(Q30501632)

English

Dinucleotide repeat polymorphisms at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenita

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scholarly article

1 reference

Europe PubMed Central

21 September 2017

Dinucleotide repeat polymorphisms at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenita (English)

1 reference

Europe PubMed Central

21 September 2017

periodic paralysis

1 reference

based on heuristic

inferred from title

hyperkalemic periodic paralysis

1 reference

based on heuristic

inferred from title

paramyotonia congenita

1 reference

based on heuristic

inferred from title

author name string

A I McClatchey

1

1 reference

Europe PubMed Central

21 September 2017

J Trofatter

2

1 reference

Europe PubMed Central

21 September 2017

D McKenna-Yasek

3

1 reference

Europe PubMed Central

21 September 2017

W Raskind

4

1 reference

Europe PubMed Central

21 September 2017

T Bird

5

1 reference

Europe PubMed Central

21 September 2017

M Pericak-Vance

6

1 reference

Europe PubMed Central

21 September 2017

J Gilchrist

7

1 reference

Europe PubMed Central

21 September 2017

K Arahata

8

1 reference

Europe PubMed Central

21 September 2017

D Radosavljevic

9

1 reference

Europe PubMed Central

21 September 2017

H G Worthen

10

1 reference

Europe PubMed Central

21 September 2017

language of work or name

0 references

publication date

1 May 1992

1 reference

Europe PubMed Central

21 September 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

21 September 2017

50

1 reference

Europe PubMed Central

21 September 2017

896-901

1 reference

Europe PubMed Central

21 September 2017

5

1 reference

Europe PubMed Central

21 September 2017

Strategies for multilocus linkage analysis in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Existence of distinct sodium channel messenger RNAs in rat brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

A rat brain Na+ channel alpha subunit with novel gating properties

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Primary structure and functional expression of a mammalian skeletal muscle sodium channel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Molecular cloning of a putative tetrodotoxin-resistant rat heart Na+ channel isoform

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Structure and function of voltage-sensitive ion channels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Probing the molecular structure of the voltage-dependent sodium channel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Schwartz-Jampel syndrome: II. Na+ channel defect causes myotonia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Primary structure and expression of a sodium channel characteristic of denervated and immature rat skeletal muscle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Assignment of a human skeletal muscle sodium channel α-subunit gene (SCN4A) to 17q23.1–25.3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

X-linked sideroblastic anemia and ataxia: linkage to phosphoglycerate kinase at Xq13

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Altered sodium channel behaviour causes myotonia in dominantly inherited myotonia congenita

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Altered gating and conductance of Na+ channels in hyperkalemic periodic paralysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Precise localization of human beta-globin gene complex on chromosome 11

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

DNA sequencing with chain-terminating inhibitors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

20 June 2018

Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

26 November 2018

Primary structure of rat brain sodium channel III deduced from the cDNA sequence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

26 November 2018

Expression of functional sodium channels from cloned cDNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682609

26 November 2018

Membrane defects in paramyotonia congenita (Eulenburg)

1 reference

https://pubmed.ncbi.nlm.nih.gov/1315122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A sodium channel defect in hyperkalemic periodic paralysis: potassium-induced failure of inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1315122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adynamia episodica hereditaria with myotonia: a non-inactivating sodium current and the effect of extracellular pH

1 reference

https://pubmed.ncbi.nlm.nih.gov/1315122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mechanism of activation of porcine pepsinogen

1 reference

https://pubmed.ncbi.nlm.nih.gov/1315122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

21 September 2017

1 reference

Europe PubMed Central

21 September 2017

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