Pages that link to "Q42635760"

The following pages link to Biochemical analyses of eight NKX2.5 homeodomain missense mutations causing atrioventricular block and cardiac anomalies (Q42635760):

Displaying 44 items.

• A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects (Q24317048) (← links)
• Crystal Structure of the Human NKX2.5 Homeodomain in Complex with DNA Target (Q27671009) (← links)
• Inherited conduction system abnormalities--one group of diseases, many genes (Q28236888) (← links)
• Slow progressive conduction and contraction defects in loss of Nkx2-5 mice after cardiomyocyte terminal differentiation (Q28508704) (← links)
• Chibby, an antagonist of the Wnt/beta-catenin pathway, facilitates cardiomyocyte differentiation of murine embryonic stem cells (Q28510953) (← links)
• Perinatal loss of Nkx2-5 results in rapid conduction and contraction defects (Q28593447) (← links)
• Ablation of Nkx2-5 at mid-embryonic stage results in premature lethality and cardiac malformation (Q30501669) (← links)
• Point mutations in murine Nkx2-5 phenocopy human congenital heart disease and induce pathogenic Wnt signaling. (Q30842375) (← links)
• Prediction and validation of protein-protein interactors from genome-wide DNA-binding data using a knowledge-based machine-learning approach (Q31133691) (← links)
• Genetic causes of human heart failure (Q33683773) (← links)
• Investigation of association between PFO complicated by cryptogenic stroke and a common variant of the cardiac transcription factor GATA4. (Q33932840) (← links)
• Integrating differentiation and cancer: the Nkx3.1 homeobox gene in prostate organogenesis and carcinogenesis (Q34786771) (← links)
• NKX2-5 mutations in an inbred consanguineous population: genetic and phenotypic diversity (Q35153273) (← links)
• Nuclear Receptor-Like Structure and Interaction of Congenital Heart Disease-Associated Factors GATA4 and NKX2-5. (Q35862534) (← links)
• NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets (Q35992694) (← links)
• Mechanics and function in heart morphogenesis (Q36097892) (← links)
• Isolated left ventricular non-compaction: the case for abnormal myocardial development (Q36744174) (← links)
• Crystallization and preliminary X-ray analysis of the NKX2.5 homeodomain in complex with DNA. (Q36968812) (← links)
• Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature (Q37248612) (← links)
• Functional characterization of a novel mutation in NKX2-5 associated with congenital heart disease and adult-onset cardiomyopathy. (Q37275558) (← links)
• Stem cell models of cardiac development and disease (Q37640325) (← links)
• Genetic origins of pediatric heart disease (Q37662207) (← links)
• NKX2-5: an update on this hypermutable homeodomain protein and its role in human congenital heart disease (CHD) (Q37781313) (← links)
• Genetic analysis of cardiac-specific transcription factors reveals novel insights into molecular causes of congenital heart disease (Q38443001) (← links)
• Congenital heart diseases and their association with the variant distribution features on susceptibility genes (Q38899973) (← links)
• An update on the molecular diagnosis of congenital heart disease: focus on loss-of-function mutations (Q38920317) (← links)
• Novel point mutation in the NKX2-5 gene in a Moroccan family with atrioventricular conduction disturbance and an atrial septal defect in the oval fossa (Q39398648) (← links)
• Mouse Model of Human Congenital Heart Disease: Progressive Atrioventricular Block Induced by a Heterozygous Nkx2-5 Homeodomain Missense Mutation (Q41808908) (← links)
• A mouse model of human congenital heart disease: high incidence of diverse cardiac anomalies and ventricular noncompaction produced by heterozygous Nkx2-5 homeodomain missense mutation (Q42186727) (← links)
• Somatic mutations in cardiac malformations (Q42975756) (← links)
• Inherited arrhythmias in children (Q43202552) (← links)
• The effect of p.Arg25Cys alteration in NKX2-5 on conotruncal heart anomalies: mutation or polymorphism? (Q46257517) (← links)
• In Vitro Modeling of Congenital Heart Defects Associated with an NKX2-5 Mutation Revealed a Dysregulation in BMP/Notch-Mediated Signaling. (Q47240623) (← links)
• Congenital heart defect causing mutation in Nkx2.5 displays in vivo functional deficit (Q51096160) (← links)
• Functional dissection of sequence-specific NKX2-5 DNA binding domain mutations associated with human heart septation defects using a yeast-based system. (Q53621281) (← links)
• Novel NKX2-5 mutations in patients with familial atrial septal defects. (Q53757791) (← links)
• Cardiac Actions of a Small Molecule Inhibitor Targeting GATA4-NKX2-5 Interaction. (Q55334799) (← links)
• Mechanism Sharing Between Genetic and Gestational Hypoxia-Induced Cardiac Anomalies (Q57091921) (← links)
• Familial congenital heart disease, progressive atrioventricular block and the cardiac homeobox transcription factor gene NKX2.5: (Q61650596) (← links)
• Nkx2-5 Second Heart Field Target Gene Ccdc117 Regulates DNA Metabolism and Proliferation (Q61797111) (← links)
• Heterozygous Mylk3 Knockout Mice Partially Recapitulate Human DCM With Heterozygous MYLK3 Mutations. (Q64980340) (← links)
• Atrial fibrillation risk loci interact to modulate Ca2+-dependent atrial rhythm homeostasis (Q90688952) (← links)
• A comprehensive in silico analysis, distribution and frequency of human Nkx2-5 mutations; A critical gene in congenital heart disease (Q91869426) (← links)
• Update of genetic variants in the NKX2-5 gene (Q94541561) (← links)