Allele-selective transcriptional repression of mutant HTT for the treatment of Huntington’s disease

Bryan Zeitler, Steven Froelich, Kimberly Marlen, +48

Nature Medicine

Transcriptional RegulationNeurodegenerative DiseasesHuntington ’Genetic DisorderMedicine +9

Impaired LRP6-TCF7L2 Activity Enhances Smooth Muscle Cell Plasticity and Causes Coronary Artery Disease

Roshni Srivastava, Jiasheng Zhang, Gwang‐woong Go, +3

Cell Reports

MicroRNAs Establish Uniform Traits during the Architecture of Vertebrate Embryos

Dionna M. Kasper, Albertomaria Moro, Emma Ristori, +11

Developmental Cell

BiologyEmbryologyDevelopmental BiologyNatural SciencesGenetics +8

Inflammatory Bowel Disease in a Rodent Model Alters Osteocyte Protein Levels Controlling Bone Turnover

Corinne E. Metzger, Anand Narayanan, David C. Zawieja, +1

Journal of Bone and Mineral Research

Analysis of Worsening Heart Failure Events in an Integrated Health Care System

Andrew P. Ambrosy, Rishi Parikh, Sue Hee Sung, +15

Journal of the American College of Cardiology

Heart FailureHealth PolicyCardiovascular DiseaseCoronary UnitPatient Safety +7

A Dicer-miR-107 Interaction Regulates Biogenesis of Specific miRNAs Crucial for Neurogenesis

Emma Ristori, Miguel Alejandro Lopez‐Ramirez, Anand Narayanan, +5

Developmental Cell

Specific Mirnas CrucialDevelopmental BiologyRna BiologyMicrorna DetectionSmall Rna +5

A Natural Language Processing–Based Approach for Identifying Hospitalizations for Worsening Heart Failure Within an Integrated Health Care Delivery System

Andrew P. Ambrosy, Rishi Parikh, Sue Hee Sung, +13

JAMA Network Open

EBV-positive Primary Pulmonary Lymphoepithelioma-like Carcinoma Response to PD-L1 Blockade

Anand Narayanan, Friedrich Knollmann, Julie Ann S. Walby, +3

Clinical Lung Cancer

Lymphoid NeoplasiaPd-l1 BlockadeMedicineImmunologyImmune Checkpoint Inhibitor +5

In vivo mutagenesis of miRNA gene families using a scalable multiplexed CRISPR/Cas9 nuclease system

Anand Narayanan, Guillermina Hill-Terán, Albertomaria Moro, +5

Scientific Reports

Mutations in the Histone Modifier PRDM6 Are Associated with Isolated Nonsyndromic Patent Ductus Arteriosus

Na Li, Lakshman Subrahmanyan, Emily Smith, +21

The American Journal of Human Genetics

ChromatinDevelopmental BiologyGenetic DisorderGeneticsPathology +4