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David Valle

Showing results (71-80 of 146) with videos related to

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Disease Models & Mechanisms|February 3, 2022
An enriched environment re-establishes metabolic homeostasis by reducing obesity-induced inflammationSol Díaz de León-Guerrero, Jonathan Salazar-León, Karla F Meza-Sosa, et al.
Genome Research|September 6, 2011
Characterization of complex chromosomal rearrangements by targeted capture and next-generation sequencingNara L M Sobreira, Veena Gnanakkan, Michael Walsh, et al.
Molecular Neuropsychiatry|September 9, 2016
Neuregulin 3 Knockout Mice Exhibit Behaviors Consistent with Psychotic DisordersLindsay N Hayes, Alexey Shevelkin, Mariela Zeledon, et al.
Epigenetics|April 1, 2016
ATRX binds to atypical chromatin domains at the 3' exons of zinc finger genes to preserve H3K9me3 enrichmentDavid Valle-García, Zulekha A Qadeer, Domhnall S McHugh, et al.
Frontiers in Genetics|June 21, 2024
Rare exonic <i>CELSR3</i> variants identified in Bladder Exstrophy Epispadias ComplexAngie C Jelin, Nikolai Sopko, Nara Sobreira, et al.
American Journal of Human Genetics|September 11, 2004
Isolated 3-methylcrotonyl-CoA carboxylase deficiency: evidence for an allele-specific dominant negative effect and responsiveness to biotin therapyMatthias R Baumgartner, M Fernanda Dantas, Terttu Suormala, et al.
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|April 12, 2023
A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2Michele Patricia Migliavacca, Rodrigo Ambrosio Fock, Nadia Almeida, et al.
Human Mutation|September 27, 2002
Mutation analysis of PEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotypeNancy Braverman, Li Chen, Paul Lin, et al.
Journal of Inherited Metabolic Disease|June 26, 2014
A detailed analysis of methylmalonic acid kinetics during hemodialysis and after combined liver/kidney transplantation in a patient with mut (0) methylmalonic acidemiaHilary J Vernon, C John Sperati, Joshua D King, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2011
Linkage and association on 8p21.2-p21.1 in schizophreniaM Daniele Fallin, Virginia K Lasseter, Yaping Liu, et al.
Pageof 15

Showing results (71-80 of 146) with videos related to

Sort By:
Pageof 15
Disease Models & Mechanisms|February 3, 2022
An enriched environment re-establishes metabolic homeostasis by reducing obesity-induced inflammationSol Díaz de León-Guerrero, Jonathan Salazar-León, Karla F Meza-Sosa, et al.
Genome Research|September 6, 2011
Characterization of complex chromosomal rearrangements by targeted capture and next-generation sequencingNara L M Sobreira, Veena Gnanakkan, Michael Walsh, et al.
Molecular Neuropsychiatry|September 9, 2016
Neuregulin 3 Knockout Mice Exhibit Behaviors Consistent with Psychotic DisordersLindsay N Hayes, Alexey Shevelkin, Mariela Zeledon, et al.
Epigenetics|April 1, 2016
ATRX binds to atypical chromatin domains at the 3' exons of zinc finger genes to preserve H3K9me3 enrichmentDavid Valle-García, Zulekha A Qadeer, Domhnall S McHugh, et al.
Frontiers in Genetics|June 21, 2024
Rare exonic <i>CELSR3</i> variants identified in Bladder Exstrophy Epispadias ComplexAngie C Jelin, Nikolai Sopko, Nara Sobreira, et al.
American Journal of Human Genetics|September 11, 2004
Isolated 3-methylcrotonyl-CoA carboxylase deficiency: evidence for an allele-specific dominant negative effect and responsiveness to biotin therapyMatthias R Baumgartner, M Fernanda Dantas, Terttu Suormala, et al.
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|April 12, 2023
A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2Michele Patricia Migliavacca, Rodrigo Ambrosio Fock, Nadia Almeida, et al.
Human Mutation|September 27, 2002
Mutation analysis of PEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotypeNancy Braverman, Li Chen, Paul Lin, et al.
Journal of Inherited Metabolic Disease|June 26, 2014
A detailed analysis of methylmalonic acid kinetics during hemodialysis and after combined liver/kidney transplantation in a patient with mut (0) methylmalonic acidemiaHilary J Vernon, C John Sperati, Joshua D King, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2011
Linkage and association on 8p21.2-p21.1 in schizophreniaM Daniele Fallin, Virginia K Lasseter, Yaping Liu, et al.
Pageof 15