Mark D. Matteucci - Concepedia

Author

Mark D. Matteucci

Gilead Sciences (United States)

Also Known As

M D Matteucci, M. D. MATTEUCCI, M. D. Matteucci, M.D. Matteucci, MARK D. MATTEUCCI, Mark D Matteucci, Mark D. Matteucci

Publications

6.2K

Citations

H-Index

Concepts

All Affiliations

Gilead Sciences (United States)Threshold Pharmaceuticals (United States)University of Colorado Boulder

About

Mark D. Matteucci is an author at Gilead Sciences (United States) specializing in natural sciences, molecular biology, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	23	29	3.4K
2	Biochemistry	18	23	2.8K
3	Medicine	16	16	2K
4	Engineering	10	10	1.6K
5	Biomolecular Engineering	10	11	661

Mark D. Matteucci

Publications

5.5K

Citations

H-Index

Page 1

	Year	Citations
Synthesis of deoxyoligonucleotides on a polymer support Mark D. Matteucci, M. H. CARUTHERS Journal of the American Chemical Society Dna NanotechnologyMolecular CharacterizationMolecular SciencesBioorganic ChemistryEngineering	1981	874
Antisense Gene Inhibition by Oligonucleotides Containing C-5 Propyne Pyrimidines Richard W. Wagner, Mark D. Matteucci, Jason G. Lewis, Science Melting TemperatureBiochemistryAntisense Gene InhibitionC-5 Propyne AnalogsNatural Sciences	1993	406
Synthesis of DNA via deoxynudeoside H-phosphonate Intermediates Brian C. Froehler, Peter G. Ng, Mark D. Matteucci Nucleic Acids Research Biological ActivityDna SequencingBiosynthesisBioorganic ChemistryNucleic Acid Chemistry	1986	345
A serum-resistant cytofectin for cellular delivery of antisense oligodeoxynucleotides and plasmid DNA. John G. Lewis, Kun Lin, A Kothavale, Proceedings of the National Academy of Sciences Cellular DeliveryNanomedicineGene TherapiesLipid PreparationMedicine	1996	259
Nucleosides with a Twist. Can Fixed Forms of Sugar Ring Pucker Influence Biological Activity in Nucleosides and Oligonucleotides? Víctor E. Márquez, M. Arshad Siddiqui, Abdallah Ezzitouni, Journal of Medicinal Chemistry	1996	247
Molecular and Cellular Pharmacology of the Hypoxia-Activated Prodrug TH-302 Fanying Meng, James Evans, Deepthi Bhupathi, Molecular Cancer Therapeutics PharmacotherapyRedox BiologyOxidative StressMolecular PharmacologyRedox Regulator	2011	203
Selective Tumor Hypoxia Targeting by Hypoxia-Activated Prodrug TH-302 Inhibits Tumor Growth in Preclinical Models of Cancer Jessica D. Sun, Qian Liu, Jingli Wang, Clinical Cancer Research	2011	194
Nucleoside h-phosphonates: Valuable intermediates in the synthesis of deoxyoligonucleotides Brian C. Froehler, Mark D. Matteucci Tetrahedron Letters Bioorganic ChemistryValuable IntermediatesNatural SciencesOligonucleotideMolecular Biology	1986	185
Triple helix formation inhibits transcription elongation in vitro. Stuart Young, S. H. KRAWCZYK, Mark D. Matteucci, Proceedings of the National Academy of Sciences ChromatinTranscriptional RegulationChromatin StructureMedicineNatural Sciences	1991	171
An assessment of the antisense properties of RNase H-competent and steric-blocking oligomers Michele A. Bonham, Stephen Brown, Ann L. Boyd, Nucleic Acids Research	1995	170

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