Tan ZP - Search Results

1

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.

2

19p13.2 Microdeletion including NFIX associated with overgrowth and intellectual disability suggestive of Malan syndrome.

Dong HY, Zeng H, Hu YQ, Xie L, Wang J, Wang XY, Yang YF, Tan ZP. Dong HY, et al. Among authors: tan zp. Mol Cytogenet. 2016 Sep 22;9:71. doi: 10.1186/s13039-016-0282-4. eCollection 2016. Mol Cytogenet. 2016. PMID: 27688808 Free PMC article.

3

A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.

Zeng H, Tang JG, Yang YF, Tan ZP, Tan JQ. Zeng H, et al. Among authors: tan jq, tan zp. Cytogenet Genome Res. 2017;152(1):16-21. doi: 10.1159/000477428. Epub 2017 Jun 29. Cytogenet Genome Res. 2017. PMID: 28658676

4

Interleukin-6, tumor necrosis factor-alpha and receptor activator of nuclear factor kappa ligand are elevated in hypertrophic gastric mucosa of pachydermoperiostosis.

Huang H, Wang Y, Cao Y, Wu B, Li Y, Fan L, Tan Z, Jiang Y, Tang J, Hu J, Shi X. Huang H, et al. Sci Rep. 2017 Aug 29;7(1):9686. doi: 10.1038/s41598-017-09671-7. Sci Rep. 2017. PMID: 28851954 Free PMC article.

5

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.

6

A Novel Nonsense MMP21 Variant Causes Dextrocardia and Congenital Heart Disease in a Han Chinese Patient.

Yuan ZZ, Fan LL, Jiang ZC, Yang YF, Tan ZP. Yuan ZZ, et al. Among authors: tan zp. Front Cardiovasc Med. 2020 Nov 9;7:582350. doi: 10.3389/fcvm.2020.582350. eCollection 2020. Front Cardiovasc Med. 2020. PMID: 33240936 Free PMC article.

7

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.

8

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

9

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.

10

Identification of a novel MYO1D variant associated with laterality defects, congenital heart diseases, and sperm defects in humans.

Yuan Z, Zhu X, Xie X, Wang C, Gu H, Yang J, Fan L, Xiang R, Yang Y, Tan Z. Yuan Z, et al. Front Med. 2024 Jun;18(3):558-564. doi: 10.1007/s11684-023-1042-6. Epub 2024 Apr 30. Front Med. 2024. PMID: 38684630

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