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La ricerca find articoli where authors phrase all words ' JAISSLE G' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 11 riferimenti
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    1. Seeliger, MW; Grimm, C; Stahlberg, F; Friedburg, C; Jaissle, G; Zrenner, E; Guo, H; Reme, CE; Humphries, P; Hofmann, F; Biel, M; Fariss, RN; Redmond, TM; Wenzel, A
      New views on RPE65 deficiency: the rod system is the source of vision in amouse model of Leber congenital amaurosis

      NATURE GENETICS
    2. Spiwoks-Becker, I; Vollrath, L; Seeliger, MW; Jaissle, G; Eshkind, LG; Leube, RE
      Synaptic vesicle alterations in rod photoreceptors of synaptophysin-deficient mice

      NEUROSCIENCE
    3. Wenzel, A; Grimm, C; Seeliger, MW; Jaissle, G; Hafezi, F; Kretschmer, R; Zrenner, E; Reme, CE
      Prevention of photoreceptor apoptosis by activation of the glucocorticoid receptor

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    4. Incerti, B; Cortese, K; Pizzigoni, A; Surace, EM; Varani, S; Coppola, M; Jeffery, G; Seeliger, M; Jaissle, G; Bennett, DC; Marigo, V; Schiaffino, MV; Tacchetti, C; Ballabio, A
      Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1

      HUMAN MOLECULAR GENETICS
    5. Biel, M; Seeliger, M; Pfeifer, A; Kohler, K; Gerstner, A; Ludwig, A; Jaissle, G; Fauser, S; Zrenner, E; Hofmann, F
      Selective loss of cone function in mice lacking the cyclic nucleotide-gated channel CNG3

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    6. VANDENHURK JAJM; HENDRIKS W; VANDEPOL DJR; OERLEMANS F; JAISSLE G; RUTHER K; KOHLER K; HARTMANN J; ZRENNER E; VANBOKHOVEN H; WIERINGA B; ROPERS HH; CREMERS FPM
      MOUSE CHOROIDEREMIA GENE MUTATION CAUSES PHOTORECEPTOR CELL DEGENERATION AND IS NOT TRANSMITTED THROUGH THE FEMALE GERMLINE

      Human molecular genetics
    7. CREMERS FPM; VANDENHURK JAJM; HENDRIKS W; VANDEPOL TJR; OERLEMANS F; JAISSLE G; KOHLER K; RUTHER K; HARTMANN J; ZRENNER E; WIERINGA B; ROPERS HH
      THE CHOROIDEREMIA MUTATION RESULTS IN PHOTORECEPTOR CELL DEGENERATIONIN CHIMERIC MICE BUT IS EMBRYONIC LETHAL IN HEMIZYGOTIC MICE

      The FASEB journal
    8. RUETHER K; VANDEPOL D; JAISSLE G; BERGER W; TORNOW RP; ZRENNER E
      RETINOSCHISISLIKE ALTERATIONS IN THE MOUSE EYE CAUSED BY GENE TARGETING OF THE NORRIE DISEASE GENE

      Investigative ophthalmology & visual science
    9. RUETHER K; VANDERPOL D; BERGER W; JAISSLE G; ZRENNER E
      PREFERENTIAL LOSS OF ERG B-WAVE AMPLITUDE IN A TRANSGENIC MOUSE MODELOF NORRIE DISEASE (ND)

      Investigative ophthalmology & visual science
    10. JAISSLE G; RUETHER K; VANDENHURK J; CREMERS F; ZRENNER E
      ELECTROPHYSIOLOGICAL AND MORPHOLOGICAL FINDINGS IN MICE HETEROZYGOUS FOR A CHOROIDEREMIA (CHM) GENE MUTATION

      Investigative ophthalmology & visual science
    11. VANDENHURK J; OERLEMANS F; VANDEPOL D; JAISSLE G; RUTHER K; ROPERS HH; WIERINGA B; CREMERS F; HENDRIKS W
      MATERNAL TRANSMISSION OF A CHOROIDEREMIA MUTATION IN MICE IS EMBRYONIC LETHAL

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/01/21 alle ore 22:54:41