about
Expression and evolutionary conservation of the tescalcin gene during developmentIdentification of SOX3 as an XX male sex reversal gene in mice and humansDefective survival of proliferating Sertoli cells and androgen receptor function in a mouse model of the ATR-X syndromeSignaling through the TGF beta-activin receptors ALK4/5/7 regulates testis formation and male germ cell developmentUsing ROADMAP Data to Identify Enhancers Associated with Disorders of Sex Development.Conserved expression of a novel gene during gonadal development.The cerebellin 4 precursor gene is a direct target of SRY and SOX9 in miceCloning and expression of R-Spondin1 in different vertebrates suggests a conserved role in ovarian developmentHeterogeneity of Human Neutrophil CD177 Expression Results from CD177P1 Pseudogene ConversionRapid high-throughput analysis of DNaseI hypersensitive sites using a modified Multiplex Ligation-dependent Probe Amplification approachNormalizing gene expression levels in mouse fetal germ cells.Painful ovulation in a 46,XX SRY -ve adult male with SOX9 duplication.Ex vivo magnetofection: a novel strategy for the study of gene function in mouse organogenesis.Copy number variation in patients with disorders of sex development due to 46,XY gonadal dysgenesis.Development of retroviral vectors for tissue-restricted expression in chicken embryonic gonadsMutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determinationSRY mutation analysis by next generation (deep) sequencing in a cohort of chromosomal Disorders of Sex Development (DSD) patients with a mosaic karyotype.Whole exome sequencing combined with linkage analysis identifies a novel 3 bp deletion in NR5A1Three-dimensional visualization of testis cord morphogenesis, a novel tubulogenic mechanism in developmentSex determination: insights from the chicken.Identification of candidate gonadal sex differentiation genes in the chicken embryo using RNA-seqHormonal evaluation in relation to phenotype and genotype in 286 patients with a disorder of sex development from Indonesia.Disorders of sex development: insights from targeted gene sequencing of a large international patient cohort.Variants in congenital hypogonadotrophic hypogonadism genes identified in an Indonesian cohort of 46,XY under-virilised boys.Human embryonic stem cell research: an Australian perspective.Onset of meiosis in the chicken embryo; evidence of a role for retinoic acid.The Genetic and Environmental Factors Underlying Hypospadias.The potential role of microRNAs in regulating gonadal sex differentiation in the chicken embryo.The molecular genetics of ovarian differentiation in the avian model.The genetics of disorders of sex development in humans.Genetic regulation of mammalian gonad development.Molecular mechanisms associated with 46,XX disorders of sex development.Premature Ovarian Insufficiency: New Perspectives on Genetic Cause and Phenotypic Spectrum.Review disorders of sex development: The evolving role of genomics in diagnosis and gene discovery.The proto-oncogene Ret is required for male foetal germ cell survival.FGF9, activin and TGFβ promote testicular characteristics in an XX gonad organ culture model.Females battle to suppress their inner male.Genetic evidence against a role for W-linked histidine triad nucleotide binding protein (HINTW) in avian sex determination.WNT/β-catenin and p27/FOXL2 differentially regulate supporting cell proliferation in the developing ovary.Characterisation of urogenital ridge gene expression in the human embryonal carcinoma cell line NT2/D1.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Andrew H Sinclair
@ast
Andrew H Sinclair
@en
Andrew H Sinclair
@es
Andrew H Sinclair
@nl
Andrew H Sinclair
@sl
type
label
Andrew H Sinclair
@ast
Andrew H Sinclair
@en
Andrew H Sinclair
@es
Andrew H Sinclair
@nl
Andrew H Sinclair
@sl
prefLabel
Andrew H Sinclair
@ast
Andrew H Sinclair
@en
Andrew H Sinclair
@es
Andrew H Sinclair
@nl
Andrew H Sinclair
@sl
P106
P21
P31
P496
0000-0003-2741-7992