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H Shaikh

Showing results (211-220 of 236) with videos related to

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Human Molecular Genetics|April 28, 2017
Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalitiesAnita M Quintana, Hung-Chun Yu, Alison Brebner, et al.
Molecular Psychiatry|March 2, 2011
Rare structural variation of synapse and neurotransmission genes in autismX Gai, H M Xie, J C Perin, et al.
Oral Oncology|October 2, 2024
Loss of MACROD2 drives radioresistance but not cisplatin resistance in HPV-positive head and neck cancerAlice Dawson, Amir Hossein Karimi, Mushfiq H Shaikh, et al.
Pediatric Neurology|April 2, 2017
X-Linked Cobalamin Disorder (HCFC1) Mimicking Nonketotic Hyperglycinemia With Increased Both Cerebrospinal Fluid Glycine and Methylmalonic AcidEmmanuel Scalais, Elise Osterheld, Christiane Weitzel, et al.
Human Mutation|December 6, 2008
SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variationBinita M Kamath, Brian D Thiel, Xiaowu Gai, et al.
Oral Oncology|December 9, 2025
NOTCH1 loss promotes chemo and radio-resistance in head and neck cancerMushfiq H Shaikh, Walid Gazala, Cindy Zheng, et al.
Journal of Medical Genetics|March 20, 2015
Mutations in the mitochondrial cysteinyl-tRNA synthase gene, CARS2, lead to a severe epileptic encephalopathy and complex movement disorderCurtis R Coughlin, Gunter H Scharer, Marisa W Friederich, et al.
Genome Research|September 5, 2019
The 22q11 low copy repeats are characterized by unprecedented size and structural variabilityWolfram Demaerel, Yulia Mostovoy, Feyza Yilmaz, et al.
American Journal of Human Genetics|August 3, 2010
A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21)Molly B Sheridan, Takema Kato, Chad Haldeman-Englert, et al.
Head & Neck|February 21, 2022
Tumor molecular differences associated with outcome disparities of Black patients with head and neck cancerHugh A J Kim, Peter Y F Zeng, Alana Sorgini, et al.
Pageof 24

Showing results (211-220 of 236) with videos related to

Sort By:
Pageof 24
Human Molecular Genetics|April 28, 2017
Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalitiesAnita M Quintana, Hung-Chun Yu, Alison Brebner, et al.
Molecular Psychiatry|March 2, 2011
Rare structural variation of synapse and neurotransmission genes in autismX Gai, H M Xie, J C Perin, et al.
Oral Oncology|October 2, 2024
Loss of MACROD2 drives radioresistance but not cisplatin resistance in HPV-positive head and neck cancerAlice Dawson, Amir Hossein Karimi, Mushfiq H Shaikh, et al.
Pediatric Neurology|April 2, 2017
X-Linked Cobalamin Disorder (HCFC1) Mimicking Nonketotic Hyperglycinemia With Increased Both Cerebrospinal Fluid Glycine and Methylmalonic AcidEmmanuel Scalais, Elise Osterheld, Christiane Weitzel, et al.
Human Mutation|December 6, 2008
SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variationBinita M Kamath, Brian D Thiel, Xiaowu Gai, et al.
Oral Oncology|December 9, 2025
NOTCH1 loss promotes chemo and radio-resistance in head and neck cancerMushfiq H Shaikh, Walid Gazala, Cindy Zheng, et al.
Journal of Medical Genetics|March 20, 2015
Mutations in the mitochondrial cysteinyl-tRNA synthase gene, CARS2, lead to a severe epileptic encephalopathy and complex movement disorderCurtis R Coughlin, Gunter H Scharer, Marisa W Friederich, et al.
Genome Research|September 5, 2019
The 22q11 low copy repeats are characterized by unprecedented size and structural variabilityWolfram Demaerel, Yulia Mostovoy, Feyza Yilmaz, et al.
American Journal of Human Genetics|August 3, 2010
A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21)Molly B Sheridan, Takema Kato, Chad Haldeman-Englert, et al.
Head & Neck|February 21, 2022
Tumor molecular differences associated with outcome disparities of Black patients with head and neck cancerHugh A J Kim, Peter Y F Zeng, Alana Sorgini, et al.
Pageof 24