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Raman Sood

Showing results (71-80 of 79) with videos related to

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The Journal of Clinical Investigation|March 27, 2012
Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesisRivka A Rachel, Helen L May-Simera, Shobi Veleri, et al.
American Journal of Human Genetics|July 5, 2003
Localization of a novel melanoma susceptibility locus to 1p22Elizabeth Gillanders, Suh-Hang Hank Juo, Elizabeth A Holland, et al.
Journal of Neurogenetics|May 10, 2021
Compound heterozygous <i>KCTD7</i> variants in progressive myoclonus epilepsyElizabeth A Burke, Morgan Sturgeon, Diane B Zastrow, et al.
The New England Journal of Medicine|June 7, 2013
A congenital neutrophil defect syndrome associated with mutations in VPS45Thierry Vilboux, Atar Lev, May Christine V Malicdan, et al.
Nature Genetics|April 22, 2003
Melanoma mouse model implicates metabotropic glutamate signaling in melanocytic neoplasiaPamela M Pollock, Karine Cohen-Solal, Raman Sood, et al.
Genomics|February 6, 2002
Physical and transcript map of the hereditary prostate cancer region at xq27Dietrich A Stephan, Gareth R Howell, Tanya M Teslovich, et al.
Annals of the Rheumatic Diseases|January 24, 2018
Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitorsAngeliki Giannelou, Hongying Wang, Qing Zhou, et al.
Blood Advances|July 5, 2023
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41Claire C Homan, Michael W Drazer, Kai Yu, et al.
The New England Journal of Medicine|February 21, 2014
Early-onset stroke and vasculopathy associated with mutations in ADA2Qing Zhou, Dan Yang, Amanda K Ombrello, et al.
Pageof 8

Showing results (71-80 of 79) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 79 results.
The Journal of Clinical Investigation|March 27, 2012
Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesisRivka A Rachel, Helen L May-Simera, Shobi Veleri, et al.
American Journal of Human Genetics|July 5, 2003
Localization of a novel melanoma susceptibility locus to 1p22Elizabeth Gillanders, Suh-Hang Hank Juo, Elizabeth A Holland, et al.
Journal of Neurogenetics|May 10, 2021
Compound heterozygous <i>KCTD7</i> variants in progressive myoclonus epilepsyElizabeth A Burke, Morgan Sturgeon, Diane B Zastrow, et al.
The New England Journal of Medicine|June 7, 2013
A congenital neutrophil defect syndrome associated with mutations in VPS45Thierry Vilboux, Atar Lev, May Christine V Malicdan, et al.
Nature Genetics|April 22, 2003
Melanoma mouse model implicates metabotropic glutamate signaling in melanocytic neoplasiaPamela M Pollock, Karine Cohen-Solal, Raman Sood, et al.
Genomics|February 6, 2002
Physical and transcript map of the hereditary prostate cancer region at xq27Dietrich A Stephan, Gareth R Howell, Tanya M Teslovich, et al.
Annals of the Rheumatic Diseases|January 24, 2018
Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitorsAngeliki Giannelou, Hongying Wang, Qing Zhou, et al.
Blood Advances|July 5, 2023
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41Claire C Homan, Michael W Drazer, Kai Yu, et al.
The New England Journal of Medicine|February 21, 2014
Early-onset stroke and vasculopathy associated with mutations in ADA2Qing Zhou, Dan Yang, Amanda K Ombrello, et al.
Pageof 8