(Q34373577)

1 August 2017

title

Mutational analysis of the human SLC26A8 gene: exclusion as a candidate for male infertility due to primary spermatogenic failure (English)

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1 August 2017

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6

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1 August 2017

Mäkelä S

1

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1 August 2017

Eklund R

2

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1 August 2017

Lähdetie J

3

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1 August 2017

Mikkola M

4

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1 August 2017

Hovatta O

5

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1 August 2017

publication date

3 December 2004

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Molecular Human Reproduction

1 August 2017

published in

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1 August 2017

volume

11

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1 August 2017

issue

2

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1 August 2017

page(s)

129-132

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A Drosophila rotund transcript expressed during spermatogenesis and imaginal disc morphogenesis encodes a protein which is similar to human Rac GTPase-activating (racGAP) proteins.

1 August 2017

cites work

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https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

RotundRacGAP functions with Ras during spermatogenesis and retinal differentiation in Drosophila melanogaster

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

Molecular Analysis of the Pds Gene in Pendred Syndrome (Sensorineural Hearing Loss and Goitre)

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

Mutations of the Down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

Functional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

SLC26A3 mutations in congenital chloride diarrhea

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

Familial t(6;21)(p21.1;p13) translocation associated with male-only sterility

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

Intracellular pH regulation by HCO3-/Cl- exchange is activated during early mouse zygote development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

On the allelic spectrum of human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

Mutations in the diastrophic dysplasia sulfate transporter (DTDST) gene (SLC26A2): 22 novel mutations, mutation review, associated skeletal phenotypes, and diagnostic relevance

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

Tat1, a novel sulfate transporter specifically expressed in human male germ cells and potentially linked to rhogtpase signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

Two frequent missense mutations in Pendred syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

The Sensitivity of Single-Strand Conformation Polymorphism Analysis for the Detection of Single Base Substitutions

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FMOLEHR%2FGAH140

21 January 2018

Identifiers

DOI

10.1093/MOLEHR/GAH140

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1 August 2017

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