(Q28295517)

English

Genetic disorders of the red cell membranes

scientific article

In more languages

edit

Statements

0 references

1 reference

Europe PubMed Central

title

Genetic disorders of the red cell membranes (English)

0 references

author name string

J Delaunay

series ordinal

1

0 references

language of work or name

English

0 references

publication date

1 August 1995

0 references

published in

FEBS Letters

0 references

volume

369

0 references

issue

1

0 references

page(s)

34-7

0 references

cites work

NF-kappa B and related proteins: Rel/dorsal homologies meet ankyrin-like repeats

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2F0014-5793%2895%2900460-Q

retrieved

21 January 2018

Erythrocyte spectrin is comprised of many homologous triple helical segments

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2F0014-5793%2895%2900460-Q

retrieved

21 January 2018

Analysis of the three-alpha-helix motif in the spectrin superfamily of proteins

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2F0014-5793%2895%2900460-Q

retrieved

21 January 2018

A nonsense mutation 1669Glu-->Ter within the regulatory domain of human erythroid ankyrin leads to a selective deficiency of the major ankyrin isoform (band 2.1) and a phenotype of autosomal dominant hereditary spherocytosis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2F0014-5793%2895%2900460-Q

retrieved

21 January 2018

Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2F0014-5793%2895%2900460-Q

retrieved

21 January 2018

Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE).

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2F0014-5793%2895%2900460-Q

retrieved

21 January 2018

Defective anion transport activity of the abnormal band 3 in hereditary ovalocytic red blood cells

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2F0014-5793%2895%2900460-Q

retrieved

21 January 2018

A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemia

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2F0014-5793%2895%2900460-Q

retrieved

21 January 2018

Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2F0014-5793%2895%2900460-Q

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2F0014-5793%2895%2900460-Q

retrieved

21 January 2018

Low expression allele alpha LELY of red cell spectrin is associated with mutations in exon 40 (alpha V/41 polymorphism) and intron 45 and with partial skipping of exon 46.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2F0014-5793%2895%2900460-Q

retrieved

21 January 2018

Homozygous 4.1(-) hereditary elliptocytosis associated with a point mutation in the downstream initiation codon of protein 4.1 gene

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2F0014-5793%2895%2900460-Q

retrieved

21 January 2018

Protein 4.1 deficiency associated with an altered binding to the spectrin-actin complex of the red cell membrane skeleton

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2F0014-5793%2895%2900460-Q

retrieved

21 January 2018

Red cell membrane sialoglycoprotein beta in homozygous and heterozygous 4.1(-) hereditary elliptocytosis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2F0014-5793%2895%2900460-Q

retrieved

21 January 2018

Identifiers

DOI

10.1016/0014-5793(95)00460-Q

0 references

Fatcat ID

release_ugzeod2nxbdyzdpgagv7uqna2e

0 references

PubMed ID

7641880

0 references

(Q28295517)

Genetic disorders of the red cell membranes

Statements

Identifiers

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)