(Q34265298)

English

Sp alpha V/41: a common spectrin polymorphism at the alpha IV-alpha V domain junction. Relevance to the expression level of hereditary elliptocytosis due to alpha-spectrin variants located in trans

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

1 August 2017

Sp alpha V/41: a common spectrin polymorphism at the alpha IV-alpha V domain junction. Relevance to the expression level of hereditary elliptocytosis due to alpha-spectrin variants located in trans (English)

1 reference

Europe PubMed Central

1 August 2017

hereditary elliptocytosis

1 reference

based on heuristic

inferred from title

author name string

N Alloisio

1

1 reference

Europe PubMed Central

1 August 2017

L Morlé

2

1 reference

Europe PubMed Central

1 August 2017

J Maréchal

3

1 reference

Europe PubMed Central

1 August 2017

A F Roux

4

1 reference

Europe PubMed Central

1 August 2017

M T Ducluzeau

5

1 reference

Europe PubMed Central

1 August 2017

D Guetarni

6

1 reference

Europe PubMed Central

1 August 2017

B Pothier

7

1 reference

Europe PubMed Central

1 August 2017

F Baklouti

8

1 reference

Europe PubMed Central

1 August 2017

A Ghanem

9

1 reference

Europe PubMed Central

1 August 2017

R Kastally

10

1 reference

Europe PubMed Central

1 August 2017

J Delaunay

11

1 reference

Europe PubMed Central

1 August 2017

language of work or name

0 references

publication date

1 June 1991

1 reference

Europe PubMed Central

1 August 2017

Journal of Clinical Investigation

1 reference

Europe PubMed Central

1 August 2017

87

1 reference

Europe PubMed Central

1 August 2017

6

1 reference

Europe PubMed Central

1 August 2017

2169-2177

1 reference

Europe PubMed Central

1 August 2017

Common structural polymorphisms in human erythrocyte spectrin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

Hereditary elliptocytosis and related disorders.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

Sp alpha I/65 hereditary elliptocytosis in North Africa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

Synthesis and assembly of membrane skeletal proteins in mammalian red cell precursors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

Molecular determinants of clinical expression of hereditary elliptocytosis and pyropoikilocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

Abnormal oxidant sensitivity and beta-chain structure of spectrin in hereditary spherocytosis associated with defective spectrin-protein 4.1 binding

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

Spectrin Tunis (alpha I/78): a new alpha I variant that causes asymptomatic hereditary elliptocytosis in the heterozygous state

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

From genes to structural morphogenesis: the genesis and epigenesis of a red blood cell

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

The alpha-spectrin gene is on chromosome 1 in mouse and man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

Spectrin Oran (alpha II/21), a new spectrin variant concerning the alpha II domain and causing severe elliptocytosis in the homozygous state

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

Three RFLPs are detected by an alpha spectrin genomic clone

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

Molecular basis of Sp alpha I/65 hereditary elliptocytosis in North Africa: insertion of a TTG triplet between codons 147 and 149 in the alpha-spectrin gene from five unrelated families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

The red cell skeleton and its genetic disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

Two elliptocytogenic alpha I/74 variants of the spectrin alpha I domain. Spectrin Culoz (GGT----GTT; alpha I 40 Gly----Val) and spectrin Lyon (CTT----TTT; alpha I 43 Leu---Phe).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

Genetics of the red cell membrane skeleton

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin allele

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296976

6 July 2018

A structural model of human erythrocyte spectrin. Alignment of chemical and functional domains

1 reference

https://pubmed.ncbi.nlm.nih.gov/2040699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrin-alpha I/61: a new structural variant of alpha-spectrin in a double-heterozygous form of hereditary pyropoikilocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2040699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain

1 reference

https://pubmed.ncbi.nlm.nih.gov/2040699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two distinct variants of erythrocyte spectrin beta IV domain

1 reference

https://pubmed.ncbi.nlm.nih.gov/2040699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain

1 reference

https://pubmed.ncbi.nlm.nih.gov/2040699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of Sp alpha I/74 hereditary elliptocytosis to the alpha- or beta-chain of spectrin through in vitro dimer reconstitution

1 reference

https://pubmed.ncbi.nlm.nih.gov/2040699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI115250

1 reference

Europe PubMed Central

1 August 2017

1 reference

Europe PubMed Central

1 August 2017

1 reference

Europe PubMed Central

1 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34265298&oldid=1980334636"