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Marcella Devoto

Showing results (81-90 of 122) with videos related to

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Biorxiv : the Preprint Server for Biology|October 10, 2024
TNFSF13 insufficiency disrupts human colonic epithelial cell-mediated B cell differentiationXianghui Ma, Noor Dawany, Ayano Kondo, et al.
Human Reproduction (Oxford, England)|July 26, 2015
Pathway analysis supports association of nonsyndromic cryptorchidism with genetic loci linked to cytoskeleton-dependent functionsJulia Spencer Barthold, Yanping Wang, Thomas F Kolon, et al.
NPJ Parkinson'S Disease|February 10, 2026
Genetic co-regulation of neopterin and Parkinson's diseaseValeria Orrù, Michele Marongiu, Maristella Steri, et al.
BMC Urology|October 23, 2016
Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidismYanping Wang, Jin Li, Thomas F Kolon, et al.
Gastroenterology|July 21, 2015
Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel diseaseJudith R Kelsen, Noor Dawany, Christopher J Moran, et al.
Nature Genetics|May 18, 2004
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-BIan D Krantz, Jennifer McCallum, Cheryl DeScipio, et al.
Nature|August 30, 2008
Identification of ALK as a major familial neuroblastoma predisposition geneYaël P Mossé, Marci Laudenslager, Luca Longo, et al.
JAMA Neurology|May 5, 2015
Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended FamilyKristen Zukosky, Katherine Meilleur, Bryan J Traynor, et al.
European Journal of Neurology|October 19, 2022
Mutations in MYO9B are associated with Charcot-Marie-Tooth disease type 2 neuropathies and isolated optic atrophySilvia Cipriani, Marta Guerrero-Valero, Stefano Tozza, et al.
The Journal of Allergy and Clinical Immunology. in Practice|April 24, 2021
Immune Dysregulation in Human ITCH Deficiency Successfully Treated with Hematopoietic Cell TransplantationTrusha Patel, Sarah E Henrickson, Emily K Moser, et al.
Pageof 13

Showing results (81-90 of 122) with videos related to

Sort By:
Pageof 13
Biorxiv : the Preprint Server for Biology|October 10, 2024
TNFSF13 insufficiency disrupts human colonic epithelial cell-mediated B cell differentiationXianghui Ma, Noor Dawany, Ayano Kondo, et al.
Human Reproduction (Oxford, England)|July 26, 2015
Pathway analysis supports association of nonsyndromic cryptorchidism with genetic loci linked to cytoskeleton-dependent functionsJulia Spencer Barthold, Yanping Wang, Thomas F Kolon, et al.
NPJ Parkinson'S Disease|February 10, 2026
Genetic co-regulation of neopterin and Parkinson's diseaseValeria Orrù, Michele Marongiu, Maristella Steri, et al.
BMC Urology|October 23, 2016
Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidismYanping Wang, Jin Li, Thomas F Kolon, et al.
Gastroenterology|July 21, 2015
Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel diseaseJudith R Kelsen, Noor Dawany, Christopher J Moran, et al.
Nature Genetics|May 18, 2004
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-BIan D Krantz, Jennifer McCallum, Cheryl DeScipio, et al.
Nature|August 30, 2008
Identification of ALK as a major familial neuroblastoma predisposition geneYaël P Mossé, Marci Laudenslager, Luca Longo, et al.
JAMA Neurology|May 5, 2015
Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended FamilyKristen Zukosky, Katherine Meilleur, Bryan J Traynor, et al.
European Journal of Neurology|October 19, 2022
Mutations in MYO9B are associated with Charcot-Marie-Tooth disease type 2 neuropathies and isolated optic atrophySilvia Cipriani, Marta Guerrero-Valero, Stefano Tozza, et al.
The Journal of Allergy and Clinical Immunology. in Practice|April 24, 2021
Immune Dysregulation in Human ITCH Deficiency Successfully Treated with Hematopoietic Cell TransplantationTrusha Patel, Sarah E Henrickson, Emily K Moser, et al.
Pageof 13