107 related articles for article (PubMed ID: 15565366)
21. Kinetics of blood glucose in mice carrying hemizygous Pax6.
Nitta Y; Shigeyoshi Y; Nakagata N; Kaneko T; Nitta K; Harada T; Ishizaki F; Townsend J
Exp Anim; 2009 Apr; 58(2):105-12. PubMed ID: 19448333
[TBL] [Abstract][Full Text] [Related]
22. Mutation analysis of PAX6 gene in a large Chinese family with aniridia.
Song SJ; Liu YZ; Cong RC; Jin Y; Hou ZQ; Ma ZZ; Ren GC; Li LS
Chin Med J (Engl); 2005 Feb; 118(4):302-6. PubMed ID: 15740668
[TBL] [Abstract][Full Text] [Related]
23. Pax6 is crucial for β-cell function, insulin biosynthesis, and glucose-induced insulin secretion.
Gosmain Y; Katz LS; Masson MH; Cheyssac C; Poisson C; Philippe J
Mol Endocrinol; 2012 Apr; 26(4):696-709. PubMed ID: 22403172
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. Variants in TRIM44 Cause Aniridia by Impairing PAX6 Expression.
Zhang X; Qin G; Chen G; Li T; Gao L; Huang L; Zhang Y; Ouyang K; Wang Y; Pang Y; Zeng B; Yu L
Hum Mutat; 2015 Dec; 36(12):1164-7. PubMed ID: 26394807
[TBL] [Abstract][Full Text] [Related]
27. [PAX6 mutation caused brain abnormalities in humans].
Song SJ; Liu YZ; Cong RC; Zhang XY; Yang ZJ; Li LS
Beijing Da Xue Xue Bao Yi Xue Ban; 2005 Feb; 37(1):48-50. PubMed ID: 15719041
[TBL] [Abstract][Full Text] [Related]
28. [Two neonates with congenital aniridia: the necessity of genetic investigation].
van Os E; Niemarkt HJ; Verreussel MJ; Cruysberg JR; Bok LA; Spruijt L
Ned Tijdschr Geneeskd; 2008 Mar; 152(10):569-73. PubMed ID: 18402324
[TBL] [Abstract][Full Text] [Related]
29. Mutant PAX6 downregulates prohormone convertase 2 expression in mouse islets.
Chen Y; Cao W; Zhou S; Shen L; Wen J
Exp Biol Med (Maywood); 2013 Nov; 238(11):1259-64. PubMed ID: 24047795
[TBL] [Abstract][Full Text] [Related]
30. Aniridia with preserved visual function: a report of four cases with no mutations in PAX6.
Traboulsi EI; Ellison J; Sears J; Maumenee IH; Avallone J; Mohney BG
Am J Ophthalmol; 2008 Apr; 145(4):760-4. PubMed ID: 18243151
[TBL] [Abstract][Full Text] [Related]
31. Pituitary function and glucose tolerance in a family with a PAX6 mutation.
Hergott-Faure L; Borot S; Kleinclauss C; Abitbol M; Penfornis A
Ann Endocrinol (Paris); 2012 Dec; 73(6):510-4. PubMed ID: 23146210
[TBL] [Abstract][Full Text] [Related]
32. [Study of genetic mutation locus in a family with congenital aniridia].
Cong RC; Song SJ; Liu YZ
Zhonghua Yan Ke Za Zhi; 2006 Dec; 42(12):1113-7. PubMed ID: 17415970
[TBL] [Abstract][Full Text] [Related]
33. PAX6 analysis of two unrelated families from the Arabian Peninsula with classic hereditary aniridia.
Khan AO; Aldahmesh MA
Ophthalmic Genet; 2008 Sep; 29(3):145-8. PubMed ID: 18766996
[TBL] [Abstract][Full Text] [Related]
34. A case of aniridia with unilateral Peters anomaly.
Sawada M; Sato M; Hikoya A; Wang C; Minoshima S; Azuma N; Hotta Y
J AAPOS; 2011 Feb; 15(1):104-6. PubMed ID: 21397818
[TBL] [Abstract][Full Text] [Related]
35. Familial peripheral keratopathy without PAX6 mutation.
Smith WM; Lange JM; Sturm AC; Tanner SM; Mauger TF
Cornea; 2012 Feb; 31(2):130-3. PubMed ID: 22146551
[TBL] [Abstract][Full Text] [Related]
36. Comparison between aniridia with and without PAX6 mutations: clinical and molecular analysis in 14 Korean patients with aniridia.
Lim HT; Seo EJ; Kim GH; Ahn H; Lee HJ; Shin KH; Lee JK; Yoo HW
Ophthalmology; 2012 Jun; 119(6):1258-64. PubMed ID: 22361317
[TBL] [Abstract][Full Text] [Related]
37. Microphthalmia, late onset keratitis, and iris coloboma/aniridia in a family with a novel PAX6 mutation.
Xiao X; Li S; Zhang Q
Ophthalmic Genet; 2012 Jun; 33(2):119-21. PubMed ID: 22171686
[TBL] [Abstract][Full Text] [Related]
38. PAX6 3' deletion in a family with aniridia.
Wawrocka A; Budny B; Debicki S; Jamsheer A; Sowinska A; Krawczynski MR
Ophthalmic Genet; 2012 Mar; 33(1):44-8. PubMed ID: 21985185
[TBL] [Abstract][Full Text] [Related]
39. A deletion 3' to the PAX6 gene in familial aniridia cases.
D'Elia AV; Pellizzari L; Fabbro D; Pianta A; Divizia MT; Rinaldi R; Grammatico B; Grammatico P; Arduino C; Damante G
Mol Vis; 2007 Jul; 13():1245-50. PubMed ID: 17679951
[TBL] [Abstract][Full Text] [Related]
40. Developmental and cellular factors underlying corneal epithelial dysgenesis in the Pax6+/- mouse model of aniridia.
Ramaesh T; Ramaesh K; Martin Collinson J; Chanas SA; Dhillon B; West JD
Exp Eye Res; 2005 Aug; 81(2):224-35. PubMed ID: 16080917
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]