Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis

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The molecular basis of disorders of the red cell membrane Imaging of the diffusion of single band 3 molecules on normal and mutant erythrocytes.

P2860

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P2860

Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis

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http://www.wikidata.org/entity/Q35881989

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1996 nî lūn-bûn

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1996年の論文

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1996年論文

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1996年論文

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1996年論文

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1996年論文

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1996年論文

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1996年论文

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1996年论文

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1996年论文

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name

Molecular basis and haplotypin ...... cytosis and pyropoikilocytosis

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Molecular basis and haplotypin ...... cytosis and pyropoikilocytosis

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Molecular basis and haplotypin ...... cytosis and pyropoikilocytosis

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Molecular basis and haplotypin ...... cytosis and pyropoikilocytosis

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Molecular basis and haplotypin ...... cytosis and pyropoikilocytosis

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Molecular basis and haplotypin ...... cytosis and pyropoikilocytosis

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P1476

Molecular basis and haplotypin ...... cytosis and pyropoikilocytosis

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Curtis PJ

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Forget BG

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Gallagher PG

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Kotula L

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Marchesi SL

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

Speicher DW

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

Wang Y

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P2860

A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple he

Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis

The exon-intron organization of the human erythrocyte alpha-spectrin gene

Spectrin genes in health and disease

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

Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis

Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide

Growth of Plasmodium falciparum in human erythrocytes containing abnormal membrane proteins.

Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis.

Identification of proteolytically resistant domains of human erythrocyte spectrin.

P304

351-359

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scholarly article

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English

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1996-08-01T00:00:00Z

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8755921

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P932

1914747

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Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis

about

P2860

P2860

Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P407

P433

P478

P577

P698

P932

P1433

P1476

P2093

P2860

P304

P31

P407

P433

P478

P577

P698

P932