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Vincent R Harley

Showing results (71-80 of 76) with videos related to

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Clinical Genetics|November 9, 2022
FGF9 variant in 46,XY DSD patient suggests a role for dimerization in sex determinationBrittany Croft, Anthony D Bird, Makoto Ono, et al.
Plos One|March 8, 2013
Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental diseaseGeorgina Caruana, Peter G Farlie, Adam H Hart, et al.
Plos One|July 21, 2012
A 46,XY female DSD patient with bilateral gonadoblastoma, a novel SRY missense mutation combined with a WT1 KTS splice-site mutationRemko Hersmus, Yvonne G van der Zwan, Hans Stoop, et al.
Biorxiv : the Preprint Server for Biology|February 17, 2023
A "Four Core Genotypes" rat model to distinguish mechanisms underlying sex-biased phenotypes and diseasesArthur P Arnold, Xuqi Chen, Michael N Grzybowski, et al.
Biology of Sex Differences|February 21, 2026
Sry-modified laboratory rat lines to study sex-chromosome effects underlying sex differences in physiology and disease: four core genotypes and moreArthur P Arnold, Xuqi Chen, Michael N Grzybowski, et al.
Nature Communications|August 7, 2024
Male autism spectrum disorder is linked to brain aromatase disruption by prenatal BPA in multimodal investigations and 10HDA ameliorates the related mouse phenotypeChristos Symeonides, Kristina Vacy, Sarah Thomson, et al.
Pageof 8

Showing results (71-80 of 76) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 76 results.
Clinical Genetics|November 9, 2022
FGF9 variant in 46,XY DSD patient suggests a role for dimerization in sex determinationBrittany Croft, Anthony D Bird, Makoto Ono, et al.
Plos One|March 8, 2013
Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental diseaseGeorgina Caruana, Peter G Farlie, Adam H Hart, et al.
Plos One|July 21, 2012
A 46,XY female DSD patient with bilateral gonadoblastoma, a novel SRY missense mutation combined with a WT1 KTS splice-site mutationRemko Hersmus, Yvonne G van der Zwan, Hans Stoop, et al.
Biorxiv : the Preprint Server for Biology|February 17, 2023
A "Four Core Genotypes" rat model to distinguish mechanisms underlying sex-biased phenotypes and diseasesArthur P Arnold, Xuqi Chen, Michael N Grzybowski, et al.
Biology of Sex Differences|February 21, 2026
Sry-modified laboratory rat lines to study sex-chromosome effects underlying sex differences in physiology and disease: four core genotypes and moreArthur P Arnold, Xuqi Chen, Michael N Grzybowski, et al.
Nature Communications|August 7, 2024
Male autism spectrum disorder is linked to brain aromatase disruption by prenatal BPA in multimodal investigations and 10HDA ameliorates the related mouse phenotypeChristos Symeonides, Kristina Vacy, Sarah Thomson, et al.
Pageof 8