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Clinical Genetics
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November 9, 2022
FGF9 variant in 46,XY DSD patient suggests a role for dimerization in sex determination
Brittany 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 disease
Georgina 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 mutation
Remko 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 diseases
Arthur 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 more
Arthur 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 phenotype
Christos Symeonides, Kristina Vacy, Sarah Thomson, et al.
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Search research articles
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Showing results (71-80 of 76) with videos related to
Sort By:
Page
of 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 determination
Brittany 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 disease
Georgina 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 mutation
Remko 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 diseases
Arthur 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 more
Arthur 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 phenotype
Christos Symeonides, Kristina Vacy, Sarah Thomson, et al.
Page
of 8