Depletion of SLC4A11 causes cell death by apoptosis in an immortalized human corneal endothelial cell line (Q33556321)

28 July 2017

title

Depletion of SLC4A11 causes cell death by apoptosis in an immortalized human corneal endothelial cell line (English)

1 reference

28 July 2017

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Jeppe Praetorius

7

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Tin Aung

9

object named as

Tin Aung

1 reference

28 July 2017

Jun Liu

1

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28 July 2017

Li-Fong Seet

2

1 reference

28 July 2017

Li Wei Koh

3

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28 July 2017

Anandalakshmi Venkatraman

4

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28 July 2017

Divya Venkataraman

5

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28 July 2017

Rajiv R Mohan

6

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28 July 2017

Joseph A Bonanno

8

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28 July 2017

Eranga N Vithana

10

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28 July 2017

language of work or name

English

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publication date

5 June 2012

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Investigative Ophthalmology Visual Science

28 July 2017

published in

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28 July 2017

volume

53

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28 July 2017

issue

7

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28 July 2017

page(s)

3270-3279

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Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by SLC4A11 mutations

28 July 2017

cites work

1 reference

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An alpha 2 collagen VIII transgenic knock-in mouse model of Fuchs endothelial corneal dystrophy shows early endothelial cell unfolded protein response and apoptosis

21 June 2018

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Role of Bcl-2 family proteins and caspases in the regulation of apoptosis.

21 June 2018

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SLC4A11 prevents osmotic imbalance leading to corneal endothelial dystrophy, deafness, and polyuria.

21 June 2018

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Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities

21 June 2018

1 reference

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Molecular physiology and genetics of Na+-independent SLC4 anion exchangers

21 June 2018

1 reference

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Bicarbonate transport in cell physiology and disease

21 June 2018

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Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome)

21 June 2018

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Autosomal recessive CHED associated with novel compound heterozygous mutations in SLC4A11.

21 June 2018

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Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy

21 June 2018

1 reference

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Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11

21 June 2018

1 reference

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Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).

21 June 2018

1 reference

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Molecular pathophysiology of SLC4 bicarbonate transporters

21 June 2018

1 reference

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NaBC1 is a ubiquitous electrogenic Na+ -coupled borate transporter essential for cellular boron homeostasis and cell growth and proliferation

21 June 2018

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Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

21 June 2018

1 reference

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Corneal endothelial cell apoptosis in patients with Fuchs' dystrophy

21 June 2018

1 reference

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Fuchs' endothelial dystrophy of the cornea

21 June 2018

1 reference

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Congenital hereditary corneal oedema of Maumenee: its clinical features, management, and pathology

21 June 2018

1 reference

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Clinical Differentiation of Recessive Congenital Hereditary Endothelial Dystrophy and Dominant Hereditary Endothelial Dystrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007482

A biochemical framework for SLC4A11, the plasma membrane protein defective in corneal dystrophies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007482

SLC4A7 sodium bicarbonate co-transporter controls mitochondrial apoptosis in ischaemic coronary endothelial cells.

31 October 2018

1 reference

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SLC4A11 mutations in Fuchs endothelial corneal dystrophy.

31 October 2018

1 reference

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Borate transport and cell growth and proliferation. Not only in plants.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007482

The role of apoptosis in the pathogenesis of Fuchs endothelial dystrophy of the cornea

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007482

Isolation and characterization of a mouse monoclonal antibody against human corneal endothelial cells

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007482

Bone morphogenic proteins 2 and 4 and their receptors in the adult human cornea.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007482

Development of genetically engineered tet HPV16-E6/E7 transduced human corneal epithelial clones having tight regulation of proliferation and normal differentiation

31 October 2018

1 reference

12 December 2020

Endothelial repair in the rat cornea

1 reference

12 December 2020

Expression of cell cycle-associated proteins in human and rabbit corneal endothelium in situ

1 reference

12 December 2020

A morphological and functional study of Congenital Hereditary Endothelial Dystrophy

1 reference

12 December 2020

Molecular expression of SLC4-derived Na+-dependent anion transporters in selected human tissues

1 reference

12 December 2020

Identifiers

DOI

10.1167/IOVS.11-8724

1 reference

28 July 2017

1 reference

28 July 2017

1 reference