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SLC4A11 gene
Known as:
BICARBONATE TRANSPORTER-RELATED PROTEIN 1
, solute carrier family 4 member 11
, BTR1
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National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Interaction of Fluorescently Labeled Cadherin G Protein-coupled Receptor with the Cry1Ab Toxin of Bacillus thuringiensis
Li Liu
,
Stefanie Boyd
,
M. Kavoussi
,
L. Bulla
,
Duane D. Winkler
Journal of Proteomics & Bioinformatics
2018
Corpus ID: 49862720
The Cry1Ab toxin produced by Bacillus thuringiensis binds to a conserved structural motif in the 12th ectodomain module (EC12) of…
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2017
2017
SLC4A11 depletion impairs NRF2 mediated antioxidant signaling and increases reactive oxygen species in human corneal endothelial cells during oxidative stress
Sanjukta Guha
,
S. Chaurasia
,
Charanya Ramachandran
,
Sanhita Roy
Scientific Reports
2017
Corpus ID: 256914348
Corneal endothelial dystrophy is a progressive disease with gradual loss of vision and characterized by degeneration and…
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2017
2017
High SLC4A11 expression is an independent predictor for poor overall survival in grade 3/4 serous ovarian cancer
L. Qin
,
Ting Li
,
Yuhua Liu
PLoS ONE
2017
Corpus ID: 27745383
In this study, we aimed to examine the expression of SLC4A11 in ovarian cancer and in normal ovarian tissues, its prognostic…
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2016
2016
2 Functional Assessment of SLC 4 A 11 , an Integral Membrane Protein Mutated in Corneal 3 Dystrophies 4 5
S. Loganathan
,
Hans-Peter Schneider
,
P. Morgan
,
W. Joachim
,
Deitmer
,
Joseph R. Casey
2016
Corpus ID: 264738561
1 2 Functional Assessment of SLC4A11, an Integral Membrane Protein Mutated in Corneal 3 Dystrophies 4 5 Sampath K. Loganathan…
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Review
2016
Review
2016
Focus on “ Mouse Slc 4 a 11 expressed in Xenopus oocytes is an ideally selective H / OH conductance pathway that is stimulated by rises in intracellular and extracellular pH ”
K. Nehrke
2016
Corpus ID: 4574763
CONGENITAL HEREDITARY ENDOTHELIAL DYSTROPHY (CHED; OMIM no. 217700) is a rare disorder of the corneal endothelium that results in…
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2014
2014
Two novel mutations including a large deletion of the SLC4A11 gene causing autosomal recessive hereditary endothelial dystrophy
V. Puangsricharern
,
Patra Yeetong
,
Chonthicha Charumalai
,
K. Suphapeetiporn
,
V. Shotelersuk
British Journal of Ophthalmology
2014
Corpus ID: 22911458
Congenital hereditary endothelial dystrophy (CHED) is an inherited disorder of the corneal endothelium characterised by bilateral…
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2011
2011
A biochemical framework for SLC4A11, the plasma membrane protein defective in corneal dystrophies.
Gonzalo L. Vilas
,
P. Morgan
,
S. Loganathan
,
A. Quon
,
J. Casey
Biochemistry
2011
Corpus ID: 33243448
Mutations in the SLC4A11 protein, reported as a sodium-coup-led borate transporter of the human plasma membrane, are responsible…
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2009
2009
Analysis of the Effects of SLC4A11 (CHED2) Gene Depletion on Corneal Endothelial Cell Growth and Proliferation
E. Vithana
,
Anandalakshmi Venkatraman
,
L. Koh
,
R. Mohan
,
L. Seet
2009
Corpus ID: 83169220
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