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Deepak Narayan

Showing results (121-130 of 125) with videos related to

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The Journal of Clinical Investigation|September 13, 2016
ABC transporters and NR4A1 identify a quiescent subset of tissue-resident memory T cellsChandra Sekhar Boddupalli, Shiny Nair, Simon M Gray, et al.
Hepatology (Baltimore, Md.)|August 31, 2010
A common variant in the patatin-like phospholipase 3 gene (PNPLA3) is associated with fatty liver disease in obese children and adolescentsNicola Santoro, Romy Kursawe, Ebe D'Adamo, et al.
The Journal of Investigative Dermatology|October 26, 2012
Whole-exome sequencing reveals somatic mutations in HRAS and KRAS, which cause nevus sebaceusJonathan L Levinsohn, Li C Tian, Lynn M Boyden, et al.
Nature Genetics|July 28, 2015
Exome sequencing identifies recurrent mutations in NF1 and RASopathy genes in sun-exposed melanomasMichael Krauthammer, Yong Kong, Antonella Bacchiocchi, et al.
Nature Genetics|July 31, 2012
Exome sequencing identifies recurrent somatic RAC1 mutations in melanomaMichael Krauthammer, Yong Kong, Byung Hak Ha, et al.
Pageof 13

Showing results (121-130 of 125) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 125 results.
The Journal of Clinical Investigation|September 13, 2016
ABC transporters and NR4A1 identify a quiescent subset of tissue-resident memory T cellsChandra Sekhar Boddupalli, Shiny Nair, Simon M Gray, et al.
Hepatology (Baltimore, Md.)|August 31, 2010
A common variant in the patatin-like phospholipase 3 gene (PNPLA3) is associated with fatty liver disease in obese children and adolescentsNicola Santoro, Romy Kursawe, Ebe D'Adamo, et al.
The Journal of Investigative Dermatology|October 26, 2012
Whole-exome sequencing reveals somatic mutations in HRAS and KRAS, which cause nevus sebaceusJonathan L Levinsohn, Li C Tian, Lynn M Boyden, et al.
Nature Genetics|July 28, 2015
Exome sequencing identifies recurrent mutations in NF1 and RASopathy genes in sun-exposed melanomasMichael Krauthammer, Yong Kong, Antonella Bacchiocchi, et al.
Nature Genetics|July 31, 2012
Exome sequencing identifies recurrent somatic RAC1 mutations in melanomaMichael Krauthammer, Yong Kong, Byung Hak Ha, et al.
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