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Il giacimento bentonitico di "Pedra de Fogu" (Sardegna). Nota conclusiva
Authors: PIETRACAPRINA A NOVELLI G RINALDI A
Citation: A. Pietracaprina et al., Il giacimento bentonitico di "Pedra de Fogu" (Sardegna). Nota conclusiva, Memorie della Societa Geologica Italiana , 8, 1969, pp. 205-218
Tracce di DNA in un Myctophidae del Messiniano di Mondaino (Forlì) (nota preliminare)
Authors: BIZZARINI F NOVELLI G ZANOTTI A
Citation: F. Bizzarini et al., Tracce di DNA in un Myctophidae del Messiniano di Mondaino (Forlì) (nota preliminare), Bollettino della Societa paleontologica italiana , 29(2), 1990, pp. 249-250
HUMAN UDP-GALACTOSE 4'-EPIMERASE (GALE) GENE AND IDENTIFICATION OF 5 MISSENSE MUTATIONS IN PATIENTS WITH EPIMERASE-DEFICIENCY GALACTOSEMIA
Authors: MACERATESI P DAUDE N DALLAPICCOLA B NOVELLI G ALLEN R OKANO Y REICHARDT J
Citation: P. Maceratesi et al., HUMAN UDP-GALACTOSE 4'-EPIMERASE (GALE) GENE AND IDENTIFICATION OF 5 MISSENSE MUTATIONS IN PATIENTS WITH EPIMERASE-DEFICIENCY GALACTOSEMIA, MOLECULAR GENETICS AND METABOLISM, 63(1), 1998, pp. 26-30
IDENTIFICATION OF 5 NEW MUTATIONS AND 3 NOVEL POLYMORPHISMS IN THE MUSCLE CHLORIDE CHANNEL GENE (CLCN1) IN 20 ITALIAN PATIENTS WITH DOMINANT AND RECESSIVE MYOTONIA-CONGENITA
Authors: SANGIUOLO F BOTTA A MESORACA A SERVIDEI S MERLINI L FRATTA G NOVELLI G DALLAPICCOLA B
Citation: F. Sangiuolo et al., IDENTIFICATION OF 5 NEW MUTATIONS AND 3 NOVEL POLYMORPHISMS IN THE MUSCLE CHLORIDE CHANNEL GENE (CLCN1) IN 20 ITALIAN PATIENTS WITH DOMINANT AND RECESSIVE MYOTONIA-CONGENITA, Human mutation, 11(4), 1998, pp. 331-331
A SINGLE POLYMERASE CHAIN REACTION-BASED PROTOCOL FOR DETECTING NORMAL AND EXPANDED ALLELES IN MYOTONIC-DYSTROPHY
Authors: GENNARELLI M PAVONI M AMICUCCI P NOVELLI G DALLAPICCOLA B
Citation: M. Gennarelli et al., A SINGLE POLYMERASE CHAIN REACTION-BASED PROTOCOL FOR DETECTING NORMAL AND EXPANDED ALLELES IN MYOTONIC-DYSTROPHY, Diagnostic molecular pathology, 7(3), 1998, pp. 135-137
POSITIVE CORRELATION OF CTG EXPANSION AND PHARYNGOESOPHAGEAL ALTERATIONS IN MYOTONIC-DYSTROPHY PATIENTS
Authors: MARCON M BRIANI C ERMANI M MENEGAZZO E IURILLI V FELTRIN GP NOVELLI G GENNARELLI M ANGELINI C
Citation: M. Marcon et al., POSITIVE CORRELATION OF CTG EXPANSION AND PHARYNGOESOPHAGEAL ALTERATIONS IN MYOTONIC-DYSTROPHY PATIENTS, Italian journal of neurological sciences, 19(2), 1998, pp. 75-80
GENOMIC INSTABILITY ASSOCIATED WITH MYOTONIC-DYSTROPHY DOES NOT INVOLVE P53 EXPRESSION AND ACTIVITY
Authors: GENNARELLI M LUCARELLI M AMICUCCI P SODDU S NOVELLI G DALLAPICCOLA B
Citation: M. Gennarelli et al., GENOMIC INSTABILITY ASSOCIATED WITH MYOTONIC-DYSTROPHY DOES NOT INVOLVE P53 EXPRESSION AND ACTIVITY, Cell biochemistry and function, 16(2), 1998, pp. 117-122
FIRST-TRIMESTER PRENATAL-DIAGNOSIS OF ELLIS-VAN-CREVELD-SYNDROME USING LINKED MICROSATELLITE MARKERS
Authors: TORRENTE I MANGINO M DELUCA A MINGARELLI R GENNARELLI M GIANNOTTI A NOVELLI G DALLAPICCOLA B
Citation: I. Torrente et al., FIRST-TRIMESTER PRENATAL-DIAGNOSIS OF ELLIS-VAN-CREVELD-SYNDROME USING LINKED MICROSATELLITE MARKERS, Prenatal diagnosis, 18(5), 1998, pp. 504-506
STRUCTURE AND EXPRESSION OF THE HUMAN UBIQUITIN FUSION DEGRADATION GENE (UFD1L)
Authors: NOVELLI G MARI A AMATI F COLOSIMO A SANGIUOLO F BENGALA M CONTI E RATTI A BORDONI R PIZZUTI A BALDINI A CRINELLI R PANDOLFI F MAGNANI M DALLAPICCOLA B
Citation: G. Novelli et al., STRUCTURE AND EXPRESSION OF THE HUMAN UBIQUITIN FUSION DEGRADATION GENE (UFD1L), Biochimica et biophysica acta, N. Gene structure and expression, 1396(2), 1998, pp. 158-162
A HIGHLY POLYMORPHIC CA GT REPEAT (LIMK1GT) WITHIN THE WILLIAMS-SYNDROME CRITICAL REGION/
Authors: MARI A AMATI F CONTI E BENGALA M NOVELLI G DALLAPICCOLA B
Citation: A. Mari et al., A HIGHLY POLYMORPHIC CA GT REPEAT (LIMK1GT) WITHIN THE WILLIAMS-SYNDROME CRITICAL REGION/, Clinical genetics, 53(3), 1998, pp. 226-227
EXPRESSION STUDY OF SURVIVAL MOTOR-NEURON GENE IN HUMAN FETAL TISSUES
Authors: NOVELLI G CALZA L AMICUCCI P GIARDINO L POZZA M SILANI V PIZZUTI A GENNARELLI M PIOMBO G CAPON F DALLAPICCOLA B
Citation: G. Novelli et al., EXPRESSION STUDY OF SURVIVAL MOTOR-NEURON GENE IN HUMAN FETAL TISSUES, Biochemical and molecular medicine, 61(1), 1997, pp. 102-106
RECOMBINANT CFTR DETECTION IN CF TRACHEAL EPITHELIAL-CELLS FOLLOWING IN-VITRO LIPOSOME-MEDIATED GENE-TRANSFER
Authors: COLOSIMO A SCARPINO S SANGIUOLO F DISARIO S MOSSA G NOVELLI G DALLAPICCOLA B
Citation: A. Colosimo et al., RECOMBINANT CFTR DETECTION IN CF TRACHEAL EPITHELIAL-CELLS FOLLOWING IN-VITRO LIPOSOME-MEDIATED GENE-TRANSFER, Biochemistry and molecular biology international, 42(4), 1997, pp. 723-729
UFD1L, A DEVELOPMENTALLY EXPRESSED UBIQUITINATION GENE, IS DELETED INCATCH-22-SYNDROME
Authors: PIZZUTI A NOVELLI G RATTI A AMATI F MARI A CALABRESE G NICOLIS S SILANI V MARINO B SCARLATO G OTTOLENGHI S DALLAPICCOLA B
Citation: A. Pizzuti et al., UFD1L, A DEVELOPMENTALLY EXPRESSED UBIQUITINATION GENE, IS DELETED INCATCH-22-SYNDROME, Human molecular genetics, 6(2), 1997, pp. 259-265
ASSIGNMENT OF THE GENE FOR A UBIQUITIN FUSION DEGRADATION PROTEIN (UFD1L) MOUSE-CHROMOSOME 16B1-B4, SYNTENIC WITH THE TUPLE-1 GENE
Authors: BOTTA A JURECIC V PIZZUTI A NOVELLI G DALLAPICCOLA B BALDINI A
Citation: A. Botta et al., ASSIGNMENT OF THE GENE FOR A UBIQUITIN FUSION DEGRADATION PROTEIN (UFD1L) MOUSE-CHROMOSOME 16B1-B4, SYNTENIC WITH THE TUPLE-1 GENE, Cytogenetics and cell genetics, 77(3-4), 1997, pp. 264-265
2 NEW MISSENSE MUTATIONS (A105T AND C110G) IN THE NORRIN GENE IN 2 ITALIAN FAMILIES WITH NORRIE-DISEASE AND FAMILIAL EXUDATIVE VITREORETINOPATHY
Authors: TORRENTE I MANGINO M GENNARELLI M NOVELLI G GIANNOTTI A VADALA P DALLAPICCOLA B
Citation: I. Torrente et al., 2 NEW MISSENSE MUTATIONS (A105T AND C110G) IN THE NORRIN GENE IN 2 ITALIAN FAMILIES WITH NORRIE-DISEASE AND FAMILIAL EXUDATIVE VITREORETINOPATHY, American journal of medical genetics, 72(2), 1997, pp. 242-244
TRICUSPID-ATRESIA AND 22Q11 DELETION
Authors: MARINO B DIGILIO MC NOVELLI G GIANNOTTI A DALLAPICCOLA B
Citation: B. Marino et al., TRICUSPID-ATRESIA AND 22Q11 DELETION, American journal of medical genetics, 72(1), 1997, pp. 40-42
ANALYSIS OF 160 CONSECUTIVE LIVING UNRELATED KIDNEY-TRANSPLANTS - 1983-1997
Authors: ALFANI D PRETAGOSTINI R ROSSI M POLI L DESIMONE P CELONNELLO M NOVELLI G URBANO D VENETTONI S PERSIJN G SMITS J CORTESINI R
Citation: D. Alfani et al., ANALYSIS OF 160 CONSECUTIVE LIVING UNRELATED KIDNEY-TRANSPLANTS - 1983-1997, Transplantation proceedings, 29(8), 1997, pp. 3399-3401
COGNITIVE DYSFUNCTION AND SPECT AND PET IMAGING IN 30 GENETICALLY DEFINED MYOTONIC-DYSTROPHY PATIENTS
Authors: MENEGAZZO E PERINI G GREGIANIN M FERRUZZA E MARCADELLA S ANGELINI C INFANTOLINO D CHIERICHETTI F FERLIN G GENNARELLI M NOVELLI G
Citation: E. Menegazzo et al., COGNITIVE DYSFUNCTION AND SPECT AND PET IMAGING IN 30 GENETICALLY DEFINED MYOTONIC-DYSTROPHY PATIENTS, Neurology, 48(3), 1997, pp. 6118-6118
ISOLATION OF AN UBIQUITINATION GENE, CANDIDATE FOR THE SENSORINEURAL DEAFNESS IN CATCH22 PATIENTS
Authors: RATTI A NOVELLI G DALLAPICCOLA B CALABRESE G SILANI V CIAMMOLA A BRAGA M SCARLATO G NICOLIS S PIZZUTI A
Citation: A. Ratti et al., ISOLATION OF AN UBIQUITINATION GENE, CANDIDATE FOR THE SENSORINEURAL DEAFNESS IN CATCH22 PATIENTS, Neurology, 48(3), 1997, pp. 67009-67009
CONOTRUNCAL HEART-DEFECTS AND CHROMOSOME 22Q11 MICRODELETION
Authors: DIGILIO MC MARINO B GIANNOTTI A NOVELLI G DALLAPICCOLA B
Citation: Mc. Digilio et al., CONOTRUNCAL HEART-DEFECTS AND CHROMOSOME 22Q11 MICRODELETION, The Journal of pediatrics, 130(4), 1997, pp. 675-677
SPECTRUM OF CLINICAL-FEATURES ASSOCIATED WITH INTERSTITIAL CHROMOSOME22Q11 DELETIONS - A EUROPEAN COLLABORATIVE STUDY
Authors: RYAN AK GOODSHIP JA WILSON DI PHILIP N LEVY A SEIDEL H SCHUFFENHAUER S OECHSLER H BELOHRADSKY B PRIEUR M AURIAS A RAYMOND FL CLAYTONSMITH J HATCHWELL E MCKEOWN C BEEMER FA DALLAPICCOLA B NOVELLI G HURST JA IGNATIUS J GREEN AJ WINTER RM BRUETON L BRONDUMNIELSEN K STEWART F VANESSEN T PATTON M PATERSON J SCAMBLER PJ
Citation: Ak. Ryan et al., SPECTRUM OF CLINICAL-FEATURES ASSOCIATED WITH INTERSTITIAL CHROMOSOME22Q11 DELETIONS - A EUROPEAN COLLABORATIVE STUDY, Journal of Medical Genetics, 34(10), 1997, pp. 798-804
EXPRESSION OF RECEPTORS FOR NATIVE AND CHEMICALLY-MODIFIED LOW-DENSITY LIPOPROTEINS IN BRAIN MICROVESSELS
Authors: LUCARELLI M GENNARELLI M CARDELLI P NOVELLI G SCARPA S DALLAPICCOLA B STROM R
Citation: M. Lucarelli et al., EXPRESSION OF RECEPTORS FOR NATIVE AND CHEMICALLY-MODIFIED LOW-DENSITY LIPOPROTEINS IN BRAIN MICROVESSELS, FEBS letters, 401(1), 1997, pp. 53-58
SCANNING OF PSORIASIS SUSCEPTIBILITY GENES IN THE ITALIAN POPULATION AND ASSIGNMENT OF A NEW LOCUS TO CHROMOSOME 1CEN-Q21
Authors: CAPON F NOVELLI G SEMPRINI S CLEMENTI M NUDO M VULTAGGIO P BOTTA A FABRIZI G DALLAPICCOLA B
Citation: F. Capon et al., SCANNING OF PSORIASIS SUSCEPTIBILITY GENES IN THE ITALIAN POPULATION AND ASSIGNMENT OF A NEW LOCUS TO CHROMOSOME 1CEN-Q21, American journal of human genetics, 61(4), 1997, pp. 216-216
IDENTIFICATION OF A NOVEL NONCODING NUCLEAR-RNA FROM THE DIGEORGE-SYNDROME CRITICAL REGION AT 22Q11
Authors: NOVELLI G PIZZUTI A AMATI F RATTI A MARI A FOGH I CONTI E BENGALA M BORDONI R BELLONE E MANDICH P COLOSIMO A PANDOLFI F DALLAPICCOLA B
Citation: G. Novelli et al., IDENTIFICATION OF A NOVEL NONCODING NUCLEAR-RNA FROM THE DIGEORGE-SYNDROME CRITICAL REGION AT 22Q11, American journal of human genetics, 61(4), 1997, pp. 2232-2232
SPINAL MUSCULAR-ATROPHY - RESOURCES AVAILABLE ON THE WORLD-WIDE-WEB
Authors: NOVELLI G
Citation: G. Novelli, SPINAL MUSCULAR-ATROPHY - RESOURCES AVAILABLE ON THE WORLD-WIDE-WEB, Molecular medicine today, 2(9), 1996, pp. 369-369
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