Wang Z - Search Results

1

Ovotesticular disorders of sex development in FGF9 mouse models of human synostosis syndromes.

Bird AD, Croft BM, Harada M, Tang L, Zhao L, Ming Z, Bagheri-Fam S, Koopman P, Wang Z, Akita K, Harley VR. Bird AD, et al. Among authors: wang z. Hum Mol Genet. 2020 Aug 3;29(13):2148-2161. doi: 10.1093/hmg/ddaa100. Hum Mol Genet. 2020. PMID: 32452519

2

Multiple synostoses syndrome is due to a missense mutation in exon 2 of FGF9 gene.

Wu XL, Gu MM, Huang L, Liu XS, Zhang HX, Ding XY, Xu JQ, Cui B, Wang L, Lu SY, Chen XY, Zhang HG, Huang W, Yuan WT, Yang JM, Gu Q, Fei J, Chen Z, Yuan ZM, Wang ZG. Wu XL, et al. Among authors: wang zg, wang l. Am J Hum Genet. 2009 Jul;85(1):53-63. doi: 10.1016/j.ajhg.2009.06.007. Am J Hum Genet. 2009. PMID: 19589401 Free PMC article.

3

Prss37 is required for male fertility in the mouse.

Shen C, Kuang Y, Liu J, Feng J, Chen X, Wu W, Chi J, Tang L, Wang Y, Fei J, Wang Z. Shen C, et al. Among authors: wang z, wang y. Biol Reprod. 2013 May 16;88(5):123. doi: 10.1095/biolreprod.112.107086. Print 2013 May. Biol Reprod. 2013. PMID: 23553430

4

A point mutation in Fgf9 impedes joint interzone formation leading to multiple synostoses syndrome.

Tang L, Wu X, Zhang H, Lu S, Wu M, Shen C, Chen X, Wang Y, Wang W, Shen Y, Gu M, Ding X, Jin X, Fei J, Wang Z. Tang L, et al. Among authors: wang w, wang z, wang y. Hum Mol Genet. 2017 Apr 1;26(7):1280-1293. doi: 10.1093/hmg/ddx029. Hum Mol Genet. 2017. PMID: 28169396

5

Lacking of palladin leads to multiple cellular events changes which contribute to NTD.

Tan J, Chen XJ, Shen CL, Zhang HX, Tang LY, Lu SY, Wu WT, Kuang Y, Fei J, Wang ZG. Tan J, et al. Neural Dev. 2017 Mar 24;12(1):4. doi: 10.1186/s13064-017-0081-6. Neural Dev. 2017. PMID: 28340616 Free PMC article.

6

Gpr110 deficiency decelerates carcinogen-induced hepatocarcinogenesis via activation of the IL-6/STAT3 pathway.

Ma B, Zhu J, Tan J, Mao Y, Tang L, Shen C, Zhang H, Kuang Y, Fei J, Yang X, Wang Z. Ma B, et al. Among authors: wang z. Am J Cancer Res. 2017 Mar 1;7(3):433-447. eCollection 2017. Am J Cancer Res. 2017. PMID: 28401002 Free PMC article.

7

Nhe5 deficiency enhances learning and memory via upregulating Bdnf/TrkB signaling in mice.

Chen X, Wang X, Tang L, Wang J, Shen C, Liu J, Lu S, Zhang H, Kuang Y, Fei J, Wang Z. Chen X, et al. Among authors: wang x, wang j, wang z. Am J Med Genet B Neuropsychiatr Genet. 2017 Dec;174(8):828-838. doi: 10.1002/ajmg.b.32600. Epub 2017 Oct 5. Am J Med Genet B Neuropsychiatr Genet. 2017. PMID: 28981195

8

Identification of MAVS as a Novel Risk Factor for the Development of Osteoarthritis.

Liu J, Tang LY, Wang YG, Lu SY, Zhang EN, Wang ZG, Zhang HX. Liu J, et al. Aging Dis. 2018 Feb 1;9(1):40-50. doi: 10.14336/AD.2017.0308. eCollection 2018 Feb. Aging Dis. 2018. PMID: 29392080 Free PMC article.

9

DHTKD1 Deficiency Causes Charcot-Marie-Tooth Disease in Mice.

Xu WY, Zhu H, Shen Y, Wan YH, Tu XD, Wu WT, Tang L, Zhang HX, Lu SY, Jin XL, Fei J, Wang ZG. Xu WY, et al. Mol Cell Biol. 2018 Jun 14;38(13):e00085-18. doi: 10.1128/MCB.00085-18. Print 2018 Jul 1. Mol Cell Biol. 2018. PMID: 29661920 Free PMC article.

10

Tafa-2 plays an essential role in neuronal survival and neurobiological function in mice.

Wang X, Shen C, Chen X, Wang J, Cui X, Wang Y, Zhang H, Tang L, Lu S, Fei J, Wang Z. Wang X, et al. Among authors: wang j, wang z, wang y. Acta Biochim Biophys Sin (Shanghai). 2018 Oct 1;50(10):984-995. doi: 10.1093/abbs/gmy097. Acta Biochim Biophys Sin (Shanghai). 2018. PMID: 30137205 Free PMC article.

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