Acquired haemoglobin H disease. - Test2 - elhamkhani - TriplyDB

Acquired haemoglobin H disease.

Acquired haemoglobin H disease.

http://www.wikidata.org/entity/Q36307579

about

Hemoglobin H disease in Muscat, Oman - A 5 year study

P2860

Q35765429-A039EF63-43C2-4677-B723-6B5A13D194F2

P2860

Acquired haemoglobin H disease.

http://www.wikidata.org/entity/Q36307579

description

2005 nî lūn-bûn

@nan

2005年の論文

@ja

2005年学术文章

@wuu

2005年学术文章

@zh-cn

2005年学术文章

@zh-hans

2005年学术文章

@zh-my

2005年学术文章

@zh-sg

2005年學術文章

@yue

2005年學術文章

@zh

2005年學術文章

@zh-hant

name

Acquired haemoglobin H disease.

@ast

Acquired haemoglobin H disease.

@en

type

label

Acquired haemoglobin H disease.

@ast

Acquired haemoglobin H disease.

@en

prefLabel

Acquired haemoglobin H disease.

@ast

Acquired haemoglobin H disease.

@en

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Q36307579-B57DFF6A-B567-4007-8E9F-C1F35A5CF43F

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P2860

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Q36307579-60591877-8F51-4E99-AD69-906118984E7A

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Q36307579-6F9FB175-6BE7-47B3-8213-CD0D12A447C4

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Q36307579-104D45BC-C8D4-4D82-8F50-5F9D881A05ED

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Q36307579-595D21DF-BC95-450C-9A02-7202D1732764

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Q36307579-DA9A9B5D-DD9C-44BD-A99F-BDC206B3DBB6

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Q36307579-D3A01FFE-9595-4EEF-A907-1114F382C703

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10245330500141689

P1433

P1476

Acquired haemoglobin H disease.

@en

P2093

Nazeer A Alli

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

P2860

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)

The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies

Increased alpha:non-alpha globin chain synthesis ratios in myelodysplastic syndromes and myeloid leukaemia

Molecular-clinical spectrum of the ATR-X syndrome.

S1 nuclease analysis of alpha-globin gene expression in preleukemic patients with acquired hemoglobin H disease after transfer to mouse erythroleukemia cells.

Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes.

Acquired alpha-thalassemia in preleukemia is due to decreased expression of all four alpha-globin genes.

Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations.

Negro alpha-thalassaemia is caused by deletion of a single alpha-globin gene.

Hemoglobin Constant Spring, and unusual alpha-chain variant involved in the etiology of hemoglobin H disease.

P304

413-418

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

P31

scholarly article

P356

10.1080/10245330500141689

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P433

5

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

P478

10

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

P577

2005-10-01T00:00:00Z

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

P698

16273735

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