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American Journal of Human Genetics|April 2, 2019
Truncating Mutations in UBAP1 Cause Hereditary Spastic ParaplegiaMohammad Ali Farazi Fard, Adriana P Rebelo, Elena Buglo, et al.
Methods (San Diego, Calif.)|February 21, 2015
Methodological aspects of the molecular and histological study of prostate cancer: focus on PTENAitziber Ugalde-Olano, Ainara Egia, Sonia Fernández-Ruiz, et al.
Reumatologia Clinica|March 12, 2013
Different clinical expression of patients with ankylosing spondylitis according to gender in relation to time since onset of disease. Data from REGISPONSERRafaela Ortega Castro, Pilar Font Ugalde, M Carmen Castro Villegas, et al.
Nature Communications|May 30, 2026
COXFA4L2 upregulation preserves residual cytochrome c oxidase activity in COXFA4-related Leigh-like encephalopathyMicol Falabella, Sandra Lopez Calcerrada, Jana Aref, et al.
Astrobiology|March 20, 2024
Planetary Protection Knowledge Gap Closure Enabling Crewed Missions to MarsJames A Spry, Bette Siegel, Corien Bakermans, et al.
Journal of Clinical Laboratory Analysis|June 2, 2026
Beta-Thalassemia in Spain: Results From the National Thalassemia Registry and Molecular Analysis of Patients With Transfusion-Dependent ThalassemiaAna Villegas, Paloma Ropero, Fernando Ataulfo González, et al.
Nature Genetics|August 6, 2013
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and miceAnnika Keller, Ana Westenberger, Maria J Sobrido, et al.
Nature Communications|June 16, 2026
Fibroblastic aspartoacylase suppresses TGFβ-mediated responses and cancer progressionIanire Astobiza, Catalina Capó-Serra, Cristina Viera, et al.
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