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American Journal of Human Genetics|May 16, 2007
RAB23 mutations in Carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesityDagan Jenkins, Dominik Seelow, Fernanda S Jehee, et al.
Plos One|April 24, 2025
Collaborative metabolic curation of an emerging model marine bacterium, Alteromonas macleodii ATCC 27126Daniel Sher, Emma E George, Matthias Wietz, et al.
Pediatric Pulmonology|October 23, 2025
Vaccine Coverage Among People With Cystic Fibrosis: A National Multicenter Cross-Sectional Study in IsraelLior Tsviban, Nofar Amitai, Hagit Levine, et al.
Science (New York, N.Y.)|February 19, 2021
De novo design of transmembrane β barrelsAnastassia A Vorobieva, Paul White, Binyong Liang, et al.
Nature Genetics|January 25, 2011
Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndromeCaroline Rooryck, Anna Diaz-Font, Daniel P S Osborn, et al.
Journal of Medical Genetics|January 30, 2026
Expanding the phenotypic spectrum of MECOM-associated syndrome: rare variants are associated with syndromic pulmonary arterial hypertensionCarrie L Welch, Meriel McEntagart, Shahin Moledina, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 18, 2023
The new face of cystic fibrosis in the era of population genetic carrier screeningMiri Dotan, Hannah Blau, Amihood Singer, et al.
British Journal of Clinical Pharmacology|November 28, 2022
The effect of TRV027 on coagulation in COVID-19: A pilot randomized, placebo-controlled trialAlexander J Robbins, Nur Amalina Che Bakri, Edward Toke-Bjolgerud, et al.
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