(Q35767774)

English

Molecular basis of spectrin deficiency in beta spectrin Durham. A deletion within beta spectrin adjacent to the ankyrin-binding site precludes spectrin attachment to the membrane in hereditary spherocytosis

scientific article published on December 1995

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Molecular basis of spectrin deficiency in beta spectrin Durham. A deletion within beta spectrin adjacent to the ankyrin-binding site precludes spectrin attachment to the membrane in hereditary spherocytosis (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

author name string

H Hassoun

1

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

J N Vassiliadis

2

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

J Murray

3

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

S J Yi

4

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

M Hanspal

5

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

R E Ware

6

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

S S Winter

7

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

S S Chiou

8

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

J Palek

9

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

language of work or name

0 references

publication date

1 December 1995

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Journal of Clinical Investigation

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

96

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

2623-2629

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Mutations involving the spectrin heterodimer contact site: clinical expression and alterations in specific function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

The spectrin-based membrane skeleton and micron-scale organization of the plasma membrane

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

Crystal structure of the repetitive segments of spectrin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

Altered spectrin dimer-dimer association and instability of erythrocyte membrane skeletons in hereditary pyropoikilocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

Self-assembly of spectrin oligomers in vitro: a basis for a dynamic cytoskeleton

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

Identification of functional domains of human erythrocyte spectrin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

Erythrocyte spectrin is comprised of many homologous triple helical segments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

Partial deficiency of erythrocyte spectrin in hereditary spherocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 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=185967

27 July 2018

Hereditary elliptocytosis, spherocytosis and related disorders: consequences of a deficiency or a mutation of membrane skeletal proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

Deficiency of protein 4.2 in erythrocytes from a patient with a Coombs negative hemolytic anemia. Evidence for a role of protein 4.2 in stabilizing ankyrin on the membrane

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

A haemolytic syndrome associated with the complete absence of red cell membrane protein 4.2 in two Tunisian siblings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

Full-length sequence of the cDNA for human erythroid beta-spectrin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

Ankyrin binds to the 15th repetitive unit of erythroid and nonerythroid beta-spectrin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

Properties of human red cell spectrin heterodimer (side-to-side) assembly and identification of an essential nucleation site

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

Mutations of the red blood cell membrane proteins: from clinical evaluation to detection of the underlying genetic defect

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

Identification and partial purification of ankyrin, the high affinity membrane attachment site for human erythrocyte spectrin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 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=185967

27 July 2018

Selective association of spectrin with the cytoplasmic surface of human erythrocyte plasma membranes. Quantitative determination with purified (32P)spectrin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

27 July 2018

Solubilization and purification of enzymatically active glutathione S-transferase (pGEX) fusion proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

25 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=185967

25 September 2018

Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8675627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8675627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular structure of human erythrocyte spectrin

1 reference

https://pubmed.ncbi.nlm.nih.gov/8675627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA analysis in the diagnosis of hemoglobin disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/8675627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficient red-cell spectrin in severe, recessively inherited spherocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8675627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8675627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA in heritable disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8675627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of spectrin subunits and reassociation in vitro. Analysis by fluorescence polarization

1 reference

https://pubmed.ncbi.nlm.nih.gov/8675627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial spectrin deficiency in hereditary pyropoikilocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8675627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8675627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proliferation and maturation of human erythroid progenitors in liquid culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/8675627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genetic defect of erythrocyte band 4.2 protein associated with hereditary spherocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8675627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary spherocytosis characterized by increased spectrin/band 3 ratio

1 reference

https://pubmed.ncbi.nlm.nih.gov/8675627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Asynchronous synthesis of membrane skeletal proteins during terminal maturation of murine erythroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/8675627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human erythrocyte protein 4.2 deficiency associated with hemolytic anemia and a homozygous 40glutamic acid-->lysine substitution in the cytoplasmic domain of band 3 (band 3Montefiore)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8675627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8675627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI118327

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

ResearchGate publication ID

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