189 related articles for article (PubMed ID: 21858719)
1. A spontaneous mutation in Srebf2 leads to cataracts and persistent skin wounds in the lens opacity 13 (lop13) mouse.
Merath KM; Chang B; Dubielzig R; Jeannotte R; Sidjanin DJ
Mamm Genome; 2011 Dec; 22(11-12):661-73. PubMed ID: 21858719
[TBL] [Abstract][Full Text] [Related]
2. Functional analysis of the Hsf4(lop11) allele responsible for cataracts in lop11 mice.
Liang L; Liegel R; Endres B; Ronchetti A; Chang B; Sidjanin DJ
Mol Vis; 2011; 17():3062-71. PubMed ID: 22162625
[TBL] [Abstract][Full Text] [Related]
3. Breakdown of interlocking domains may contribute to formation of membranous globules and lens opacity in ephrin-A5(-/-) mice.
Biswas S; Son A; Yu Q; Zhou R; Lo WK
Exp Eye Res; 2016 Apr; 145():130-139. PubMed ID: 26643403
[TBL] [Abstract][Full Text] [Related]
4. A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice.
Chang B; Wang X; Hawes NL; Ojakian R; Davisson MT; Lo WK; Gong X
Hum Mol Genet; 2002 Mar; 11(5):507-13. PubMed ID: 11875045
[TBL] [Abstract][Full Text] [Related]
5. p62 expression and autophagy in αB-crystallin R120G mutant knock-in mouse model of hereditary cataract.
Wignes JA; Goldman JW; Weihl CC; Bartley MG; Andley UP
Exp Eye Res; 2013 Oct; 115():263-73. PubMed ID: 23872361
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. A 1-bp deletion in the gammaC-crystallin leads to dominant cataracts in mice.
Zhao L; Li K; Bao S; Zhou Y; Liang Y; Zhao G; Chen Y; Xiao J
Mamm Genome; 2010 Aug; 21(7-8):361-9. PubMed ID: 20686773
[TBL] [Abstract][Full Text] [Related]
8. A novel spontaneous mutation of BCAR3 results in extrusion cataracts in CF#1 mouse strain.
Kondo T; Nakamori T; Nagai H; Takeshita A; Kusakabe KT; Okada T
Mamm Genome; 2016 Oct; 27(9-10):451-9. PubMed ID: 27364350
[TBL] [Abstract][Full Text] [Related]
9. Microphakia and congenital cataract formation in a novel Lim2(C51R) mutant mouse.
Puk O; Ahmad N; Wagner S; de Angelis MH; Graw J
Mol Vis; 2011; 17():1164-71. PubMed ID: 21617753
[TBL] [Abstract][Full Text] [Related]
10. A deletion in a cis element of Foxe3 causes cataracts and microphthalmia in rct mice.
Wada K; Maeda YY; Watanabe K; Oshio T; Ueda T; Takahashi G; Yokohama M; Saito J; Seki Y; Takahama S; Ishii R; Shitara H; Taya C; Yonekawa H; Kikkawa Y
Mamm Genome; 2011 Dec; 22(11-12):693-702. PubMed ID: 22002806
[TBL] [Abstract][Full Text] [Related]
11. Autophagy and UPR in alpha-crystallin mutant knock-in mouse models of hereditary cataracts.
Andley UP; Goldman JW
Biochim Biophys Acta; 2016 Jan; 1860(1 Pt B):234-9. PubMed ID: 26071686
[TBL] [Abstract][Full Text] [Related]
12. AlphaA-crystallin R49Cneo mutation influences the architecture of lens fiber cell membranes and causes posterior and nuclear cataracts in mice.
Andley UP
BMC Ophthalmol; 2009 Jul; 9():4. PubMed ID: 19619312
[TBL] [Abstract][Full Text] [Related]
13. Domain disruption and mutation of the bZIP transcription factor, MAF, associated with cataract, ocular anterior segment dysgenesis and coloboma.
Jamieson RV; Perveen R; Kerr B; Carette M; Yardley J; Heon E; Wirth MG; van Heyningen V; Donnai D; Munier F; Black GC
Hum Mol Genet; 2002 Jan; 11(1):33-42. PubMed ID: 11772997
[TBL] [Abstract][Full Text] [Related]
14. Blind sterile 2 (bs2), a hypomorphic mutation in Agps, results in cataracts and male sterility in mice.
Liegel R; Chang B; Dubielzig R; Sidjanin DJ
Mol Genet Metab; 2011 May; 103(1):51-9. PubMed ID: 21353609
[TBL] [Abstract][Full Text] [Related]
15. SREBP-2-deficient and hypomorphic mice reveal roles for SREBP-2 in embryonic development and SREBP-1c expression.
Vergnes L; Chin RG; de Aguiar Vallim T; Fong LG; Osborne TF; Young SG; Reue K
J Lipid Res; 2016 Mar; 57(3):410-21. PubMed ID: 26685326
[TBL] [Abstract][Full Text] [Related]
16. Qki activates Srebp2-mediated cholesterol biosynthesis for maintenance of eye lens transparency.
Shin S; Zhou H; He C; Wei Y; Wang Y; Shingu T; Zeng A; Wang S; Zhou X; Li H; Zhang Q; Mo Q; Long J; Lan F; Chen Y; Hu J
Nat Commun; 2021 May; 12(1):3005. PubMed ID: 34021134
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples.
Le Hellard S; Mühleisen TW; Djurovic S; Fernø J; Ouriaghi Z; Mattheisen M; Vasilescu C; Raeder MB; Hansen T; Strohmaier J; Georgi A; Brockschmidt FF; Melle I; Nenadic I; Sauer H; Rietschel M; Nöthen MM; Werge T; Andreassen OA; Cichon S; Steen VM
Mol Psychiatry; 2010 May; 15(5):463-72. PubMed ID: 18936756
[TBL] [Abstract][Full Text] [Related]
19. Lens crystallin modifications and cataract in transgenic mice overexpressing acylpeptide hydrolase.
Santhoshkumar P; Xie L; Raju M; Reneker L; Sharma KK
J Biol Chem; 2014 Mar; 289(13):9039-52. PubMed ID: 24554718
[TBL] [Abstract][Full Text] [Related]
20. Refractive defects and cataracts in mice lacking lens intrinsic membrane protein-2.
Shiels A; King JM; Mackay DS; Bassnett S
Invest Ophthalmol Vis Sci; 2007 Feb; 48(2):500-8. PubMed ID: 17251442
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]