Detalhe da pesquisa
1.
Paternal USP26 mutations raise Klinefelter syndrome risk in the offspring of mice and humans.
EMBO J
; 40(13): e106864, 2021 07 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33978233
2.
A Novel Exon Polymorphism of TP53 Associated with Recurrent Pregnancy Loss in a Chinese Han Population.
Clin Lab
; 67(10)2021 Oct 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34655190
3.
Variation analysis of tousled like kinase 1 gene in patients with sporadic premature ovarian insufficiency.
Gynecol Endocrinol
; 36(1): 33-35, 2020 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-31362519
4.
Mutational analysis of IZUMO1R in women with fertilization failure and polyspermy after in vitro fertilization.
J Assist Reprod Genet
; 35(3): 539-544, 2018 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-29243140
5.
Kisspeptin: a new marker for human pre-ovulation.
Gynecol Endocrinol
; 33(7): 560-563, 2017 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-28266227
6.
Variation analysis of EXO1 gene in Chinese patients with premature ovarian failure.
Reprod Biomed Online
; 32(3): 329-33, 2016 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-26774993
7.
Polycystic ovary syndrome susceptibility single nucleotide polymorphisms in women with a single PCOS clinical feature.
Hum Reprod
; 30(3): 732-6, 2015 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-25586784
8.
Activin A promotes human trophoblast invasion by upregulating integrin ß3 via ALK4-SMAD4 signaling.
Placenta
; 129: 62-69, 2022 11.
Artigo
Inglês
| MEDLINE | ID: mdl-36244196
9.
PCOS-GWAS Susceptibility Variants in THADA, INSR, TOX3, and DENND1A Are Associated With Metabolic Syndrome or Insulin Resistance in Women With PCOS.
Front Endocrinol (Lausanne)
; 11: 274, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-32425888
10.
Novel WEE2 gene variants identified in patients with fertilization failure and female infertility.
Fertil Steril
; 111(3): 519-526, 2019 03.
Artigo
Inglês
| MEDLINE | ID: mdl-30827524
11.
ERBB4 Confers Risk for Polycystic Ovary Syndrome in Han Chinese.
Sci Rep
; 7: 42000, 2017 02 14.
Artigo
Inglês
| MEDLINE | ID: mdl-28195137
12.
Novel zona pellucida gene variants identified in patients with oocyte anomalies.
Fertil Steril
; 107(6): 1364-1369, 2017 06.
Artigo
Inglês
| MEDLINE | ID: mdl-28577617
13.
Family-based analysis of eight susceptibility loci in polycystic ovary syndrome.
Sci Rep
; 5: 12619, 2015 Jul 29.
Artigo
Inglês
| MEDLINE | ID: mdl-26220222
14.
Gene therapy of malignant solid tumors by targeting erbB2 receptors and by activating T cells.
Cancer Biother Radiopharm
; 27(10): 711-8, 2012 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-22988969