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

Worobec AS; Akin C; Scott LM; Metcalfe DD

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

机译：细胞遗传学异常及其与肥大细胞增多症发病机理中Asp816Val c-kit突变的缺乏相关性。

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来源
《The Journal of Allergy and Clinical Immunology》 |1998年第3期|共2页
作者
Worobec AS; Akin C; Scott LM; Metcalfe DD;
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原文格式 PDF
正文语种 eng
中图分类医学免疫学;
关键词
Chromosome Aberrations; Mastocytosis; Point Mutation; Proto Oncogene Protein c kit genetics; 染色体畸变; 肥大细胞增多; 点突变;

机译：Chromosome Aberrations;Mastocytosis;Point Mutation;Proto Oncogene Protein c kit genetics;染色体畸变;肥大细胞增多;点突变;

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专利

1. Cytogenetic abnormalities and their lack of relationship to the Asp816Val c-kit mutation in the pathogenesis of mastocytosis. [J] . Worobec AS, Akin C, Scott LM, The Journal of Allergy and Clinical Immunology . 1998,第3期

机译：细胞遗传学异常及其与肥大细胞增多症发病机理中Asp816Val c-kit突变的缺乏相关性。
2. Expression of the C-kit receptor (CD117) is a feature of almost all subtypes of de novo acute myeloblastic leukemia (AML), including cytogenetically good-risk AML, and lacks prognostic significance. [J] . Schwartz S, Heinecke A, Zimmermann M, Leukemia and lymphoma . 1999,第1a2期

机译：C-kit受体（CD117）的表达是几乎所有新生代急性粒细胞性白血病（AML）的特征，包括细胞遗传学上的高危AML，并且缺乏预后意义。
3. c-kit遺伝子に点突然変異(Asp816Val)を認めた肥満細胞症の3例 [J] . 小沢桂, 菊池智, 折笠玲子, 日本皮膚科学会雑誌 . 2005,第7期

机译：c-kit基因点突变（Asp816 Val）引起的三例肥胖细胞病
4. Review of Pathophysiology on GIST:The Role of Immunohistochemical Staining and c-KIT Mutational Analysis [C] . S. Hirot International Gastric Cancer Congress . 2005

机译：GIST病理生理学述评：免疫组织化学染色和C-kit突变分析的作用
5. The role of c-KIT mutations in tumorigenesis in humans and dogs [D] . Thaiwong, Tuddow 2012

机译：c-KIT突变在人和狗的肿瘤发生中的作用
6. Relationship between gene mutations and protein expressions of PDGFR α and C-kit in gastrointestinal stromal tumors [O] . Jun-Yi He, HX Tong, Y Zhang, 2015

机译：胃肠道间质瘤中PDGFRα和C-kit基因突变与蛋白表达的关系
7. Lack of apparent hematologic abnormalities in human patients with c-kit (stem cell factor receptor) gene mutations letter [O] . RA Spritz 1992

机译：人类C-kit（干细胞因子受体）基因突变缺乏明显的血液管病，基因突变字母

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

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