The genetic advantage hypothesis in cystic fibrosis heterozygotes: a murine study (Q24530092)

2

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R Ratcliff

3

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W H Colledge

4

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M J Evans

Toxigenic diarrheas, congenital diarrheas, and cystic fibrosis: disorders of intestinal ion transport

5

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language of work or name

English

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publication date

15 January 1995

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published in

Journal of Physiology

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volume

482 ( Pt 2)

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page(s)

449-54

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cites work

1 reference

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Human genetics. What is good about cystic fibrosis?

27 September 2017

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Cystic fibrosis heterozygote resistance to cholera toxin in the cystic fibrosis mouse model

27 September 2017

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Gates of Janus: cystic fibrosis and diarrhea

27 September 2017

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Activation of intestinal CFTR Cl- channel by heat-stable enterotoxin and guanylin via cAMP-dependent protein kinase.

27 September 2017

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Cystic fibrosis: molecular biology and therapeutic implications

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Diffusion of drugs through stationary water layers as the rate limiting process in their action at membrane receptors

27 September 2017

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Chloride secretion in response to guanylin in colonic epithelial from normal and transgenic cystic fibrosis mice

27 September 2017

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Failure to induce secretion in jejunal biopsies from children with cystic fibrosis

30 May 2018

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Altered intestinal chloride transport in cystic fibrosis

30 May 2018

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Abnormal epithelial transport in cystic fibrosis jejunum

30 May 2018

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Ion-transporting activity in the murine colonic epithelium of normal animals and animals with cystic fibrosis

30 May 2018

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Production of a severe cystic fibrosis mutation in mice by gene targeting

29 November 2018

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Kinin-stimulated chloride secretion in mouse colon requires the participation of CFTR chloride channels

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Cystic fibrosis and chloride-secreting diarrhoea

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Accounting for cystic fibrosis

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Hyposecretion of beta-adrenergically induced sweating in cystic fibrosis heterozygotes

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