[Detection of pathogenic gene mutations in thirteen cases of congenital bilateral absence of vas deferens infertility patients]. [PDF]
Tang Y, Zhang Y, Wu D, Lin Y, Lan F.
europepmc +1 more source
[Type of CEBPA mutations in acute myeloid leukemia and their effect on prognosis]. [PDF]
Mao YY +6 more
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Gene mutations in children with permanent congenital hypothyroidism in Yunnan, China. [PDF]
Gong Y +7 more
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摘 要 应用受体的放射配基结合分析(RBA)和多聚酶链反应-单链构象多态分析(PCR-S SCP)技术对未 经治疗的16 例前列腺癌和23 例前列腺增生症组织中雄激素受体的表达水平和雄激素受体基因第8 外显子突 变情况作检测。结果显示, 前列腺癌中雄激素受体的平均水平明显高于前列腺增生症, 在2 例前列腺癌和1 例 前列腺增生症标本中检出雄激素受体基因第8 外显子突变, 前列腺癌中雄激素受体的表达水平与雄素受体基 因突变和前列腺癌临床分期具有相关性。结果表明,在前列腺癌中雄激素受体有过量表达 ...
doaj
Early-onset Parkinson's disease with mutations in both the PRKN gene and the APOB gene: A case report. [PDF]
Bing S, Yi X, Tang X.
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[Analysis of the association between pre- and post-treatment genetic mutation status and treatment efficacy and survival in patients with newly diagnosed myelodysplastic syndromes with excess blasts receiving hypomethylating agent therapy]. [PDF]
Zhong T +8 more
europepmc +1 more source
基因<italic>nif</italic>A产物对肺炎克氏杆菌(<italic>Klebsiella pneumoniae</italic>)<italic>gln</italic>突变型的<italic>Nif</italic><sup>-</sup>表型的校正和固氮酶的组成型合成的作用 [PDF]
丽雯 王 +4 more
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