Complex interdependence regulates heterotypic transcription factor distribution and coordinates cardiogenesis
Transcription factors (TFs) are thought to function with partners to achieve specificity and
precise quantitative outputs. In the develo** heart, heterotypic TF interactions, such as …
precise quantitative outputs. In the develo** heart, heterotypic TF interactions, such as …
The transcriptional regulator HDP1 controls expansion of the inner membrane complex during early sexual differentiation of malaria parasites
Transmission of Plasmodium falciparum and other malaria parasites requires their
differentiation from asexual blood stages into gametocytes, the non-replicative sexual stage …
differentiation from asexual blood stages into gametocytes, the non-replicative sexual stage …
A novel NKX2. 5 loss-of-function mutation associated with congenital bicuspid aortic valve
XK Qu, XB Qiu, F Yuan, J Wang, CM Zhao… - The American journal of …, 2014 - Elsevier
Bicuspid aortic valve (BAV) is the most common form of congenital cardiovascular defect in
humans and is associated with substantial morbidity and mortality. Emerging evidence …
humans and is associated with substantial morbidity and mortality. Emerging evidence …
Functional Characterization of a Novel Mutation in NKX2-5 Associated With Congenital Heart Disease and Adult-Onset Cardiomyopathy
MW Costa, G Guo, O Wolstein, M Vale… - Circulation …, 2013 - Am Heart Assoc
Background—The transcription factor NKX2-5 is crucial for heart development, and
mutations in this gene have been implicated in diverse congenital heart diseases and …
mutations in this gene have been implicated in diverse congenital heart diseases and …
DNA binding analysis of rare variants in homeodomains reveals homeodomain specificity-determining residues
Homeodomains (HDs) are the second largest class of DNA binding domains (DBDs) among
eukaryotic sequence-specific transcription factors (TFs) and are the TF structural class with …
eukaryotic sequence-specific transcription factors (TFs) and are the TF structural class with …
Disease-associated non-coding variants alter NKX2-5 DNA-binding affinity
Genome-wide association studies (GWAS) have mapped over 90% of disease-or trait-
associated variants within the non-coding genome, like cis-regulatory elements (CREs). Non …
associated variants within the non-coding genome, like cis-regulatory elements (CREs). Non …
Experimental approaches to investigate biophysical interactions between homeodomain transcription factors and DNA
Homeodomain transcription factors (TFs) bind to specific DNA sequences to regulate the
expression of target genes. Structural work has provided insight into molecular identities and …
expression of target genes. Structural work has provided insight into molecular identities and …
A direct fate exclusion mechanism by Sonic hedgehog-regulated transcriptional repressors
Y Nishi, X Zhang, J Jeong, KA Peterson… - …, 2015 - journals.biologists.com
Sonic hedgehog (Shh) signaling patterns the vertebrate spinal cord by activating a group of
transcriptional repressors in distinct neural progenitors of somatic motor neuron and …
transcriptional repressors in distinct neural progenitors of somatic motor neuron and …
A mouse model of human congenital heart disease: high incidence of diverse cardiac anomalies and ventricular noncompaction produced by heterozygous Nkx2-5 …
H Ashraf, L Pradhan, EI Chang, R Terada… - Circulation …, 2014 - Am Heart Assoc
Background—Heterozygous human mutations of NKX2-5 are highly penetrant and
associated with varied congenital heart defects. The heterozygous knockout of murine Nkx2 …
associated with varied congenital heart defects. The heterozygous knockout of murine Nkx2 …
Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac Death
G Sveinbjornsson, EF Olafsdottir… - Circulation: Genomic …, 2018 - Am Heart Assoc
Background: Dilated cardiomyopathy (DCM) is an important cause of heart failure. Variants
in> 50 genes have been reported to cause DCM, but causative variants have been found in …
in> 50 genes have been reported to cause DCM, but causative variants have been found in …