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David R Fitzpatrick

Showing results (31-40 of 153) with videos related to

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Pediatrics|April 4, 2018
NALCN Dysfunction as a Cause of Disordered Respiratory Rhythm With Central ApneaJamie Campbell, David R FitzPatrick, Tara Azam, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 12, 2004
Evolutionarily conserved sequence elements that positively regulate IFN-gamma expression in T cellsMaria Shnyreva, William M Weaver, Mathieu Blanchette, et al.
Plos One|September 3, 2010
Bilateral renal agenesis/hypoplasia/dysplasia (BRAHD): postmortem analysis of 45 cases with breakpoint mapping of two de novo translocationsLouise Harewood, Monica Liu, Jean Keeling, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 21, 2006
Rapid demethylation of the IFN-gamma gene occurs in memory but not naive CD8 T cellsEllen N Kersh, David R Fitzpatrick, Kaja Murali-Krishna, et al.
Wellcome Open Research|March 21, 2017
Returning genome sequences to research participants: Policy and practiceCaroline F Wright, Anna Middleton, Jeffrey C Barrett, et al.
Genome Research|August 21, 2021
Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genomeVera B Kaiser, Lana Talmane, Yatendra Kumar, et al.
American Journal of Medical Genetics. Part A|July 19, 2016
Status dystonicus in two patients with SOX2-anophthalmia syndrome and nonsense mutationsKathleen M Gorman, Sally A Lynch, Adele Schneider, et al.
Nature Communications|May 26, 2021
Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defectGabrielle Olley, Madapura M Pradeepa, Graeme R Grimes, et al.
Open Biology|June 12, 2015
Warburg Micro syndrome is caused by RAB18 deficiency or dysregulationMark T Handley, Sarah M Carpanini, Girish R Mali, et al.
American Journal of Medical Genetics. Part A|May 18, 2007
Cornelia de Lange syndrome: clinical review, diagnostic and scoring systems, and anticipatory guidanceAntonie D Kline, Ian D Krantz, Annemarie Sommer, et al.
Pageof 16

Showing results (31-40 of 153) with videos related to

Sort By:
Pageof 16
Pediatrics|April 4, 2018
NALCN Dysfunction as a Cause of Disordered Respiratory Rhythm With Central ApneaJamie Campbell, David R FitzPatrick, Tara Azam, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 12, 2004
Evolutionarily conserved sequence elements that positively regulate IFN-gamma expression in T cellsMaria Shnyreva, William M Weaver, Mathieu Blanchette, et al.
Plos One|September 3, 2010
Bilateral renal agenesis/hypoplasia/dysplasia (BRAHD): postmortem analysis of 45 cases with breakpoint mapping of two de novo translocationsLouise Harewood, Monica Liu, Jean Keeling, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 21, 2006
Rapid demethylation of the IFN-gamma gene occurs in memory but not naive CD8 T cellsEllen N Kersh, David R Fitzpatrick, Kaja Murali-Krishna, et al.
Wellcome Open Research|March 21, 2017
Returning genome sequences to research participants: Policy and practiceCaroline F Wright, Anna Middleton, Jeffrey C Barrett, et al.
Genome Research|August 21, 2021
Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genomeVera B Kaiser, Lana Talmane, Yatendra Kumar, et al.
American Journal of Medical Genetics. Part A|July 19, 2016
Status dystonicus in two patients with SOX2-anophthalmia syndrome and nonsense mutationsKathleen M Gorman, Sally A Lynch, Adele Schneider, et al.
Nature Communications|May 26, 2021
Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defectGabrielle Olley, Madapura M Pradeepa, Graeme R Grimes, et al.
Open Biology|June 12, 2015
Warburg Micro syndrome is caused by RAB18 deficiency or dysregulationMark T Handley, Sarah M Carpanini, Girish R Mali, et al.
American Journal of Medical Genetics. Part A|May 18, 2007
Cornelia de Lange syndrome: clinical review, diagnostic and scoring systems, and anticipatory guidanceAntonie D Kline, Ian D Krantz, Annemarie Sommer, et al.
Pageof 16