Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis. - Wikidata - awgldk - TriplyDB

Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.

Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.

http://www.wikidata.org/entity/Q34565862

about

Red cell membrane: past, present, and future Multiple protein 4.1 isoforms produced by alternative splicing in human erythroid cells The membrane skeleton of erythrocytes. A percolation model.Sp alpha V/41: a common spectrin polymorphism at the alpha IV-alpha V domain junction. Relevance to the expression level of hereditary elliptocytosis due to alpha-spectrin variants located in trans Modulation of erythrocyte membrane mechanical stability by 2,3-diphosphoglycerate in the neonatal poikilocytosis/elliptocytosis syndrome.Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis.Shear-response of the spectrin dimer-tetramer equilibrium in the red blood cell membrane.Measurements of three-dimensional refractive index tomography and membrane deformability of live erythrocytes from Pelophylax nigromaculatus.

P2860

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P2860

Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.

http://www.wikidata.org/entity/Q34565862

description

1987 nî lūn-bûn

@nan

1987 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

1987 թվականի մարտին հրատարակված գիտական հոդված

@hy

1987年の論文

@ja

1987年論文

@yue

1987年論文

@zh-hant

1987年論文

@zh-hk

1987年論文

@zh-mo

1987年論文

@zh-tw

1987年论文

@wuu

name

Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.

@ast

Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.

@en

Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.

@nl

type

label

Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.

@ast

Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.

@en

Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.

@nl

prefLabel

Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.

@ast

Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.

@en

Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.

@nl

P1433

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P1476

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P2093

Q34565862-2CA0ED5F-6178-48AD-84F7-712E386A3579

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P2860

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P304

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P31

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P356

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P407

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P433

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P478

Q34565862-2DCB038D-4C96-4FC3-A233-625A8171968D

P577

Q34565862-FFE98CF5-3918-4C85-AE06-F8E57BDC47D7

P5875

Q34565862-F51DE611-1689-45A5-96CB-8B59C52D31E1

P698

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P932

Q34565862-0A5CFB58-704C-47B4-91E4-4389AAEE560A

P356

P1433

Journal of Clinical Investigation

P1476

Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.

@en

P2093

N Mohandas

http://www.w3.org/2001/XMLSchema#string

P A Lane

http://www.w3.org/2001/XMLSchema#string

R L Shew

http://www.w3.org/2001/XMLSchema#string

T A Iarocci

http://www.w3.org/2001/XMLSchema#string

T Hays

http://www.w3.org/2001/XMLSchema#string

W C Mentzer

http://www.w3.org/2001/XMLSchema#string

P2860

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

High resolution two-dimensional electrophoresis of proteins

Cleavage of structural proteins during the assembly of the head of bacteriophage T4

"Western blotting": electrophoretic transfer of proteins from sodium dodecyl sulfate--polyacrylamide gels to unmodified nitrocellulose and radiographic detection with antibody and radioiodinated protein A

A genetic defect in the binding of protein 4.1 to spectrin in a kindred with hereditary spherocytosis

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

Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane

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

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

Defective spectrin dimer-dimer association with hereditary elliptocytosis

P304

989-996

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1172/JCI112911

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P407

P433

3

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P478

79

http://www.w3.org/2001/XMLSchema#string

P577

1987-03-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

19342895

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P698

3818958

http://www.w3.org/2001/XMLSchema#string

P932

424257

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