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W Scherer

Showing results (651-660 of 915) with videos related to

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BMC Medical Genomics|January 12, 2023
Disruption of DDX53 coding sequence has limited impact on iPSC-derived human NGN2 neuronsMuhammad Faheem, Eric Deneault, Roumiana Alexandrova, et al.
Communications Biology|July 22, 2023
Decreased left heart flow in fetal lambs causes left heart hypoplasia and pro-fibrotic tissue remodelingMiriam S Reuter, Dustin J Sokolowski, J Javier Diaz-Mejia, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1998
Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration siteD Mishmar, A Rahat, S W Scherer, et al.
Genome Research|November 24, 2006
Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arraysDaisuke Komura, Fan Shen, Shumpei Ishikawa, et al.
Journal of Clinical Immunology|August 15, 2013
Combined de-novo mutation and non-random X-chromosome inactivation causing Wiskott-Aldrich syndrome in a female with thrombocytopeniaBoonchai Boonyawat, Santhosh Dhanraj, Fahad Al Abbas, et al.
Journal of Neurodevelopmental Disorders|July 5, 2024
An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructureJane Summers, Danielle Baribeau, Polina Perlman, et al.
Autism Research : Official Journal of the International Society for Autism Research|August 1, 2023
Linkage of whole genome sequencing and administrative health data in autism: A proof of concept studyDanielle A Baribeau, Jasleen Arneja, Xuesong Wang, et al.
Journal of Medical Genetics|October 18, 2018
Biallelic mutations in EXOC3L2 cause a novel syndrome that affects the brain, kidney and bloodAdel Shalata, Supanun Lauhasurayotin, Zvi Leibovitz, et al.
Genomics|February 7, 2002
Molecular genetic studies of human chromosome 7 in Russell-Silver syndromeKazuhiko Nakabayashi, Bridget A Fernandez, Ikuko Teshima, et al.
Genome Research|February 18, 2011
A novel approach identifies new differentially methylated regions (DMRs) associated with imprinted genesSanaa Choufani, Jonathan S Shapiro, Martha Susiarjo, et al.
Pageof 92

Showing results (651-660 of 915) with videos related to

Sort By:
Pageof 92
BMC Medical Genomics|January 12, 2023
Disruption of DDX53 coding sequence has limited impact on iPSC-derived human NGN2 neuronsMuhammad Faheem, Eric Deneault, Roumiana Alexandrova, et al.
Communications Biology|July 22, 2023
Decreased left heart flow in fetal lambs causes left heart hypoplasia and pro-fibrotic tissue remodelingMiriam S Reuter, Dustin J Sokolowski, J Javier Diaz-Mejia, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1998
Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration siteD Mishmar, A Rahat, S W Scherer, et al.
Genome Research|November 24, 2006
Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arraysDaisuke Komura, Fan Shen, Shumpei Ishikawa, et al.
Journal of Clinical Immunology|August 15, 2013
Combined de-novo mutation and non-random X-chromosome inactivation causing Wiskott-Aldrich syndrome in a female with thrombocytopeniaBoonchai Boonyawat, Santhosh Dhanraj, Fahad Al Abbas, et al.
Journal of Neurodevelopmental Disorders|July 5, 2024
An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructureJane Summers, Danielle Baribeau, Polina Perlman, et al.
Autism Research : Official Journal of the International Society for Autism Research|August 1, 2023
Linkage of whole genome sequencing and administrative health data in autism: A proof of concept studyDanielle A Baribeau, Jasleen Arneja, Xuesong Wang, et al.
Journal of Medical Genetics|October 18, 2018
Biallelic mutations in EXOC3L2 cause a novel syndrome that affects the brain, kidney and bloodAdel Shalata, Supanun Lauhasurayotin, Zvi Leibovitz, et al.
Genomics|February 7, 2002
Molecular genetic studies of human chromosome 7 in Russell-Silver syndromeKazuhiko Nakabayashi, Bridget A Fernandez, Ikuko Teshima, et al.
Genome Research|February 18, 2011
A novel approach identifies new differentially methylated regions (DMRs) associated with imprinted genesSanaa Choufani, Jonathan S Shapiro, Martha Susiarjo, et al.
Pageof 92