Shao B - Search Results

1

Loss of SUN1 function in spermatocytes disrupts the attachment of telomeres to the nuclear envelope and contributes to non-obstructive azoospermia in humans.

Meng Q, Shao B, Zhao D, Fu X, Wang J, Li H, Zhou Q, Gao T. Meng Q, et al. Among authors: shao b. Hum Genet. 2023 Apr;142(4):531-541. doi: 10.1007/s00439-022-02515-z. Epub 2023 Mar 18. Hum Genet. 2023. PMID: 36933034

2

Unraveling the proteomic profile of mice testis during the initiation of meiosis.

Shao B, Guo Y, Wang L, Zhou Q, Gao T, Zheng B, Zheng H, Zhou T, Zhou Z, Guo X, Huang X, Sha J. Shao B, et al. J Proteomics. 2015 Apr 29;120:35-43. doi: 10.1016/j.jprot.2015.02.015. Epub 2015 Mar 7. J Proteomics. 2015. PMID: 25753125

3

Somatic Angiotensin I-Converting Enzyme Regulates Self-Renewal of Mouse Spermatogonial Stem Cells Through the Mitogen-Activated Protein Kinase Signaling Pathway.

Gao T, Zhao X, Liu C, Shao B, Zhang X, Li K, Cai J, Wang S, Huang X. Gao T, et al. Among authors: shao b. Stem Cells Dev. 2018 Aug 1;27(15):1021-1032. doi: 10.1089/scd.2017.0287. Epub 2018 Jun 29. Stem Cells Dev. 2018. PMID: 29792376

4

BMI1 promotes steroidogenesis through maintaining redox homeostasis in mouse MLTC-1 and primary Leydig cells.

Gao T, Lin M, Shao B, Zhou Q, Wang Y, Chen X, Zhao D, Dai X, Shen C, Cheng H, Yang S, Li H, Zheng B, Zhong X, Yu J, Chen L, Huang X. Gao T, et al. Among authors: shao b. Cell Cycle. 2020 Aug;19(15):1884-1898. doi: 10.1080/15384101.2020.1779471. Epub 2020 Jun 28. Cell Cycle. 2020. PMID: 32594840 Free PMC article.

5

TRIM59 is required for mouse GC-1 cell maintenance through modulating the ubiquitination of AXIN1.

Wu T, Zhou H, Wang L, Tan J, Gao W, Wu Y, Zhao D, Shen C, Zheng B, Huang X, Shao B. Wu T, et al. Among authors: shao b. Heliyon. 2024 Aug 23;10(17):e36744. doi: 10.1016/j.heliyon.2024.e36744. eCollection 2024 Sep 15. Heliyon. 2024. PMID: 39263074 Free PMC article.

6

A De Novo Mutation in DYRK1A Causes Syndromic Intellectual Disability: A Chinese Case Report.

Qiao F, Shao B, Wang C, Wang Y, Zhou R, Liu G, Meng L, Hu P, Xu Z. Qiao F, et al. Among authors: shao b. Front Genet. 2019 Nov 19;10:1194. doi: 10.3389/fgene.2019.01194. eCollection 2019. Front Genet. 2019. PMID: 31803247 Free PMC article.

7

Case Report: Prenatal Whole-Exome Sequencing to Identify a Novel Heterozygous Synonymous Variant in NIPBL in a Fetus With Cornelia de Lange Syndrome.

Qiao F, Zhang C, Wang Y, Liu G, Shao B, Hu P, Xu Z. Qiao F, et al. Among authors: shao b. Front Genet. 2021 Feb 9;12:628890. doi: 10.3389/fgene.2021.628890. eCollection 2021. Front Genet. 2021. PMID: 33633789 Free PMC article.

8

A De Novo heterozygous frameshift mutation identified in BCL11B causes neurodevelopmental disorder by whole exome sequencing.

Qiao F, Wang C, Luo C, Wang Y, Shao B, Tan J, Hu P, Xu Z. Qiao F, et al. Among authors: shao b. Mol Genet Genomic Med. 2019 Sep;7(9):e897. doi: 10.1002/mgg3.897. Epub 2019 Jul 25. Mol Genet Genomic Med. 2019. PMID: 31347296 Free PMC article. Clinical Trial.

9

Current attitudes and preconceptions towards expanded carrier screening in the Eastern Chinese reproductive-aged population.

Zhang F, Tan J, Shao B, Jiang T, Zhou R, Wang Y, Zhang J, Qiao F, Ji X, Wang Y, Hu P, Xu Z. Zhang F, et al. Among authors: shao b. J Assist Reprod Genet. 2021 Mar;38(3):697-707. doi: 10.1007/s10815-020-02032-w. Epub 2021 Jan 6. J Assist Reprod Genet. 2021. PMID: 33409754 Free PMC article.

10

Molecular diagnostic in fetuses with isolated congenital anomalies of the kidney and urinary tract by whole-exome sequencing.

Zhou X, Wang Y, Shao B, Wang C, Hu P, Qiao F, Xu Z. Zhou X, et al. Among authors: shao b. J Clin Lab Anal. 2020 Nov;34(11):e23480. doi: 10.1002/jcla.23480. Epub 2020 Aug 11. J Clin Lab Anal. 2020. PMID: 32779812 Free PMC article.

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