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Nature|September 18, 2009
Genetic variation in IL28B and spontaneous clearance of hepatitis C virusDavid L Thomas, Chloe L Thio, Maureen P Martin, et al.Alzheimer'S & Dementia (New York, N. Y.)|February 1, 2021
The association of circulating amylin with β-amyloid in familial Alzheimer's diseaseHan Ly, Nirmal Verma, Savita Sharma, et al.The Journal of Clinical Investigation|September 4, 2013
Epithelial stem cell mutations that promote squamous cell carcinoma metastasisRuth A White, Jill M Neiman, Anand Reddi, et al.Cellr4-- Repair, Replacement, Regeneration, & Reprogramming|June 24, 2021
Umbilical Cord-derived Mesenchymal Stem Cells for COVID-19 Patients with Acute Respiratory Distress Syndrome (ARDS)G Lanzoni, E Linetsky, D Correa, et al.American Journal of Respiratory and Critical Care Medicine|April 13, 2022
Rare and Common Variants in <i>KIF15</i> Contribute to Genetic Risk of Idiopathic Pulmonary FibrosisDavid Zhang, Gundula Povysil, Philippe H Kobeissy, et al.Stroke|December 4, 2010
Guidelines for the primary prevention of stroke: a guideline for healthcare professionals from the American Heart Association/American Stroke AssociationLarry B Goldstein, Cheryl D Bushnell, Robert J Adams, et al.American Journal of Human Genetics|August 7, 2012
Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophreniaAnna C Need, Joseph P McEvoy, Massimo Gennarelli, et al.Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2006
The alpha-synuclein gene in multiple system atrophyT Ozawa, D G Healy, P M Abou-Sleiman, et al.Digestive Diseases and Sciences|May 1, 2012
The association of genetic variants with hepatic steatosis in patients with genotype 1 chronic hepatitis C infectionPaul J Clark, Alexander J Thompson, Qianqian Zhu, et al.Scientific Reports|December 6, 2023
The diagnostic yield of exome sequencing in liver diseases from a curated gene panelXiao-Fei Kong, Kelsie Bogyo, Sheena Kapoor, et al.Pageof 144