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Showing results (721-730 of 726) with videos related to

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Cell|August 6, 2013
AMPD2 regulates GTP synthesis and is mutated in a potentially treatable neurodegenerative brainstem disorderNaiara Akizu, Vincent Cantagrel, Jana Schroth, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterationsEllen S Regalado, Lauren Mellor-Crummey, Julie De Backer, et al.
Nature Genetics|September 13, 2011
Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1Scott A LeMaire, Merry-Lynn N McDonald, Dong-Chuan Guo, et al.
Molecular Metabolism|March 18, 2014
Identification of a novel mitochondrial uncoupler that does not depolarize the plasma membraneBrandon M Kenwood, Janelle L Weaver, Amandeep Bajwa, et al.
Cancer Research|December 19, 2024
A Pan-RAS Inhibitor with a Unique Mechanism of Action Blocks Tumor Growth and Induces Antitumor Immunity in Gastrointestinal CancerJeremy B Foote, Tyler E Mattox, Adam B Keeton, et al.
American Journal of Human Genetics|November 9, 2022
EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesisChristin S Adamo, Aude Beyens, Alvise Schiavinato, et al.
Pageof 73

Showing results (721-730 of 726) with videos related to

Sort By:
Pageof 73
You have reached the last page of results.This site can display upto 726 results.
Cell|August 6, 2013
AMPD2 regulates GTP synthesis and is mutated in a potentially treatable neurodegenerative brainstem disorderNaiara Akizu, Vincent Cantagrel, Jana Schroth, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterationsEllen S Regalado, Lauren Mellor-Crummey, Julie De Backer, et al.
Nature Genetics|September 13, 2011
Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1Scott A LeMaire, Merry-Lynn N McDonald, Dong-Chuan Guo, et al.
Molecular Metabolism|March 18, 2014
Identification of a novel mitochondrial uncoupler that does not depolarize the plasma membraneBrandon M Kenwood, Janelle L Weaver, Amandeep Bajwa, et al.
Cancer Research|December 19, 2024
A Pan-RAS Inhibitor with a Unique Mechanism of Action Blocks Tumor Growth and Induces Antitumor Immunity in Gastrointestinal CancerJeremy B Foote, Tyler E Mattox, Adam B Keeton, et al.
American Journal of Human Genetics|November 9, 2022
EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesisChristin S Adamo, Aude Beyens, Alvise Schiavinato, et al.
Pageof 73