Sfoglia per Autore
CORRELATION BETWEEN CLINICAL AND MOLECULAR-FEATURES IN MYOTONIC-DYSTROPHY
1993-01-01 Angelini, C; Menegazzo, E; Mostacciuolo, Ml; Melacini, P; Novelli, G; Gennarelli, Massimo; Dallapiccola, B.
FAILURE IN DETECTING mRNA TRANSCRIPTS FROM THE MUTATED ALLELE IN MYOTONIC DYSTROPHY MUSCLE.
1993-01-01 Novelli, G.; Gennarelli, Massimo; Zelano, G.; Pizzuti, A.; Fattorini, C.; Caskey, C. T.; Dallapiccola, B.
MEIOTIC DRIVE AT THE MYOTONIC DYSTROPHY LOCUS.
1994-01-01 Gennarelli, Massimo; Dallapiccola, B.; Baiget, M.; Martorell, L.; Novelli, G.
NORTH EURASIAN ORIGIN OF THE MYOTONIC DYSTROPHY MUTATION.
1994-01-01 Novelli, G.; Spedini, G.; DESTRO BISOL, G.; Gennarelli, Massimo; Fattorini, C.; Dallapiccola, B.
EXCLUSION OF LINKAGE WITH CHROMOSOME 21 IN FAMILIES WITH RECURRENCE OF NON-DOWN ATRIOVEENTRICULAR CANAL.
1994-01-01 Gennarelli, Massimo; Novelli, G.; Digilio, M. C.; Giannotti, A.; Marino, B.; Dallapiccola, B.
MALE HYPOGONADISM IN MYOTONIC DYSTROPHY IS RELATED TO (CTG)n TRIPLET MUTATION.
1994-01-01 Mastrogiacomo, I.; Pagani, E.; Novelli, G.; Angelini, C.; Gennarelli, Massimo; Menegazzo, E.; Bonanni, G.; Dallapiccola, B.
FIRST TRIMESTER PRENATAL DIAGNOSIS OF SPINAL MUSCOLAR ATROPHY USING MICROSATELLITE MARKERS.
1994-01-01 LO CICERO, S.; Capon, F.; Melchionda, S.; Gennarelli, Massimo; Novelli, G.; Dallapiccola, B.
TWO PEDIGREES OF AUTOSOMAL DOMINANT ATRIOVENTRICULAR CANAL DEFECT (AVCD): EXCLUSION FROM THE CRITICAL REGION ON 8p.
1995-01-01 Amati, F.; Mari, A.; Mingarelli, R.; Gennarelli, Massimo; DI GIGLIO, M. C.; Giannotti, A.; Marino, B.; Novelli, G.; Dallapiccola, B.
DIFFERENT EXPRESSION OF THE MYOTONIC PROTEIN KINASE GENE IN DISCRETE AREAS OF HUMAN BRAIN.
1995-01-01 Gennarelli, Massimo; Luccarellim, ; Zelano, G.; Pizzuti, A.; Novelli, G.; Dallapiccola, B.
Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation.
1995-01-01 Wang, J; Pegoraro, E; Menegazzo, E; Gennarelli, Massimo; Hoop, Rc; Angelini, C; Hoffman, Ep
DISCORDANT CLINICAL OUTCOME IN MYOTONIC DYSTROPHY RELATIVES SHOWING (CTG)n>700 REPEATS.
1995-01-01 Novelli, G.; Gennarelli, Massimo; Menegazzo, E.; Angelini, C.; Dallapiccola, B.
IDENTIFICATION OF MULTIPLE TRANSCRIBED SEQUENCES FROM THE SPINAL MUSCULAR ATROPHY REGION ON HUMAN CHROMOSOME 5.
1995-01-01 Pizzuti, A.; Colosimo, A.; Ratti, A.; Capon, F.; Gennarelli, Massimo; Silani, V.; Ghezzi, C.; LO CICERO, S.; Calabrese, G.; Palka, G.; Scarlato, G.; Novelli, G.
Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients.
1995-01-01 Gennarelli, Massimo; M., Lucarelli; F., Capon; A., Pizzuti; L., Merlini; C., Angelini; G., Novelli; B., Dallapiccola
TROPHOBLAST AND SKELETAL-MUSCLE SMN GENE-EXPRESSION IN SPINAL MUSCULAR-ATROPHY
1995-01-01 Dallapiccola, B; Capon, F; Lucarelli, M; Gennarelli, Massimo; Levato, C; Angelini, C; Merlini, L; Novelli, G.
LINKAGE ANALYSIS IN FAMILIES WITH LYNCH-II SYNDROME IDENTIFIES HEALTHY-SUBJECTS AT RISK
1995-01-01 Piepoli, A; Santoro, R; Cristofaro, G; Siena, D; Accadia, L; Gennarelli, Massimo; Andriulli, A; Peltomaki, P; Delachapelle, A.
POSTZYGOTIC INSTABILITY OF MYOTONIC DYSTROPHY p[AGC]n REPEAT SUPPORTED BY LARGER EXPANSIONS IN MUSCLE AND REDUCED AMPLIFICATIONS IN SPERMS.
1995-01-01 Massari, A.; Gennarelli, Massimo; Menegazzo, E.; Pizzuti, A.; Silani, V.; Mastrogiacomo, I.; Pagani, E.; Angelini, C.; Scarlato, G.; Novelli, G.; Dallapiccola, B.
Sfi I MACRORESTRICTION ENDONUCLEASE FINGERPRINTING ANALYSIS OF CANDIDA PARAPSILOSIS ISOLATES: CORRELATION WITH THEIR ISOLATION SOURCE.
1996-01-01 Pontieri, E.; Gregori, L.; Gennarelli, Massimo; Ceddia, T.; Novelli, G.; Dallapiccola, B.; DE BERNARDIS, F.; Carruba, G.
CLINICAL AND HORMONAL ASPECTS OF MALEHYPOGONADISM IN MYOTONIC DYSTROPHY.
1996-01-01 Mastrogiacomo, I.; Bonanni, G.; Menegazzo, E.; Santarosa, C.; Pagani, E.; Gennarelli, Massimo; Angelini, C.
Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeats.
1996-01-01 Gennarelli, Massimo; Novelli, G; ANDREASI BASSI, F; Martorell, L; Cornet, M; Menegazzo, E; Mostacciuolo, Ml; Martinez, Jm; Angelini, C; Pizzuti, A; Baiget, M; Dallapiccola, B.
LINKAGE ANLYSIS IDENTIFIES GENE CARRIERS AMONG MEMBERS OF HNPCC
1996-01-01 Piepoli, A.; Santoro, R.; Cristofaro, G.; Traversa, G.; Gennarelli, Massimo; Accadia, L.; Siena, D.; Lynch, H. T.; Peltomaki, P.; Andriulli, A.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
CORRELATION BETWEEN CLINICAL AND MOLECULAR-FEATURES IN MYOTONIC-DYSTROPHY | 1-gen-1993 | Angelini, C; Menegazzo, E; Mostacciuolo, Ml; Melacini, P; Novelli, G; Gennarelli, Massimo; Dallapiccola, B. | |
FAILURE IN DETECTING mRNA TRANSCRIPTS FROM THE MUTATED ALLELE IN MYOTONIC DYSTROPHY MUSCLE. | 1-gen-1993 | Novelli, G.; Gennarelli, Massimo; Zelano, G.; Pizzuti, A.; Fattorini, C.; Caskey, C. T.; Dallapiccola, B. | |
MEIOTIC DRIVE AT THE MYOTONIC DYSTROPHY LOCUS. | 1-gen-1994 | Gennarelli, Massimo; Dallapiccola, B.; Baiget, M.; Martorell, L.; Novelli, G. | |
NORTH EURASIAN ORIGIN OF THE MYOTONIC DYSTROPHY MUTATION. | 1-gen-1994 | Novelli, G.; Spedini, G.; DESTRO BISOL, G.; Gennarelli, Massimo; Fattorini, C.; Dallapiccola, B. | |
EXCLUSION OF LINKAGE WITH CHROMOSOME 21 IN FAMILIES WITH RECURRENCE OF NON-DOWN ATRIOVEENTRICULAR CANAL. | 1-gen-1994 | Gennarelli, Massimo; Novelli, G.; Digilio, M. C.; Giannotti, A.; Marino, B.; Dallapiccola, B. | |
MALE HYPOGONADISM IN MYOTONIC DYSTROPHY IS RELATED TO (CTG)n TRIPLET MUTATION. | 1-gen-1994 | Mastrogiacomo, I.; Pagani, E.; Novelli, G.; Angelini, C.; Gennarelli, Massimo; Menegazzo, E.; Bonanni, G.; Dallapiccola, B. | |
FIRST TRIMESTER PRENATAL DIAGNOSIS OF SPINAL MUSCOLAR ATROPHY USING MICROSATELLITE MARKERS. | 1-gen-1994 | LO CICERO, S.; Capon, F.; Melchionda, S.; Gennarelli, Massimo; Novelli, G.; Dallapiccola, B. | |
TWO PEDIGREES OF AUTOSOMAL DOMINANT ATRIOVENTRICULAR CANAL DEFECT (AVCD): EXCLUSION FROM THE CRITICAL REGION ON 8p. | 1-gen-1995 | Amati, F.; Mari, A.; Mingarelli, R.; Gennarelli, Massimo; DI GIGLIO, M. C.; Giannotti, A.; Marino, B.; Novelli, G.; Dallapiccola, B. | |
DIFFERENT EXPRESSION OF THE MYOTONIC PROTEIN KINASE GENE IN DISCRETE AREAS OF HUMAN BRAIN. | 1-gen-1995 | Gennarelli, Massimo; Luccarellim, ; Zelano, G.; Pizzuti, A.; Novelli, G.; Dallapiccola, B. | |
Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation. | 1-gen-1995 | Wang, J; Pegoraro, E; Menegazzo, E; Gennarelli, Massimo; Hoop, Rc; Angelini, C; Hoffman, Ep | |
DISCORDANT CLINICAL OUTCOME IN MYOTONIC DYSTROPHY RELATIVES SHOWING (CTG)n>700 REPEATS. | 1-gen-1995 | Novelli, G.; Gennarelli, Massimo; Menegazzo, E.; Angelini, C.; Dallapiccola, B. | |
IDENTIFICATION OF MULTIPLE TRANSCRIBED SEQUENCES FROM THE SPINAL MUSCULAR ATROPHY REGION ON HUMAN CHROMOSOME 5. | 1-gen-1995 | Pizzuti, A.; Colosimo, A.; Ratti, A.; Capon, F.; Gennarelli, Massimo; Silani, V.; Ghezzi, C.; LO CICERO, S.; Calabrese, G.; Palka, G.; Scarlato, G.; Novelli, G. | |
Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients. | 1-gen-1995 | Gennarelli, Massimo; M., Lucarelli; F., Capon; A., Pizzuti; L., Merlini; C., Angelini; G., Novelli; B., Dallapiccola | |
TROPHOBLAST AND SKELETAL-MUSCLE SMN GENE-EXPRESSION IN SPINAL MUSCULAR-ATROPHY | 1-gen-1995 | Dallapiccola, B; Capon, F; Lucarelli, M; Gennarelli, Massimo; Levato, C; Angelini, C; Merlini, L; Novelli, G. | |
LINKAGE ANALYSIS IN FAMILIES WITH LYNCH-II SYNDROME IDENTIFIES HEALTHY-SUBJECTS AT RISK | 1-gen-1995 | Piepoli, A; Santoro, R; Cristofaro, G; Siena, D; Accadia, L; Gennarelli, Massimo; Andriulli, A; Peltomaki, P; Delachapelle, A. | |
POSTZYGOTIC INSTABILITY OF MYOTONIC DYSTROPHY p[AGC]n REPEAT SUPPORTED BY LARGER EXPANSIONS IN MUSCLE AND REDUCED AMPLIFICATIONS IN SPERMS. | 1-gen-1995 | Massari, A.; Gennarelli, Massimo; Menegazzo, E.; Pizzuti, A.; Silani, V.; Mastrogiacomo, I.; Pagani, E.; Angelini, C.; Scarlato, G.; Novelli, G.; Dallapiccola, B. | |
Sfi I MACRORESTRICTION ENDONUCLEASE FINGERPRINTING ANALYSIS OF CANDIDA PARAPSILOSIS ISOLATES: CORRELATION WITH THEIR ISOLATION SOURCE. | 1-gen-1996 | Pontieri, E.; Gregori, L.; Gennarelli, Massimo; Ceddia, T.; Novelli, G.; Dallapiccola, B.; DE BERNARDIS, F.; Carruba, G. | |
CLINICAL AND HORMONAL ASPECTS OF MALEHYPOGONADISM IN MYOTONIC DYSTROPHY. | 1-gen-1996 | Mastrogiacomo, I.; Bonanni, G.; Menegazzo, E.; Santarosa, C.; Pagani, E.; Gennarelli, Massimo; Angelini, C. | |
Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeats. | 1-gen-1996 | Gennarelli, Massimo; Novelli, G; ANDREASI BASSI, F; Martorell, L; Cornet, M; Menegazzo, E; Mostacciuolo, Ml; Martinez, Jm; Angelini, C; Pizzuti, A; Baiget, M; Dallapiccola, B. | |
LINKAGE ANLYSIS IDENTIFIES GENE CARRIERS AMONG MEMBERS OF HNPCC | 1-gen-1996 | Piepoli, A.; Santoro, R.; Cristofaro, G.; Traversa, G.; Gennarelli, Massimo; Accadia, L.; Siena, D.; Lynch, H. T.; Peltomaki, P.; Andriulli, A. |
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