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Marcella Devoto

Showing results (71-80 of 122) with videos related to

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International Journal of Pediatric Otorhinolaryngology|November 6, 2012
A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patientsJosine C C Widdershoven, Mark Bowser, Molly B Sheridan, 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.
Molecular Human Reproduction|October 28, 2015
Polygenic inheritance of cryptorchidism susceptibility in the LE/orl ratJulia Spencer Barthold, Joan Pugarelli, Madolyn L MacDonald, et al.
Plos Genetics|August 14, 2018
A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1Ying Chen, Melissa A Gilbert, Christopher M Grochowski, et al.
Frontiers in Immunology|February 9, 2026
<i>CMTM8</i> variants influence BNT162b2 COVID-19 vaccination response by regulating granulocytic/polymorphonuclear myeloid-derived suppressor cell activityAlessandro Testori, Antonella Mulas, Mara Marongiu, et al.
Plos Genetics|March 26, 2011
Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility LociLe B Nguyen, Sharon J Diskin, Mario Capasso, 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.
Cellular and Molecular Gastroenterology and Hepatology|January 17, 2017
<i>THBS2</i> Is a Candidate Modifier of Liver Disease Severity in Alagille SyndromeEllen A Tsai, Melissa A Gilbert, Christopher M Grochowski, et al.
European Journal of Human Genetics : EJHG|January 28, 2016
Variants of the ACTG2 gene correlate with degree of severity and presence of megacystis in chronic intestinal pseudo-obstructionIvana Matera, Marta Rusmini, Yiran Guo, et al.
Human Molecular Genetics|December 17, 2013
Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and miceYaqun Zou, Daniela Zwolanek, Yayoi Izu, et al.
Pageof 13

Showing results (71-80 of 122) with videos related to

Sort By:
Pageof 13
International Journal of Pediatric Otorhinolaryngology|November 6, 2012
A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patientsJosine C C Widdershoven, Mark Bowser, Molly B Sheridan, 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.
Molecular Human Reproduction|October 28, 2015
Polygenic inheritance of cryptorchidism susceptibility in the LE/orl ratJulia Spencer Barthold, Joan Pugarelli, Madolyn L MacDonald, et al.
Plos Genetics|August 14, 2018
A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1Ying Chen, Melissa A Gilbert, Christopher M Grochowski, et al.
Frontiers in Immunology|February 9, 2026
<i>CMTM8</i> variants influence BNT162b2 COVID-19 vaccination response by regulating granulocytic/polymorphonuclear myeloid-derived suppressor cell activityAlessandro Testori, Antonella Mulas, Mara Marongiu, et al.
Plos Genetics|March 26, 2011
Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility LociLe B Nguyen, Sharon J Diskin, Mario Capasso, 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.
Cellular and Molecular Gastroenterology and Hepatology|January 17, 2017
<i>THBS2</i> Is a Candidate Modifier of Liver Disease Severity in Alagille SyndromeEllen A Tsai, Melissa A Gilbert, Christopher M Grochowski, et al.
European Journal of Human Genetics : EJHG|January 28, 2016
Variants of the ACTG2 gene correlate with degree of severity and presence of megacystis in chronic intestinal pseudo-obstructionIvana Matera, Marta Rusmini, Yiran Guo, et al.
Human Molecular Genetics|December 17, 2013
Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and miceYaqun Zou, Daniela Zwolanek, Yayoi Izu, et al.
Pageof 13