Ji Z - Search Results

1

A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review.

Sha Y, Zheng L, Ji Z, Mei L, Ding L, Lin S, Wang X, Yang X, Li P. Sha Y, et al. Among authors: ji z. BMC Med Genet. 2018 Apr 16;19(1):63. doi: 10.1186/s12881-018-0570-4. BMC Med Genet. 2018. PMID: 29661171 Free PMC article. Review.

2

Genetic factors contributing to human primary ciliary dyskinesia and male infertility.

Ji ZY, Sha YW, Ding L, Li P. Ji ZY, et al. Asian J Androl. 2017 Sep-Oct;19(5):515-520. doi: 10.4103/1008-682X.181227. Asian J Androl. 2017. PMID: 27270341 Free PMC article. Review.

3

A successful pregnancy by intracytoplasmic sperm injection using ejaculate sperm from an infertile man with 46, XX/46, XY true hermaphrodite.

Sha YW, Sha YK, Ding L, Lin SB, Ji ZY, Wang X, Song YQ, Li P. Sha YW, et al. Asian J Androl. 2017 Nov-Dec;19(6):721-722. doi: 10.4103/1008-682X.190329. Asian J Androl. 2017. PMID: 27905326 Free PMC article. No abstract available.

4

Diagnosis of a Chinese man with 45,X/46,X,i(Y)(q10)/47,X,i(Y) (q10) ×2 mosaic Turner syndrome.

Sha YW, Ding L, Ji ZY, Ge YS, Kong H, Zhang Q, Zhou YL, Li P. Sha YW, et al. Asian J Androl. 2018 Mar-Apr;20(2):205-207. doi: 10.4103/1008-682X.193162. Asian J Androl. 2018. PMID: 28091398 Free PMC article. No abstract available.

5

Comprehensive Genome Profiling of Single Sperm Cells by Multiple Annealing and Looping-Based Amplification Cycles and Next-Generation Sequencing from Carriers of Robertsonian Translocation.

Sha Y, Sha Y, Ji Z, Ding L, Zhang Q, Ouyang H, Lin S, Wang X, Shao L, Shi C, Li P, Song Y. Sha Y, et al. Among authors: ji z. Ann Hum Genet. 2017 Mar;81(2):91-97. doi: 10.1111/ahg.12187. Ann Hum Genet. 2017. PMID: 28205220

6

Globozoospermic infertility associated with balanced DPY19L2 translocation/gene deletion at the chromosomal breakpoint.

Sha YW, Mei LB, Zheng LK, Tian RH, Ding L, Ji ZY, Zhang Q, Li P. Sha YW, et al. Asian J Androl. 2018 Mar-Apr;20(2):210-211. doi: 10.4103/1008-682X.196314. Asian J Androl. 2018. PMID: 28272055 Free PMC article. No abstract available.

7

DNAH1 gene mutations and their potential association with dysplasia of the sperm fibrous sheath and infertility in the Han Chinese population.

Sha Y, Yang X, Mei L, Ji Z, Wang X, Ding L, Li P, Yang S. Sha Y, et al. Among authors: ji z. Fertil Steril. 2017 Jun;107(6):1312-1318.e2. doi: 10.1016/j.fertnstert.2017.04.007. Fertil Steril. 2017. PMID: 28577616 Free article.

8

A novel mutation in HAUS7 results in severe oligozoospermia in two brothers.

Li L, Sha YW, Su ZY, Mei LB, Ji ZY, Zhang Q, Lin SB, Wang X, Qiu PP, Li P, Yin C. Li L, et al. Gene. 2018 Jan 10;639:106-110. doi: 10.1016/j.gene.2017.10.014. Epub 2017 Oct 7. Gene. 2018. PMID: 29017965

9

[Familial fragile X syndrome: A pedigree analysis].

Sha YW, Ding L, Ji ZY, Mei LB, Li P, Li Z. Sha YW, et al. Among authors: ji zy. Zhonghua Nan Ke Xue. 2016 Sep;22(9):797-804. Zhonghua Nan Ke Xue. 2016. PMID: 29071876 Chinese.

10

Novel Mutations in CFAP44 and CFAP43 Cause Multiple Morphological Abnormalities of the Sperm Flagella (MMAF).

Sha YW, Wang X, Xu X, Su ZY, Cui Y, Mei LB, Huang XJ, Chen J, He XM, Ji ZY, Bao H, Yang X, Li P, Li L. Sha YW, et al. Reprod Sci. 2019 Jan;26(1):26-34. doi: 10.1177/1933719117749756. Epub 2017 Dec 25. Reprod Sci. 2019. PMID: 29277146

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