BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

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]
    of 10.