(Q34258409)

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Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. I. Biochemical identification of rearrangements in the spectrin/actin binding domain and functional characterizations

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Europe PubMed Central

PubMed publication ID

31 July 2017

Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. I. Biochemical identification of rearrangements in the spectrin/actin binding domain and functional characterizations (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

author name string

S L Marchesi

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

J Conboy

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

P Agre

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

J T Letsinger

4

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

V T Marchesi

5

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

D W Speicher

6

1 reference

Europe PubMed Central

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31 July 2017

N Mohandas

7

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

language of work or name

0 references

publication date

1 August 1990

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Journal of Clinical Investigation

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Europe PubMed Central

PubMed publication ID

31 July 2017

86

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Europe PubMed Central

PubMed publication ID

31 July 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

516-523

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

The hereditary elliptocytoses: clinical and linkage data

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296754

6 July 2018

https://pubmed.ncbi.nlm.nih.gov/2384597

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monoclonal antibodies as probes of domain structure of the spectrin alpha subunit

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296754

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296754

6 July 2018

Identification and Location of Brain Protein 4.1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296754

6 July 2018

An analogue of the erythroid membrane skeletal protein 4.1 in nonerythroid cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296754

6 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=296754

6 July 2018

The heterozygous form of 4.1(-) hereditary elliptocytosis [the 4.1(-) trait].

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296754

6 July 2018

Synapsin I is a spectrin-binding protein immunologically related to erythrocyte protein 4.1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296754

6 July 2018

Restoration of normal membrane stability to unstable protein 4.1-deficient erythrocyte membranes by incorporation of purified protein 4.1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296754

6 July 2018

Structure of the spectrin-actin binding site of erythrocyte protein 4.1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296754

6 July 2018

Molecular cloning of protein 4.1, a major structural element of the human erythrocyte membrane skeleton

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296754

6 July 2018

Selective expression of an erythroid-specific isoform of protein 4.1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296754

6 July 2018

Multiple protein 4.1 isoforms produced by alternative splicing in human erythroid cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296754

6 July 2018

The kinetics of resealing of washed erythrocyte ghosts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296754

6 July 2018

Molecular basis of hereditary elliptocytosis due to protein 4.1 deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=296754

28 July 2018

Distinct variants of erythrocyte protein 4.1 inherited in linkage with elliptocytosis and Rh type in three white families

1 reference

https://pubmed.ncbi.nlm.nih.gov/2384597

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hybrid erythrocytes for membrane studies in sickle cell disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/2384597

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[1st instance of the absence of an erythrocyte membrane protein (band 4(1)) in a case of familial elliptocytic anemia]

1 reference

https://pubmed.ncbi.nlm.nih.gov/2384597

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2384597

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A shortened variant of red cell membrane protein 4.1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2384597

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A protein immunologically related to erythrocyte band 4.1 is found on stress fibres of non-erythroid cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/2384597

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A structural model of human erythrocyte protein 4.1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2384597

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of spectrin and protein 4.1-like proteins in mammalian lens

1 reference

https://pubmed.ncbi.nlm.nih.gov/2384597

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Platelets contain proteins immunologically related to red cell spectrin and protein 4.1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2384597

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2384597

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential phosphorylation of multiple sites in protein 4.1 and protein 4.9 by phorbol ester-activated and cyclic AMP-dependent protein kinases

1 reference

https://pubmed.ncbi.nlm.nih.gov/2384597

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of the functional site of erythrocyte protein 4.1 involved in spectrin-actin associations

1 reference

https://pubmed.ncbi.nlm.nih.gov/2384597

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanisms of cytoskeletal regulation: modulation of aortic endothelial cell protein band 4.1 by the extracellular matrix

1 reference

https://pubmed.ncbi.nlm.nih.gov/2384597

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A molecular study of heterozygous protein 4.1 deficiency in hereditary elliptocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2384597

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI114738

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

ResearchGate publication ID

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