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Nature Cell Biology|July 1, 2020
Unrestrained ESCRT-III drives micronuclear catastrophe and chromosome fragmentationMarina Vietri, Sebastian W Schultz, Aurélie Bellanger, et al.
Nature Communications|February 2, 2019
Remodeling of secretory lysosomes during education tunes functional potential in NK cellsJodie P Goodridge, Benedikt Jacobs, Michelle L Saetersmoen, et al.
American Journal of Human Genetics|March 18, 2008
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndromeGregor D Gilfillan, Kaja K Selmer, Ingrid Roxrud, et al.
Nature Immunology|September 15, 2020
Author Correction: STEEP mediates STING ER exit and activation of signalingBao-Cun Zhang, Ramya Nandakumar, Line S Reinert, et al.
Nature Immunology|July 22, 2020
STEEP mediates STING ER exit and activation of signalingBao-Cun Zhang, Ramya Nandakumar, Line S Reinert, et al.
American Journal of Human Genetics|February 29, 2024
Bi-allelic variants in SNF8 cause a disease spectrum ranging from severe developmental and epileptic encephalopathy to syndromic optic atrophyMelanie Brugger, Antonella Lauri, Yan Zhen, et al.
Autophagy|January 12, 2008
Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotesDaniel J Klionsky, Hagai Abeliovich, Patrizia Agostinis, et al.
Autophagy|September 12, 2012
Guidelines for the use and interpretation of assays for monitoring autophagyDaniel J Klionsky, Fabio C Abdalla, Hagai Abeliovich, et al.
Autophagy|February 26, 2021
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1Daniel J Klionsky, Amal Kamal Abdel-Aziz, Sara Abdelfatah, et al.
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