(Q34565862)

3 August 2017

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

1 reference

3 August 2017

P A Lane

1

1 reference

3 August 2017

R L Shew

2

1 reference

3 August 2017

T A Iarocci

3

1 reference

3 August 2017

N Mohandas

4

1 reference

3 August 2017

T Hays

5

1 reference

3 August 2017

W C Mentzer

6

1 reference

3 August 2017

language of work or name

English

0 references

publication date

1 March 1987

1 reference

Journal of Clinical Investigation

3 August 2017

1 reference

3 August 2017

79

1 reference

3 August 2017

3

1 reference

3 August 2017

989-996

1 reference

Tryptic digestion of spectrin in variants of hereditary elliptocytosis

3 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Molecular defect of spectrin in hereditary pyropoikilocytosis. Alterations in the trypsin-resistant domain involved in spectrin self-association

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Spectrin beta-chain variant associated with hereditary elliptocytosis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Defective spectrin dimer-dimer association with hereditary elliptocytosis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stability

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Coexpression of a mutant beta-actin and the two normal beta- and gamma-cytoplasmic actins in a stably transformed human cell line

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Molecular and functional changes in spectrin from patients with hereditary pyropoikilocytosis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

A molecular defect of spectrin in a subset of patients with hereditary elliptocytosis. Alterations in the alpha-subunit domain involved in spectrin self-association

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

A molecular defect in two families with hemolytic poikilocytic anemia: reduction of high affinity membrane binding sites for ankyrin

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

The influence of membrane skeleton on red cell deformability, membrane material properties, and shape

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

The red cell membrane skeleton: recent progress

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

“Western Blotting”: Electrophoretic transfer of proteins from sodium dodecyl sulfate-polyacrylamide gels to unmodified nitrocellulose and radiographic detection with antibody and radioiodinated protein A

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Defective binding of spectrin to ankyrin in a kindred with recessively inherited hereditary elliptocytosis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Synthesis and assembly of spectrin during avian erythropoiesis: stoichiometric assembly but unequal synthesis of alpha and beta spectrin.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

A Genetic Defect in the Binding of Protein 4.1 to Spectrin in a Kindred with Hereditary Spherocytosis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

A new abnormal variant of spectrin in black patients with hereditary elliptocytosis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Hereditary elliptocytosis and related disorders.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

The removal of leukocytes and platelets from whole blood.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Influence of single amino acid substitutions on electrophoretic mobility of sodium dodecyl sulfate-protein complexes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

A single amino acid substitution in a histidine-transport protein drastically alters its mobility in sodium dodecyl sulfate-polyacrylamide gel electrophoresis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Spectrin-actin membrane skeleton of normal and abnormal red blood cells

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

High resolution two-dimensional electrophoresis of proteins

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Quantification of Coomassie Blue stained proteins in polyacrylamide gels based on analyses of eluted dye

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Spontaneous, reversible protein cross-linking in the human erythrocyte membrane. Temperature and pH dependence

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Sp alpha I/65: a new variant of the alpha subunit of spectrin in hereditary elliptocytosis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=424257

Homozygous Hereditary Elliptocytosis as the Cause of Haemolytic Anemia in Infancy

27 October 2018

1 reference

12 December 2020

The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes

1 reference

12 December 2020

Analyses of phosphorylated tryptic peptide of spectrin from human erythrocyte membrane

1 reference

12 December 2020

Monovalent cation composition and ATP and lipid content of irreversibly sickled cells

1 reference

12 December 2020

A technique to detect reduced mechanical stability of red cell membranes: relevance to elliptocytic disorders

1 reference

12 December 2020

Spectrin tetramer-dimer equilibrium in hereditary elliptocytosis

1 reference

12 December 2020

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

1 reference

12 December 2020

Isolation of the chemical domains of human erythrocyte spectrin

1 reference

12 December 2020

Identification of the hereditary pyropoikilocytosis carrier state

1 reference

12 December 2020

A case of elliptocytosis associated with a truncated spectrin chain

1 reference

12 December 2020

Recessive X-linked ichthyosis: lack of immunologically detectable steroid sulfatase enzyme protein

1 reference

12 December 2020

Abnormal spectrin in hereditary elliptocytosis

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI112911

1 reference

3 August 2017

1 reference

3 August 2017

1 reference