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Alexandra M. Lopes

i3s
H指数:22
被引数:1,730

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A genetic variant in the 3′-UTR of PIWIL4 confers risk for extreme phenotypes of male infertility by altering miR-215 and miR-136 binding affinity

<i>PIWIL4</i>基因3′-UTR区域的一个遗传变异通过改变miR-215和miR-136的结合亲和力,增加了男性不育极端表型的风险。

2025-06-110
OAAI
Predicting testicular sperm extraction outcomes in non-obstructive azoospermic patients using machine learning and non-invasive biomarker detection

利用机器学习和无创生物标志物检测预测非梗阻性无精子症患者的睾丸精子提取结局

2025-06-010
OA
Diminished DNA binding affinity of DMRT1 caused by heterozygous DM domain mutations is a cause of male infertility

由杂合DM结构域突变引起的DMRT1的DNA结合亲和力降低是男性不育的原因

2025-01-080
PRE
A comprehensive study of common and rare genetic variants in spermatogenesis-related loci identifies new risk factors for idiopathic severe spermatogenic failure
2024-11-130
OAAI
Diverse monogenic subforms of human spermatogenic failure

人类生精失败的多种单基因亚形式

2022-12-2633
OAAI
Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility
2022-11-106
OAAI
Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort
2021-04-2012
OAAI
Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic men
2020-12-01101
OAAI
Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility
2020-08-0164
OAAI