVERTISEMENTS: Some of the most important techniques used in molecular biology are as follows: Molecular Biology techniques include characterization, isolation and manipulation of the molecular components of cells and organisms. These components include DNA, the repository of genetic information; RNA, functional and structural part of the translational apparatus and proteins, the major
[115] 1: Basic Molecular Biology Techniques - Royal Society of Chemistry — There have been a number of key developments in molecular biology techniques but the one that has had the greatest impact in recent years has been the polymerase chain reaction (PCR). One of the reasons for the adoption of the PCR is the elegant simplicity of the reaction and the relative ease of the practical manipulation steps.
[116] What Are the Basic Techniques in Molecular Biology? — Molecular biology is a rapidly evolving field that has revolutionized our understanding of the molecular basis of biological activity. The techniques used in molecular biology are diverse and powerful, enabling researchers to study the structure, function, and regulation of biological molecules at the molecular level.
[117] Molecular Biology: Top 9 Methods and Techniques used in Molecular Biology — The following points highlight the nine main methods and techniques of molecular biology. The methods are:- 1. DNA Ligation 2. Elution of DNA Fragments from Agarose 3. Phenol Purification of DNA from Low Melting Agarose 4. Polymerase Chain Reaction 5. SDS-Polyacrylamide Gel Electrophoresis 6. Iso-Electric Focusing (IEF) of Proteins 7. Trypsin Digestion of Protein Gel 8. Protein Dialysis […]
[118] 10 Essential Molecular Biology Techniques You Need to Know — Molecular biology is a branch of biology that studies the molecular basis of biological activity. The techniques used in molecular biology are essential for a wide range of biological research, including genetics, genomics, biotechnology, and biochemistry.In this article, we will discuss the 10 essential molecular biology techniques that every biologist needs to know.
[123] Building Evidence and Measuring Clinical Outcomes for Genomic Medicine — A vision of genomic medicine is the use of newer broad-based genetic testing by individuals and their health practitioners to enhance routine clinical activities including diagnosis, risk assessment, tailored therapy, and more precise prognosis.1,2 Rapid advances in laboratory technologies, particularly next generation sequencing, have introduced relatively inexpensive approaches to acquiring a large set of genetic data with potential applications across many specialties of medicine.3 Both widespread marketing of genomic medicine services and health system implementations have increased the availability of testing to patients and their clinicians.4–6 However, investigations of the clinical utility of genetic testing have often not kept pace, leading to uncertainty about the value of returning findings not related to the original indication and concerns about unintended consequences.7 A lack of clinical outcome data has been cited as one significant factor to the slow uptake of genetic testing into clinical guidelines and inconsistent payer reimbursement policies.8–11 As some clinicians await further study of verification of benefits, and others adopt testing more readily, the assessment of outcomes is increasingly critical to the future practice of genomic medicine.
[124] PCR Techniques: Clinical Impact and Diagnostic Limitations — PCR Techniques: Clinical Impact and Diagnostic Limitations - BiologyInsights Polymerase Chain Reaction (PCR) has transformed molecular biology by enabling precise DNA sequence amplification and detection. Real-time monitoring of the amplification process, often achieved through fluorescent dyes or probes, allows for quantitative analysis, making RT-PCR a powerful tool for both diagnostic and research applications. In clinical settings, RT-PCR is indispensable for detecting and monitoring viral infections. Real-time quantitative PCR (qPCR) is the predominant method for viral load quantification, leveraging its capacity to measure DNA or cDNA during each amplification cycle. By enabling the detection of minute quantities of genetic material, PCR has expanded diagnostic capabilities beyond conventional methods, allowing healthcare providers to identify infections and genetic anomalies with accuracy.
[125] Impact of Genetic Testing on Human Health: - PubMed Central (PMC) — The mission of the Precision Medicine Program at Nemours Children’s Health is to integrate the application of genetic information into patient care and to provide colleagues across our institution with the resources and knowledge base to adapt to the growing genetic and genomic landscape that impacts modern patient care. In a few short years, this program has been shown to increase access to genetic testing and provide prompt diagnoses and supportive care.5 The Nemours Pharmacogenomics Service Program, comprised of trained PharmD specialists, provides education, clinical decision support tools, and best practice alerts in the electronic health record (EHR).6,7 The Nemours Biomedical Research Informatics Center deployed a learning health system model, developing analytic tools to improve use of existing EHR data for outcomes research, and natural language processing and machine learning tools to make maximal use of unstructured medical data.8,9 The Biobank and Molecular Analysis Program offers a biorepository for storage of pediatric tissue samples as well as guidance and scientific support to investigators in the conduct of clinical research.
[126] Implementation and utilization of genetic testing in personalized ... — Pharmacogenetics is the study of the genetic determinants of drug response variability, and increasing enthusiasm for implementing clinical pharmacogenetic testing is evidenced by the personalized medicine programs that are now preemptively genotyping germline pharmacogenetic variants1 and the recent availability of clinical practice guidelines when pharmacogenetic test results are available.2 Other developments supporting the implementation of pharmacogenetic testing include the recent availability of rapid sample-to-answer genotyping platforms that could potentially be used at the point-of-care3 and the increasing use of clinical decision support (CDS) for health care providers deployed through electronic health records (EHRs).4 This review aims to summarize the current state of the personalized medicine genetic testing field, with an emphasis on pharmacogenetic testing and clinical implementation.
[127] Advancements in Molecular Techniques for Cutting-Edge Research — Explore the latest molecular techniques driving innovation in research, from gene editing to advanced sequencing technologies. The landscape of DNA sequencing technologies has evolved dramatically, offering researchers tools to decode the genetic blueprint of organisms with speed and accuracy. CRISPR-Cas9 has emerged as a transformative tool in genetic engineering, offering a precise method to modify DNA sequences in living organisms. Polymerase Chain Reaction (PCR) has long been a staple technique in molecular biology, renowned for its ability to amplify DNA sequences. This process has been harnessed in research and therapeutic settings, providing a versatile tool for studying gene function and developing treatments for diseases. Single-cell RNA sequencing (scRNA-seq) has emerged as a groundbreaking technique, offering insights into cellular diversity and function.
[128] Next-Generation Sequencing Technology: Current Trends and Advancements ... — This review article provides an overview of NGS technology and its impact on various areas of research, such as clinical genomics, cancer, infectious diseases, and the study of the microbiome. These second-generation sequencing technologies have significantly increased the throughput and speed of DNA sequencing, enabling a wide range of applications in genomics research and clinical diagnostics . 192.Abel H.J., Duncavage E.J. Detection of structural DNA variation from next generation sequencing data: A review of informatic approaches. 203.Hajibabaei M., Shokralla S., Zhou X., Singer G.A.C., Baird D.J. Environmental Barcoding: A Next-Generation Sequencing Approach for Biomonitoring Applications Using River Benthos. 208.Minogue T.D., Koehler J.W., Stefan C.P., Conrad T.A. Next-Generation Sequencing for Biodefense: Biothreat Detection, Forensics, and the Clinic.
[129] Top 10 Biotechnology Breakthroughs Transforming Our World — By tweaking the genetic makeup of crops, biotechnology companies have developed plant varieties that are resistant to diseases, pests, and environmental conditions. Synthetic biology can enhance agricultural practices by engineering crops with improved yield, resistance to pests and environmental stress, and higher nutritional value, contributing to sustainable food production. Synthetic biology significantly impacts biomanufacturing by creating tailored organisms that can produce complex chemicals, pharmaceuticals, and materials more sustainably and efficiently. Synthetic biology has the potential to revolutionize industries by enabling the development of innovative products and solutions, offering new ways to address environmental issues, and creating more efficient manufacturing processes.
[148] A Framework to Guide Undergraduate Education in Interdisciplinary ... — The NSF has accepted the definition of “interdisciplinary research” set forth in a report from the National Academy of Sciences, National Academy of Engineering, and Institute of Medicine (NASEM, 2005): “Interdisciplinary research is a mode of research by teams or individuals that integrates information, data, techniques, tools, perspectives, concepts, and/or theories from two or more disciplines or bodies of specialized knowledge to advance fundamental understanding or to solve problems whose solutions are beyond the scope of a single discipline or area of research practice” (p. 2). Example curriculum applying the IDSF to an interdisciplinary course assignment: Students in an upper-division environmental course are tasked to address the decline in honeybee populations via an activity and assignment in which they are asked to construct a proposal to mitigate this issue and are scored on the inclusion of the five IDSF criteria in their response
[149] Building bridges through collaboration - a pathway for ... — The contributions of Linus Pauling, considered by many to be the father of molecular biology, similarly illustrate the power of interdisciplinary research .For example, in the late 1930s, he first applied the newly emerging discipline of quantum mechanics, which had largely focused on descriptions of simple atomic structures, to address the chemical bond in the context of molecular structure
[151] PDF — The integration of cutting-edge technologies and interdisciplinary approaches continues to propel molecular biology forward, paving the way for new insights into the complexities of life at the molecular level Keywords: Molecular Biology; CRISPR-Cas9 Gene; Nucleic Acid Sequencing; Genomics; Signaling Pathways Annals of Experimental and Molecular Biology 2 Bhuvana D, et al. Genomics, the study of an organism’s entire DNA sequence, has been a focal point of recent advances in molecular biology. In addition to elucidating the complexities of biological systems, recent advances in molecular biology have spurred the development of transformative technologies for genome editing and manipulation. Gene Correction: CRISPR-Cas9 can facilitate the precise correction of disease-causing mutations by inducing DSBs at specific genomic loci, followed by HDR-mediated repair Annals of Experimental and Molecular Biology 3 Bhuvana D, et al.
[153] Recent Advances in Cellular and Molecular Bioengineering for Building ... — In the field of cellular and molecular bioengineering (CMBE), engineering biological systems is one of the fastest-growing areas, especially with recent research breakthroughs simultaneously in multiple fields, including stem cell research, tissue engineering, gene editing, synthetic biology, omics, and biomanufacturing. Efforts have also been focused on engineering lymphoid cells and organs, including bone marrow, thymus tissue, and lymph nodes.49 For instance, recreating the bone marrow niche allows for the maintenance and expansion of the CD34+ cell population.28,65 Recapitulating the interaction of stromal cells (genetically engineered to express DLL1 for Notch activation) and human hematopoietic stem cells (HSCs) enables the long-term maintenance of lymphoid progenitors and improves the efficiency of differentiation and positive selection of human T cells.93 Activated B cells can be produced from engineered immune organoids mimicking the germinal center.2,67,74,80 The development of these in vitro systems provides an opportunity for investigating the physiology and pathology of immune systems and for
[154] Bioinformatics 101: Understanding the Key Principles and Applications — Bioinformatics plays a critical role in understanding health and disease by leveraging data from genomics and molecular biology. It helps improve treatments, identify disease mechanisms, and design personalized medicine strategies. Pharmacogenomics and Personalized Medicine. Pharmacogenomics examines how genes affect a person's response to drugs.
[155] The role and application of bioinformatics techniques and tools in drug ... — Bioinformatics tools and multi-omics combined analysis have played an important role in responding to new disease outbreaks and developing new drugs. By analyzing the genomic information of pathogens, researchers can track the spread, evolution, and drug resistance of pathogens, which has important implications for controlling infectious diseases.
[156] Role of Bioinformatics in Biological Sciences | SpringerLink — Bioinformatics is characterized as the use of computational and analytical instruments to identify and analyze biological data. It is an interdisciplinary field that takes advantage of computer science, mathematics, chemistry, physics, and biology. Bioinformatics is important for data management in modern biology and medicine.
[159] Integration of Biochemistry and Cell Biology: Molecular Mechanism - Longdom — Biochemistry focuses on the study of chemical processes within and relating to living organisms, while cell biology investigates the structure and function of cells, the basic units of life.The integration of these disciplines enables researchers to explain molecular mechanisms and cellular functions. For instance, the elucidation of signal
[171] Thermodynamics and Statistical Mechanics - 545.630 — In this course we will aim for understanding the thermodynamics of chemical and biomolecular systems. We will first review classical, macroscopic thermodynamics, covering concepts such as equilibrium, stability, and the role of thermodynamic potentials. ... Statistical mechanics provides a link between the mechanics of atoms and macroscopic
[172] 3.1: The Laws of Thermodynamics - Biology LibreTexts — Similarly in a cell, the potential energy in a chemical bond can be released and then used for processes such as putting smaller molecules together into larger molecules, or causing a molecular motor to spin or bend - actions that could lead to pumping of protons or the contraction of muscle cells, respectively.
[173] Thermodynamics of Biological Processes - ScienceDirect — There is a long and rich tradition of using ideas from both equilibrium thermodynamics and its microscopic partner theory of equilibrium statistical mechanics. In this chapter, we provide some background on the origins of the seemingly unreasonable effectiveness of ideas from both thermodynamics and statistical mechanics in biology. After making a description of these foundational issues, we
[174] Thermodynamics - an overview | ScienceDirect Topics — The first and second laws of thermodynamics apply to all living organisms. A living organism represents an open thermodynamic system that continuously exchanges compounds and heat with the environment, performs mechanical work, and disposes of internal entropy production.
[176] Advancements in Molecular Techniques for Cutting-Edge Research — Explore the latest molecular techniques driving innovation in research, from gene editing to advanced sequencing technologies. The landscape of DNA sequencing technologies has evolved dramatically, offering researchers tools to decode the genetic blueprint of organisms with speed and accuracy. CRISPR-Cas9 has emerged as a transformative tool in genetic engineering, offering a precise method to modify DNA sequences in living organisms. Polymerase Chain Reaction (PCR) has long been a staple technique in molecular biology, renowned for its ability to amplify DNA sequences. This process has been harnessed in research and therapeutic settings, providing a versatile tool for studying gene function and developing treatments for diseases. Single-cell RNA sequencing (scRNA-seq) has emerged as a groundbreaking technique, offering insights into cellular diversity and function.
[178] Past, present, and future of CRISPR genome editing technologies — Genome editing—the precise and targeted modification of the genetic material of living organisms—represents one of the most significant advancements in molecular biology. It has far-reaching applications, from unraveling fundamental biological processes to driving advancements in medicine, agriculture, and biotechnology.
[179] Artificial intelligence and bioinformatics: a journey from traditional ... — Personalize Medicine: Diagnostic, Prognostic, and Predictive biomarkers | Genomic data, clinical data, biomarker levels | 1- Machine Learning models (Logistic Regression, Random Forests): Predict disease risk based on an individual's genetic data. The keywords used were: ("Artificial Intelligence" OR "AI" OR "Machine Intelligence") AND ("Bioinformatics" OR "Biological Data Analysis") AND ("Machine Learning" OR "ML") AND ("Deep Learning" OR "DL") AND ("Natural Language Processing" OR "NLP") AND ("Genome Sequencing" OR "Genomic Analysis") AND ("Protein Structure Prediction") AND ("Drug Discovery") AND ("System Biology") AND ("Personalized Medicine") AND ("Imaging") AND ("Signal Processing") AND ("Text Mining"). Our examination encompassed the diverse applications of AI techniques such as ML, DL, and NLP, elucidating their contributions to tasks such as genome sequencing, protein structure prediction, drug discovery, system biology, personalized medicine, imaging, signal processing, and text mining.
[180] Artificial Intelligence in Biological Sciences - PMC - PubMed Central (PMC) — The current review article highlights how Artificial Intelligence, and its components could be used in the medical, agricultural, and bio-based industrial sectors to make human life more sustainable. 9.Sarker I.H. AI-Based Modeling: Techniques, Applications and Research Issues Towards Automation, Intelligent and Smart Systems. 62.El-Sappagh S., Alonso J.M., Islam S.M.R., Sultan A.M., Kwak K.S. A Multilayer Multimodal Detection and Prediction Model Based on Explainable Artificial Intelligence for Alzheimer’s Disease. 78.Abràmoff M.D., Lavin P.T., Birch M., Shah N., Folk J.C. Pivotal Trial of an Autonomous AI-Based Diagnostic System for Detection of Diabetic Retinopathy in Primary Care Offices. 118.Liu L.W., Lu C.T., Wang Y.M., Lin K.H., Ma X., Lin W.S. Rice (Oryza sativa L.) Growth Modeling Based on Growth Degree Day (GDD) and Artificial Intelligence Algorithms.
[182] Next Generation DNA Sequencing and the Future of Genomic Medicine — 2. Next generation DNA sequencing. The commercially available next generation sequencing platforms differ from traditional Sanger sequencing technology in a number of ways. First, the DNA sequencing libraries are clonally amplified in vitro, obviating the need for time consuming and laborious cloning of the DNA library into bacteria. Second
[183] PDF — the future of DNA sequencing. History of DNA sequencing technologies . The development of DNA sequencing technologies has a rich history, with multiple paradigm shifts occurring within a few decades. Below, we review early efforts to sequence biopolymers, the invention of electro-phoretic methods for DNA sequencing and their scaling to the Human
[184] DNA sequencing at 40: past, present and future - Nature — The history and future potential of DNA sequencing, including the development of the underlying technologies and the expansion of its areas of application, are reviewed.
[187] Ethical Issues Regarding CRISPR Mediated Genome Editing — Ethical Issues Regarding CRISPR Mediated Genome Editing - PubMed Search: Search Your saved search Name of saved search: Ethical Issues Regarding CRISPR Mediated Genome Editing Ethical Issues Regarding CRISPR Mediated Genome Editing CRISPR-Cas9 has emerged as a simple, precise and most rapid genome editing technology. The most contentious issues concerning human germline modifications are the challenges to human safety and morality such as risk of unforeseen, undesirable effects in clinical applications particularly to correct or prevent genetic diseases, matter of informed consent and the risk of exploitation for eugenics. Optimization of genome editing through CRISPR-Cas9 engineering. [CRISPR/CAS9, the King of Genome Editing Tools]. CRISPR/Cas9 in Genome Editing and Beyond. Salsman J, et al. Advancement of animal and poultry nutrition: Harnessing the power of CRISPR-Cas genome editing technology.
[188] Ethics, Values, and Responsibility in Human Genome Editing — Citation PDF Altmetric CRISPR/Cas9 genome editing is an inexpensive and efficient tool to introduce changes in DNA. Its ease of use sets virtually no limits on potential scientific and clinical applications. Genome editing at the beginning of embryonic life means that any genomic alteration introduced will pass on to the germline and propagate through future generations. These possibilities have sparked considerable debate about germline genome editing ethics, governance, and the scope of responsible use of germline interventions.4 An announcement by Chinese researchers in April 20155 that they had edited human embryos initiated public controversy and fear about germline genome editing.6 In November 2018, He Jiankui announced the birth of twin girls with a modified version of the CCR5 gene,7 an alteration that could confer resistance to HIV infection. It has been argued that ethics and governance debates should go beyond the imperative of clinical innovation by paying attention to respect for human rights11 and dignity12 and by carefully considering unknown consequences for gene-edited people and future generations, both in terms of safety and possible eugenic uses of this technology.13 Others have pointed to the availability of safer and more ethically acceptable means of preventing congenital genetic defects, such as pre-implantation genetic diagnosis.14 Still others fear that, if anything goes wrong with human germline editing, research on and clinical use of somatic cell therapy could face reputational crises.15 Consensus has gradually emerged in the scientific community about the need for an international moratorium on premature clinical uses of human germline editing.16,17,18 Public dialogue aimed at reaching “broad societal consensus”16 on uses of genome editing has also emerged as key to the legitimacy of governance decisions about such controversial technology.19 Given that the first clinical trials involving somatic uses of CRISPR/Cas9 are underway,20,21 genome editing is primed to foster dramatic innovation in patient care provided that it is used responsibly.
[189] What are the Ethical Concerns of Genome Editing? — Most of the ethical discussions related to genome editing center around human germline because editing changes made in the germline would be passed down to future generations. Overview The debate about genome editing is not a new one but has regained attention following the discovery that CRISPR has the potential to make such editing more accurate and even "easy" in comparison to older technologies. As of 2014, there were about 40 countries that discouraged or banned research on germline editing, including 15 nations in Western Europe, because of ethical and safety concerns.3 There is also an international effort led by the US, UK, and China to harmonize regulation of the application of genome editing technologies. Researchers and ethicists who have written and spoken about genome editing, such as those present at the International Summit on Human Gene Editing, generally agree that until germline genome editing is deemed safe through research, it should not be used for clinical reproductive purposes; the risk cannot be justified by the potential benefit. Researchers and bioethicists also worry about the possibility of obtaining truly informed consent from prospective parents as long as the risks of germline therapy are unknown.10 Justice and Equity As with many new technologies, there is concern that genome editing will only be accessible to the wealthy and will increase existing disparities in access to health care and other interventions.