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

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Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations.

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

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http://www.wikidata.org/entity/Q48762756

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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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

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2016年學術文章

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2016年學術文章

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name

CD44 as a potential screening ...... and hereditary spherocytosis.

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CD44 as a potential screening ...... and hereditary spherocytosis.

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type

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CD44 as a potential screening ...... and hereditary spherocytosis.

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CD44 as a potential screening ...... and hereditary spherocytosis.

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CD44 as a potential screening ...... and hereditary spherocytosis.

@en

CD44 as a potential screening ...... and hereditary spherocytosis.

@nl

P1476

CD44 as a potential screening ...... and hereditary spherocytosis.

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P2093

A Bomford

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A Guest

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B K Singleton

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C A Green

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F Seeney

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H Heimpel

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L Ranjha

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M-J King

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P Mehta

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R Mushens

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P2860

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

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer

Detection of hereditary pyropoikilocytosis by the eosin-5-maleimide (EMA)-binding test is attributable to a marked reduction in EMA-reactive transmembrane proteins

Advances in the understanding of the congenital dyserythropoietic anaemias.

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.

Congenital dyserythropoietic anemia type II: epidemiology, clinical appearance, and prognosis based on long-term observation.

Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics.

Mutational spectrum in congenital dyserythropoietic anemia type II: identification of 19 novel variants in SEC23B gene.

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

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312-326

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scholarly article

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10.1002/CYTO.B.21488

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Momin R Ahmed

M Wozniak

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2016-10-26T00:00:00Z

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27784127

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

about

P2860

P2860

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

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