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David Valle

Showing results (81-90 of 146) with videos related to

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Prenatal Diagnosis|January 30, 2020
The utility of exome sequencing for fetal pleural effusionsAngie C Jelin, Nara Sobreira, Elizabeth Wohler, et al.
Journal of Neuroscience Research|February 10, 2025
Klf10 Regulates the Emergence of Glial Phenotypes During Hypothalamic DevelopmentNorma Angelica Garduño-Tamayo, Jorge Luis Almazán, Rubí Romo-Rodríguez, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 25, 2021
Immunotherapy for breast cancer using EpCAM aptamer tumor-targeted gene knockdownYing Zhang, Xuemei Xie, Pourya Naderi Yeganeh, et al.
American Journal of Human Genetics|July 24, 2004
Replication study supports evidence for linkage to 9p24 in obsessive-compulsive disorderVirginia L Willour, Yin Yao Shugart, Jack Samuels, et al.
Molecular Neuropsychiatry|November 4, 2015
Identification and functional studies of regulatory variants responsible for the association of <i>NRG3</i> with a delusion phenotype in schizophreniaMariela Zeledón, Nicole Eckart, Margaret Taub, et al.
Molecular Syndromology|January 8, 2015
Novel Deletion of SERPINF1 Causes Autosomal Recessive Osteogenesis Imperfecta Type VI in Two Brazilian FamiliesRenata Moldenhauer Minillo, Nara Sobreira, Maria de Fatima de Faria Soares, et al.
Genetic Epidemiology|June 23, 2010
Detection of SNP-SNP interactions in trios of parents with schizophrenic childrenQing Li, M Daniele Fallin, Thomas A Louis, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 15, 2023
The SET oncoprotein promotes estrogen-induced transcription by facilitating establishment of active chromatinChangying Guo, Karla F Meza-Sosa, David Valle-Garcia, et al.
American Journal of Medical Genetics. Part A|May 26, 2012
The Centers for Mendelian Genomics: a new large-scale initiative to identify the genes underlying rare Mendelian conditionsMichael J Bamshad, Jay A Shendure, David Valle, et al.
Human Mutation|July 16, 2015
GeneMatcher aids in the identification of a new malformation syndrome with intellectual disability, unique facial dysmorphisms, and skeletal and connective tissue abnormalities caused by de novo variants in HNRNPKP Y Billie Au, Jing You, Oana Caluseriu, et al.
Pageof 15

Showing results (81-90 of 146) with videos related to

Sort By:
Pageof 15
Prenatal Diagnosis|January 30, 2020
The utility of exome sequencing for fetal pleural effusionsAngie C Jelin, Nara Sobreira, Elizabeth Wohler, et al.
Journal of Neuroscience Research|February 10, 2025
Klf10 Regulates the Emergence of Glial Phenotypes During Hypothalamic DevelopmentNorma Angelica Garduño-Tamayo, Jorge Luis Almazán, Rubí Romo-Rodríguez, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 25, 2021
Immunotherapy for breast cancer using EpCAM aptamer tumor-targeted gene knockdownYing Zhang, Xuemei Xie, Pourya Naderi Yeganeh, et al.
American Journal of Human Genetics|July 24, 2004
Replication study supports evidence for linkage to 9p24 in obsessive-compulsive disorderVirginia L Willour, Yin Yao Shugart, Jack Samuels, et al.
Molecular Neuropsychiatry|November 4, 2015
Identification and functional studies of regulatory variants responsible for the association of <i>NRG3</i> with a delusion phenotype in schizophreniaMariela Zeledón, Nicole Eckart, Margaret Taub, et al.
Molecular Syndromology|January 8, 2015
Novel Deletion of SERPINF1 Causes Autosomal Recessive Osteogenesis Imperfecta Type VI in Two Brazilian FamiliesRenata Moldenhauer Minillo, Nara Sobreira, Maria de Fatima de Faria Soares, et al.
Genetic Epidemiology|June 23, 2010
Detection of SNP-SNP interactions in trios of parents with schizophrenic childrenQing Li, M Daniele Fallin, Thomas A Louis, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 15, 2023
The SET oncoprotein promotes estrogen-induced transcription by facilitating establishment of active chromatinChangying Guo, Karla F Meza-Sosa, David Valle-Garcia, et al.
American Journal of Medical Genetics. Part A|May 26, 2012
The Centers for Mendelian Genomics: a new large-scale initiative to identify the genes underlying rare Mendelian conditionsMichael J Bamshad, Jay A Shendure, David Valle, et al.
Human Mutation|July 16, 2015
GeneMatcher aids in the identification of a new malformation syndrome with intellectual disability, unique facial dysmorphisms, and skeletal and connective tissue abnormalities caused by de novo variants in HNRNPKP Y Billie Au, Jing You, Oana Caluseriu, et al.
Pageof 15