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David Valle

Showing results (61-70 of 146) with videos related to

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American Journal of Human Genetics|August 21, 2003
Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22M Daniele Fallin, Virginia K Lasseter, Paula S Wolyniec, et al.
Bioinformatics (Oxford, England)|January 31, 2012
SynaptomeDB: an ontology-based knowledgebase for synaptic genesMehdi Pirooznia, Tao Wang, Dimitrios Avramopoulos, et al.
Molecular Cell|July 8, 2019
PCIF1 Catalyzes m6Am mRNA Methylation to Regulate Gene ExpressionErdem Sendinc, David Valle-Garcia, Abhinav Dhall, et al.
Molecular and Cellular Biochemistry|July 29, 2006
Overexpression of proline oxidase induces proline-dependent and mitochondria-mediated apoptosisChien-an A Hu, Steven P Donald, Jian Yu, et al.
Ophthalmic Genetics|July 20, 2022
A possible ocular biomarker for response to hyperornithinemia in gyrate atrophy: the effect of pyridoxine, lysine, and arginine-restricted diet in a patient with advanced diseaseMariana Matioli da Palma, Cristy Ku, Austin D Igelman, et al.
Pediatrics|May 3, 2006
Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T geneStacie B Peddy, Luca A Vricella, Jane E Crosson, et al.
Pharmaceuticals (Basel, Switzerland)|August 29, 2024
Kynurenines and Inflammation: A Remarkable Axis for Multiple Sclerosis TreatmentPaul Carrillo-Mora, Carlos Landa-Solís, David Valle-Garcia, et al.
American Journal of Medical Genetics. Part A|December 12, 2023
De novo variants identified by trio whole exome sequencing of bladder exstrophy epispadias complexAngie C Jelin, Elizabeth Wohler, Renan Martin, et al.
Neurology. Genetics|February 24, 2018
Familial monophasic acute transverse myelitis due to the pathogenic variant in <i>VPS37A</i>Maureen A Mealy, Tai-Seung Nam, Santiago J Pardo, et al.
American Journal of Medical Genetics. Part A|September 24, 2015
Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblingsSalma Ben-Salem, Nara Sobreira, Nadia A Akawi, et al.
Pageof 15

Showing results (61-70 of 146) with videos related to

Sort By:
Pageof 15
American Journal of Human Genetics|August 21, 2003
Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22M Daniele Fallin, Virginia K Lasseter, Paula S Wolyniec, et al.
Bioinformatics (Oxford, England)|January 31, 2012
SynaptomeDB: an ontology-based knowledgebase for synaptic genesMehdi Pirooznia, Tao Wang, Dimitrios Avramopoulos, et al.
Molecular Cell|July 8, 2019
PCIF1 Catalyzes m6Am mRNA Methylation to Regulate Gene ExpressionErdem Sendinc, David Valle-Garcia, Abhinav Dhall, et al.
Molecular and Cellular Biochemistry|July 29, 2006
Overexpression of proline oxidase induces proline-dependent and mitochondria-mediated apoptosisChien-an A Hu, Steven P Donald, Jian Yu, et al.
Ophthalmic Genetics|July 20, 2022
A possible ocular biomarker for response to hyperornithinemia in gyrate atrophy: the effect of pyridoxine, lysine, and arginine-restricted diet in a patient with advanced diseaseMariana Matioli da Palma, Cristy Ku, Austin D Igelman, et al.
Pediatrics|May 3, 2006
Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T geneStacie B Peddy, Luca A Vricella, Jane E Crosson, et al.
Pharmaceuticals (Basel, Switzerland)|August 29, 2024
Kynurenines and Inflammation: A Remarkable Axis for Multiple Sclerosis TreatmentPaul Carrillo-Mora, Carlos Landa-Solís, David Valle-Garcia, et al.
American Journal of Medical Genetics. Part A|December 12, 2023
De novo variants identified by trio whole exome sequencing of bladder exstrophy epispadias complexAngie C Jelin, Elizabeth Wohler, Renan Martin, et al.
Neurology. Genetics|February 24, 2018
Familial monophasic acute transverse myelitis due to the pathogenic variant in <i>VPS37A</i>Maureen A Mealy, Tai-Seung Nam, Santiago J Pardo, et al.
American Journal of Medical Genetics. Part A|September 24, 2015
Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblingsSalma Ben-Salem, Nara Sobreira, Nadia A Akawi, et al.
Pageof 15