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Journal of Medical Genetics|November 13, 2024
Long-read sequencing for detection and subtyping of Prader-Willi and Angelman syndromesVahid Akbari, Sarah Dada, Yaoqing Shen, et al.
Clinical Journal of the American Society of Nephrology : CJASN|June 8, 2022
Digenic Alport SyndromeJudy Savige, Alessandra Renieri, Elisabet Ars, et al.
American Journal of Respiratory and Critical Care Medicine|July 18, 2009
Role of insulin-like growth factor binding protein-3 in allergic airway remodelingKristen L Veraldi, Bethany T Gibson, Hidekata Yasuoka, et al.
Journal of Lipid Research|October 26, 2007
Absence of stearoyl-CoA desaturase-1 ameliorates features of the metabolic syndrome in LDLR-deficient miceMarcia L E MacDonald, Roshni R Singaraja, Nagat Bissada, et al.
Cold Spring Harbor Molecular Case Studies|January 5, 2017
Optic atrophy, cataracts, lipodystrophy/lipoatrophy, and peripheral neuropathy caused by a de novo OPA3 mutationStephanie C Bourne, Katelin N Townsend, Casper Shyr, et al.
Nanoscale Advances|September 22, 2022
High shear in situ exfoliation of 2D gallium oxide sheets from centrifugally derived thin films of liquid galliumKasturi Vimalanathan, Timotheos Palmer, Zoe Gardner, et al.
Journal of the American Chemical Society|May 17, 2023
Electrochemical Synthesis of Poly(trisulfides)Jasmine M M Pople, Thomas P Nicholls, Le Nhan Pham, et al.
Respiratory Physiology & Neurobiology|November 12, 2015
Absence of mutations in HCRT, HCRTR1 and HCRTR2 in patients with ROHHADSarah F Barclay, Casey M Rand, Paul A Gray, et al.
Chemsuschem|February 26, 2021
Insulating Composites Made from Sulfur, Canola Oil, and Wool*Israa Bu Najmah, Nicholas A Lundquist, Melissa K Stanfield, et al.
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