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Results: 1-25 | 26-35
Results: 1-25/35
IN-VIVO RESPONSE OF MOUSE-LIVER TO GAMMA-RADIATION ASSESSED BY THE COMET ASSAY
Authors: CARRERA P DEMIGUEL M LOPEZ J DELATORRE C NAVARETTE MH
Citation: P. Carrera et al., IN-VIVO RESPONSE OF MOUSE-LIVER TO GAMMA-RADIATION ASSESSED BY THE COMET ASSAY, Mutation research. Genetic toxicology and environmental mutagenesis, 413(1), 1998, pp. 23-31
MUTATIONAL ANALYSIS IN A MULTIGENIC SCREENING BY DG-DGGE
Authors: CREMONESI L CARRERA P FIRPO S CARDILLO E FERRARI M RIGHETTI SB RIGHETTI PG MAURI D GELFI C
Citation: L. Cremonesi et al., MUTATIONAL ANALYSIS IN A MULTIGENIC SCREENING BY DG-DGGE, European journal of human genetics, 6, 1998, pp. 1034-1034
CHARACTERIZATION OF MUTATIONS WITHIN THE CACNL1A4 GENE IN ITALIAN FAMILIES WITH FAMILIAL HEMIPLEGIC MIGRAINE (FHM)
Authors: CARRERA P STENIRRI S PIATTI M FERRARI M RIGHETTI PG MAURI D CURCIO M GELFI C
Citation: P. Carrera et al., CHARACTERIZATION OF MUTATIONS WITHIN THE CACNL1A4 GENE IN ITALIAN FAMILIES WITH FAMILIAL HEMIPLEGIC MIGRAINE (FHM), European journal of human genetics, 6, 1998, pp. 4115-4115
PREVALENCE OF MUTATION ASSOCIATED TO RESISTANCE WITH NUCLEOSIDE ANALOGS IN A COHORT OF NAIVE HIV-1 POSITIVE SUBJECTS DURING THE PERIOD 1984-1997
Authors: TAMBUSSI G BOERI E CARRERA P GIANOTTI N LAZZARIN A
Citation: G. Tambussi et al., PREVALENCE OF MUTATION ASSOCIATED TO RESISTANCE WITH NUCLEOSIDE ANALOGS IN A COHORT OF NAIVE HIV-1 POSITIVE SUBJECTS DURING THE PERIOD 1984-1997, Journal of biological regulators and homeostatic agents, 12(1-2), 1998, pp. 32-34
COMPARISON OF CLINICAL-RADIOLOGICAL AND MOLECULAR FINDINGS IN HYPOCHONDROPLASIA
Authors: PRINSTER C CARRERA P DELMASCHIO M WEBER G MAGHNIE M VIGONE MC MORA S TONINI G RIGON F BELUFFI G SEVERI F CHIUMELLO G FERRARI M
Citation: C. Prinster et al., COMPARISON OF CLINICAL-RADIOLOGICAL AND MOLECULAR FINDINGS IN HYPOCHONDROPLASIA, American journal of medical genetics, 75(1), 1998, pp. 109-112
A MODIFIER SCREEN IN THE EYE REVEALS CONTROL GENES FOR KRUPPEL ACTIVITY IN THE DROSOPHILA EMBRYO
Authors: CARRERA P ABRELL S KERBER B WALLDORF U PREISS A HOCH M JACKLE H
Citation: P. Carrera et al., A MODIFIER SCREEN IN THE EYE REVEALS CONTROL GENES FOR KRUPPEL ACTIVITY IN THE DROSOPHILA EMBRYO, Proceedings of the National Academy of Sciences of the United Statesof America, 95(18), 1998, pp. 10779-10784
DETECTION OF HIV-TYPE-1 VARIANTS RESISTANT TO MULTIPLE-DRUGS BY DRHODAMINE TERMINATORS AUTOMATED DNA DIRECT SEQUENCING IN THE CLINICAL LABORATORY
Authors: FERRARI M CRUCIANELLI R BOERI E STUCCHI S RACCA S MURONE M TAMBUSSI G LAZZARIN A CARRERA P
Citation: M. Ferrari et al., DETECTION OF HIV-TYPE-1 VARIANTS RESISTANT TO MULTIPLE-DRUGS BY DRHODAMINE TERMINATORS AUTOMATED DNA DIRECT SEQUENCING IN THE CLINICAL LABORATORY, Clinical chemistry, 44, 1998, pp. 15-15
MUTATIONAL ANALYSIS IN A MULTIGENIC SCREENING BY DG-DGGE
Authors: FERRARI M CARRERA P FIRPO S CARDILLO E CREMONESI L RIGHETTI SC RIGHETTI PG MAURI D GELFI C
Citation: M. Ferrari et al., MUTATIONAL ANALYSIS IN A MULTIGENIC SCREENING BY DG-DGGE, Clinical chemistry, 44, 1998, pp. 142-142
A FAST COMET ASSAY VARIANT FOR SOLID TISSUE-CELLS - THE ASSESSMENT OFDNA-DAMAGE IN HIGHER-PLANTS
Authors: NAVARRETE MH CARRERA P DEMIGUEL M DELATORRE C
Citation: Mh. Navarrete et al., A FAST COMET ASSAY VARIANT FOR SOLID TISSUE-CELLS - THE ASSESSMENT OFDNA-DAMAGE IN HIGHER-PLANTS, Mutation research. Genetic toxicology and environmental mutagenesis, 389(2-3), 1997, pp. 271-277
NEW POLYMORPHISM IN EXON-14 OF THE DYSTROPHIN GENE DETECTED BY RT-PCRAND DGGE
Authors: BARBIERI AM SORIANI N FERRARI M CARRERA P
Citation: Am. Barbieri et al., NEW POLYMORPHISM IN EXON-14 OF THE DYSTROPHIN GENE DETECTED BY RT-PCRAND DGGE, Molecular and cellular probes, 11(2), 1997, pp. 161-162
ARE SPONTANEOUS EXPRESSIONS AND EMOTIONS LINKED - AN EXPERIMENTAL TEST OF COHERENCE
Authors: FERNANDEZDOLS JM SANCHEZ F CARRERA P RUIZBELDA MA
Citation: Jm. Fernandezdols et al., ARE SPONTANEOUS EXPRESSIONS AND EMOTIONS LINKED - AN EXPERIMENTAL TEST OF COHERENCE, Journal of nonverbal behavior, 21(3), 1997, pp. 163-177
UNUSUAL CLINICAL-FEATURES AND EARLY BRAIN MRI LESIONS IN A FAMILY WITH CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY
Authors: MALANDRINI A CARRERA P CIACCI G GONNELLI S VILLANOVA M PALMERI S VISMARA L BRANCOLINI V SIGNORINI E FERRARI M GUAZZI GC
Citation: A. Malandrini et al., UNUSUAL CLINICAL-FEATURES AND EARLY BRAIN MRI LESIONS IN A FAMILY WITH CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY, Neurology, 48(5), 1997, pp. 1200-1203
RAPID DETECTION OF 21-HYDROXYLASE DEFICIENCY MUTATIONS BY ALLELE-SPECIFIC IN-VITRO AMPLIFICATION AND CAPILLARY-ZONE-ELECTROPHORESIS
Authors: CARRERA P BARBIERI AM FERRARI M RIGHETTI PG PEREGO M GELFI C
Citation: P. Carrera et al., RAPID DETECTION OF 21-HYDROXYLASE DEFICIENCY MUTATIONS BY ALLELE-SPECIFIC IN-VITRO AMPLIFICATION AND CAPILLARY-ZONE-ELECTROPHORESIS, Clinical chemistry, 43(11), 1997, pp. 2121-2127
LIGASE CHAIN-REACTION ASSAY FOR HUMAN MUTATIONS - THE SICKLE-CELL BY LCR ASSAY
Authors: REYES AA CARRERA P CARDILLO E UGOZZOLI L LOWERY JD LIN CIP GO M FERRARI M WALLACE RB
Citation: Aa. Reyes et al., LIGASE CHAIN-REACTION ASSAY FOR HUMAN MUTATIONS - THE SICKLE-CELL BY LCR ASSAY, Clinical chemistry, 43(1), 1997, pp. 40-44
CACN 1A4 GENE-MUTATIONS IN ITALIAN FAMILIES WITH FAMILIAL HEMIPLEGIC MIGRAINE (FHM)/
Authors: CARRERA P STENIRRI S PIATTI M FERRARI M RIGHETTI PG MAURI D CAPELLI L GELFI C
Citation: P. Carrera et al., CACN 1A4 GENE-MUTATIONS IN ITALIAN FAMILIES WITH FAMILIAL HEMIPLEGIC MIGRAINE (FHM)/, American journal of human genetics, 61(4), 1997, pp. 2393-2393
ANALYSIS OF SPANISH ACOUSTIC SURVEYS FOR SARDINE, 1991-1993 - ABUNDANCE ESTIMATES AND INTERANNUAL VARIABILITY
Authors: PORTEIRO C CARRERA P MIQUEL J
Citation: C. Porteiro et al., ANALYSIS OF SPANISH ACOUSTIC SURVEYS FOR SARDINE, 1991-1993 - ABUNDANCE ESTIMATES AND INTERANNUAL VARIABILITY, ICES journal of marine science, 53(2), 1996, pp. 429-433
7 NOVEL-ADDITIONAL SMALL MUTATIONS AND A NEW ALTERNATIVE SPLICING IN THE HUMAN DYSTROPHIN GENE DETECTED BY HETERODUPLEX ANALYSIS AND RESTRICTED RT-PCR HETERODUPLEX ANALYSIS OF ILLEGITIMATE TRANSCRIPTS
Authors: BABIERI AM SORIANI N FERLINI A MICHELATO A FERRARI M CARRERA P
Citation: Am. Babieri et al., 7 NOVEL-ADDITIONAL SMALL MUTATIONS AND A NEW ALTERNATIVE SPLICING IN THE HUMAN DYSTROPHIN GENE DETECTED BY HETERODUPLEX ANALYSIS AND RESTRICTED RT-PCR HETERODUPLEX ANALYSIS OF ILLEGITIMATE TRANSCRIPTS, European journal of human genetics, 4(3), 1996, pp. 183-187
DETECTION OF N540K MUTATIONS IN PATIENTS WITH HYPOCHONDROPLASIA
Authors: PRINSTER C MORA S WEBER G CHIUMELLO G FERRARI M CARRERA P
Citation: C. Prinster et al., DETECTION OF N540K MUTATIONS IN PATIENTS WITH HYPOCHONDROPLASIA, Journal of bone and mineral research, 11, 1996, pp. 479-479
POINT MUTATIONS IN ITALIAN PATIENTS WITH CLASSIC, NONCLASSIC, AND CRYPTIC FORMS OF STEROID 21-HYDROXYLASE DEFICIENCY
Authors: CARRERA P BORDONE L AZZANI T BRUNELLI V GARANCINI MP CHIUMELLO G FERRARI M
Citation: P. Carrera et al., POINT MUTATIONS IN ITALIAN PATIENTS WITH CLASSIC, NONCLASSIC, AND CRYPTIC FORMS OF STEROID 21-HYDROXYLASE DEFICIENCY, Human genetics, 98(6), 1996, pp. 662-665
TBP BINDS THE TRANSCRIPTIONALLY INACTIVE TA(5) SEQUENCE BUT THE RESULTING COMPLEX IS NOT EFFICIENTLY RECOGNIZED BY TFIIB AND TFIIA
Authors: BERNUES J CARRERA P AZORIN F
Citation: J. Bernues et al., TBP BINDS THE TRANSCRIPTIONALLY INACTIVE TA(5) SEQUENCE BUT THE RESULTING COMPLEX IS NOT EFFICIENTLY RECOGNIZED BY TFIIB AND TFIIA, Nucleic acids research, 24(15), 1996, pp. 2950-2958
DIFFERENT APPROACHES TO MOLECULAR SCANNING OF POINT MUTATIONS IN GENETIC-DISEASES
Authors: FERRARI M CARRERA P CREMONESI L
Citation: M. Ferrari et al., DIFFERENT APPROACHES TO MOLECULAR SCANNING OF POINT MUTATIONS IN GENETIC-DISEASES, Pure and applied chemistry, 68(10), 1996, pp. 1913-1918
A ROLE FOR N-MYRISTOYLATION IN PROTEIN TARGETING - NADH-CYTOCHROME B(5) REDUCTASE REQUIRES MYRISTIC ACID FOR ASSOCIATION WITH OUTER MITOCHONDRIAL BUT NOT ER MEMBRANES
Authors: BORGESE N AGGUJARO D CARRERA P PIETRINI G BASSETTI M
Citation: N. Borgese et al., A ROLE FOR N-MYRISTOYLATION IN PROTEIN TARGETING - NADH-CYTOCHROME B(5) REDUCTASE REQUIRES MYRISTIC ACID FOR ASSOCIATION WITH OUTER MITOCHONDRIAL BUT NOT ER MEMBRANES, The Journal of cell biology, 135(6), 1996, pp. 1501-1513
MOLECULAR DIAGNOSIS OF GENETIC-DISEASES
Authors: FERRARI M CREMONESI L CARRERA P BONINI PA
Citation: M. Ferrari et al., MOLECULAR DIAGNOSIS OF GENETIC-DISEASES, Clinical biochemistry, 29(3), 1996, pp. 201-208
CLINICOPATHOLOGICAL AND GENETIC-STUDIES OF 2 FURTHER ITALIAN FAMILIESWITH CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY
Authors: MALANDRINI A CARRERA P PALMERI S CAVALLARO T FABRIZI GM VILLANOVA M FATTAPPOSTA M VISMARA L BRANCOLINI V TANGANELLI P CALI A MOROCUTTI C ZEVIANI M FERRARI M GUAZZI GC
Citation: A. Malandrini et al., CLINICOPATHOLOGICAL AND GENETIC-STUDIES OF 2 FURTHER ITALIAN FAMILIESWITH CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY, Acta Neuropathologica, 92(2), 1996, pp. 115-122
CAG TRIPLET ANALYSIS IN FAMILIES WITH ANDROGEN INSENSITIVITY SYNDROMEBY CAPILLARY ELECTROPHORESIS IN POLYMER NETWORKS
Authors: GELFI C RIGHETTI PG LEONCINI F BRUNELLI V CARRERA P FERRARI M
Citation: C. Gelfi et al., CAG TRIPLET ANALYSIS IN FAMILIES WITH ANDROGEN INSENSITIVITY SYNDROMEBY CAPILLARY ELECTROPHORESIS IN POLYMER NETWORKS, Journal of chromatography, 706(1-2), 1995, pp. 463-468
Risultati: 1-25 | 26-35