Peripheral marginalisation of endoplasmic reticulum membranes in cultured erythroblasts of congenital dyserythropoietic anaemia type II.

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CD44 as a potential screening marker for preliminary differentiation between congenital dyserythropoietic anemia type II and hereditary spherocytosis.

P2860

Q48762756-97C30608-C9A5-45F6-81D0-7C395EB022BB

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Peripheral marginalisation of endoplasmic reticulum membranes in cultured erythroblasts of congenital dyserythropoietic anaemia type II.

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http://www.wikidata.org/entity/Q50427902

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2016 nî lūn-bûn

@nan

2016年の論文

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2016年学术文章

@wuu

2016年学术文章

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2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

@zh-hant

name

Peripheral marginalisation of ...... rythropoietic anaemia type II.

@en

Peripheral marginalisation of ...... rythropoietic anaemia type II.

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type

Item

label

Peripheral marginalisation of ...... rythropoietic anaemia type II.

@en

Peripheral marginalisation of ...... rythropoietic anaemia type II.

@nl

prefLabel

Peripheral marginalisation of ...... rythropoietic anaemia type II.

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Peripheral marginalisation of ...... rythropoietic anaemia type II.

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P1476

Peripheral marginalisation of ...... rythropoietic anaemia type II.

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P2093

C A Green

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D J P Ferguson

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M-J King

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P2860

Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts

Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship.

Maturing reticulocytes internalize plasma membrane in glycophorin A-containing vesicles that fuse with autophagosomes before exocytosis.

Characteristic phenotypes associated with congenital dyserythropoietic anemia (type II) manifest at different stages of erythropoiesis

Transcriptional divergence and conservation of human and mouse erythropoiesis.

Morphological Abnormalities in cultured erythroid colonies (BFU-E) from the blood of two patients with HEMPAS.

Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.

Homozygosity mapping reveals founder SEC23B-Y462C mutations in Indian congenital dyserythropoietic anemia type II.

Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B gene.

Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: definition of clinical and molecular spectrum and identification of new diagnostic scores.

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649-651

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scholarly article

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10.1136/JCLINPATH-2016-203611

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English

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

P478

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

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Momin R Ahmed

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2016-03-23T00:00:00Z

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27010435

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P921

endoplasmic reticulum

Peripheral marginalisation of endoplasmic reticulum membranes in cultured erythroblasts of congenital dyserythropoietic anaemia type II.

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P2860

P2860

Peripheral marginalisation of endoplasmic reticulum membranes in cultured erythroblasts of congenital dyserythropoietic anaemia type II.

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P1476

P2093

P2860

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P356

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P577

P698

P921

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P1476

P2093

P2860

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P50

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