150 related articles for article (PubMed ID: 18385073)
1. Novel allele of crybb2 in the mouse and its expression in the brain.
Ganguly K; Favor J; Neuhäuser-Klaus A; Sandulache R; Puk O; Beckers J; Horsch M; Schädler S; Vogt Weisenhorn D; Wurst W; Graw J
Invest Ophthalmol Vis Sci; 2008 Apr; 49(4):1533-41. PubMed ID: 18385073
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Targeted knockout of the mouse betaB2-crystallin gene (Crybb2) induces age-related cataract.
Zhang J; Li J; Huang C; Xue L; Peng Y; Fu Q; Gao L; Zhang J; Li W
Invest Ophthalmol Vis Sci; 2008 Dec; 49(12):5476-83. PubMed ID: 18719080
[TBL] [Abstract][Full Text] [Related]
4. Mutation analysis of congenital cataracts in Indian families: identification of SNPS and a new causative allele in CRYBB2 gene.
Santhiya ST; Manisastry SM; Rawlley D; Malathi R; Anishetty S; Gopinath PM; Vijayalakshmi P; Namperumalsamy P; Adamski J; Graw J
Invest Ophthalmol Vis Sci; 2004 Oct; 45(10):3599-607. PubMed ID: 15452067
[TBL] [Abstract][Full Text] [Related]
5. Gene conversion mutation in crystallin, beta-B2 (CRYBB2) in a Chilean family with autosomal dominant cataract.
Bateman JB; von-Bischhoffshaunsen FR; Richter L; Flodman P; Burch D; Spence MA
Ophthalmology; 2007 Mar; 114(3):425-32. PubMed ID: 17234267
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Mutation analysis in a German family identified a new cataract-causing allele in the CRYBB2 gene.
Pauli S; Söker T; Klopp N; Illig T; Engel W; Graw J
Mol Vis; 2007 Jun; 13():962-7. PubMed ID: 17653036
[TBL] [Abstract][Full Text] [Related]
8. 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]
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. A new Fgf10 mutation in the mouse leads to atrophy of the harderian gland and slit-eye phenotype in heterozygotes: a novel model for dry-eye disease?
Puk O; Esposito I; Söker T; Löster J; Budde B; Nürnberg P; Michel-Soewarto D; Fuchs H; Wolf E; Hrabé de Angelis M; Graw J
Invest Ophthalmol Vis Sci; 2009 Sep; 50(9):4311-8. PubMed ID: 19407009
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype.
Puk O; Löster J; Dalke C; Soewarto D; Fuchs H; Budde B; Nürnberg P; Wolf E; de Angelis MH; Graw J
Invest Ophthalmol Vis Sci; 2008 Apr; 49(4):1525-32. PubMed ID: 18385072
[TBL] [Abstract][Full Text] [Related]
14. Differential expression of T-type calcium channels in P/Q-type calcium channel mutant mice with ataxia and absence epilepsy.
Nahm SS; Jung KY; Enger MK; Griffith WH; Abbott LC
J Neurobiol; 2005 Feb; 62(3):352-60. PubMed ID: 15514988
[TBL] [Abstract][Full Text] [Related]
15. Crybb2 coding for βB2-crystallin affects sensorimotor gating and hippocampal function.
Sun M; Hölter SM; Stepan J; Garrett L; Genius J; Kremmer E; Hrabě de Angelis M; Wurst W; Lie DC; Bally-Cuif L; Eder M; Rujescu D; Graw J
Mamm Genome; 2013 Oct; 24(9-10):333-48. PubMed ID: 24096375
[TBL] [Abstract][Full Text] [Related]
16. Identification and mRNA expression of Ogdh, QP-C, and two predicted genes in the postnatal mouse brain.
Sadakata T; Furuichi T
Neurosci Lett; 2006 Sep; 405(3):217-22. PubMed ID: 16901643
[TBL] [Abstract][Full Text] [Related]
17. Three murine cataract mutants (Cat2) are defective in different gamma-crystallin genes.
Klopp N; Favor J; Löster J; Lutz RB; Neuhäuser-Klaus A; Prescott A; Pretsch W; Quinlan RA; Sandilands A; Vrensen GF; Graw J
Genomics; 1998 Sep; 52(2):152-8. PubMed ID: 9782080
[TBL] [Abstract][Full Text] [Related]
18. Arginine 54 and Tyrosine 118 residues of {alpha}A-crystallin are crucial for lens formation and transparency.
Xia CH; Liu H; Chang B; Cheng C; Cheung D; Wang M; Huang Q; Horwitz J; Gong X
Invest Ophthalmol Vis Sci; 2006 Jul; 47(7):3004-10. PubMed ID: 16799046
[TBL] [Abstract][Full Text] [Related]
19. Differential brain transcriptome of beta4 nAChR subunit-deficient mice: is it the effect of the null mutation or the background strain?
Kedmi M; Orr-Urtreger A
Physiol Genomics; 2007 Jan; 28(2):213-22. PubMed ID: 16985005
[TBL] [Abstract][Full Text] [Related]
20. Crygf(Rop): the first mutation in the Crygf gene causing a unique radial lens opacity.
Graw J; Klopp N; Neuhäuser-Klaus A; Favor J; Löster J
Invest Ophthalmol Vis Sci; 2002 Sep; 43(9):2998-3002. PubMed ID: 12202521
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]