SUR1‐TRPM4 and AQP4 form a heteromultimeric complex that amplifies ion/water osmotic coupling and drives astrocyte swelling

JA Stokum, MS Kwon, SK Woo, O Tsymbalyuk… - Glia, 2018 - Wiley Online Library
Astrocyte swelling occurs after central nervous system injury and contributes to brain
swelling, which can increase mortality. Mechanisms proffered to explain astrocyte swelling …

GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrum

D Škorić‐Milosavljević, FVY Tjong… - American Journal of …, 2019 - Wiley Online Library
The first human mutations in GATA6 were described in a cohort of patients with persistent
truncus arteriosus, and the phenotypic spectrum has expanded since then. This study …

Cryoinjury models of the adult and neonatal mouse heart for studies of scarring and regeneration

EG Strungs, EL Ongstad, MP O'Quinn… - … and Repair: Methods …, 2013 - Springer
A major limitation in studies of the injured heart is animal-to-animal variability in wound size
resulting from commonly used techniques such as left anterior descending coronary artery …

GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve

YJ Xu, RM Di, Q Qiao, XM Li, RT Huang, S Xue, XY Liu… - Gene, 2018 - Elsevier
Congenital bicuspid aortic valve (BAV), the most common form of birth defect in humans, is
associated with substantial morbidity and mortality. Increasing evidence demonstrates that …

Novel GATA6 Mutations Associated with Congenital Ventricular Septal Defect or Tetralogy of Fallot

J Wang, XJ Luo, YF Xin, Y Liu, ZM Liu, Q Wang… - DNA and cell …, 2012 - liebertpub.com
Congenital heart disease (CHD) is the most common form of developmental malformation
and is the leading noninfectious cause of infant mortality. Emerging evidence indicates that …

A loss-of-function and H2B-Venus transcriptional reporter allele for Gata6 in mice

L Freyer, C Schröter, N Saiz, N Schrode… - BMC developmental …, 2015 - Springer
Background The GATA-binding factor 6 (Gata6) gene encodes a zinc finger transcription
factor that often functions as a key regulator of lineage specification during development. It is …

A novel GATA6 mutation associated with congenital ventricular septal defect

GF Zheng, D Wei, H Zhao, N Zhou… - International …, 2012 - spandidos-publications.com
Ventricular septal defect (VSD) is the most common form of congenital cardiovascular
malformation and an important contributor to the substantially increased morbidity and …

Somatic mutations in the GATA6 gene underlie sporadic tetralogy of Fallot

RT Huang, S Xue, YJ Xu… - … journal of molecular …, 2013 - spandidos-publications.com
Tetralogy of Fallot (TOF) is the most common cyanotic congenital heart disease associated
with significant morbidity and mortality in humans. However, the molecular etiology …

Prevalence and spectrum of GATA6 mutations associated with familial atrial fibrillation

YQ Yang, XH Wang, HW Tan… - International …, 2012 - internationaljournalofcardiology.com
Atrial fibrillation (AF) is the most common type of cardiac arrhythmia, occurring in 1% to 2%
of the general population. The prevalence of AF increases with age, ranging from b1% in …

GATA6 loss-of-function mutation in atrial fibrillation

YQ Yang, L Li, J Wang, XL Zhang, RG Li, YJ Xu… - European journal of …, 2012 - Elsevier
Atrial fibrillation (AF) is the most common type of sustained cardiac arrhythmia and is
associated with substantial morbidity and mortality. Increasing evidence demonstrates that …