Zhi-Ping Tan[Author] - Search Results

Year	Number of Results
2002	2
2005	2
2007	2
2008	1
2010	1
2012	6
2013	2
2014	4
2015	2
2016	2
2017	4
2018	1
2020	2
2021	4
2022	2
2023	1
2024	0

1

A novel 7-chemokine-genes predictive signature for prognosis and therapeutic response in renal clear cell carcinoma.

Lin MJ, Tang XX, Yao GS, Tan ZP, Dai L, Wang YH, Zhu JQ, Xu QH, Mumin MA, Liang H, Wang Z, Deng Q, Luo JH, Wei JH, Cao JZ. Lin MJ, et al. Among authors: tan zp. Front Pharmacol. 2023 Mar 20;14:1120562. doi: 10.3389/fphar.2023.1120562. eCollection 2023. Front Pharmacol. 2023. PMID: 37021054 Free PMC article.

2

Haploinsufficiency of syncoilin leads to hypertrophic cardiomyopathy.

Fan LL, Yuan ZZ, Jiao ZJ, Zeng H, Yang YF, Tan ZP. Fan LL, et al. Among authors: tan zp. Genes Dis. 2022 Mar 23;9(6):1412-1414. doi: 10.1016/j.gendis.2022.02.011. eCollection 2022 Nov. Genes Dis. 2022. PMID: 36157493 Free PMC article. No abstract available.

3

Mutant CARD10 in a family with progressive immunodeficiency and autoimmunity.

Yang DH, Guo T, Yuan ZZ, Lei C, Ding SZ, Yang YF, Tan ZP, Luo H. Yang DH, et al. Among authors: tan zp. Cell Mol Immunol. 2020 Jul;17(7):782-784. doi: 10.1038/s41423-020-0423-x. Epub 2020 Apr 1. Cell Mol Immunol. 2020. PMID: 32238915 Free PMC article. No abstract available.

4

A novel nonsense PKD1L1 variant cause heterotaxy syndrome with congenital asplenia in a Han Chinese patient.

Gu H, Yuan ZZ, Xie XH, Yang YF, Tan ZP. Gu H, et al. Among authors: tan zp. J Hum Genet. 2022 Oct;67(10):573-577. doi: 10.1038/s10038-022-01053-w. Epub 2022 Jun 13. J Hum Genet. 2022. PMID: 35691949

5

CircRNA Microarray Profiling Reveals hsa_circ_0058493 as a Novel Biomarker for Imatinib-Resistant CML.

Zhong AN, Yin Y, Tang BJ, Chen L, Shen HW, Tan ZP, Li WQ, He Q, Sun B, Zhu Y, Xiao J, Jiang ZP, Xu P. Zhong AN, et al. Among authors: tan zp. Front Pharmacol. 2021 Sep 13;12:728916. doi: 10.3389/fphar.2021.728916. eCollection 2021. Front Pharmacol. 2021. PMID: 34588984 Free PMC article.

6

Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia.

Guo T, Tu CF, Yang DH, Ding SZ, Lei C, Wang RC, Liu L, Kang X, Shen XQ, Yang YF, Tan ZP, Tan YQ, Luo H. Guo T, et al. Among authors: tan zp. Hum Genet. 2021 May;140(5):761-773. doi: 10.1007/s00439-020-02241-4. Epub 2021 Jan 3. Hum Genet. 2021. PMID: 33389130

7

A clinical and molecular analysis of a patient with Emanuel syndrome.

Luo JW, Yang H, Tan ZP, Tu M, Luo H, Yang YF, Xie L. Luo JW, et al. Among authors: tan zp. Mol Med Rep. 2017 Mar;15(3):1348-1352. doi: 10.3892/mmr.2017.6107. Epub 2017 Jan 5. Mol Med Rep. 2017. PMID: 28075445

8

Novel mutation of EXT2 identified in a large family with multiple osteochondromas.

Chen XJ, Zhang H, Tan ZP, Hu W, Yang YF. Chen XJ, et al. Among authors: tan zp. Mol Med Rep. 2016 Nov;14(5):4687-4691. doi: 10.3892/mmr.2016.5814. Epub 2016 Oct 6. Mol Med Rep. 2016. PMID: 27748933 Free PMC article.

9

Case Report: BAF-Opathies/SSRIDDs Due to a de novo ACTL6A Variant, Previously Considered to Be Heart-Hand Syndrome.

Yuan ZZ, Xie XH, Gu H, Zhang WZ, Hu YQ, Yang YF, Tan ZP. Yuan ZZ, et al. Among authors: tan zp. Front Cardiovasc Med. 2021 Aug 13;8:708033. doi: 10.3389/fcvm.2021.708033. eCollection 2021. Front Cardiovasc Med. 2021. PMID: 34485408 Free PMC article.

10

Case Report: Mutant SCN9A Susceptible to Charcot Neuroarthropathy in a Patient With Congenital Insensitivity to Pain.

Xie XH, Tang JG, Liu ZH, Peng SJ, Yuan ZZ, Gu H, Hu YQ, Tan ZP. Xie XH, et al. Among authors: tan zp. Front Neurosci. 2021 Jul 14;15:697167. doi: 10.3389/fnins.2021.697167. eCollection 2021. Front Neurosci. 2021. PMID: 34335171 Free PMC article.

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