نتایج جستجو برای: nr5a1

تعداد نتایج: 360  

Journal: :The Journal of endocrinology 2005
Y Kamei Y Aoyama T Fujimoto N Kenmotsu C Kishi M Koushi S Sugano K Morohashi R Kamiyama R Asakai

Several steroidogenic cell lines of granulosa cells (GC) have been used to elucidate differentiation mechanisms of GC during folliculogenesis. These cell lines, however, are of limited usefulness since they have lost some of their differentiation potential. The transcription factor adrenal-4 binding protein (Ad4BP), also known as steroidogenic factor-1 or NR5A1, is essential for the expression ...

Journal: :Hormones and behavior 2012
Neza Grgurevic Tomaz Büdefeld Tanja Spanic Stuart A Tobet Gregor Majdic

Female receptivity including the immobile hormone-dependent lordosis posture is essential for successful reproduction in rodents. It is well documented that lordosis is organized during the perinatal period when the actions of androgens decrease the males' ability to display this behavior in adulthood. Conversely the absence of androgens, and the presence of low levels of prepubertal estrogens,...

2014
Juliana Gabriel Ribeiro de Andrade Antonia Paula Marques-de-Faria Helena Campos Fabbri Maricilda Palandi de Mello Gil Guerra-Júnior Andréa Trevas Maciel-Guerra

Background/Aims. Studies on 46,XY partial gonadal dysgenesis (PGD) have focused on molecular, gonadal, genital, and hormone features; little is known about follow-up. Our aim was to analyze long-term outcomes of PGD. Methods. Retrospective longitudinal study conducted at a reference service in Brazil. Ten patients were first evaluated in the 1990s and followed up until the 2010s; follow-up rang...

2007
Walter Just Algimantas Sinkus Annette Baumstark Rotraud Kuhn Daniel Ortmann Irena Andriuškevičiūtė Lina Jurkėnienė Loreta Šalomskienė

Gonadal dysgenesis with XY male-to-female sex reversal has been attributed to mutations and gene dosage differences in at least seven genes. We present a family of three sisters with a pure gonadal dysgenesis (Swyer syndrome) with an 46, XY karyotype. The sisters have a common X-chromosomal haplotype in Xp21.3-p11.3, the region of the X-chromosomal Swyer syndrome which includes NR0B1. We exclud...

2017
Iveta Yotova Emily Hsu Catherine Do Aulona Gaba Matthias Sczabolcs Sabine Dekan Lukas Kenner Rene Wenzl Benjamin Tycko

Endometriosis is characterized by growth of endometrial-like tissue outside the uterine cavity. Since its pathogenesis may involve epigenetic changes, we used Illumina 450K Methylation Beadchips to profile CpG methylation in endometriosis stromal cells compared to stromal cells from normal endometrium. We validated and extended the Beadchip data using bisulfite sequencing (bis-seq), and analyze...

Journal: :Journal of molecular endocrinology 2009
Marie France Bouchard Hiroaki Taniguchi Robert S Viger

GATA transcription factors are crucial regulators of cell-specific gene expression in many tissues including the gonads. Although clinical cases of reproductive dysfunction have yet to be formally linked to GATA gene mutations, they have begun to be reported in other systems. Heterozygous GATA4 mutations have been associated with cases of congenital heart defects. Little is known, however, abou...

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