Common polymorphisms in genes encoding the human mineralocorticoid receptor and the human amiloride-sensitive sodium channel. (Q48001072)

7 February 2018

title

Common polymorphisms in genes encoding the human mineralocorticoid receptor and the human amiloride-sensitive sodium channel. (English)

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7 February 2018

author name string

Ludwig M

1

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7 February 2018

Bolkenius U

2

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7 February 2018

Wickert L

3

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7 February 2018

Bidlingmaier F

4

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7 February 2018

publication date

1 March 1998

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7 February 2018

The Journal of Steroid Biochemistry and Molecular Biology

published in

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7 February 2018

volume

64

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7 February 2018

issue

5-6

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7 February 2018

page(s)

227-230

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7 February 2018

Molecular genetics of human blood pressure variation

cites work

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7 January 2021

A mutation in the epithelial sodium channel causing Liddle disease increases channel activity in the Xenopus laevis oocyte expression system

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7 January 2021

Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel

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7 January 2021

Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome

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7 January 2021

A de novo missense mutation of the beta subunit of the epithelial sodium channel causes hypertension and Liddle syndrome, identifying a proline-rich segment critical for regulation of channel activity

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7 January 2021

Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1

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https://api.crossref.org/works/10.1016%2FS0960-0760%2897%2900195-7

7 January 2021

A novel splice-site mutation in the gamma subunit of the epithelial sodium channel gene in three pseudohypoaldosteronism type 1 families

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https://api.crossref.org/works/10.1016%2FS0960-0760%2897%2900195-7

7 January 2021

No alteration in the primary structure of the mineralocorticoid receptor in a family with pseudohypoaldosteronism

1 reference

https://api.crossref.org/works/10.1016%2FS0960-0760%2897%2900195-7

7 January 2021

No apparent mineralocorticoid receptor defect in a series of sporadic cases of pseudohypoaldosteronism.

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7 January 2021

Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor

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7 January 2021

Cloning, chromosomal localization, and physical linkage of the beta and gamma subunits (SCNN1B and SCNN1G) of the human epithelial amiloride-sensitive sodium channel

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7 January 2021

Splicing of messenger RNA precursors

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7 January 2021

5'-Heterogeneity of the mineralocorticoid receptor messenger ribonucleic acid: differential expression and regulation of splice variants within the rat hippocampus.

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7 January 2021

An analysis of vertebrate mRNA sequences: intimations of translational control

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7 January 2021

10.1016/S0960-0760(97)00195-7

Identifiers

DOI

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7 February 2018

PubMed ID

9618022

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7 February 2018