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David A Buchner

Showing results (31-40 of 40) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|June 5, 2019
Germline USP8 Mutation Associated With Pediatric Cushing Disease and Other Clinical Features: A New SyndromeMichal Cohen, Rebecca Persky, Rachel Stegemann, et al.
Human Molecular Genetics|October 11, 2002
Molecular and pathological effects of a modifier gene on deficiency of the sodium channel Scn8a (Na(v)1.6)Jennifer A Kearney, David A Buchner, Georgius De Haan, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 4, 2012
The juxtaparanodal proteins CNTNAP2 and TAG1 regulate diet-induced obesityDavid A Buchner, Jon M Geisinger, Patricia A Glazebrook, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 19, 2021
eIF2A-knockout mice reveal decreased life span and metabolic syndromeRichard Anderson, Anchal Agarwal, Arnab Ghosh, et al.
Science Translational Medicine|September 13, 2021
Engineered nasal cartilage for the repair of osteoarthritic knee cartilage defectsLina Acevedo Rua, Marcus Mumme, Cristina Manferdini, et al.
Human Molecular Genetics|March 23, 2018
Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiencyAnlu Chen, Dov Tiosano, Tulay Guran, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 24, 2007
pak2a mutations cause cerebral hemorrhage in redhead zebrafishDavid A Buchner, Fengyun Su, Jennifer S Yamaoka, et al.
Elife|March 17, 2020
PACT-mediated PKR activation acts as a hyperosmotic stress intensity sensor weakening osmoadaptation and enhancing inflammationKenneth T Farabaugh, Dawid Krokowski, Bo-Jhih Guan, et al.
Plos Genetics|April 30, 2019
Mutations in PIK3C2A cause syndromic short stature, skeletal abnormalities, and cataracts associated with ciliary dysfunctionDov Tiosano, Hagit N Baris, Anlu Chen, et al.
Science (New York, N.Y.)|December 9, 2021
PI(3,4)P2-mediated cytokinetic abscission prevents early senescence and cataract formationFederico Gulluni, Lorenzo Prever, Huayi Li, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
The Journal of Clinical Endocrinology and Metabolism|June 5, 2019
Germline USP8 Mutation Associated With Pediatric Cushing Disease and Other Clinical Features: A New SyndromeMichal Cohen, Rebecca Persky, Rachel Stegemann, et al.
Human Molecular Genetics|October 11, 2002
Molecular and pathological effects of a modifier gene on deficiency of the sodium channel Scn8a (Na(v)1.6)Jennifer A Kearney, David A Buchner, Georgius De Haan, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 4, 2012
The juxtaparanodal proteins CNTNAP2 and TAG1 regulate diet-induced obesityDavid A Buchner, Jon M Geisinger, Patricia A Glazebrook, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 19, 2021
eIF2A-knockout mice reveal decreased life span and metabolic syndromeRichard Anderson, Anchal Agarwal, Arnab Ghosh, et al.
Science Translational Medicine|September 13, 2021
Engineered nasal cartilage for the repair of osteoarthritic knee cartilage defectsLina Acevedo Rua, Marcus Mumme, Cristina Manferdini, et al.
Human Molecular Genetics|March 23, 2018
Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiencyAnlu Chen, Dov Tiosano, Tulay Guran, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 24, 2007
pak2a mutations cause cerebral hemorrhage in redhead zebrafishDavid A Buchner, Fengyun Su, Jennifer S Yamaoka, et al.
Elife|March 17, 2020
PACT-mediated PKR activation acts as a hyperosmotic stress intensity sensor weakening osmoadaptation and enhancing inflammationKenneth T Farabaugh, Dawid Krokowski, Bo-Jhih Guan, et al.
Plos Genetics|April 30, 2019
Mutations in PIK3C2A cause syndromic short stature, skeletal abnormalities, and cataracts associated with ciliary dysfunctionDov Tiosano, Hagit N Baris, Anlu Chen, et al.
Science (New York, N.Y.)|December 9, 2021
PI(3,4)P2-mediated cytokinetic abscission prevents early senescence and cataract formationFederico Gulluni, Lorenzo Prever, Huayi Li, et al.
Pageof 4