Hereditary spherocytosis and hereditary elliptocytosis: aberrant protein sorting during erythroblast enucleation (Q34022437)

30 July 2017

title

Hereditary spherocytosis and hereditary elliptocytosis: aberrant protein sorting during erythroblast enucleation (English)

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30 July 2017

main subject

hereditary spherocytosis

1 reference

hereditary elliptocytosis

inferred from title

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4

Narla Mohandas

1 reference

30 July 2017

6

Joel Anne Chasis

1 reference

30 July 2017

5

Xiuli An

1 reference

30 July 2017

1

Marcela Salomao

1 reference

30 July 2017

Ke Chen

2

1 reference

30 July 2017

Jonathan Villalobos

series ordinal

3

1 reference

30 July 2017

language of work or name

English

0 references

publication date

25 March 2010

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30 July 2017

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30 July 2017

volume

116

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30 July 2017

issue

2

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30 July 2017

page(s)

267-269

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4.1R-deficient human red blood cells have altered phosphatidylserine exposure pathways and are deficient in CD44 and CD47 glycoproteins

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2910610

Red cell membrane: past, present, and future

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2910610

Protein 4.1R-dependent multiprotein complex: new insights into the structural organization of the red blood cell membrane

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2910610

Mechanism of protein sorting during erythroblast enucleation: role of cytoskeletal connectivity

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2910610

Rh-RhAG/ankyrin-R, a new interaction site between the membrane bilayer and the red cell skeleton, is impaired by Rh(null)-associated mutation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2910610

Protein 4.1R-deficient mice are viable but have erythroid membrane skeleton abnormalities

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2910610

Anion exchanger 1 (band 3) is required to prevent erythrocyte membrane surface loss but not to form the membrane skeleton

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2910610

An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2910610

Cytoskeletal distribution and function during the maturation and enucleation of mammalian erythroblasts

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2910610

Ankyrin and the hemolytic anemia mutation, nb, map to mouse chromosome 8: presence of the nb allele is associated with a truncated erythrocyte ankyrin

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2910610

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2910610

Complete deficiency of glycophorin A in red blood cells from mice with targeted inactivation of the band 3 (AE1) gene

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2910610

A band 3-based macrocomplex of integral and peripheral proteins in the RBC membrane

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2910610

Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrin

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20339087

12 December 2020

inferred from PubMed ID database lookup

Red Cell Membranes of Ankyrin-Deficient nb/nb Mice Lack Band 3 Tetramers but Contain Normal Membrane Skeletons

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20339087

12 December 2020

inferred from PubMed ID database lookup

Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20339087

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1182/BLOOD-2010-02-264127

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30 July 2017

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30 July 2017

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