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Christopher J Cardinale

Showing results (11-20 of 18) with videos related to

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Journal of Crohn'S & Colitis|April 10, 2020
Regulation of Janus Kinase 2 by an Inflammatory Bowel Disease Causal Non-coding Single Nucleotide PolymorphismChristopher J Cardinale, Michael E March, Xiang Lin, et al.
Scientific Reports|August 22, 2015
CNV Analysis Associates AKNAD1 with Type-2 Diabetes in Jordan SubpopulationsRana Dajani, Jin Li, Zhi Wei, et al.
Sleep|August 2, 2014
A novel BHLHE41 variant is associated with short sleep and resistance to sleep deprivation in humansRenata Pellegrino, Ibrahim Halil Kavakli, Namni Goel, et al.
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.
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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 24, 2024
Novel insights into the phenotypic spectrum and pathogenesis of Hardikar syndromeAlanna Strong, Michael E March, Christopher J Cardinale, et al.
Nature Communications|October 10, 2015
Genetic sharing and heritability of paediatric age of onset autoimmune diseasesYun R Li, Sihai D Zhao, Jin Li, et al.
Nature Medicine|August 25, 2015
Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseasesYun R Li, Jin Li, Sihai D Zhao, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Journal of Crohn'S & Colitis|April 10, 2020
Regulation of Janus Kinase 2 by an Inflammatory Bowel Disease Causal Non-coding Single Nucleotide PolymorphismChristopher J Cardinale, Michael E March, Xiang Lin, et al.
Scientific Reports|August 22, 2015
CNV Analysis Associates AKNAD1 with Type-2 Diabetes in Jordan SubpopulationsRana Dajani, Jin Li, Zhi Wei, et al.
Sleep|August 2, 2014
A novel BHLHE41 variant is associated with short sleep and resistance to sleep deprivation in humansRenata Pellegrino, Ibrahim Halil Kavakli, Namni Goel, et al.
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.
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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 24, 2024
Novel insights into the phenotypic spectrum and pathogenesis of Hardikar syndromeAlanna Strong, Michael E March, Christopher J Cardinale, et al.
Nature Communications|October 10, 2015
Genetic sharing and heritability of paediatric age of onset autoimmune diseasesYun R Li, Sihai D Zhao, Jin Li, et al.
Nature Medicine|August 25, 2015
Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseasesYun R Li, Jin Li, Sihai D Zhao, et al.
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