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E Brunkow

Showing results (11-20 of 29) with videos related to

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Nature Genetics|January 4, 2001
Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouseM E Brunkow, E W Jeffery, K A Hjerrild, et al.
Nature Genetics|January 4, 2001
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3C L Bennett, J Christie, F Ramsdell, et al.
Immunity|May 22, 2012
Disruption of Fnip1 reveals a metabolic checkpoint controlling B lymphocyte developmentHeon Park, Karen Staehling, Mark Tsang, et al.
American Journal of Medical Genetics|July 13, 2002
A 52-kb deletion in the SOST-MEOX1 intergenic region on 17q12-q21 is associated with van Buchem disease in the Dutch populationKaren Staehling-Hampton, Sean Proll, Bryan W Paeper, et al.
The Journal of Experimental Medicine|November 19, 2008
A point mutation in the murine Hem1 gene reveals an essential role for Hematopoietic protein 1 in lymphopoiesis and innate immunityHeon Park, Karen Staehling-Hampton, Mark W Appleby, et al.
The EMBO Journal|November 25, 2003
Osteocyte control of bone formation via sclerostin, a novel BMP antagonistDavid G Winkler, May Kung Sutherland, James C Geoghegan, et al.
Nature Genetics|January 4, 2001
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfyR S Wildin, F Ramsdell, J Peake, et al.
Frontiers in Genetics|March 6, 2015
Identification of copy number variants in whole-genome data using Reference Coverage ProfilesGustavo Glusman, Alissa Severson, Varsha Dhankani, et al.
Journal of the Neurological Sciences|November 19, 2024
Multi-Omic characterization of the effects of Ocrelizumab in patients with relapsing-remitting multiple sclerosisSergey A Kornilov, Nathan D Price, Richard Gelinas, et al.
American Journal of Human Genetics|October 30, 2004
Polymorphisms in the sclerosteosis/van Buchem disease gene (SOST) region are associated with bone-mineral density in elderly whitesAndre G Uitterlinden, Pascal P Arp, Bryan W Paeper, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Nature Genetics|January 4, 2001
Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouseM E Brunkow, E W Jeffery, K A Hjerrild, et al.
Nature Genetics|January 4, 2001
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3C L Bennett, J Christie, F Ramsdell, et al.
Immunity|May 22, 2012
Disruption of Fnip1 reveals a metabolic checkpoint controlling B lymphocyte developmentHeon Park, Karen Staehling, Mark Tsang, et al.
American Journal of Medical Genetics|July 13, 2002
A 52-kb deletion in the SOST-MEOX1 intergenic region on 17q12-q21 is associated with van Buchem disease in the Dutch populationKaren Staehling-Hampton, Sean Proll, Bryan W Paeper, et al.
The Journal of Experimental Medicine|November 19, 2008
A point mutation in the murine Hem1 gene reveals an essential role for Hematopoietic protein 1 in lymphopoiesis and innate immunityHeon Park, Karen Staehling-Hampton, Mark W Appleby, et al.
The EMBO Journal|November 25, 2003
Osteocyte control of bone formation via sclerostin, a novel BMP antagonistDavid G Winkler, May Kung Sutherland, James C Geoghegan, et al.
Nature Genetics|January 4, 2001
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfyR S Wildin, F Ramsdell, J Peake, et al.
Frontiers in Genetics|March 6, 2015
Identification of copy number variants in whole-genome data using Reference Coverage ProfilesGustavo Glusman, Alissa Severson, Varsha Dhankani, et al.
Journal of the Neurological Sciences|November 19, 2024
Multi-Omic characterization of the effects of Ocrelizumab in patients with relapsing-remitting multiple sclerosisSergey A Kornilov, Nathan D Price, Richard Gelinas, et al.
American Journal of Human Genetics|October 30, 2004
Polymorphisms in the sclerosteosis/van Buchem disease gene (SOST) region are associated with bone-mineral density in elderly whitesAndre G Uitterlinden, Pascal P Arp, Bryan W Paeper, et al.
Pageof 3