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H Sherr

Showing results (201-210 of 290) with videos related to

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American Journal of Medical Genetics. Part A|May 25, 2013
Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruptionAlex R Paciorkowski, Kim Keppler-Noreuil, Luther Robinson, et al.
Plos One|April 25, 2013
Quantitative trait loci for interhemispheric commissure development and social behaviors in the BTBR T⁺ tf/J mouse model of autismDorothy M Jones-Davis, Mu Yang, Eric Rider, et al.
Molecular Cancer Research : MCR|May 1, 2016
Role for the Aryl Hydrocarbon Receptor and Diverse Ligands in Oral Squamous Cell Carcinoma Migration and TumorigenesisElizabeth A Stanford, Alejandra Ramirez-Cardenas, Zhongyan Wang, et al.
Plos One|October 28, 2016
Early Predictors of Impaired Social Functioning in Male Rhesus Macaques (Macaca mulatta)Valentina Sclafani, Laura A Del Rosso, Shannon K Seil, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|October 30, 2018
Heavy Metal Neurotoxicants Induce ALS-Linked TDP-43 PathologyPeter E A Ash, Uma Dhawan, Samantha Boudeau, et al.
Endocrinology|December 19, 2002
Bax, caspase-2, and caspase-3 are required for ovarian follicle loss caused by 4-vinylcyclohexene diepoxide exposure of female mice in vivoYasushi Takai, Jacqueline Canning, Gloria I Perez, et al.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|February 9, 2020
Abnormal Auditory Mismatch Fields in Children and Adolescents With 16p11.2 Deletion and 16p11.2 DuplicationJunko Matsuzaki, Jeffrey I Berman, Lisa Blaskey, et al.
Molecular Autism|July 9, 2021
Autism-associated biomarkers: test-retest reliability and relationship to quantitative social trait variation in rhesus monkeysOzge Oztan, Catherine F Talbot, Emanuela Argilli, et al.
American Journal of Medical Genetics. Part A|July 14, 2016
16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohortKyle J Steinman, Sarah J Spence, Melissa B Ramocki, et al.
Neurology|November 9, 2005
Genomic microarray analysis identifies candidate loci in patients with corpus callosum anomaliesE H Sherr, R Owen, D G Albertson, et al.
Pageof 29

Showing results (201-210 of 290) with videos related to

Sort By:
Pageof 29
American Journal of Medical Genetics. Part A|May 25, 2013
Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruptionAlex R Paciorkowski, Kim Keppler-Noreuil, Luther Robinson, et al.
Plos One|April 25, 2013
Quantitative trait loci for interhemispheric commissure development and social behaviors in the BTBR T⁺ tf/J mouse model of autismDorothy M Jones-Davis, Mu Yang, Eric Rider, et al.
Molecular Cancer Research : MCR|May 1, 2016
Role for the Aryl Hydrocarbon Receptor and Diverse Ligands in Oral Squamous Cell Carcinoma Migration and TumorigenesisElizabeth A Stanford, Alejandra Ramirez-Cardenas, Zhongyan Wang, et al.
Plos One|October 28, 2016
Early Predictors of Impaired Social Functioning in Male Rhesus Macaques (Macaca mulatta)Valentina Sclafani, Laura A Del Rosso, Shannon K Seil, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|October 30, 2018
Heavy Metal Neurotoxicants Induce ALS-Linked TDP-43 PathologyPeter E A Ash, Uma Dhawan, Samantha Boudeau, et al.
Endocrinology|December 19, 2002
Bax, caspase-2, and caspase-3 are required for ovarian follicle loss caused by 4-vinylcyclohexene diepoxide exposure of female mice in vivoYasushi Takai, Jacqueline Canning, Gloria I Perez, et al.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|February 9, 2020
Abnormal Auditory Mismatch Fields in Children and Adolescents With 16p11.2 Deletion and 16p11.2 DuplicationJunko Matsuzaki, Jeffrey I Berman, Lisa Blaskey, et al.
Molecular Autism|July 9, 2021
Autism-associated biomarkers: test-retest reliability and relationship to quantitative social trait variation in rhesus monkeysOzge Oztan, Catherine F Talbot, Emanuela Argilli, et al.
American Journal of Medical Genetics. Part A|July 14, 2016
16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohortKyle J Steinman, Sarah J Spence, Melissa B Ramocki, et al.
Neurology|November 9, 2005
Genomic microarray analysis identifies candidate loci in patients with corpus callosum anomaliesE H Sherr, R Owen, D G Albertson, et al.
Pageof 29