about
GATA3 inhibits breast cancer metastasis through the reversal of epithelial-mesenchymal transitionGATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humansMutations in IRX5 impair craniofacial development and germ cell migration via SDF1An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidismDoes GATA3 act in tissue-specific pathways? A meta-analysis-based approachDown-regulation of GATA-3 expression during human papillomavirus-mediated immortalization and cervical carcinogenesisGATA family transcriptional factors: emerging suspects in hematologic disordersSingle-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humansLower urinary tract development and diseaseBmp4 is essential for the formation of the vestibular apparatus that detects angular head movementsGenomic analysis of the function of the transcription factor gata3 during development of the mammalian inner earThe emerging role of GATA transcription factors in development and diseaseTCR-dependent translational control of GATA-3 enhances Th2 differentiationGATA3 controls the specification of prosensory domain and neuronal survival in the mouse cochleaDevelopmental profiling of spiral ganglion neurons reveals insights into auditory circuit assembly.Gata3 is a critical regulator of cochlear wiringNephric duct insertion is a crucial step in urinary tract maturation that is regulated by a Gata3-Raldh2-Ret molecular network in miceGata3-deficient mice develop parathyroid abnormalities due to dysregulation of the parathyroid-specific transcription factor Gcm2Gcm2 is required for the differentiation and survival of parathyroid precursor cells in the parathyroid/thymus primordiaGata3 acts downstream of beta-catenin signaling to prevent ectopic metanephric kidney inductionTranscription factor GATA-3 alters pathway selection of olivocochlear neurons and affects morphogenesis of the earDifferentiation of effector CD4 T cell populations (*)GATA3 haploinsufficiency does not block allergic sensitization or atopic disease.Cellular and Molecular Underpinnings of Neuronal Assembly in the Central Auditory System during Mouse Development.A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functionsTime-dependent gene expression analysis of the developing superior olivary complex.GATA3 in development and cancer differentiation: cells GATA have it!Renal diagnosis without renal biopsy. Nephritis and sensorineural deafness.GATA factor mutations in hematologic disease.Pathway signature and cellular differentiation in clear cell renal cell carcinoma.Breast tumor specific mutation in GATA3 affects physiological mechanisms regulating transcription factor turnoverPituitary gland development and disease: from stem cell to hormone productionMutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract.Genetic kidney diseases.Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies.A focused in situ hybridization screen identifies candidate transcriptional regulators of thymic epithelial cell development and function.Seizure, deafness and renal agenesis: A rare case of barakat syndromeDeletion of the GATA domain of TRPS1 causes an absence of facial hair and provides new insights into the bone disorder in inherited tricho-rhino-phalangeal syndromes.Exploring the genetic basis of early-onset chronic kidney disease.
P2860
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P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
GATA3 haplo-insufficiency causes human HDR syndrome
@ast
GATA3 haplo-insufficiency causes human HDR syndrome
@en
GATA3 haplo-insufficiency causes human HDR syndrome
@en-gb
GATA3 haplo-insufficiency causes human HDR syndrome
@nl
type
label
GATA3 haplo-insufficiency causes human HDR syndrome
@ast
GATA3 haplo-insufficiency causes human HDR syndrome
@en
GATA3 haplo-insufficiency causes human HDR syndrome
@en-gb
GATA3 haplo-insufficiency causes human HDR syndrome
@nl
prefLabel
GATA3 haplo-insufficiency causes human HDR syndrome
@ast
GATA3 haplo-insufficiency causes human HDR syndrome
@en
GATA3 haplo-insufficiency causes human HDR syndrome
@en-gb
GATA3 haplo-insufficiency causes human HDR syndrome
@nl
P2093
P2860
P356
P1433
P1476
GATA3 haplo-insufficiency causes human HDR syndrome
@en
P2093
G Vanderlinden
H Van Esch
I Holdaway
K Devriendt
M A Nesbit
P2860
P2888
P304
P356
10.1038/35019088
P407
P577
2000-07-27T00:00:00Z
P5875
P6179
1019522979