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International Journal of Molecular Sciences|December 11, 2025
L467F;F508del Complex Allele in a Heterozygous State with CFTRdele2,3: What to Expect from CFTR Modulators?Elena Kondratyeva, Anna Efremova, Yuliya Melyanovskaya, et al.
Scientific Reports|May 25, 2021
Prematurity alters the progenitor cell program of the upper respiratory tract of neonatesJessica E Shui, Wei Wang, Helu Liu, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 8, 2009
PINK1-dependent recruitment of Parkin to mitochondria in mitophagyCristofol Vives-Bauza, Chun Zhou, Yong Huang, et al.
Ebiomedicine|September 26, 2020
Hypothermic oxygenated perfusion protects from mitochondrial injury before liver transplantationAndrea Schlegel, Xavier Muller, Matteo Mueller, et al.
International Journal of Molecular Sciences|November 25, 2023
Pathogenic Variants and Genotypes of the CFTR Gene in Russian Men with Cystic Fibrosis and CBAVD SyndromeVyacheslav Chernykh, Stanislav Krasovsky, Olga Solovova, et al.
Plos Medicine|November 9, 2021
Integrating HIV services and other health services: A systematic review and meta-analysisCaroline A Bulstra, Jan A C Hontelez, Moritz Otto, et al.
Biorxiv : the Preprint Server for Biology|January 9, 2026
A mouse model of CHCHD10 p.R15L familial ALS presents mild, age-related motor neuron degeneration without protein instability or mitochondrial dysfunctionJoonHyung Park, Anna Stepanova, Jalia Dash, et al.
Journal of Cell Science|September 3, 2017
Distinct intracellular sAC-cAMP domains regulate ER Ca2+ signaling and OXPHOS functionFederica Valsecchi, Csaba Konrad, Marilena D'Aurelio, et al.
Pigment Cell & Melanoma Research|December 22, 2025
Genetic Features of Albinism: A Comprehensive Analysis in the Russian PopulationSofya Ionova, Andrey Marakhonov, Vitaliy Kadyshev, et al.
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