Cytogenetic abnormalities and their lack of relationship to the Asp816Val c-kit mutation in the pathogenesis of mastocytosis

被引：17

作者：

Worobec, AS ^{[1
]}

Akin, C ^{[1
]}

Scott, LM ^{[1
]}

Metcalfe, DD ^{[1
]}

机构：

[1] NIAID, Lab Allerg Dis, NIH, Bethesda, MD 20892 USA

来源：

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY | 1998年 / 102卷 / 03期

关键词：

D O I：

10.1016/S0091-6749(98)70144-7

中图分类号：

R392 [医学免疫学];

学科分类号：

100102 ;

摘要：

[No abstract available]

引用

页码：523 / 524

页数：2

共 5 条

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[2] IDENTIFICATION OF A POINT MUTATION IN THE CATALYTIC DOMAIN OF THE PROTOONCOGENE C-KIT IN PERIPHERAL-BLOOD MONONUCLEAR-CELLS OF PATIENTS WHO HAVE MASTOCYTOSIS WITH AN ASSOCIATED HEMATOLOGIC DISORDER [J].

NAGATA, H ;

WOROBEC, AS ;

OH, CK ;

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METCALFE, DD .

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[3]

SWOLIN B, 1987, BLOOD, V70, P1928

[4] The protooncogene c-kit and c-kit ligand in human disease [J].

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[5]

WOROBEC AC, IN PRESS CANCER

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