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Iscience|July 17, 2024
Supernumerary proteins of the human mitochondrial ribosomal small subunit are integral for assembly and translationTaru Hilander, Ryan Awadhpersad, Geoffray Monteuuis, et al.
Life Science Alliance|August 10, 2022
Islet Gene View-a tool to facilitate islet researchOlof Asplund, Petter Storm, Vikash Chandra, et al.
Protein Science : a Publication of the Protein Society|March 21, 2024
Proinsulin folding and trafficking defects trigger a common pathological disturbance of endoplasmic reticulum homeostasisAnoop Arunagiri, Maroof Alam, Leena Haataja, et al.
Nature Genetics|July 21, 2014
Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune diseaseSarah E Flanagan, Emma Haapaniemi, Mark A Russell, et al.
EMBO Molecular Medicine|January 3, 2026
A new form of diabetes caused by INS mutations defined by zygosity, stem cell and population dataYue Tong, Marianne Becker, Ulrike Schierloh, et al.
Cell Metabolism|August 7, 2025
HNF1A and A1CF coordinate a beta cell transcription-splicing axis that is disrupted in type 2 diabetesEdgar Bernardo, Matías Gonzalo De Vas, Diego Balboa, et al.
Iscience|April 11, 2022
DUX4 is a multifunctional factor priming human embryonic genome activationSanna Vuoristo, Shruti Bhagat, Christel Hydén-Granskog, et al.
Transplantation|April 16, 2016
Executive Summary of IPITA-TTS Opinion Leaders Report on the Future of β-Cell ReplacementJames F Markmann, Stephen T Bartlett, Paul Johnson, et al.
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