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未突变慢性淋巴细胞白血病中允许存在多少免疫球蛋白可变区重链突变的测定——对不同突变百分比患者的长期随访

Determination of how many immunoglobulin variable region heavy chain mutations are allowable in unmutated chronic lymphocytic leukaemia - long-term follow up of patients with different percentages of mutations.

作者信息

Hamblin Terry J, Davis Zadie A, Oscier David G

机构信息

Department of Haematology, Royal Bournemouth Hospital, Bournemouth, UK.

出版信息

Br J Haematol. 2008 Feb;140(3):320-3. doi: 10.1111/j.1365-2141.2007.06928.x. Epub 2007 Dec 5.

Abstract

The choice of 98% sequence homology for immunoglobulin heavy chains to distinguish between mutated and unmutated versions of chronic lymphocytic leukaemia (CLL) was arbitrary and was chosen to account for supposed polymorphisms. Some authors chose 97% or even 95%. This study examined survival curves for cohorts of patients with varying degrees of sequence homology. All patients with <97% homology behaved as if mutated. Those with 97-98% homology were more aggressive than the mutated cases, but less aggressive than those with >98% homology.

摘要

选择98%的免疫球蛋白重链序列同源性来区分慢性淋巴细胞白血病(CLL)的突变型和未突变型是随意的,这样选择是为了考虑假定的多态性。一些作者选择97%甚至95%。本研究检查了具有不同程度序列同源性的患者队列的生存曲线。所有同源性<97%的患者表现得如同是突变型。同源性为97 - 98%的患者比突变型病例侵袭性更强,但比同源性>98%的患者侵袭性弱。

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