نتایج جستجو برای: gata3

تعداد نتایج: 1819  

Journal: :Development 2006
David Grote Abdallah Souabni Meinrad Busslinger Maxime Bouchard

The mammalian pro- and mesonephros are transient embryonic kidneys essential for urogenital system development. The nephric (Wolffian) duct, which is a central constituent of both structures, elongates caudally along a stereotypical path to reach the hindlimb level where it induces metanephros (adult kidney) formation, while the remaining duct gives rise to the male genital tract (epidydimis, v...

2009
Tomonori Hosoya Takashi Kuroha Takashi Moriguchi Dustin Cummings Ivan Maillard Kim-Chew Lim James Douglas Engel

Most T lymphocytes appear to arise from very rare early T lineage progenitors (ETPs) in the thymus, but the transcriptional programs that specify ETP generation are not completely known. The transcription factor GATA-3 is required for the development of T lymphocytes at multiple late differentiation steps as well as for the development of thymic natural killer cells. However, a role for GATA-3 ...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2007
Montserrat Garcia-Closas Melissa A Troester Ying Qi Anita Langerød Meredith Yeager Jolanta Lissowska Louise Brinton Robert Welch Beata Peplonska Daniela S Gerhard Inger Torhild Gram Vessela Kristensen Anne-Lise Børresen-Dale Stephen Chanock Charles M Perou

GATA-binding protein 3 (GATA3) is a transcription factor and a putative tumor suppressor that is highly expressed in normal breast luminal epithelium and estrogen receptor alpha (ER)-positive breast tumors. We hypothesized that common genetic variation in GATA3 could influence breast carcinogenesis. Four tag single-nucleotide polymorphisms (SNP) in GATA3 and its 3' flanking gene FLJ4598 were ge...

2015
Rikako Hiramatsu Yoshifumi Ubara Toshihiro Tajima Takeshi Usui Kazutaka Namba Yasuhiro Takeuchi Naoki Sawa Eiko Hasegawa Kenmei Takaichi

We describe a hemodialysis patient with hypoparathyroidism due to HDR (hypoparathyroidism, sensorineural deafness, and renal dysplasia) syndrome caused by GATA3 mutation. She presents tumoral calcinosis which is a rare complication of end-stage renal failure. A novel mutation of GATA3 is identified in this patient.

Journal: :Medicina-lithuania 2023

This study aimed to evaluate the diagnostic and prognostic roles of GATA-binding protein 3 (GATA3) immunohistochemistry in urothelial carcinoma (UC) using a meta-analysis. We investigated GATA3 immunohistochemical expression rates performed subgroup analysis based on tumor site, location, histological subtypes. The overall survival patients with GATA3-positive -negative UC were compared. estima...

2016
Sun-Young Kong Kwang-Soo Kim Jiewan Kim Min Kyeong Kim Ki Hong Lee Je-Yong Lee Nuri Oh Ji-In Park Ji-Hoon Park Sun-Hee Heo Sung Han Shim Dong Ryul Lee Keun Pil Kim Kyung-Soon Park

Triple-negative breast cancer is a highly aggressive tumor subtype that lacks effective therapeutic targets. Here, we show that ELK3 is overexpressed in a subset of breast cancers, in particular basal-like and normal-like/claudin-low cell lines. Suppression of ELK3 in MDA-MB-231 cells led to transdifferentiation from an invasive mesenchymal phenotype to a non-invasive epithelial phenotype both ...

2014
Aimée M Deaton Peter C Cook Dina De Sousa Alexander T Phythian-Adams Adrian Bird Andrew S MacDonald

Th1 and Th2 cell fates are traditionally viewed as mutually exclusive, but recent work suggests that these lineages may be more plastic than previously thought. When isolating splenic CD4(+) T cells from mice infected with the parasitic helminth Schistosoma mansoni, we observed a defined population of IFN-γ/IL-4 double-positive cells. These IFN-γ(+) IL-4(+) cells showed differences in DNA methy...

2017
Christian Krendl Dmitry Shaposhnikov Valentyna Rishko Chaido Ori Christoph Ziegenhain Steffen Sass Lukas Simon Nikola S. Müller Tobias Straub Kelsey E. Brooks Shawn L. Chavez Wolfgang Enard Fabian J. Theis Micha Drukker

To elucidate the molecular basis of BMP4-induced differentiation of human pluripotent stem cells (PSCs) toward progeny with trophectoderm characteristics, we produced transcriptome, epigenome H3K4me3, H3K27me3, and CpG methylation maps of trophoblast progenitors, purified using the surface marker APA. We combined them with the temporally resolved transcriptome of the preprogenitor phase and of ...

2013
Kelly Sheehan-Rooney Mary E. Swartz Feng Zhao Dong Liu Johann K. Eberhart

The severity of most human birth defects is highly variable. Our ability to diagnose, treat and prevent defects relies on our understanding of this variability. Mutation of the transcription factor GATA3 in humans causes the highly variable hypoparathyroidism, sensorineural deafness and renal dysplasia (HDR) syndrome. Although named for a triad of defects, individuals with HDR can also exhibit ...

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