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La ricerca find articoli where soggetti phrase all words 'RHODOPSIN MUTATION' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 17 riferimenti
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    1. Mohand-Said, S; Hicks, D; Leveillard, T; Picaud, S; Porto, F; Sahel, JA
      Rod-cone interactions: Developmental and clinical significance

      PROGRESS IN RETINAL AND EYE RESEARCH
    2. Shaw, LC; Skold, A; Wong, F; Petters, R; Hauswirth, W; Lewin, AS
      An allele-specific hammerhead ribozyme gene therapy for a porcine model ofautosomal dominant retinitis pigmentosa

      MOLECULAR VISION
    3. Pierce, EA
      Pathways to photoreceptor cell death in inherited retinal degenerations

      BIOESSAYS
    4. Shastry, BS
      Hereditary degenerative retinopathies: Optimism for somatic gene therapy

      IUBMB LIFE
    5. Liu, CD; Li, YW; Peng, M; Laties, AM; Wen, R
      Activation of caspase-3 in the retina of transgenic rats with the rhodopsin mutation S334ter during photoreceptor degeneration

      JOURNAL OF NEUROSCIENCE
    6. LEM J
      DISEASES OF G-PROTEIN-COUPLED SIGNAL-TRANSDUCTION PATHWAYS - THE MAMMALIAN VISUAL-SYSTEM AS A MODEL

      Seminars in the neurosciences
    7. SHASTRY BS
      LIGHT, SIGHT AND FIGHT FOR INSIGHT

      Biochimie
    8. YOSHII M; MURAKAMI A; AKEO K; FUJIKI K; SAGA M; MIZUKAWA A; ITOH J; OKISAKA S; YANASHIMA K; HOTTA Y; KANAI A; OGUCHI Y
      VISUAL FUNCTION IN RETINITIS-PIGMENTOSA RELATED TO A CODON-15 RHODOPSIN GENE MUTATION

      Ophthalmic research
    9. MULLER J; GONDOS B; KOSUGI S; MORI T; SHENKER A
      SEVERE TESTOTOXICOSIS PHENOTYPE ASSOCIATED WITH ASP(578)-]TYR MUTATION OF THE LUTROPHIN CHORIOGONADOTROPHIN RECEPTOR GENE/

      Journal of Medical Genetics
    10. PONJAVIC V; ABRAHAMSON M; ANDREASSON S; EHINGER B; FEX G; POLLAND W
      A MILD PHENOTYPE OF AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA IS ASSOCIATED WITH THE RHODOPSIN MUTATION PRO-267-LEU

      Ophthalmic genetics
    11. PETTERS RM; ALEXANDER CA; WELLS KD; COLLINS EB; SOMMER JR; BLANTON MR; ROJAS G; HAO Y; FLOWERS WL; BANIN E; CIDECIYAN AV; JACOBSON SG; WONG F
      GENETICALLY-ENGINEERED LARGE ANIMAL-MODEL FOR STUDYING CONE PHOTORECEPTOR SURVIVAL AND DEGENERATION IN RETINITIS-PIGMENTOSA

      Nature biotechnology
    12. CHANG GQ; GAITAN A; HAO Y; WONG F
      CORRELATION OF DNA FRAGMENTATION AND CHROMATIN CONDENSATION IN APOPTOTIC NUCLEI OF THE SER-6 MOUSE RETINA

      Microscopy research and technique
    13. CAO W; WEN R; LI F; LAVAIL MM; STEINBERG RH
      MECHANICAL INJURY INCREASES BFGF AND CNTF MRMA EXPRESSION IN THE MOUSE RETINA

      Experimental Eye Research
    14. GOTO Y; PEACHEY NS; ZIROLI NE; SEIPLE WH; GRYCZAN C; PEPPERBERG DR; NAASH MI
      ROD PHOTOTRANSDUCTION IN TRANSGENIC MICE EXPRESSING A MUTANT OPSIN GENE

      Journal of the Optical Society of America. A, Optics, image science,and vision.
    15. DAIGER SP; SULLIVAN LS; RODRIGUEZ JA
      CORRELATION OF PHENOTYPE WITH GENOTYPE IN INHERITED RETINAL DEGENERATION

      Behavioral and brain sciences
    16. VANDENBORN LI; VANSCHOONEVELD MJ; DEJONG LAMS; RIEMSLAG FCC; DEJONG PTVM; GAL A; BLEEKERWAGEMAKERS EM
      THR4LYS RHODOPSIN MUTATION IS ASSOCIATED WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA OF THE CONE-ROD TYPE IN A SMALL DUTCH FAMILY

      Ophthalmic genetics
    17. LI ZY; JACOBSON SG; MILAM AH
      AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA CAUSED BY THE THREONINE-17-METHIONINE RHODOPSIN MUTATION - RETINAL HISTOPATHOLOGY AND IMMUNOCYTOCHEMISTRY

      Experimental Eye Research


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 17/02/20 alle ore 08:24:08