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Afzal Sheikh

Showing results (51-60 of 58) with videos related to

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Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|August 8, 2012
Pheochromocytoma: a rare cause of childhood hypertensive encephalopathySommayya Aftab, Tayyba Yasmeen, M Haroon Hamid, et al.
Journal of Pediatric Surgery|June 23, 2016
Persistent mullerian duct syndrome: A 24-year experienceMuhammad Saleem, Uzma Ather, Bilal Mirza, et al.
Asian Pacific Journal of Tropical Biomedicine|September 4, 2014
Protective effects of Moringa oleifera Lam. leaves against arsenic-induced toxicity in miceAfzal Sheikh, Fouzia Yeasmin, Smita Agarwal, et al.
Arthritis and Rheumatism|September 29, 2011
Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneityYin Liu, Yuval Ramot, Antonio Torrelo, et al.
Toxicology and Applied Pharmacology|January 17, 2012
Elevated levels of plasma Big endothelin-1 and its relation to hypertension and skin lesions in individuals exposed to arsenicEkhtear Hossain, Khairul Islam, Fouzia Yeasmin, et al.
American Journal of Human Genetics|September 25, 2012
A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiencyQing Zhou, Geun-Shik Lee, Jillian Brady, et al.
The Journal of Clinical Investigation|February 2, 2016
Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN productionAnja Brehm, Yin Liu, Afzal Sheikh, et al.
The Journal of Clinical Investigation|November 3, 2015
Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN productionAnja Brehm, Yin Liu, Afzal Sheikh, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|August 8, 2012
Pheochromocytoma: a rare cause of childhood hypertensive encephalopathySommayya Aftab, Tayyba Yasmeen, M Haroon Hamid, et al.
Journal of Pediatric Surgery|June 23, 2016
Persistent mullerian duct syndrome: A 24-year experienceMuhammad Saleem, Uzma Ather, Bilal Mirza, et al.
Asian Pacific Journal of Tropical Biomedicine|September 4, 2014
Protective effects of Moringa oleifera Lam. leaves against arsenic-induced toxicity in miceAfzal Sheikh, Fouzia Yeasmin, Smita Agarwal, et al.
Arthritis and Rheumatism|September 29, 2011
Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneityYin Liu, Yuval Ramot, Antonio Torrelo, et al.
Toxicology and Applied Pharmacology|January 17, 2012
Elevated levels of plasma Big endothelin-1 and its relation to hypertension and skin lesions in individuals exposed to arsenicEkhtear Hossain, Khairul Islam, Fouzia Yeasmin, et al.
American Journal of Human Genetics|September 25, 2012
A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiencyQing Zhou, Geun-Shik Lee, Jillian Brady, et al.
The Journal of Clinical Investigation|February 2, 2016
Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN productionAnja Brehm, Yin Liu, Afzal Sheikh, et al.
The Journal of Clinical Investigation|November 3, 2015
Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN productionAnja Brehm, Yin Liu, Afzal Sheikh, et al.
Pageof 6