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A Simple Method of Blood Collection to Detect Mutational Changes BTK Gene Analysis in Vietnamese Children With XLA X-Linked Agammaglobulinemia

机译：一种简单的血液收集方法，以检测越南儿童越南儿童的突变变化BTK基因分析 X-Linked Agammaglobobulinemia

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Anh V.T. Nguyen; Le Thi Minh Huong; Gesmar Segundo; Roger Kobayashi; Nguyen Thi Van Anh; Nguyen Ngoc Quynh Le; Thuc Thanh Huyen; Le Thanh Hai; Troy R. Torgerson; Hans D. Ochs;
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专利

1. X-LINKED AGAMMAGLOBULINEMIA (XLA) DIAGNOSED IN VIETNAMESE TEENAGER WHO PRESENTED WITH GASTROINTESTINAL DISEASE AND FOUND TO HAVE A NOVEL BRUTON'S TYROSINE KINASE (BTK) GENE MUTATION [J] . Rubin Tamar N., Dokmeci Elif Journal of Clinical Immunology . 2017,第2期

机译：诊断出患有胃肠疾病的越南少年诊断的X-Linked Agammaglobulinemia（XLA）发现具有新的Bruton的酪氨酸激酶（BTK）基因突变
2. Mutation screening of the BTK gene in 56 families with X-linked agammaglobulinemia (XLA): 47 unique mutations without correlation to clinical course. [J] . Holinski-Feder E, Weiss M, Brandau O, Pediatrics: Official Publication of the American Academy of Pediatrics . 1998,第2期

机译：X连锁无球蛋白血症（XLA）的56个家庭中BTK基因的突变筛选：47个独特的突变，与临床病程无关。
3. Clinical characteristics and prenatal diagnosis for 22 families in Henan Province of China with X-linked agammaglobulinemia (XLA) related to Bruton’s tyrosine kinase (BTK) gene mutations [J] . Shanshan Gao, Shuang Hu, Huikun Duan, BMC Medical Genetics . 2020,第1期

机译：中国河南省22家家族临床特征及产前诊断与X-Conneded Agammaglobulinemia（XLA）与Bruton的酪氨酸激酶（BTK）基因突变有关
4. HPLC-ESI-MS/MS analysis of hemoglobin peptides in tryptic digests of dried-blood spot extracts detects HbS, HbC, HbD, HbE, HbO-Arab, and HbG-Philadelphia mutations [C] . Christopher A. Haynes, Stephanie Guerra, Jessalyn Fontana, American Society for Mass Spectrometry Conference on Mass Spectrometry and Allied Topics . 2013

机译：HPLC-ESI-MS / MS分析干血斑提取物中的胰蛋白酶杂草肽中的血红蛋白肽检测HBS，HBC，HBD，HBE，HBO-Arab和HBG-Fhildelphia突变
5. Correction of Btk deficiency in murine models of X-linked agammaglobulinemia by retroviral mediated gene therapy. [D] . Yu, Phyllis W. 2004

机译：通过逆转录病毒介导的基因疗法纠正X连锁的丙种球蛋白血症小鼠模型中Btk缺乏症。
6. Clinical characteristics and prenatal diagnosis for 22 families in Henan Province of China with X-linked agammaglobulinemia (XLA) related to Bruton’s tyrosine kinase (BTK) gene mutations [O] . Shanshan Gao, Shuang Hu, Huikun Duan, 2020

机译：中国河南省22家家族临床特征及产前诊断与X-Conneded Agammaglobulinemia（XLA）与Bruton的酪氨酸激酶（BTK）基因突变有关
7. Analysis of Btk mutations in patients with X-linked agammaglobulinaemia (XLA) and determination of carrier status in normal female relatives: a nationwide study of Btk deficiency in Greece [O] . Speletas M, Kanariou M, Kanakoudi-Tsakalidou F, 2001

机译：分析X连锁性丙种球蛋白血症（XLa）患者的Btk突变和正常女性亲属的携带者状态测定：希腊Btk缺乏的全国性研究

A Simple Method of Blood Collection to Detect Mutational Changes BTK Gene Analysis in Vietnamese Children With XLA X-Linked Agammaglobulinemia

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