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B Agrawal

Showing results (251-260 of 360) with videos related to

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Newborn (Clarksville, Md.)|June 24, 2022
Current Understanding of Transfusion-associated Necrotizing Enterocolitis: Review of Clinical and Experimental Studies and a Call for More Definitive EvidenceMinesh Khashu, Christof Dame, Pascal M Lavoie, et al.
American Journal of Human Genetics|July 24, 2012
Dominant mutation of CCDC78 in a unique congenital myopathy with prominent internal nuclei and atypical coresKaren Majczenko, Ann E Davidson, Sandra Camelo-Piragua, et al.
Basic Research in Cardiology|December 25, 2023
Striated preferentially expressed gene deficiency leads to mitochondrial dysfunction in developing cardiomyocytesGu Li, He Huang, Yanshuang Wu, et al.
American Journal of Medical Genetics. Part A|February 6, 2020
A phenotypically severe, biochemically "silent" case of HIBCH deficiency in a newborn diagnosed by rapid whole exome sequencing and enzymatic testingAlissa M D'Gama, William J Brucker, Tian Zhang, et al.
European Journal of Human Genetics : EJHG|January 23, 2023
Reanalysis of clinical exome identifies the second variant in two individuals with recessive disordersQifei Li, Rohan Agrawal, Klaus Schmitz-Abe, et al.
Advanced Genetics (Hoboken, N.J.)|March 13, 2023
Mendelian Disorders in an Interstitial Cystitis/Bladder Pain Syndrome CohortElicia Estrella, Shira Rockowitz, Marielle Thorne, et al.
Scientific Reports|July 26, 2019
Etiology and Outcome of non-immune Hydrops Fetalis in Southern China: report of 1004 casesDahua Meng, Qifei Li, Xuehua Hu, et al.
Neuromuscular Disorders : NMD|May 8, 2012
Congenital myopathy caused by a novel missense mutation in the CFL2 geneC W Ockeloen, H J Gilhuis, R Pfundt, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 6, 2006
A study to determine the effects of food and multiple dosing on the pharmacokinetics of vorinostat given orally to patients with advanced cancerEric H Rubin, Nancy G B Agrawal, Evan J Friedman, et al.
Annals of Neurology|July 6, 2004
Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutationsPankaj B Agrawal, Corinne D Strickland, Charles Midgett, et al.
Pageof 36

Showing results (251-260 of 360) with videos related to

Sort By:
Pageof 36
Newborn (Clarksville, Md.)|June 24, 2022
Current Understanding of Transfusion-associated Necrotizing Enterocolitis: Review of Clinical and Experimental Studies and a Call for More Definitive EvidenceMinesh Khashu, Christof Dame, Pascal M Lavoie, et al.
American Journal of Human Genetics|July 24, 2012
Dominant mutation of CCDC78 in a unique congenital myopathy with prominent internal nuclei and atypical coresKaren Majczenko, Ann E Davidson, Sandra Camelo-Piragua, et al.
Basic Research in Cardiology|December 25, 2023
Striated preferentially expressed gene deficiency leads to mitochondrial dysfunction in developing cardiomyocytesGu Li, He Huang, Yanshuang Wu, et al.
American Journal of Medical Genetics. Part A|February 6, 2020
A phenotypically severe, biochemically "silent" case of HIBCH deficiency in a newborn diagnosed by rapid whole exome sequencing and enzymatic testingAlissa M D'Gama, William J Brucker, Tian Zhang, et al.
European Journal of Human Genetics : EJHG|January 23, 2023
Reanalysis of clinical exome identifies the second variant in two individuals with recessive disordersQifei Li, Rohan Agrawal, Klaus Schmitz-Abe, et al.
Advanced Genetics (Hoboken, N.J.)|March 13, 2023
Mendelian Disorders in an Interstitial Cystitis/Bladder Pain Syndrome CohortElicia Estrella, Shira Rockowitz, Marielle Thorne, et al.
Scientific Reports|July 26, 2019
Etiology and Outcome of non-immune Hydrops Fetalis in Southern China: report of 1004 casesDahua Meng, Qifei Li, Xuehua Hu, et al.
Neuromuscular Disorders : NMD|May 8, 2012
Congenital myopathy caused by a novel missense mutation in the CFL2 geneC W Ockeloen, H J Gilhuis, R Pfundt, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 6, 2006
A study to determine the effects of food and multiple dosing on the pharmacokinetics of vorinostat given orally to patients with advanced cancerEric H Rubin, Nancy G B Agrawal, Evan J Friedman, et al.
Annals of Neurology|July 6, 2004
Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutationsPankaj B Agrawal, Corinne D Strickland, Charles Midgett, et al.
Pageof 36