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Elife|February 12, 2019
Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motilityWondwossen M Yeshaw, Marianne van der Zwaag, Francesco Pinto, et al.Nature Genetics|March 18, 1999
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier diseaseA Sakuntabhai, V Ruiz-Perez, S Carter, et al.Journal of Endocrinological Investigation|January 24, 2022
Testosterone positively regulates vagina NO-induced relaxation: an experimental study in ratsI Cellai, S Filippi, P Comeglio, et al.Annals of Neurology|August 5, 2004
Chorein detection for the diagnosis of chorea-acanthocytosisCarol Dobson-Stone, Antonio Velayos-Baeza, Lea A Filippone, et al.Translational Psychiatry|July 26, 2017
The DCDC2 deletion is not a risk factor for dyslexiaT S Scerri, E Macpherson, A Martinelli, et al.Archives of Neurology|April 13, 2005
Early clinical heterogeneity in choreoacanthocytosisAlexander Lossos, Carol Dobson-Stone, Anthony P Monaco, et al.Journal of Endocrinological Investigation|February 15, 2021
Treatment potential of LPCN 1144 on liver health and metabolic regulation in a non-genomic, high fat diet induced NASH rabbit modelP Comeglio, E Sarchielli, S Filippi, et al.Plos One|December 5, 2012
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structureThomas S Scerri, Fahimeh Darki, Dianne F Newbury, et al.Plos Genetics|September 27, 2013
Common variants in left/right asymmetry genes and pathways are associated with relative hand skillWilliam M Brandler, Andrew P Morris, David M Evans, et al.American Journal of Human Genetics|October 30, 2004
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United StatesClyde Francks, Silvia Paracchini, Shelley D Smith, et al.Pageof 59