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La ricerca find articoli where authors phrase all words 'BYKHOVSKAYA Y' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 13 riferimenti
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    1. Bykhovskaya, Y; Yang, HY; Taylor, K; Hang, T; Tun, RYM; Estivill, X; Casano, RAMS; Majamaa, K; Shohat, M; Fischel-Ghodsian, N
      Modifier locus for mitochondrial DNA disease: Linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness

      GENETICS IN MEDICINE
    2. Johnson, KR; Zheng, QY; Bykhovskaya, Y; Spirina, O; Fischel-Ghodsian, N
      A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

      NATURE GENETICS
    3. Spirina, O; Bykhovskaya, Y; Kajava, AV; O'Brien, TW; Nierlich, DP; Mougey, EB; Sylvester, JE; Graack, HR; Wittmann-Liebold, B; Fischel-Ghodsian, N
      Heart-specific splice-variant of a human mitochondrial ribosomal protein (mRNA processing; tissue specific splicing)

      GENE
    4. Chen, XG; Bykhovskaya, Y; Tidow, N; Hamon, M; Bercovitz, Z; Spirina, O; Fischel-Ghodsian, N
      The Familial Mediterranean Fever protein interacts and colocalizes with a putative Golgi transporter

      PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE
    5. Bykhovskaya, Y; Estivill, X; Taylor, K; Hang, T; Hamon, M; Casano, RAMS; Yang, HY; Rotter, JI; Shohat, M; Fischel-Ghodsian, N
      Candidate locus for a nuclear modifier gene for maternally inherited deafness

      AMERICAN JOURNAL OF HUMAN GENETICS
    6. Casano, RAMS; Johnson, DF; Bykhovskaya, Y; Torricelli, F; Bigozzi, M; Fischel-Ghodsian, N
      Inherited susceptibility to aminoglycoside ototoxicity: Genetic heterogeneity and clinical implications

      AMERICAN JOURNAL OF OTOLARYNGOLOGY
    7. Friedman, RA; Bykhovskaya, Y; Sue, CM; DiMauro, S; Bradley, R; Fallis-Cunningham, R; Paradies, N; Pensak, ML; Smith, RJ; Groden, J; Li, XYC; Fischel-Ghodsian, N
      Maternally inherited nonsyndromic hearing loss

      AMERICAN JOURNAL OF MEDICAL GENETICS
    8. CASANO RAMS; BYKHOVSKAYA Y; JOHNSON DF; HAMON M; TORRICELLI F; BIGOZZI M; FISCHELGHODSIAN N
      HEARING-LOSS DUE TO THE MITOCHONDRIAL A1555G MUTATION IN ITALIAN FAMILIES

      American journal of medical genetics
    9. BYKHOVSKAYA Y; SHOHAT M; EHRENMAN K; JOHNSON D; HAMON M; CANTOR RM; AOUIZERAT B; BU XD; ROTTER JI; JABER L; FISCHELGHODSIAN N
      EVIDENCE FOR COMPLEX NUCLEAR INHERITANCE IN A PEDIGREE WITH NONSYNDROMIC DEAFNESS DUE TO A HOMOPLASMIC MITOCHONDRIAL MUTATION

      American journal of medical genetics
    10. SEVIOR KB; HATAMOCHI A; STEWART IA; BYKHOVSKAYA Y; ALLENPOWELL DR; FISCHELGHODSIAN N; MAW MA
      MITOCHONDRIAL A7445G MUTATION IN 2 PEDIGREES WITH PALMOPLANTAR KERATODERMA AND DEAFNESS

      American journal of medical genetics
    11. FISCHELGHODSIAN N; BYKHOVSKAYA Y; TAYLOR K; KAHEN T; CANTOR R; EHRENMAN K; SMITH R; KEITHLEY E
      TEMPORAL BONE ANALYSIS OF PATIENTS WITH PRESBYCUSIS REVEALS HIGH-FREQUENCY OF MITOCHONDRIAL MUTATIONS

      Hearing research
    12. FRIEDMAN RA; BYKHOVSKAYA Y; TU G; TALBOT JM; WILSON DF; PARNES LS; FISCHELGHODSIAN N
      MOLECULAR ANALYSIS OF THE POU3F4 GENE IN PATIENTS WITH CLINICAL AND RADIOGRAPHIC EVIDENCE OF X-LINKED MIXED DEAFNESS WITH PERILYMPHATIC GUSHER

      The Annals of otology, rhinology & laryngology
    13. BYKHOVSKAYA Y; EHRENMAN K; JOHNSON D; HAMON M; CANTOR R; TAYLOR K; BU X; JABER L; ROTTER JI; SHOHAT M; FISCHELGHODSIAN N
      LACK OF EVIDENCE FOR LINKAGE TO A NUCLEAR LOCUS IN A PEDIGREE WITH NONSYNDROMIC DEAFNESS DUE TO A HOMOPLASMIC MITOCHONDRIAL MUTATION

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 31/10/20 alle ore 08:57:43