Tang W - Search Results

1

Crosstalk between colorectal CSCs and immune cells in tumorigenesis, and strategies for targeting colorectal CSCs.

Zhao Q, Zong H, Zhu P, Su C, Tang W, Chen Z, Jin S. Zhao Q, et al. Among authors: tang w. Exp Hematol Oncol. 2024 Jan 22;13(1):6. doi: 10.1186/s40164-024-00474-x. Exp Hematol Oncol. 2024. PMID: 38254219 Free PMC article. Review.

2

Novel Clinical Manifestation and Favorable Treatment Outcome of Cochlear Implant in a Chinese Family With Likely Pathogenic Variant of the P2RX2 Gene.

Li Q, Sun S, Zuo B, Lian C, Tang W, Xu H, Lu W. Li Q, et al. Among authors: tang w. Am J Med Genet A. 2025 Jan;197(1):e63877. doi: 10.1002/ajmg.a.63877. Epub 2024 Sep 11. Am J Med Genet A. 2025. PMID: 39258340

3

A likely pathogenic POLD1 variant associated with mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome in a Chinese patient.

Zuo B, Xu H, Pan Z, Mao L, Feng H, Zeng B, Tang W, Lu W. Zuo B, et al. Among authors: tang w. BMC Med Genomics. 2022 Oct 21;15(1):220. doi: 10.1186/s12920-022-01374-x. BMC Med Genomics. 2022. PMID: 36280868 Free PMC article.

4

Phenotypic variability in two female siblings with oocyte maturation arrest due to a TUBB8 variant.

Dou Q, Xu H, Ma L, Tan L, Tang W. Dou Q, et al. Among authors: tang w. BMC Med Genomics. 2023 Oct 30;16(1):271. doi: 10.1186/s12920-023-01712-7. BMC Med Genomics. 2023. PMID: 37904145 Free PMC article.

5

Molecular diagnosis of hereditary deafness and application of stepwise testing strategy.

Zeng BP, Xu HG, Mao L, Tang WX. Zeng BP, et al. Yi Chuan. 2023 Jan 20;45(1):29-41. doi: 10.16288/j.yczz.22-206. Yi Chuan. 2023. PMID: 36927636 Review.

6

Defining the sensitivity landscape of EGFR variants to tyrosine kinase inhibitors.

An L, Wang Y, Wu G, Wang Z, Shi Z, Liu C, Wang C, Yi M, Niu C, Duan S, Li X, Tang W, Wu K, Chen S, Xu H. An L, et al. Among authors: tang w. Transl Res. 2023 May;255:14-25. doi: 10.1016/j.trsl.2022.11.002. Epub 2022 Nov 5. Transl Res. 2023. PMID: 36347492 Free article.

7

Novel compound heterozygous pathogenic variants in the SLC3A1 gene in a Chinese family with cystinuria.

Liu D, Zhao Y, Xue X, Hou X, Xu H, Zhao X, Tian Y, Tang W, Guo J, Xu C. Liu D, et al. Among authors: tang w. BMC Med Genomics. 2023 Dec 19;16(1):333. doi: 10.1186/s12920-023-01767-6. BMC Med Genomics. 2023. PMID: 38114997 Free PMC article.

8

Molecular Mechanisms and Clinical Phenotypes of GJB2 Missense Variants.

Mao L, Wang Y, An L, Zeng B, Wang Y, Frishman D, Liu M, Chen Y, Tang W, Xu H. Mao L, et al. Among authors: tang w. Biology (Basel). 2023 Mar 27;12(4):505. doi: 10.3390/biology12040505. Biology (Basel). 2023. PMID: 37106706 Free PMC article. Review.

9

Increased diagnostic yield in a cohort of hearing loss families using a comprehensive stepwise strategy of molecular testing.

Zeng B, Xu H, Yu Y, Li S, Tian Y, Li T, Yang Z, Wang H, Wang G, Chang M, Tang W. Zeng B, et al. Among authors: tang w. Front Genet. 2022 Dec 7;13:1057293. doi: 10.3389/fgene.2022.1057293. eCollection 2022. Front Genet. 2022. PMID: 36568381 Free PMC article.

10

A novel nonsense variant of the AGXT identified in a Chinese family: special variant research in the Chinese reference genome.

Xu CB, Zhou XD, Xu HE, Zhao YL, Zhao XH, Liu DH, Tian YA, Hu XX, Guan JY, Guo JC, Tang WX, Xue X. Xu CB, et al. BMC Nephrol. 2021 Mar 10;22(1):83. doi: 10.1186/s12882-021-02276-3. BMC Nephrol. 2021. PMID: 33691640 Free PMC article.

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