Associated Papers
Apocrine carcinoma of the breast: distinctive metabolic reprogramming and high-frequency PIK3CA mutations revealed by molecular and immunohistochemical analysis.
Nakamura H et al.
Histopathology, 2025
Summarizing the human genes and their variants causative of non-obstructive azoospermia uncovered using whole genome/exome sequencing.
Ibrahim R et al.
Reproductive Biology, 2025
Implication of androgen receptor gene dysfunction in human Müllerian duct anomalies.
Li L et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology, 2024
Comprehensive germline and somatic genomic profiles of Chinese patients with biliary tract cancer.
Yu H et al.
Frontiers in Oncology, 2022
36072793 (PubMed )
Supplement: Table_2.xlsx › germline_alterations
Germline and somatic variants in ovarian carcinoma: A next-generation sequencing (NGS) analysis.
Andrikopoulou A et al.
Frontiers in Oncology, 2022
Structural analysis of the impact of a novel androgen receptor gene mutation in two adult patients with mild androgen insensitivity syndrome.
Hage M et al.
Andrologia, 2021
Androgen receptor gene mutations are associated with male infertility in Northeast China: Clinical features and identification of two novel mutations.
Li L et al.
Andrologia, 2019
Identification of mutations in patients with acquired pure red cell aplasia.
Zhang X et al.
Acta Biochimica Et Biophysica Sinica, 2018
AR mutations in 28 patients with androgen insensitivity syndrome (Prader grade 0-3).
Wang Y et al.
Science China. Life Sciences, 2017
Next-generation sequencing reveals somatic mutations that confer exceptional response to everolimus.
Lim SM et al.
Oncotarget, 2016
26859683 (PubMed )
Supplement: oncotarget-07-10547-s002.pdf
Molecular basis of non-syndromic hypospadias: systematic mutation screening and genome-wide copy-number analysis of 62 patients.
Kon M et al.
Human Reproduction (oxford, England), 2015
Select a paper to view details