Xia Y - Search Results

1

A novel mutation in PCD-associated gene DNAAF3 causes male infertility due to asthenozoospermia.

Wan F, Yu L, Qu X, Xia Y, Feng K, Zhang L, Zhang N, Zhao G, Zhang C, Guo H. Wan F, et al. Among authors: xia y. J Cell Mol Med. 2023 Oct;27(20):3107-3116. doi: 10.1111/jcmm.17881. Epub 2023 Aug 3. J Cell Mol Med. 2023. PMID: 37537752 Free PMC article.

2

Overexpression of long non-coding RNA H19 promotes invasion and autophagy via the PI3K/AKT/mTOR pathways in trophoblast cells.

Xu J, Xia Y, Zhang H, Guo H, Feng K, Zhang C. Xu J, et al. Among authors: xia y. Biomed Pharmacother. 2018 May;101:691-697. doi: 10.1016/j.biopha.2018.02.134. Epub 2018 Mar 22. Biomed Pharmacother. 2018. PMID: 29522949

3

Surface Engineering of Metal-Organic Framework as pH-/NIR-Responsive Nanocarrier for Imaging-Guided Chemo-Photothermal Therapy.

Guo H, Xia Y, Feng K, Qu X, Zhang C, Wan F. Guo H, et al. Among authors: xia y. Int J Nanomedicine. 2020 May 7;15:3235-3250. doi: 10.2147/IJN.S239910. eCollection 2020. Int J Nanomedicine. 2020. PMID: 32440121 Free PMC article.

4

[Sperm-hyaluronan binding assay in in vitro fertilization and embryo transfer].

Qu XW, Xia S, Feng K, Xia YQ, Wan F, Zhang CL, Guo HB. Qu XW, et al. Zhonghua Nan Ke Xue. 2020 Sep;26(9):803-806. Zhonghua Nan Ke Xue. 2020. PMID: 33377703 Chinese.

5

A Novel Noncanonical Splicing Mutation of ANOS1 Gene in Siblings with Kallmann Syndrome Identified by Whole-Exome Sequencing.

Xia Y, Guo H, Ge H, Feng K, Qu X, Wan F, Zhang C, Yang J. Xia Y, et al. Reprod Sci. 2022 Feb;29(2):475-479. doi: 10.1007/s43032-021-00672-6. Epub 2021 Jul 6. Reprod Sci. 2022. PMID: 34231177

6

[Genetic analysis of three cases of acephalic spermatozoa syndrome caused by SUN5 mutation and the outcome of assisted reproductive technology].

Feng K, Ni JJ, Xia YQ, Qu XW, Zhang HJ, Wan F, Hong K, Zhang CL, Guo HB. Feng K, et al. Among authors: xia yq. Beijing Da Xue Xue Bao Yi Xue Ban. 2021 Aug 18;53(4):803-807. doi: 10.19723/j.issn.1671-167X.2021.04.031. Beijing Da Xue Xue Bao Yi Xue Ban. 2021. PMID: 34393249 Free PMC article. Chinese.

7

[Analysis of DNAH1 gene variant in two infertile males with multiple morphological abnormalities of sperm flagella].

Feng K, Wan F, Xia Y, Yang K, Qu X, Xia S, Guo H, Zhang C, Wu D. Feng K, et al. Among authors: xia y, xia s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Sep 10;38(9):849-852. doi: 10.3760/cma.j.cn511374-20200424-00302. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34487528 Chinese.

8

Correlation between CFTR variants and outcomes of ART in patients with CAVD in Central China.

Qu X, Li L, Cui C, Feng K, Xia Y, Wan F, Zhang C, Guo H. Qu X, et al. Among authors: xia y. Sci Rep. 2023 Jan 5;13(1):64. doi: 10.1038/s41598-022-26384-8. Sci Rep. 2023. PMID: 36604502 Free PMC article.

9

Compound heterozygous mutations in CFTR causing congenital bilateral absence of the vas deferens in a Chinese pedigree.

Li L, Qu X, Cui C, Feng K, Xia Y, Wan F, Ge H, Fang Y, Zhang C, Guo H. Li L, et al. Among authors: xia y. Mol Genet Genomic Med. 2024 Jan;12(1):e2364. doi: 10.1002/mgg3.2364. Mol Genet Genomic Med. 2024. PMID: 38284450 Free PMC article.

10

[Clinical characteristics and genetic analysis of a patient with Acephalic spermatozoa syndrome due to variant of PMFBP1 gene].

Feng K, Xia Y, Qu X, Wan F, Yang K, Xu J, Zhang C, Guo H. Feng K, et al. Among authors: xia y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024 Jun 10;41(6):749-752. doi: 10.3760/cma.j.cn511374-20220323-00199. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024. PMID: 38818563 Chinese.

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