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Marcella Devoto

Showing results (61-70 of 122) with videos related to

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Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|August 21, 2004
A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutationsMarkus Pfister, Holger Thiele, Guy Van Camp, et al.
Carcinogenesis|December 11, 2012
Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibilityMario Capasso, Sharon J Diskin, Francesca Totaro, et al.
The American Journal of Gastroenterology|February 4, 2006
Contribution of IBD5 locus to clinical features of IBD patientsAnna Latiano, O Palmieri, Rossella M Valvano, et al.
BMC Gastroenterology|November 20, 2015
A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case reportJudith R Kelsen, Noor Dawany, Alejandro Martinez, et al.
Human Reproduction (Oxford, England)|April 5, 2018
Subphenotype meta-analysis of testicular cancer genome-wide association study data suggests a role for RBFOX family genes in cryptorchidism susceptibilityYanping Wang, Dione R Gray, Alan K Robbins, et al.
International Journal of Cancer|August 23, 2018
Fine mapping of 2q35 high-risk neuroblastoma locus reveals independent functional risk variants and suggests full-length BARD1 as tumor-suppressorFlora Cimmino, Marianna Avitabile, Sharon J Diskin, et al.
Gastroenterology|June 8, 2020
Impaired Redox and Protein Homeostasis as Risk Factors and Therapeutic Targets in Toxin-Induced Biliary AtresiaXiao Zhao, Kristin Lorent, Diana Escobar-Zarate, et al.
European Journal of Human Genetics : EJHG|May 10, 2007
A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23-q24Alessia Deglincerti, Roberto De Giorgio, Kivanc Cefle, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 16, 2011
Computerized neurocognitive profile in young people with 22q11.2 deletion syndrome compared to youths with schizophrenia and at-risk for psychosisPaula C Goldenberg, Monica E Calkins, Jan Richard, et al.
Genes|September 5, 2019
Exploring Shared Susceptibility between Two Neural Crest Cells Originating Conditions: Neuroblastoma and Congenital Heart DiseaseAlessandro Testori, Vito A Lasorsa, Flora Cimmino, et al.
Pageof 13

Showing results (61-70 of 122) with videos related to

Sort By:
Pageof 13
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|August 21, 2004
A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutationsMarkus Pfister, Holger Thiele, Guy Van Camp, et al.
Carcinogenesis|December 11, 2012
Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibilityMario Capasso, Sharon J Diskin, Francesca Totaro, et al.
The American Journal of Gastroenterology|February 4, 2006
Contribution of IBD5 locus to clinical features of IBD patientsAnna Latiano, O Palmieri, Rossella M Valvano, et al.
BMC Gastroenterology|November 20, 2015
A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case reportJudith R Kelsen, Noor Dawany, Alejandro Martinez, et al.
Human Reproduction (Oxford, England)|April 5, 2018
Subphenotype meta-analysis of testicular cancer genome-wide association study data suggests a role for RBFOX family genes in cryptorchidism susceptibilityYanping Wang, Dione R Gray, Alan K Robbins, et al.
International Journal of Cancer|August 23, 2018
Fine mapping of 2q35 high-risk neuroblastoma locus reveals independent functional risk variants and suggests full-length BARD1 as tumor-suppressorFlora Cimmino, Marianna Avitabile, Sharon J Diskin, et al.
Gastroenterology|June 8, 2020
Impaired Redox and Protein Homeostasis as Risk Factors and Therapeutic Targets in Toxin-Induced Biliary AtresiaXiao Zhao, Kristin Lorent, Diana Escobar-Zarate, et al.
European Journal of Human Genetics : EJHG|May 10, 2007
A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23-q24Alessia Deglincerti, Roberto De Giorgio, Kivanc Cefle, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 16, 2011
Computerized neurocognitive profile in young people with 22q11.2 deletion syndrome compared to youths with schizophrenia and at-risk for psychosisPaula C Goldenberg, Monica E Calkins, Jan Richard, et al.
Genes|September 5, 2019
Exploring Shared Susceptibility between Two Neural Crest Cells Originating Conditions: Neuroblastoma and Congenital Heart DiseaseAlessandro Testori, Vito A Lasorsa, Flora Cimmino, et al.
Pageof 13