Characterization of GATA3 Mutations in the Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) Syndrome-Reference-Cited by-同舟云学术

Characterization of GATA3 Mutations in the Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) Syndrome

Published:2004-05 Issue:21 Volume:279 Page:22624-22634
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Nesbit M. Andrew,Bowl Michael R.,Harding Brian,Ali Asif,Ayala Alejandro,Crowe Carol,Dobbie Angus,Hampson Geeta,Holdaway Ian,Levine Michael A.,McWilliams Robert,Rigden Susan,Sampson Julian,Williams Andrew J.,Thakker Rajesh V.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference63 articles.

1. Targeted disruption of the GATA3 gene causes severe abnormalities in the nervous system and in fetal liver haematopoiesis

2. GATA4 transcription factor is required for ventral morphogenesis and heart tube formation.

3. Gotta have GATA

4. GATA-binding transcription factors in hematopoietic cells

5. FOG, a Multitype Zinc Finger Protein, Acts as a Cofactor for Transcription Factor GATA-1 in Erythroid and Megakaryocytic Differentiation

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