Back to search

Novel Point Mutation in the Cardiac Transcription Factor CSX/NKX2.5 Associated With Congenital Heart Disease.

Data up to Jan 2025

Published2002
Citations90
References18

Total Citations Per Year

Abstract

References (18)

Congenital Heart Disease Caused by Mutations in the Transcription Factor NKX2-5

1998 • 1,284 citations

Myogenic and morphogenetic defects in the heart tubes of murine embryos lacking the homeo box gene Nkx2-5.

1995 • 1,130 citations

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

1999 • 667 citations

The cardiac transcription factors Nkx2-5 and GATA-4 are mutual cofactors

1997 • 660 citations

The cardiac homeobox gene Csx/Nkx2.5 lies genetically upstream of multiple genes essential for heart development

1999 • 552 citations

Csx: a murine homeobox-containing gene specifically expressed in the developing heart.

1993 • 533 citations

Fashioning the vertebrate heart: earliest embryonic decisions

1997 • 490 citations

Molecular Pathways Controlling Heart Development

1996 • 485 citations

Recruitment of the Tinman Homolog Nkx-2.5 by Serum Response Factor Activates Cardiac α-Actin Gene Transcription

1996 • 277 citations

Building the heart piece by piece: modularity of cis-elements regulating Nkx2-5 transcription

1999 • 184 citations

Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease

2000 • 164 citations

Parsing the Heart: Genetic Modules for Organ Assembly

1997 • 163 citations

Identification of the In Vivo Casein Kinase II Phosphorylation Site within the Homeodomain of the Cardiac Tisue-Specifying Homeobox Gene Product Csx/Nkx2.5

1999 • 90 citations

Molecular Cloning and Characterization of Human Cardiac Homeobox Gene CSX1

1996 • 73 citations

Vertebrate homologs oftinman andbagpipe: Roles of the homeobox genes in cardiovascular development

1998 • 73 citations

Functional Analyses of Three Csx/Nkx-2.5 Mutations That Cause Human Congenital Heart Disease

2000 • 59 citations

Familial Atrial Septal Defect and Atrioventricular Conduction Disturbance Associated With a Point Mutation in the Cardiac Homeobox Gene <i>CSX/NKX2-5</i> in a Japanese Patient

1999 • 56 citations

Assignment of Cardiac Homeobox Gene CSX to Human Chromosome 5q34

1995 • 41 citations

Cited By (0)

Loading...
Novel Point Mutation in the Cardiac Transcription Factor CSX/NKX2.5 Associated With… (2002) – Circulation Journal | Metascience Observatory Explorer