(Q33706340)

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Analysis of novel sph (spherocytosis) alleles in mice reveals allele-specific loss of band 3 and adducin in alpha-spectrin-deficient red cells

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Europe PubMed Central

PubMed publication ID

28 July 2017

Analysis of novel sph (spherocytosis) alleles in mice reveals allele-specific loss of band 3 and adducin in alpha-spectrin-deficient red cells (English)

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Europe PubMed Central

PubMed publication ID

28 July 2017

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Amy J Lambert

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Europe PubMed Central

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28 July 2017

Luanne L Peters

8

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Luanne L Peters

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28 July 2017

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Raymond F Robledo

1

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Europe PubMed Central

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28 July 2017

Connie S Birkenmeier

3

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Europe PubMed Central

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28 July 2017

Marius V Cirlan

4

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Europe PubMed Central

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28 July 2017

Andreea Flavia M Cirlan

5

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28 July 2017

Dean R Campagna

6

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28 July 2017

Samuel E Lux

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28 July 2017

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7 January 2010

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Europe PubMed Central

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28 July 2017

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28 July 2017

115

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28 July 2017

9

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Europe PubMed Central

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28 July 2017

1804-1814

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Europe PubMed Central

PubMed publication ID

28 July 2017

Adducin forms a bridge between the erythrocyte membrane and its cytoskeleton and regulates membrane cohesion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Red cell membrane: past, present, and future

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Targeted deletion of alpha-adducin results in absent beta- and gamma-adducin, compensated hemolytic anemia, and lethal hydrocephalus in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Disorders of red cell membrane

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Tropomyosin modulates erythrocyte membrane stability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Characterization and prediction of alternative splice sites

1 reference

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14 July 2018

Mechanistic links between nonsense-mediated mRNA decay and pre-mRNA splicing in mammalian cells

1 reference

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14 July 2018

Nonsense-mediated mRNA decay in mammals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Reduced pigmentation (rp), a mouse model of Hermansky-Pudlak syndrome, encodes a novel component of the BLOC-1 complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Hereditary elliptocytosis: spectrin and protein 4.1R.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Cappuccino, a mouse model of Hermansky-Pudlak syndrome, encodes a novel protein that is part of the pallidin-muted complex (BLOC-1)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Murine recessive hereditary spherocytosis, sph/sph, is caused by a mutation in the erythroid alpha-spectrin gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Ca2+-independent binding of an EF-hand domain to a novel motif in the alpha-actinin-titin complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Targeted disruption of the beta adducin gene (Add2) causes red blood cell spherocytosis in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Mild spherocytosis and altered red cell ion transport in protein 4. 2-null mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Hematologically important mutations: spectrin and ankyrin variants in hereditary spherocytosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Location of the human red cell spectrin tetramer binding site and detection of a related "closed" hairpin loop dimer using proteolytic footprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

The junctional complex of the membrane skeleton.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 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=2832806

14 July 2018

The C-terminal domain of alpha-spectrin is structurally related to calmodulin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Ank3 (epithelial ankyrin), a widely distributed new member of the ankyrin gene family and the major ankyrin in kidney, is expressed in alternatively spliced forms, including forms that lack the repeat domain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Molecular mechanism of the calcium-induced conformational change in the spectrin EF-hands.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Spectrin deficient inherited hemolytic anemias in the mouse: Characterization by spectrin synthesis and mRNA activity in reticulocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 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=2832806

14 July 2018

The organization of proteins in the human red blood cell membrane. A review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 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=2832806

14 July 2018

Autoimmune syndromes in major histocompatibility complex (MHC) congenic strains of nonobese diabetic (NOD) mice. The NOD MHC is dominant for insulitis and cyclophosphamide-induced diabetes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

Analysis of human red cell spectrin tetramer (head-to-head) assembly using complementary univalent peptides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

14 July 2018

The erythrocyte skeletons of beta-adducin deficient mice have altered levels of tropomyosin, tropomodulin and EcapZ.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

30 October 2018

Eosin-5-maleimide binding to band 3 and Rh-related proteins forms the basis of a screening test for hereditary spherocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

30 October 2018

Role of Ras signaling in erythroid differentiation of mouse fetal liver cells: functional analysis by a flow cytometry-based novel culture system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

30 October 2018

Role of terminal nonhomologous domains in initiation of human red cell spectrin dimerization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2832806

30 October 2018

Mutations in the murine erythroid alpha-spectrin gene alter spectrin mRNA and protein levels and spectrin incorporation into the red blood cell membrane skeleton

1 reference

https://pubmed.ncbi.nlm.nih.gov/20056793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unequal alpha and beta globin mRNA in reticulocytes of normal and mutant f/f fetal mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/20056793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional characterization of human erythrocyte spectrin alpha and beta chains: association with actin and erythrocyte protein 4.1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20056793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fetal compensation of the hemolytic anemia in mice homozygous for the normoblastosis (nb) mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20056793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restriction by ankyrin of band 3 rotational mobility in human erythrocyte membranes and reconstituted lipid vesicles

1 reference

https://pubmed.ncbi.nlm.nih.gov/20056793

12 December 2020

based on heuristic

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

https://pubmed.ncbi.nlm.nih.gov/20056793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hematologically important mutations: ankyrin variants in hereditary spherocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20056793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Initiation of spectrin dimerization involves complementary electrostatic interactions between paired triple-helical bundles

1 reference

https://pubmed.ncbi.nlm.nih.gov/20056793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mild spherocytic hereditary elliptocytosis and altered levels of alpha- and gamma-adducins in beta-adducin-deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/20056793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20056793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1182/BLOOD-2009-07-232199

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

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