(Q24648422)

3

object named as

Prashant Garg

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author name string

Xiaodong Jiao

1

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Afia Sultana

2

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Balasubramanya Ramamurthy

4

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Nibaran Gangopadhyay

6

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J Fielding Hejtmancik

7

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Chitra Kannabiran

Journal of Medical Genetics

8

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language of work or name

English

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publication date

January 2007

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published in

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volume

44

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issue

1

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page(s)

64-8

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cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597914

Genetic linkage of Bietti crystallin corneoretinal dystrophy to chromosome 4q35

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597914

The SLC4 family of HCO 3 - transporters

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597914

A perfect message: RNA surveillance and nonsense-mediated decay

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597914

Faster sequential genetic linkage computations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597914

Easy calculations of lod scores and genetic risks on small computers

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597914

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597914

Molecular pathophysiology of SLC4 bicarbonate transporters

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597914

VSX1: a gene for posterior polymorphous dystrophy and keratoconus

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597914

Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597914

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597914

Exclusion of Usher syndrome gene from much of chromosome 4.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597914

Linkage of congenital hereditary endothelial dystrophy to chromosome 20.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597914

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

19 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2597914

A morphological and functional study of Congenital Hereditary Endothelial Dystrophy

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16825429

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Congenital hereditary corneal dystrophy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16825429

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Comparison between posterior polymorphous dystrophy and congenital hereditary endothelial dystrophy of the cornea

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16825429

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.2006.044644

1 reference

1 reference

1 reference

PubMed publication ID

16825429

1 reference