These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
265 related articles for article (PubMed ID: 11414759)
1. A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi mice. Sidjanin DJ; Parker-Wilson DM; Neuhäuser-Klaus A; Pretsch W; Favor J; Deen PM; Ohtaka-Maruyama C; Lu Y; Bragin A; Skach WR; Chepelinsky AB; Grimes PA; Stambolian DE Genomics; 2001 Jun; 74(3):313-9. PubMed ID: 11414759 [TBL] [Abstract][Full Text] [Related]
2. Mutations in the founder of the MIP gene family underlie cataract development in the mouse. Shiels A; Bassnett S Nat Genet; 1996 Feb; 12(2):212-5. PubMed ID: 8563764 [TBL] [Abstract][Full Text] [Related]
3. Mutation in the betaA3/A1-crystallin encoding gene Cryba1 causes a dominant cataract in the mouse. Graw J; Jung M; Löster J; Klopp N; Soewarto D; Fella C; Fuchs H; Reis A; Wolf E; Balling R; Hrabé de Angelis M Genomics; 1999 Nov; 62(1):67-73. PubMed ID: 10585769 [TBL] [Abstract][Full Text] [Related]
4. Lim2(To3) transgenic mice establish a causative relationship between the mutation identified in the lim2 gene and cataractogenesis in the To3 mouse mutant. Steele EC; Wang JH; Lo WK; Saperstein DA; Li X; Church RL Mol Vis; 2000 Jun; 6():85-94. PubMed ID: 10851259 [TBL] [Abstract][Full Text] [Related]
5. A 6-bp deletion in the Crygc gene leading to a nuclear and radial cataract in the mouse. Graw J; Neuhäuser-Klaus A; Löster J; Favor J Invest Ophthalmol Vis Sci; 2002 Jan; 43(1):236-40. PubMed ID: 11773036 [TBL] [Abstract][Full Text] [Related]
6. Structural function of MIP/aquaporin 0 in the eye lens; genetic defects lead to congenital inherited cataracts. Chepelinsky AB Handb Exp Pharmacol; 2009; (190):265-97. PubMed ID: 19096783 [TBL] [Abstract][Full Text] [Related]
7. Aey2, a new mutation in the betaB2-crystallin-encoding gene of the mouse. Graw J; Löster J; Soewarto D; Fuchs H; Reis A; Wolf E; Balling R; Hrabé de Angelis M Invest Ophthalmol Vis Sci; 2001 Jun; 42(7):1574-80. PubMed ID: 11381063 [TBL] [Abstract][Full Text] [Related]
8. Mutation of Dock5, a member of the guanine exchange factor Dock180 superfamily, in the rupture of lens cataract mouse. Omi N; Kiyokawa E; Matsuda M; Kinoshita K; Yamada S; Yamada K; Matsushima Y; Wang Y; Kawai J; Suzuki M; Hayashizaki Y; Hiai H Exp Eye Res; 2008 May; 86(5):828-34. PubMed ID: 18396277 [TBL] [Abstract][Full Text] [Related]
9. Characterization of a new, dominant V124E mutation in the mouse alphaA-crystallin-encoding gene. Graw J; Löster J; Soewarto D; Fuchs H; Meyer B; Reis A; Wolf E; Balling R; Hrabé de Angelis M Invest Ophthalmol Vis Sci; 2001 Nov; 42(12):2909-15. PubMed ID: 11687536 [TBL] [Abstract][Full Text] [Related]
10. Abnormal eye development associated with Cat4a, a dominant mouse cataract mutation on chromosome 8. Grimes PA; Koeberlein B; Favor J; Neuhäuser-Klaus A; Stambolian D Invest Ophthalmol Vis Sci; 1998 Sep; 39(10):1863-9. PubMed ID: 9727409 [TBL] [Abstract][Full Text] [Related]
11. Temporal expression of three mouse lens fiber cell membrane protein genes during early development. Zhou L; Chen T; Church RL Mol Vis; 2002 Jun; 8():143-8. PubMed ID: 12097863 [TBL] [Abstract][Full Text] [Related]
12. Characterization of a 1-bp deletion in the gammaE-crystallin gene leading to a nuclear and zonular cataract in the mouse. Klopp N; Löster J; Graw J Invest Ophthalmol Vis Sci; 2001 Jan; 42(1):183-7. PubMed ID: 11133865 [TBL] [Abstract][Full Text] [Related]
14. [A novel missense mutation in MIP gene resulted in polymorphic cataract]. Lin H; Wang L; Zhou N; Su H; Gu J; Qi Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb; 25(1):6-10. PubMed ID: 18247294 [TBL] [Abstract][Full Text] [Related]
15. Specific interaction between lens MIP/Aquaporin-0 and two members of the gamma-crystallin family. Fan J; Fariss RN; Purkiss AG; Slingsby C; Sandilands A; Quinlan R; Wistow G; Chepelinsky AB Mol Vis; 2005 Jan; 11():76-87. PubMed ID: 15692460 [TBL] [Abstract][Full Text] [Related]
16. Dense nuclear cataract caused by the gammaB-crystallin S11R point mutation. Li L; Chang B; Cheng C; Chang D; Hawes NL; Xia CH; Gong X Invest Ophthalmol Vis Sci; 2008 Jan; 49(1):304-9. PubMed ID: 18172107 [TBL] [Abstract][Full Text] [Related]
17. Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16. Sidjanin DJ; Grimes PA; Pretsch W; Neuhäuser-Klaus A; Favor J; Stambolian DE Invest Ophthalmol Vis Sci; 1997 Nov; 38(12):2502-7. PubMed ID: 9375568 [TBL] [Abstract][Full Text] [Related]
18. Characterization of a mutation in the lens-specific MP70 encoding gene of the mouse leading to a dominant cataract. Graw J; Löster J; Soewarto D; Fuchs H; Meyer B; Reis A; Wolf E; Balling R; Hrabé de Angelis M Exp Eye Res; 2001 Dec; 73(6):867-76. PubMed ID: 11846517 [TBL] [Abstract][Full Text] [Related]