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Peter L Nagy

Showing results (11-20 of 44) with videos related to

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Plos One|November 12, 2020
Blood group typing from whole-genome sequencing dataJulien Paganini, Peter L Nagy, Nicholas Rouse, et al.
Journal of Clinical Immunology|June 17, 2014
Tetratricopeptide repeat domain 7A (TTC7A) mutation in a newborn with multiple intestinal atresia and combined immunodeficiencyNiti Sardana Agarwal, Lesley Northrop, Kwame Anyane-Yeboa, et al.
BMC Veterinary Research|December 29, 2018
Inherited selective cobalamin malabsorption in Komondor dogs associated with a CUBN splice site variantJohn C Fyfe, Shelby L Hemker, Alycia Frampton, et al.
Nucleic Acids Research|September 24, 2014
Tls1 regulates splicing of shelterin components to control telomeric heterochromatin assembly and telomere lengthJiyong Wang, Xavier Tadeo, Haitong Hou, et al.
Cell|August 30, 2014
Axonally synthesized ATF4 transmits a neurodegenerative signal across brain regionsJimena Baleriola, Chandler A Walker, Ying Y Jean, et al.
Neurobiology of Aging|October 6, 2012
C9ORF72 repeat expansions not detected in a group of patients with schizophreniaEdward D Huey, Peter L Nagy, Laura Rodriguez-Murillo, et al.
Human Molecular Genetics|December 22, 2011
LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscleGeorge Dialynas, Kaitlin M Flannery, Luka N Zirbel, et al.
Neurology. Genetics|February 12, 2020
A novel noncoding <i>FKRP</i> mutation in early onset limb-girdle muscular dystrophyEzgi Saylam, Steven A Moore, Akilandeswari Aravindhan, et al.
Neurobiology of Disease|May 12, 2015
Isoform-level brain expression profiling of the spermidine/spermine N1-Acetyltransferase1 (SAT1) gene in major depression and suicideSpiro P Pantazatos, Stuart J Andrews, Jane Dunning-Broadbent, et al.
Human Molecular Genetics|September 17, 2010
Discovery of the BMPR1A promoter and germline mutations that cause juvenile polyposisDaniel Calva-Cerqueira, Fadi S Dahdaleh, George Woodfield, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
Plos One|November 12, 2020
Blood group typing from whole-genome sequencing dataJulien Paganini, Peter L Nagy, Nicholas Rouse, et al.
Journal of Clinical Immunology|June 17, 2014
Tetratricopeptide repeat domain 7A (TTC7A) mutation in a newborn with multiple intestinal atresia and combined immunodeficiencyNiti Sardana Agarwal, Lesley Northrop, Kwame Anyane-Yeboa, et al.
BMC Veterinary Research|December 29, 2018
Inherited selective cobalamin malabsorption in Komondor dogs associated with a CUBN splice site variantJohn C Fyfe, Shelby L Hemker, Alycia Frampton, et al.
Nucleic Acids Research|September 24, 2014
Tls1 regulates splicing of shelterin components to control telomeric heterochromatin assembly and telomere lengthJiyong Wang, Xavier Tadeo, Haitong Hou, et al.
Cell|August 30, 2014
Axonally synthesized ATF4 transmits a neurodegenerative signal across brain regionsJimena Baleriola, Chandler A Walker, Ying Y Jean, et al.
Neurobiology of Aging|October 6, 2012
C9ORF72 repeat expansions not detected in a group of patients with schizophreniaEdward D Huey, Peter L Nagy, Laura Rodriguez-Murillo, et al.
Human Molecular Genetics|December 22, 2011
LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscleGeorge Dialynas, Kaitlin M Flannery, Luka N Zirbel, et al.
Neurology. Genetics|February 12, 2020
A novel noncoding <i>FKRP</i> mutation in early onset limb-girdle muscular dystrophyEzgi Saylam, Steven A Moore, Akilandeswari Aravindhan, et al.
Neurobiology of Disease|May 12, 2015
Isoform-level brain expression profiling of the spermidine/spermine N1-Acetyltransferase1 (SAT1) gene in major depression and suicideSpiro P Pantazatos, Stuart J Andrews, Jane Dunning-Broadbent, et al.
Human Molecular Genetics|September 17, 2010
Discovery of the BMPR1A promoter and germline mutations that cause juvenile polyposisDaniel Calva-Cerqueira, Fadi S Dahdaleh, George Woodfield, et al.
Pageof 5