AAAAAA

   
Results: 1-8 |
Results: 8
CLINICAL AND MOLECULAR CHARACTERIZATION OF A NOVEL INCL MUTATION IN AN ITALIAN PATIENT
Authors: SANTORELLI FM CARROZZO R PETRUZZELLA V ZEVIANI M BERTINI ES
Citation: Fm. Santorelli et al., CLINICAL AND MOLECULAR CHARACTERIZATION OF A NOVEL INCL MUTATION IN AN ITALIAN PATIENT, European journal of human genetics, 6, 1998, pp. 1004-1004
COMPLEMENTATION TESTS AND SEQUENCE-ANALYSIS OF 7 GENES-CONTROLLING THE FORMATION OF CYTOCHROME-C-OXIDASE IN LEIGH-DISEASE
Authors: ZEVIANI M PETRUZZELLA V IANNA P FERNANDEZ P TIRANTI V
Citation: M. Zeviani et al., COMPLEMENTATION TESTS AND SEQUENCE-ANALYSIS OF 7 GENES-CONTROLLING THE FORMATION OF CYTOCHROME-C-OXIDASE IN LEIGH-DISEASE, Neurology, 50(4), 1998, pp. 4117-4117
ALTERATION OF MITOCHONDRIAL-DNA AND RNA LEVEL IN HUMAN FIBROBLASTS WITH IMPAIRED VITAMIN-B12 COENZYME SYNTHESIS
Authors: CANTATORE P PETRUZZELLA V NICOLETTI C PAPADIA F FRACASSO F RUSTIN P GADALETA MN
Citation: P. Cantatore et al., ALTERATION OF MITOCHONDRIAL-DNA AND RNA LEVEL IN HUMAN FIBROBLASTS WITH IMPAIRED VITAMIN-B12 COENZYME SYNTHESIS, FEBS letters, 432(3), 1998, pp. 173-178
A NOVEL INSERTION MUTATION (A(169I)) IN THE CLN1 GENE IS ASSOCIATED WITH INFANTILE NEURONAL CEROID-LIPOFUSCINOSIS IN AN ITALIAN PATIENT
Authors: SANTORELLI FM BERTINI E PETRUZZELLA V DICAPUA M CALVIERI S GASPARINI P ZEVIANI M
Citation: Fm. Santorelli et al., A NOVEL INSERTION MUTATION (A(169I)) IN THE CLN1 GENE IS ASSOCIATED WITH INFANTILE NEURONAL CEROID-LIPOFUSCINOSIS IN AN ITALIAN PATIENT, Biochemical and biophysical research communications, 245(2), 1998, pp. 519-522
DISORDERS OF NUCLEAR-MITOCHONDRIAL INTERGENOMIC SIGNALING
Authors: ZEVIANI M PETRUZZELLA V CARROZZO R
Citation: M. Zeviani et al., DISORDERS OF NUCLEAR-MITOCHONDRIAL INTERGENOMIC SIGNALING, Journal of bioenergetics and biomembranes, 29(2), 1997, pp. 121-130
IDENTIFICATION OF A NOVEL MUTATION OF THE CNL1 GENE LEADING TO INFANTILE NEURONAL CEROID-LIPOFUSCINOSIS IN AN ITALIAN PATIENT
Authors: SANTORELLI F BERTINI E PETRUZZELLA V DICAPUA M GASPARINI P ZEVIANI M
Citation: F. Santorelli et al., IDENTIFICATION OF A NOVEL MUTATION OF THE CNL1 GENE LEADING TO INFANTILE NEURONAL CEROID-LIPOFUSCINOSIS IN AN ITALIAN PATIENT, American journal of human genetics, 61(4), 1997, pp. 1516-1516
DECREASE OF D-LOOP FREQUENCY IN HEART AND CEREBRAL HEMISPHERES MITOCHONDRIAL-DNA OF AGED RAT
Authors: PETRUZZELLA V FRACASSO F GADALETA MN CANTATORE P
Citation: V. Petruzzella et al., DECREASE OF D-LOOP FREQUENCY IN HEART AND CEREBRAL HEMISPHERES MITOCHONDRIAL-DNA OF AGED RAT, Molecular and chemical neuropathology, 24(2-3), 1995, pp. 193-202
EXTREMELY HIGH-LEVELS OF MUTANT MTDNAS CO-LOCALIZE WITH CYTOCHROME-C OXIDASE-NEGATIVE RAGGED-RED FIBERS IN PATIENTS HARBORING A POINT MUTATION AT NT-3243
Authors: PETRUZZELLA V MORAES CT SANO MC BONILLA E DIMAURO S SCHON EA
Citation: V. Petruzzella et al., EXTREMELY HIGH-LEVELS OF MUTANT MTDNAS CO-LOCALIZE WITH CYTOCHROME-C OXIDASE-NEGATIVE RAGGED-RED FIBERS IN PATIENTS HARBORING A POINT MUTATION AT NT-3243, Human molecular genetics, 3(3), 1994, pp. 449-454
Risultati: 1-8 |