231 related articles for article (PubMed ID: 11756345)
1. PAX6 mutation as a genetic factor common to aniridia and glucose intolerance.
Yasuda T; Kajimoto Y; Fujitani Y; Watada H; Yamamoto S; Watarai T; Umayahara Y; Matsuhisa M; Gorogawa S; Kuwayama Y; Tano Y; Yamasaki Y; Hori M
Diabetes; 2002 Jan; 51(1):224-30. PubMed ID: 11756345
[TBL] [Abstract][Full Text] [Related]
2. Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities.
Dansault A; David G; Schwartz C; Jaliffa C; Vieira V; de la Houssaye G; Bigot K; Catin F; Tattu L; Chopin C; Halimi P; Roche O; Van Regemorter N; Munier F; Schorderet D; Dufier JL; Marsac C; Ricquier D; Menasche M; Penfornis A; Abitbol M
Mol Vis; 2007 Apr; 13():511-23. PubMed ID: 17417613
[TBL] [Abstract][Full Text] [Related]
3. A case of novel de novo paired box gene 6 (PAX6) mutation with early-onset diabetes mellitus and aniridia.
Nishi M; Sasahara M; Shono T; Saika S; Yamamoto Y; Ohkawa K; Furuta H; Nakao T; Sasaki H; Nanjo K
Diabet Med; 2005 May; 22(5):641-4. PubMed ID: 15842522
[TBL] [Abstract][Full Text] [Related]
4. Mutation analysis of paired box 6 gene in inherited aniridia in northern China.
Chen P; Zang X; Sun D; Wang Y; Wang Y; Zhao X; Zhang M; Xie L
Mol Vis; 2013; 19():1169-77. PubMed ID: 23734086
[TBL] [Abstract][Full Text] [Related]
5. Two novel PAX6 mutations identified in northeastern Chinese patients with aniridia.
Yuan H; Kang Y; Shao Z; Li Y; Yang G; Xu N
Mol Vis; 2007 Aug; 13():1555-61. PubMed ID: 17893655
[TBL] [Abstract][Full Text] [Related]
6. Identification of novel mutant PAX6 alleles in Indian cases of familial aniridia.
Neethirajan G; Nallathambi J; Krishnadas SR; Vijayalakshmi P; Shashikanth S; Collinson JM; Sundaresan P
BMC Ophthalmol; 2006 Jun; 6():28. PubMed ID: 16803629
[TBL] [Abstract][Full Text] [Related]
7. A recurrent PAX6 mutation is associated with aniridia and congenital progressive cataract in a Chinese family.
Jin C; Wang Q; Li J; Zhu Y; Shentu X; Yao K
Mol Vis; 2012; 18():465-70. PubMed ID: 22393272
[TBL] [Abstract][Full Text] [Related]
8. A novel PAX6 deletion in a Chinese family with congenital aniridia.
Chen JH; Lin W; Sun G; Huang C; Huang Y; Chen H; Pang CP; Zhang M
Mol Vis; 2012; 18():989-95. PubMed ID: 22550392
[TBL] [Abstract][Full Text] [Related]
9. [Identification of a novel PAX6 mutation in a family with congenital aniridia].
Li J; Zhao L; Cai XJ; Lu L; Li G
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Oct; 30(5):579-81. PubMed ID: 24078574
[TBL] [Abstract][Full Text] [Related]
10. [A novel mutation of the PAX6 gene in a Chinese family with aniridia].
Kang Y; Yuan HP; Li X; Li QJ; Wu Q; Hu Q
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Aug; 27(4):376-80. PubMed ID: 20677140
[TBL] [Abstract][Full Text] [Related]
11. Paired box 6 (PAX6) regulates glucose metabolism via proinsulin processing mediated by prohormone convertase 1/3 (PC1/3).
Wen JH; Chen YY; Song SJ; Ding J; Gao Y; Hu QK; Feng RP; Liu YZ; Ren GC; Zhang CY; Hong TP; Gao X; Li LS
Diabetologia; 2009 Mar; 52(3):504-13. PubMed ID: 19034419
[TBL] [Abstract][Full Text] [Related]
12. Molecular analysis of the PAX6 gene for congenital aniridia in the Korean population: identification of four novel mutations.
Park SH; Kim MS; Chae H; Kim Y; Kim M
Mol Vis; 2012; 18():488-94. PubMed ID: 22393275
[TBL] [Abstract][Full Text] [Related]
13. [A novel mutation of the PAX6 gene identified in a northeastern Chinese family with congenital aniridia].
Kang Y; Yuan HP; Li YY
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Apr; 25(2):172-5. PubMed ID: 18393239
[TBL] [Abstract][Full Text] [Related]
14. A novel PAX6 deletion in a Chinese family with congenital aniridia.
Liu Q; Wan W; Liu Y; Liu Y; Hu Z; Guo H; Xia K; Jin X
Gene; 2015 May; 563(1):41-4. PubMed ID: 25746674
[TBL] [Abstract][Full Text] [Related]
15. Mutation analysis of PAX6 in a Chinese family and a patient with a presumed sporadic case of congenital aniridia.
Luo F; Zhou L; Ma X; He Y; Zou L; Jie Y; Liu J; Pan Z
Ophthalmic Res; 2012; 47(1):27-31. PubMed ID: 21691140
[TBL] [Abstract][Full Text] [Related]
16. A 556 kb deletion in the downstream region of the PAX6 gene causes familial aniridia and other eye anomalies in a Chinese family.
Cheng F; Song W; Kang Y; Yu S; Yuan H
Mol Vis; 2011 Feb; 17():448-55. PubMed ID: 21321669
[TBL] [Abstract][Full Text] [Related]
17. Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia.
Dubey SK; Mahalaxmi N; Vijayalakshmi P; Sundaresan P
Mol Vis; 2015; 21():88-97. PubMed ID: 25678763
[TBL] [Abstract][Full Text] [Related]
18. [R240X mutation of the PAX6 gene in a Chinese family with congenital aniridia].
Wang LM; Ying M; Wang X; Wang YC; Hao P; Li ND
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct; 26(5):546-9. PubMed ID: 19806579
[TBL] [Abstract][Full Text] [Related]
19. A novel PAX6 mutation in a large Chinese family with aniridia and congenital cataract.
Cai F; Zhu J; Chen W; Ke T; Wang F; Tu X; Zhang Y; Jin R; Wu X
Mol Vis; 2010 Jun; 16():1141-5. PubMed ID: 20664694
[TBL] [Abstract][Full Text] [Related]
20. Mutation spectrum of PAX6 in Chinese patients with aniridia.
Zhang X; Wang P; Li S; Xiao X; Guo X; Zhang Q
Mol Vis; 2011; 17():2139-47. PubMed ID: 21850189
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
