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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Whole exome sequencing in families with CLL detects a variant in Integrin beta 2 associated with disease susceptibility

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Whole exome sequencing in families with CLL detects a variant in Integrin beta 2 associated with disease susceptibility

机译：具有CLL的家庭的全外显子组测序检测到整合素β2的变异与疾病易感性相关

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《Blood: The Journal of the American Society of Hematology》 |2016年第18期|共3页
作者
Goldin Lynn R.; McMaster Mary L.; Rotunno Melissa; Herman Sarah E. M.; Jones Kristine; Zhu Bin; Boland Joseph; Burdett Laurie; Hicks Belynda; Ravichandran Sarangan; Luke Brian T.; Yeager Meredith; Fontaine Laura; Goldstein Alisa M.; Chanock Stephen J.; Tucker Margaret A.; Wiestner Adrian; Marti Gerald; Caporaso Neil E.;
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1. Whole exome sequencing in families with CLL detects a variant in Integrin beta 2 associated with disease susceptibility [J] . Goldin Lynn R., McMaster Mary L., Rotunno Melissa, Blood: The Journal of the American Society of Hematology . 2016,第18期

机译：在具有CLL的家庭中的整个外壳测序检测到与疾病易感性相关的整联蛋白β2中的变体
2. Whole exome sequencing in high-risk chronic lymphocytic leukemia families: do rare germline variants in somatically altered genes or GWAS genes contribute to susceptibility? [J] . Goldin Lynn R., Rotunno Melissa, McMaster Mary L., Genetic epidemiology. . 2015,第7期

机译：高危慢性淋巴细胞性白血病家族中的全外显子组测序：体细胞改变的基因或GWAS基因中罕见的种系变异是否易感？
3. Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorder [J] . Cristiana Cruceanu, Amirthagowri Ambalavanan, Dan Spiegelman, Genome . 2013,第10期

机译：基于家庭的外显子组测序方法可确定锂反应性双相情感障碍的罕见易感性变异
4. Homozygosity Mapping using Whole-Exome Sequencing: A Valuable Approach for Pathogenic Variant Identification in Genetic Diseases [C] . Jorge Oliveira, Rute Pereira, Rosario Santos, International Conference on Bioinformatics Models, Methods and Algorithms . 2017

机译：纯合子映射使用全exome测序：一种有价值的遗传疾病致病变异鉴定的方法
5. Statistical Analysis of Genetic Sequence Variants in Whole Exome Sequencing Data from Patients with Prostate Cancer [D] . Ofori-Minta, Kelvin. 2021

机译：从前列腺癌患者的整个外壳测序数据中遗传序列变异的统计分析
6. Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility [O] . Lynn R. Goldin, Mary L. McMaster, Melissa Rotunno, -1

机译：具有CLL的家庭的全外显子组测序检测到与疾病易感性相关的整合素β2变异
7. Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorder [O] . Cristiana Cruceanu, Amirthagowri Ambalavanan, Dan Spiegelman, 2013

机译：基于家族的EXMES测序方法识别锂响应双相障碍的罕见易感性变体

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