Tan Z - Search Results

1

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. Among authors: tan z. Front Med. 2024 Jun;18(3):558-564. doi: 10.1007/s11684-023-1042-6. Epub 2024 Apr 30. Front Med. 2024. PMID: 38684630

2

Experimental study of the effects of marrow mesenchymal stem cells transfected with hypoxia-inducible factor-1alpha gene.

Yang J, Tang T, Li F, Zhou W, Liu J, Tan Z, Zheng W, Yang Y, Zhou X, Hu J. Yang J, et al. Among authors: tan z. J Biomed Biotechnol. 2009;2009:128627. doi: 10.1155/2009/128627. Epub 2009 Jul 1. J Biomed Biotechnol. 2009. PMID: 19587827 Free PMC article.

3

[Noonan syndrome: a case report and literature review].

Chen J, Yang Y, Tan Z, Wang Y, Tang X, Gong Y. Chen J, et al. Among authors: tan z. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2009 Dec;34(12):1261-5. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2009. PMID: 20045924 Review. Chinese. No abstract available.

4

Mutations of the TGFBR2 gene in Chinese patients with Marfan-related syndrome.

Chen J, Li B, Yang Y, Hu J, Zhao T, Gong Y, Tan Z. Chen J, et al. Among authors: tan z. Clin Invest Med. 2010 Feb 1;33(1):E14-21. doi: 10.25011/cim.v33i1.11833. Clin Invest Med. 2010. PMID: 20144264

5

Clinical and molecular delineation of 16p13.3 duplication in a patient with congenital heart defect and multiple congenital anomalies.

Chen JL, Yang YF, Huang C, Wang J, Yang JF, Tan ZP. Chen JL, et al. Am J Med Genet A. 2012 Mar;158A(3):685-8. doi: 10.1002/ajmg.a.34434. Epub 2012 Feb 3. Am J Med Genet A. 2012. PMID: 22307725 No abstract available.

6

Congenital heart defect and mental retardation in a patient with a 13q33.1-34 deletion.

Huang C, Yang YF, Yin N, Chen JL, Wang J, Zhang H, Tan ZP. Huang C, et al. Gene. 2012 May 1;498(2):308-10. doi: 10.1016/j.gene.2012.01.083. Epub 2012 Feb 16. Gene. 2012. PMID: 22366306

7

Identification of anaplastic lymphoma kinase as a potential therapeutic target in ovarian cancer.

Ren H, Tan ZP, Zhu X, Crosby K, Haack H, Ren JM, Beausoleil S, Moritz A, Innocenti G, Rush J, Zhang Y, Zhou XM, Gu TL, Yang YF, Comb MJ. Ren H, et al. Cancer Res. 2012 Jul 1;72(13):3312-23. doi: 10.1158/0008-5472.CAN-11-3931. Epub 2012 May 8. Cancer Res. 2012. PMID: 22570254

8

Microduplication of 3p25.2 encompassing RAF1 associated with congenital heart disease suggestive of Noonan syndrome.

Luo C, Yang YF, Yin BL, Chen JL, Huang C, Zhang WZ, Wang J, Zhang H, Yang JF, Tan ZP. Luo C, et al. Am J Med Genet A. 2012 Aug;158A(8):1918-23. doi: 10.1002/ajmg.a.35471. Epub 2012 Jul 11. Am J Med Genet A. 2012. PMID: 22786616

9

Duplication of 8q12 encompassing CHD7 is associated with a distinct phenotype but without duane anomaly.

Luo H, Xie L, Wang SZ, Chen JL, Huang C, Wang J, Yang JF, Zhang WZ, Yang YF, Tan ZP. Luo H, et al. Eur J Med Genet. 2012 Nov;55(11):646-9. doi: 10.1016/j.ejmg.2012.07.006. Epub 2012 Jul 31. Eur J Med Genet. 2012. PMID: 22902603

10

A 1.1Mb deletion in distal 13q deletion syndrome region with congenital heart defect and postaxial polydactyly: additional support for a CHD locus at distal 13q34 region.

Yang YF, Ai Q, Huang C, Chen JL, Wang J, Xie L, Zhang WZ, Yang JF, Tan ZP. Yang YF, et al. Gene. 2013 Oct 1;528(1):51-4. doi: 10.1016/j.gene.2013.03.145. Epub 2013 Apr 29. Gene. 2013. PMID: 23639964

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