Liu P - Search Results

1

Congenital anterior polar cataract associated with a missense mutation in the human alpha crystallin gene CRYAA.

Zhang L, Zhang Y, Liu P, Cao W, Tang X, Su S. Zhang L, et al. Among authors: liu p. Mol Vis. 2011;17:2693-7. Epub 2011 Oct 15. Mol Vis. 2011. PMID: 22065922 Free PMC article.

2

The E233del mutation in BFSP2 causes a progressive autosomal dominant congenital cataract in a Chinese family.

Cui X, Gao L, Jin Y, Zhang Y, Bai J, Feng G, Gao W, Liu P, He L, Fu S. Cui X, et al. Among authors: liu p. Mol Vis. 2007 Oct 24;13:2023-9. Mol Vis. 2007. PMID: 17982427

3

Reduced penetrance in familial Avellino corneal dystrophy associated with TGFBI mutations.

Cao W, Ge H, Cui X, Zhang L, Bai J, Fu S, Liu P. Cao W, et al. Among authors: liu p. Mol Vis. 2009;15:70-5. Epub 2009 Jan 14. Mol Vis. 2009. PMID: 19145249 Free PMC article.

4

A novel nonsense mutation in CRYGC is associated with autosomal dominant congenital nuclear cataracts and microcornea.

Zhang L, Fu S, Ou Y, Zhao T, Su Y, Liu P. Zhang L, et al. Among authors: liu p. Mol Vis. 2009;15:276-82. Epub 2009 Feb 6. Mol Vis. 2009. PMID: 19204787 Free PMC article.

5

[Gene mapping and mutation detection in a family with congenital nuclear cataract].

Liu P, Zhang L, Ouyang S, Gao LH, He L, Fu SB. Liu P, et al. Zhonghua Yan Ke Za Zhi. 2009 Mar;45(3):234-8. Zhonghua Yan Ke Za Zhi. 2009. PMID: 19575918 Chinese.

6

Expression changes in DNA repair enzymes and mitochondrial DNA damage in aging rat lens.

Zhang Y, Zhang L, Zhang L, Bai J, Ge H, Liu P. Zhang Y, et al. Among authors: liu p. Mol Vis. 2010 Aug 27;16:1754-63. Mol Vis. 2010. PMID: 20808729 Free PMC article.

7

A new locus in chromosome 2q37-qter is associated with posterior polar cataract.

Ouyang S, Gao L, Zhang L, Zheng Y, Cao W, Feng G, He L, Liu P. Ouyang S, et al. Among authors: liu p. Graefes Arch Clin Exp Ophthalmol. 2012 Jun;250(6):907-13. doi: 10.1007/s00417-011-1781-y. Epub 2011 Sep 1. Graefes Arch Clin Exp Ophthalmol. 2012. PMID: 21881846

8

[Gene mapping and mutation detection in a family with congenital anterior polar cataract].

Zhang L, Liu P, Zhang Y, Su S, Tang XL, Bai J. Zhang L, et al. Among authors: liu p. Zhonghua Yan Ke Za Zhi. 2011 Aug;47(8):721-5. Zhonghua Yan Ke Za Zhi. 2011. PMID: 22169612 Chinese.

9

A novel mutation in GJA3 associated with congenital Coppock-like cataract in a large Chinese family.

Zhang L, Qu X, Su S, Guan L, Liu P. Zhang L, et al. Among authors: liu p. Mol Vis. 2012;18:2114-8. Epub 2012 Jul 26. Mol Vis. 2012. PMID: 22876138 Free PMC article.

10

Blocking neuropilin-2 enhances corneal allograft survival by selectively inhibiting lymphangiogenesis on vascularized beds.

Tang XL, Sun JF, Wang XY, Du LL, Liu P. Tang XL, et al. Among authors: liu p. Mol Vis. 2010 Nov 9;16:2354-61. Mol Vis. 2010. PMID: 21139694 Free PMC article.

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