BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 18385073)

  • 41. Sequence analysis and expression mapping of the rat clustered protocadherin gene repertoires.
    Zou C; Huang W; Ying G; Wu Q
    Neuroscience; 2007 Jan; 144(2):579-603. PubMed ID: 17110050
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Identification of novel striatal genes by expression profiling in adult mouse brain.
    Ghate A; Befort K; Becker JA; Filliol D; Bole-Feysot C; Demebele D; Jost B; Koch M; Kieffer BL
    Neuroscience; 2007 May; 146(3):1182-92. PubMed ID: 17395390
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Distinct expression and subcellular localization patterns of Na+/HCO3- cotransporter (SLC 4A4) variants NBCe1-A and NBCe1-B in mouse brain.
    Rickmann M; Orlowski B; Heupel K; Roussa E
    Neuroscience; 2007 May; 146(3):1220-31. PubMed ID: 17433553
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Analysis of the Pax-3 gene in the mouse mutant splotch.
    Goulding M; Sterrer S; Fleming J; Balling R; Nadeau J; Moore KJ; Brown SD; Steel KP; Gruss P
    Genomics; 1993 Aug; 17(2):355-63. PubMed ID: 8406486
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Interaction and biophysical properties of human lens Q155* betaB2-crystallin mutant.
    Liu BF; Liang JJ
    Mol Vis; 2005 Apr; 11():321-7. PubMed ID: 15889016
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Crybb2 associates with Tmsb4X and is crucial for dendrite morphogenesis.
    Sun M; Ahmad N; Zhang R; Graw J
    Biochem Biophys Res Commun; 2018 Sep; 503(1):123-130. PubMed ID: 29864422
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Chemical mutagenesis induced two high bone density mouse mutants map to a concordant distal chromosome 4 locus.
    Mohan S; Chest V; Chadwick RB; Wergedal JE; Srivastava AK
    Bone; 2007 Nov; 41(5):860-8. PubMed ID: 17884746
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Mutation of Dock5, a member of the guanine exchange factor Dock180 superfamily, in the rupture of lens cataract mouse.
    Omi N; Kiyokawa E; Matsuda M; Kinoshita K; Yamada S; Yamada K; Matsushima Y; Wang Y; Kawai J; Suzuki M; Hayashizaki Y; Hiai H
    Exp Eye Res; 2008 May; 86(5):828-34. PubMed ID: 18396277
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Identification of a novel CRYBB2 missense mutation causing congenital autosomal dominant cataract.
    Weisschuh N; Aisenbrey S; Wissinger B; Riess A
    Mol Vis; 2012; 18():174-80. PubMed ID: 22312185
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Standardized quantitative in situ hybridization using radioactive oligonucleotide probes for detecting relative levels of mRNA transcripts verified by real-time PCR.
    Broide RS; Trembleau A; Ellison JA; Cooper J; Lo D; Young WG; Morrison JH; Bloom FE
    Brain Res; 2004 Mar; 1000(1-2):211-22. PubMed ID: 15053970
    [TBL] [Abstract][Full Text] [Related]  

  • 51. The expression of Troponin T1 gene is induced by ketamine in adult mouse brain.
    Lowe XR; Lu X; Marchetti F; Wyrobek AJ
    Brain Res; 2007 Oct; 1174():7-17. PubMed ID: 17850769
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Insertion of an intracisternal A particle retrotransposon element in plasma membrane calcium ATPase 2 gene attenuates its expression and produces an ataxic phenotype in joggle mutant mice.
    Sun XY; Chen ZY; Hayashi Y; Kanou Y; Takagishi Y; Oda S; Murata Y
    Gene; 2008 Mar; 411(1-2):94-102. PubMed ID: 18280673
    [TBL] [Abstract][Full Text] [Related]  

  • 53. crv4, a mouse model for human ataxia associated with kyphoscoliosis caused by an mRNA splicing mutation of the metabotropic glutamate receptor 1 (Grm1).
    Conti V; Aghaie A; Cilli M; Martin N; Caridi G; Musante L; Candiano G; Castagna M; Fairen A; Ravazzolo R; Guenet JL; Puliti A
    Int J Mol Med; 2006 Oct; 18(4):593-600. PubMed ID: 16964410
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Specific expression of Gsta4 in mouse cochlear melanocytes: a novel role for hearing and melanocyte differentiation.
    Uehara S; Izumi Y; Kubo Y; Wang CC; Mineta K; Ikeo K; Gojobori T; Tachibana M; Kikuchi T; Kobayashi T; Shibahara S; Taya C; Yonekawa H; Shiroishi T; Yamamoto H
    Pigment Cell Melanoma Res; 2009 Feb; 22(1):111-9. PubMed ID: 18983533
    [TBL] [Abstract][Full Text] [Related]  

  • 55. A CRYBB2 mutation in a Taiwanese family with autosomal dominant cataract.
    Ching YH; Yeh JI; Fan WL; Chen KC; Yeh MC; Woon PY; Lee YC
    J Formos Med Assoc; 2019 Jan; 118(1 Pt 1):57-63. PubMed ID: 29395391
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Identification of possible candidate biomarkers for local or whole body radiation exposure in C57BL/6 mice.
    Lee HJ; Lee M; Kang CM; Jeoung D; Bae S; Cho CK; Lee YS
    Int J Radiat Oncol Biol Phys; 2007 Nov; 69(4):1272-81. PubMed ID: 17967317
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Caytaxin deficiency causes generalized dystonia in rats.
    Xiao J; Ledoux MS
    Brain Res Mol Brain Res; 2005 Nov; 141(2):181-92. PubMed ID: 16246457
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Differential gene expression in Ndph-knockout mice in retinal development.
    Schäfer NF; Luhmann UF; Feil S; Berger W
    Invest Ophthalmol Vis Sci; 2009 Feb; 50(2):906-16. PubMed ID: 18978344
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Differential expression of extracellular matrix and adhesion molecule genes in the brain of juvenile versus adult mice in responses to intracerebroventricular administration of IL-1.
    Ching S; Zhang H; Chen Q; Quan N
    Neuroimmunomodulation; 2007; 14(1):46-56. PubMed ID: 17700040
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A novel mutation in CRYBB2 responsible for inherited coronary cataract.
    Lou D; Tong JP; Zhang LY; Chiang SW; Lam DS; Pang CP
    Eye (Lond); 2009 May; 23(5):1213-20. PubMed ID: 18617901
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.