BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

340 related articles for article (PubMed ID: 8125718)

  • 21. Retarding photoreceptor degeneration in Pdegtm1/Pdegtml mice by an apoptosis suppressor gene.
    Tsang SH; Chen J; Kjeldbye H; Li WS; Simon MI; Gouras P; Goff SP
    Invest Ophthalmol Vis Sci; 1997 Apr; 38(5):943-50. PubMed ID: 9112990
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Morphological characterization of the retinal degeneration in three strains of mice carrying the rd-3 mutation.
    Linberg KA; Fariss RN; Heckenlively JR; Farber DB; Fisher SK
    Vis Neurosci; 2005; 22(6):721-34. PubMed ID: 16469183
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Retinal degeneration in the pcd cerebellar mutant mouse. I. Light microscopic and autoradiographic analysis.
    LaVail MM; Blanks JC; Mullen RJ
    J Comp Neurol; 1982 Dec; 212(3):217-30. PubMed ID: 7153374
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Profound infantile neuroretinal dysfunction in a heterozygote for the CLN3 genetic defect.
    de los Reyes E; Dyken PR; Phillips P; Brodsky M; Bates S; Glasier C; Mrak RE
    J Child Neurol; 2004 Jan; 19(1):42-6. PubMed ID: 15032383
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Noninvasive imaging by optical coherence tomography to monitor retinal degeneration in the mouse.
    Li Q; Timmers AM; Hunter K; Gonzalez-Pola C; Lewin AS; Reitze DH; Hauswirth WW
    Invest Ophthalmol Vis Sci; 2001 Nov; 42(12):2981-9. PubMed ID: 11687546
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The mouse lysosomal membrane protein 1 gene as a candidate for the motorneuron degeneration (mnd) locus.
    Bermingham NA; Martin JE; Fisher EM
    Genomics; 1996 Mar; 32(2):266-71. PubMed ID: 8833154
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Ceroid lipofuscinosis in the border collie dog: retinal lesions in an animal model of juvenile Batten disease.
    Taylor RM; Farrow BR
    Am J Med Genet; 1992 Feb; 42(4):622-7. PubMed ID: 1319117
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Retinal degeneration in the pcd cerebellar mutant mouse. II. Electron microscopic analysis.
    Blanks JC; Mullen RJ; LaVail MM
    J Comp Neurol; 1982 Dec; 212(3):231-46. PubMed ID: 7153375
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9.
    Bronson RT; Donahue LR; Johnson KR; Tanner A; Lane PW; Faust JR
    Am J Med Genet; 1998 May; 77(4):289-97. PubMed ID: 9600738
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Retinal degeneration in the rd mouse in the absence of c-fos.
    Hafezi F; Abegg M; Grimm C; Wenzel A; Munz K; Stürmer J; Farber DB; Remé CE
    Invest Ophthalmol Vis Sci; 1998 Nov; 39(12):2239-44. PubMed ID: 9804131
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Suppression of developmental retinal cell death but not of photoreceptor degeneration in Bax-deficient mice.
    Mosinger Ogilvie J; Deckwerth TL; Knudson CM; Korsmeyer SJ
    Invest Ophthalmol Vis Sci; 1998 Aug; 39(9):1713-20. PubMed ID: 9699561
    [TBL] [Abstract][Full Text] [Related]  

  • 32. In-utero and post-delivery supplementation of motor neuron degeneration mutant mice with polyunsaturated fatty acids does not alter the clinical or pathological course.
    Bennett MJ; Boriack RL; Birch DG
    Neuropediatrics; 1997 Feb; 28(1):82-4. PubMed ID: 9151333
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Visual electrophysiological features of two naturally occurring mouse models with retinal dysfunction.
    Miyamoto M; Imai R; Sugimoto S; Aoki M; Nagai H; Ando T
    Curr Eye Res; 2006 Apr; 31(4):329-35. PubMed ID: 16603466
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Rescue of photoreceptor function by AAV-mediated gene transfer in a mouse model of inherited retinal degeneration.
    Jomary C; Vincent KA; Grist J; Neal MJ; Jones SE
    Gene Ther; 1997 Jul; 4(7):683-90. PubMed ID: 9282169
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Caspase-3 inhibitor reduces apototic photoreceptor cell death during inherited retinal degeneration in tubby mice.
    Bode C; Wolfrum U
    Mol Vis; 2003 Apr; 9():144-50. PubMed ID: 12724642
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Ceroid-lipofuscinosis (Batten's disease). Sequential electrophysiologic and pathologic changes in the retina of the ovine model.
    Graydon RJ; Jolly RD
    Invest Ophthalmol Vis Sci; 1984 Mar; 25(3):294-301. PubMed ID: 6538190
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Tibetan terrier model of canine ceroid lipofuscinosis.
    Riis RC; Cummings JF; Loew ER; de Lahunta A
    Am J Med Genet; 1992 Feb; 42(4):615-21. PubMed ID: 1609844
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Caspase-3 inhibitor transiently delays inherited retinal degeneration in C3H mice carrying the rd gene.
    Yoshizawa K; Kiuchi K; Nambu H; Yang J; Senzaki H; Kiyozuka Y; Shikata N; Tsubura A
    Graefes Arch Clin Exp Ophthalmol; 2002 Mar; 240(3):214-9. PubMed ID: 11935279
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8.
    Ranta S; Zhang Y; Ross B; Lonka L; Takkunen E; Messer A; Sharp J; Wheeler R; Kusumi K; Mole S; Liu W; Soares MB; Bonaldo MF; Hirvasniemi A; de la Chapelle A; Gilliam TC; Lehesjoki AE
    Nat Genet; 1999 Oct; 23(2):233-6. PubMed ID: 10508524
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Accumulation of the adenosine triphosphate synthase subunit C in the mnd mutant mouse. A model for neuronal ceroid lipofuscinosis.
    Pardo CA; Rabin BA; Palmer DN; Price DL
    Am J Pathol; 1994 Apr; 144(4):829-35. PubMed ID: 8160780
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.