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Showing results (31-40 of 78) with videos related to

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BMC Musculoskeletal Disorders|November 11, 2016
Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing studyChristopher J Cardinale, Dong Li, Lifeng Tian, et al.
Plos Genetics|May 26, 2017
Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastomaLee D McDaniel, Karina L Conkrite, Xiao Chang, et al.
Plos Genetics|October 10, 2009
From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetesZhi Wei, Kai Wang, Hui-Qi Qu, et al.
American Journal of Medical Genetics. Part A|May 7, 2021
A new syndrome of moyamoya disease, kidney dysplasia, aminotransferase elevation, and skin disease associated with de novo variants in RNF213Alanna Strong, Gina O'Grady, Evelyn Shih, et al.
American Journal of Medical Genetics. Part A|October 16, 2021
A novel MBTPS2 variant associated with BRESHECK syndrome impairs sterol-regulated transcription and the endoplasmic reticulum stress responseAlanna Strong, Michael E March, Christopher J Cardinale, et al.
Nature Genetics|September 4, 2012
Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastomaSharon J Diskin, Mario Capasso, Robert W Schnepp, et al.
The Journal of Allergy and Clinical Immunology|March 28, 2016
Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorderMichael D Keller, Rahul Pandey, Dong Li, et al.
The Journal of Allergy and Clinical Immunology|April 19, 2011
Genome-wide association identifies diverse causes of common variable immunodeficiencyJordan S Orange, Joseph T Glessner, Elena Resnick, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 19, 2015
Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food AllergyJin Li, Irene Fung, Joseph T Glessner, et al.
Obesity (Silver Spring, Md.)|March 19, 2013
The missense variation landscape of FTO, MC4R, and TMEM18 in obese children of African AncestrySandra Deliard, Saarene Panossian, Frank D Mentch, et al.
Pageof 8

Showing results (31-40 of 78) with videos related to

Sort By:
Pageof 8
BMC Musculoskeletal Disorders|November 11, 2016
Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing studyChristopher J Cardinale, Dong Li, Lifeng Tian, et al.
Plos Genetics|May 26, 2017
Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastomaLee D McDaniel, Karina L Conkrite, Xiao Chang, et al.
Plos Genetics|October 10, 2009
From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetesZhi Wei, Kai Wang, Hui-Qi Qu, et al.
American Journal of Medical Genetics. Part A|May 7, 2021
A new syndrome of moyamoya disease, kidney dysplasia, aminotransferase elevation, and skin disease associated with de novo variants in RNF213Alanna Strong, Gina O'Grady, Evelyn Shih, et al.
American Journal of Medical Genetics. Part A|October 16, 2021
A novel MBTPS2 variant associated with BRESHECK syndrome impairs sterol-regulated transcription and the endoplasmic reticulum stress responseAlanna Strong, Michael E March, Christopher J Cardinale, et al.
Nature Genetics|September 4, 2012
Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastomaSharon J Diskin, Mario Capasso, Robert W Schnepp, et al.
The Journal of Allergy and Clinical Immunology|March 28, 2016
Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorderMichael D Keller, Rahul Pandey, Dong Li, et al.
The Journal of Allergy and Clinical Immunology|April 19, 2011
Genome-wide association identifies diverse causes of common variable immunodeficiencyJordan S Orange, Joseph T Glessner, Elena Resnick, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 19, 2015
Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food AllergyJin Li, Irene Fung, Joseph T Glessner, et al.
Obesity (Silver Spring, Md.)|March 19, 2013
The missense variation landscape of FTO, MC4R, and TMEM18 in obese children of African AncestrySandra Deliard, Saarene Panossian, Frank D Mentch, et al.
Pageof 8