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 *

221 related articles for article (PubMed ID: 8563764)

  • 1. 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]  

  • 2. 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]  

  • 3. Missense mutations in MIP underlie autosomal dominant 'polymorphic' and lamellar cataracts linked to 12q.
    Berry V; Francis P; Kaushal S; Moore A; Bhattacharya S
    Nat Genet; 2000 May; 25(1):15-7. PubMed ID: 10802646
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. The MIP family of integral membrane channel proteins: sequence comparisons, evolutionary relationships, reconstructed pathway of evolution, and proposed functional differentiation of the two repeated halves of the proteins.
    Reizer J; Reizer A; Saier MH
    Crit Rev Biochem Mol Biol; 1993; 28(3):235-57. PubMed ID: 8325040
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. The transcription factor Sp3 interacts with promoter elements of the lens specific MIP gene.
    Kim S; Ge H; Ohtaka-Maruyama C; Chepelinsky AB
    Mol Vis; 1999 Jul; 5():12. PubMed ID: 10407063
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Interaction of major intrinsic protein (aquaporin-0) with fiber connexins in lens development.
    Yu XS; Jiang JX
    J Cell Sci; 2004 Feb; 117(Pt 6):871-80. PubMed ID: 14762116
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 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 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]  

  • 13. 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]  

  • 14. [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]  

  • 15. The mouse lens fiber-cell intrinsic membrane protein MP19 gene (Lim2) and granule membrane protein GMP-17 gene (Nkg7): Isolation and sequence analysis of two neighboring genes.
    Zhou L; Li X; Church RL
    Mol Vis; 2001 Apr; 7():79-88. PubMed ID: 11290961
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataract.
    Cohen D; Bar-Yosef U; Levy J; Gradstein L; Belfair N; Ofir R; Joshua S; Lifshitz T; Carmi R; Birk OS
    Invest Ophthalmol Vis Sci; 2007 May; 48(5):2208-13. PubMed ID: 17460281
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. A dominant mutation within the DNA-binding domain of the bZIP transcription factor Maf causes murine cataract and results in selective alteration in DNA binding.
    Lyon MF; Jamieson RV; Perveen R; Glenister PH; Griffiths R; Boyd Y; Glimcher LH; Favor J; Munier FL; Black GC
    Hum Mol Genet; 2003 Mar; 12(6):585-94. PubMed ID: 12620964
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Modifications to rat lens major intrinsic protein in selenite-induced cataract.
    Schey KL; Fowler JG; Shearer TR; David L
    Invest Ophthalmol Vis Sci; 1999 Mar; 40(3):657-67. PubMed ID: 10067969
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The ocular lens fiber membrane specific protein MIP/Aquaporin 0.
    Chepelinsky AB
    J Exp Zool A Comp Exp Biol; 2003 Nov; 300(1):41-6. PubMed ID: 14598384
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.