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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 15016766)

  • 41. Pathogenic mechanism of congenital cataract caused by the CRYBA1/A3-G91del variant and related intervention strategies.
    Xu J; Wang H; Wu C; Wang A; Wu W; Xu J; Luo C; Ni S; Yao K; Chen X
    Int J Biol Macromol; 2021 Oct; 189():44-52. PubMed ID: 34419537
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [The genetics of hereditary cataract].
    Beby F; Morle L; Michon L; M B; Edery P; Burillon C; Denis P
    J Fr Ophtalmol; 2003 Apr; 26(4):400-8. PubMed ID: 12843900
    [TBL] [Abstract][Full Text] [Related]  

  • 43. The identification and characterization of the p.G91 deletion in CRYBA1 in a Chinese family with congenital cataracts.
    Li D; Jing Q; Jiang Y
    BMC Med Genet; 2019 Sep; 20(1):153. PubMed ID: 31488069
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Cataract-causing G91del mutant destabilised βA3 heteromers formation linking with structural stability and cellular viability.
    Wang H; Tian Q; Xu J; Xu W; Yao K; Chen X
    Br J Ophthalmol; 2022 Oct; 106(10):1473-1478. PubMed ID: 34489339
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Characterization of a mutant R11H αB-crystallin associated with human inherited cataract.
    Chen Q; Yan M; Xiang F; Zhou X; Liu Y; Zheng F
    Biol Chem; 2010 Dec; 391(12):1391-400. PubMed ID: 21087083
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Creation of a new eye lens crystallin (Gambeta) through structure-guided mutagenic grafting of the surface of betaB2 crystallin onto the hydrophobic core of gammaB crystallin.
    Kapoor D; Singh B; Subramanian K; Guptasarma P
    FEBS J; 2009 Jun; 276(12):3341-53. PubMed ID: 19438717
    [TBL] [Abstract][Full Text] [Related]  

  • 47. AlphaA-crystallin expression prevents gamma-crystallin insolubility and cataract formation in the zebrafish cloche mutant lens.
    Goishi K; Shimizu A; Najarro G; Watanabe S; Rogers R; Zon LI; Klagsbrun M
    Development; 2006 Jul; 133(13):2585-93. PubMed ID: 16728471
    [TBL] [Abstract][Full Text] [Related]  

  • 48. An alphaA-crystallin gene mutation, Arg12Cys, causing inherited cataract-microcornea exhibits an altered heat-shock response.
    Zhang LY; Yam GH; Tam PO; Lai RY; Lam DS; Pang CP; Fan DS
    Mol Vis; 2009 Jun; 15():1127-38. PubMed ID: 19503744
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Progress in pathogenic genes and their functions of congenital cataract].
    Wang KJ; Zhu SQ; Cheng J
    Zhonghua Yan Ke Za Zhi; 2010 Mar; 46(3):280-4. PubMed ID: 20450675
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Unfolding crystallins: the destabilizing role of a beta-hairpin cysteine in betaB2-crystallin by simulation and experiment.
    MacDonald JT; Purkiss AG; Smith MA; Evans P; Goodfellow JM; Slingsby C
    Protein Sci; 2005 May; 14(5):1282-92. PubMed ID: 15840832
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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]  

  • 52. Mapping of four mouse genes encoding eye lens-specific structural, gap junction, and integral membrane proteins: Cryba1 (crystallin beta A3/A1), Crybb2 (crystallin beta B2), Gja8 (MP70), and Lim2 (MP19).
    Kerscher S; Church RL; Boyd Y; Lyon MF
    Genomics; 1995 Sep; 29(2):445-50. PubMed ID: 8666393
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Special fasciculiform cataract caused by a mutation in the gammaD-crystallin gene.
    Shentu X; Yao K; Xu W; Zheng S; Hu S; Gong X
    Mol Vis; 2004 Mar; 10():233-9. PubMed ID: 15064679
    [TBL] [Abstract][Full Text] [Related]  

  • 54. The importance of the last strand at the C-terminus in βB2-crystallin stability and assembly.
    Zhang K; Zhao WJ; Leng XY; Wang S; Yao K; Yan YB
    Biochim Biophys Acta; 2014 Jan; 1842(1):44-55. PubMed ID: 24120835
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Identification of a missense mutation in the alphaA-crystallin gene of the lop18 mouse.
    Chang B; Hawes NL; Roderick TH; Smith RS; Heckenlively JR; Horwitz J; Davisson MT
    Mol Vis; 1999 Sep; 5():21. PubMed ID: 10493778
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Characterization of a familial t(16;22) balanced translocation associated with congenital cataract leads to identification of a novel gene, TMEM114, expressed in the lens and disrupted by the translocation.
    Jamieson RV; Farrar N; Stewart K; Perveen R; Mihelec M; Carette M; Grigg JR; McAvoy JW; Lovicu FJ; Tam PP; Scambler P; Lloyd IC; Donnai D; Black GC
    Hum Mutat; 2007 Oct; 28(10):968-77. PubMed ID: 17492639
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A missense mutation in CRYBB2 leads to progressive congenital membranous cataract by impacting the solubility and function of βB2-crystallin.
    Chen W; Chen X; Hu Z; Lin H; Zhou F; Luo L; Zhang X; Zhong X; Yang Y; Wu C; Lin Z; Ye S; Liu Y;
    PLoS One; 2013; 8(11):e81290. PubMed ID: 24312286
    [TBL] [Abstract][Full Text] [Related]  

  • 58. 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]  

  • 59. Proteomic analysis of water insoluble proteins from normal and cataractous human lenses.
    Harrington V; Srivastava OP; Kirk M
    Mol Vis; 2007 Sep; 13():1680-94. PubMed ID: 17893670
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A second gene for cerulean cataracts maps to the beta crystallin region on chromosome 22.
    Kramer P; Yount J; Mitchell T; LaMorticella D; Carrero-Valenzuela R; Lovrien E; Maumenee I; Litt M
    Genomics; 1996 Aug; 35(3):539-42. PubMed ID: 8812489
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.