Related references
Note: Only part of the references are listed.Missense mutation in SLC4A11 in two Pakistani families affected with congenital hereditary endothelial dystrophy (CHED2)
Haiba Kaul et al.
CLINICAL AND EXPERIMENTAL OPTOMETRY (2016)
The cytoplasmic domain is essential for transport function of the integral membrane transport protein SLC4A11
Sampath K. Loganathan et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2016)
Human SLC4A11-C functions as a DIDS-stimulatable H+ (OH-) permeation pathway: partial correction of R109H mutant transport
Liyo Kao et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2015)
Human SLC4A11 Is a Novel NH3/H+ Co-transporter
Wenlin Zhang et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2015)
SLC4A11 and the Pathophysiology of Congenital Hereditary Endothelial Dystrophy
Sangita P. Patel et al.
BIOMED RESEARCH INTERNATIONAL (2015)
Two novel mutations including a large deletion of the SLC4A11 gene causing autosomal recessive hereditary endothelial dystrophy
Vilavun Puangsricharern et al.
BRITISH JOURNAL OF OPHTHALMOLOGY (2014)
Congenital Hereditary Endothelial Dystrophy Caused by SLC4A11 Mutations Progresses to Harboyan Syndrome
Salina Siddiqui et al.
CORNEA (2014)
Corneal Dystrophy-Causing SLC4A11 Mutants: Suitability for Folding-Correction Therapy
Sampath K. Loganathan et al.
HUMAN MUTATION (2014)
Bicarbonate Transport in Health and Disease
Kumari Alka et al.
IUBMB LIFE (2014)
Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophy
Nagasamy Soumittra et al.
JOURNAL OF HUMAN GENETICS (2014)
SLC4A11 is an EIPA-sensitive Na+ permeable pHi regulator
Diego G. Ogando et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2013)
Genetics of the corneal endothelial dystrophies: an evidence-based review
A. J. Aldave et al.
CLINICAL GENETICS (2013)
Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases
Gonzalo L. Vilas et al.
HUMAN MOLECULAR GENETICS (2013)
Ion Transport Function of SLC4A11 in Corneal Endothelium
Supriya S. Jalimarada et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2013)
Molecular mechanisms underlying the corneal endothelial pump
Joseph A. Bonanno
EXPERIMENTAL EYE RESEARCH (2012)
A Biochemical Framework for SLC4A11, the Plasma Membrane Protein Defective in Corneal Dystrophies
Gonzalo L. Vilas et al.
BIOCHEMISTRY (2011)
Role of NH3 and NH4+ transporters in renal acid-base transport
I. David Weiner et al.
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY (2011)
SLC4A11 Prevents Osmotic Imbalance Leading to Corneal Endothelial Dystrophy, Deafness, and Polyuria
Nicole Groeger et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Cave Canalem: How endogenous ion channels may interfere with heterologous expression in Xenopus oocytes
Jan Terhag et al.
METHODS (2010)
Slc4a11 Gene Disruption in Mice CELLULAR TARGETS OF SENSORINEURONAL ABNORMALITIES
Ivan A. Lopez et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Corneal dystrophies
Gordon K Klintworth
Orphanet Journal of Rare Diseases (2009)
Mutational Spectrum of SLC4A11 in Autosomal Recessive CHED in Saudi Arabia
Mohammed A. Aldahmesh et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2009)
Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophy
Boomiraj Hemadevi et al.
ARCHIVES OF OPHTHALMOLOGY (2008)
SLC4A11 mutations in Fuchs endothelial corneal dystrophy
Eranga N. Vithana et al.
HUMAN MOLECULAR GENETICS (2008)
Molecular expression of SLC4-derived Na+-dependent anion transporters in selected human tissues
Helle Hasager Damkier et al.
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY (2007)
Autosomal recessive CHED associated with novel compound heterozygous mutations in SLC4A11
Anthony J. Aldave et al.
CORNEA (2007)
Transport and regulatory characteristics of the yeast bicarbonate transporter homolog Bor1p
Michael L. Jennings et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2007)
Carbonic anhydrase II increases the activity of the human electrogenic Na+/HCO-3 cotransporter
Holger M. Becker et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy
Julie Desir et al.
JOURNAL OF MEDICAL GENETICS (2007)
Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11
Xiaodong Jiao et al.
JOURNAL OF MEDICAL GENETICS (2007)
Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
Eranga N. Vithana et al.
NATURE GENETICS (2006)
The Arabidopsis major intrinsic protein NIP5;1 is essential for efficient boron uptake and plant development under boron limitation
Junpei Takano et al.
PLANT CELL (2006)
NaBC1 is a ubiquitous electrogenic Na+-coupled borate transporter essential for cellular boron homeostasis and cell growth and proliferation
M Park et al.
MOLECULAR CELL (2004)
Facilitated lactate transport by MCT1 when coexpressed with the sodium bicarbonate cotransporter (NBC) in Xenopus oocytes
HM Becker et al.
BIOPHYSICAL JOURNAL (2004)
Share Paper
