Qu X - Search Results

1

[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: qu x. 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.

2

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: qu x. 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.

3

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. Among authors: qu x. Reprod Sci. 2022 Feb;29(2):475-479. doi: 10.1007/s43032-021-00672-6. Epub 2021 Jul 6. Reprod Sci. 2022. PMID: 34231177

4

[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: qu xw. 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.

5

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. Sci Rep. 2023 Jan 5;13(1):64. doi: 10.1038/s41598-022-26384-8. Sci Rep. 2023. PMID: 36604502 Free PMC article.

6

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: qu x. 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.

7

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: qu x. Mol Genet Genomic Med. 2024 Jan;12(1):e2364. doi: 10.1002/mgg3.2364. Mol Genet Genomic Med. 2024. PMID: 38284450 Free PMC article.

8

[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: qu x. 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.

9

Correlation study between the polymorphism of repetitive sequence in gene CAG of androgen receptor and the occurrence and progression of prostate cancer.

Zhai XL, Qu XW, Guo L, Ha QH. Zhai XL, et al. Asian Pac J Trop Med. 2014 Apr;7(4):301-4. doi: 10.1016/S1995-7645(14)60043-2. Asian Pac J Trop Med. 2014. PMID: 24507681 Free article.

10

An Efficient and Flexible Bifunctional Dual-Band Electrochromic Device Integrating with Energy Storage.

Huang Z, Peng Y, Zhao J, Zhang S, Qi P, Qu X, Yan F, Ding B, Xuan Y, Zhang X. Huang Z, et al. Among authors: qu x. Nanomicro Lett. 2024 Dec 27;17(1):98. doi: 10.1007/s40820-024-01604-0. Nanomicro Lett. 2024. PMID: 39729147

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