Niu Y - Search Results

1

Corrigendum to "SEMA4D acts as a novel oligogenic pathogenic gene of idiopathic hypogonadotropic hypogonadism through the PlexinB1/MET/RND1/RHOA/RAF1/MAPK signaling axis" [Genes & Diseases 10 (2023) 65-68].

Wang D, Niu Y, Tan J, Wang J, Ling L, Chen Y, Gong J, Xu H, Ling Q, Liu J, Liu J. Wang D, et al. Among authors: niu y. Genes Dis. 2024 Mar 22;11(4):101273. doi: 10.1016/j.gendis.2024.101273. eCollection 2024 Jul. Genes Dis. 2024. PMID: 38742143 Free PMC article.

2

Novel FGFR1 and KISS1R Mutations in Chinese Kallmann Syndrome Males with Cleft Lip/Palate.

Xu H, Niu Y, Wang T, Liu S, Xu H, Wang S, Liu J, Ye Z. Xu H, et al. Among authors: niu y. Biomed Res Int. 2015;2015:649698. doi: 10.1155/2015/649698. Epub 2015 Jun 25. Biomed Res Int. 2015. PMID: 26199944 Free PMC article.

3

Testosterone improves erectile function through inhibition of reactive oxygen species generation in castrated rats.

Li R, Meng X, Zhang Y, Wang T, Yang J, Niu Y, Cui K, Wang S, Liu J, Rao K. Li R, et al. Among authors: niu y. PeerJ. 2016 May 3;4:e2000. doi: 10.7717/peerj.2000. eCollection 2016. PeerJ. 2016. PMID: 27168996 Free PMC article.

4

Novel interstitial deletion in Xp22.3 in a typical X-linked recessive family with Kallmann syndrome.

Niu Y, Zhou C, Xu H, Wang D, Chen Y, Li Z, Wang T, Pokhrel G, Wang DW, Liu J. Niu Y, et al. Andrologia. 2018 Feb 14. doi: 10.1111/and.12961. Online ahead of print. Andrologia. 2018. PMID: 29441621

5

Effect of adjuvant drug therapy after varicocelectomy on fertility outcome in males with varicocele-associated infertility: Systematic review and meta-analysis.

Chen YW, Niu YH, Wang DQ, Li H, Pokhrel G, Xu H, Wang T, Wang SG, Liu JH. Chen YW, et al. Andrologia. 2018 Oct;50(8):e13070. doi: 10.1111/and.13070. Epub 2018 Jul 11. Andrologia. 2018. PMID: 29993131

6

Comparison of clinical outcome of bilateral and unilateral varicocelectomy in infertile males with left clinical and right subclinical varicocele: A meta-analysis of randomised controlled trials.

Niu Y, Wang D, Chen Y, Pokhrel G, Xu H, Wang T, Wang S, Liu J. Niu Y, et al. Andrologia. 2018 Nov;50(9):e13078. doi: 10.1111/and.13078. Epub 2018 Jul 19. Andrologia. 2018. PMID: 30024042

7

Mutation profiles and clinical characteristics of Chinese males with isolated hypogonadotropic hypogonadism.

Zhou C, Niu Y, Xu H, Li Z, Wang T, Yang W, Wang S, Wang DW, Liu J. Zhou C, et al. Among authors: niu y. Fertil Steril. 2018 Aug;110(3):486-495.e5. doi: 10.1016/j.fertnstert.2018.04.010. Fertil Steril. 2018. PMID: 30098700 Free article.

8

Testosterone undecanoate supplementation together with human chorionic gonadotropin does not impair spermatogenesis in males with isolated hypogonadotropic hypogonadism: a retrospective study.

Chen YW, Niu YH, Xu H, Wang DQ, Jiang HY, Pokhrel G, Wang T, Wang SG, Liu JH. Chen YW, et al. Asian J Androl. 2019 Jul-Aug;21(4):413-418. doi: 10.4103/aja.aja_107_18. Asian J Androl. 2019. PMID: 30604694 Free PMC article.

9

Correlations Among Genotype and Outcome in Chinese Male Patients With Congenital Hypogonadotropic Hypogonadism Under HCG Treatment.

Chen Y, Sun T, Niu Y, Wang D, Xiong Z, Li C, Liu K, Qiu Y, Sun Y, Gong J, Wang T, Wang S, Xu H, Liu J. Chen Y, et al. Among authors: niu y. J Sex Med. 2020 Apr;17(4):645-657. doi: 10.1016/j.jsxm.2020.01.011. Epub 2020 Mar 12. J Sex Med. 2020. PMID: 32171629

CONCLUSION: Among all P/LP RSVs, P/LP PROKR2 RSVs might correlate with poor responses in CHH under hCG treatment; our study supports the pathogenicity assessment of American College of Medical Genetics and Genomics criteria in genetic counseling, to improve management of patients …

CONCLUSION: Among all P/LP RSVs, P/LP PROKR2 RSVs might correlate with poor responses in CHH under hCG treatment; our study supports the pat …

10

Combined in vitro and in silico analyses of FGFR1 variants: genotype-phenotype study in idiopathic hypogonadotropic hypogonadism.

Wang D, Niu Y, Tan J, Chen Y, Xu H, Ling Q, Gong J, Ling L, Wang J, Wang T, Liu J. Wang D, et al. Among authors: niu y. Clin Genet. 2020 Oct;98(4):341-352. doi: 10.1111/cge.13814. Epub 2020 Aug 16. Clin Genet. 2020. PMID: 32666525

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