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Results: 1-20 |
Results: 20
BRCA1 AND BRCA2 GERMLINE MUTATIONS IN EARLY-ONSET BREAST-CARCINOMA PATIENTS
Authors: CONTI AR DEBENEDETTI MVG STAGI L MONDINI P PASINI B PENSOTTI V SPATTI GB RILKE F PIEROTTI MA RADICE P
Citation: Ar. Conti et al., BRCA1 AND BRCA2 GERMLINE MUTATIONS IN EARLY-ONSET BREAST-CARCINOMA PATIENTS, European journal of cancer, 34, 1998, pp. 7-7
FULL ACTIVATION OF MEN2B MUTANT RET BY AN ADDITIONAL MEN2A MUTATION OR BY LIGAND GDNF STIMULATION
Authors: BONGARZONE I VIGANO E ALBERTI L BORRELLO MG PASINI B GRECO A MONDELLINI P SMITH DP PONDER BAJ ROMEO G PIEROTTI MA
Citation: I. Bongarzone et al., FULL ACTIVATION OF MEN2B MUTANT RET BY AN ADDITIONAL MEN2A MUTATION OR BY LIGAND GDNF STIMULATION, Oncogene, 16(18), 1998, pp. 2295-2301
FREQUENCY OF RET MUTATIONS IN LONG-SEGMENT AND SHORT-SEGMENT HIRSCHSPRUNG DISEASE
Authors: SERI M YIN L BARONE V BOLINO A CELLI I BOCCIARDI R PASINI B CECCHERINI I LERONE M KRISTOFFERSSON U LARSSON LT CASASA JM CASS DT ABRAMOWICZ MJ VANDERWINDEN JM KRAVCENKIENE I BARIC I SILENGO M MARTUCCIELLO G ROMEO G
Citation: M. Seri et al., FREQUENCY OF RET MUTATIONS IN LONG-SEGMENT AND SHORT-SEGMENT HIRSCHSPRUNG DISEASE, Human mutation, 9(3), 1997, pp. 243-249
THE MULTIPLE ENDOCRINE NEOPLASIA TYPE 2B POINT MUTATION SWITCHES THE SPECIFICITY OF THE RET TYROSINE KINASE TOWARDS CELLULAR SUBSTRATES THAT ARE SUSCEPTIBLE TO INTERACT WITH CRK AND NCK
Authors: BOCCIARDI R MOGRABI B PASINI B BORRELLO MG PIEROTTI MA BOURGET I FISCHER S ROMEO G ROSSI B
Citation: R. Bocciardi et al., THE MULTIPLE ENDOCRINE NEOPLASIA TYPE 2B POINT MUTATION SWITCHES THE SPECIFICITY OF THE RET TYROSINE KINASE TOWARDS CELLULAR SUBSTRATES THAT ARE SUSCEPTIBLE TO INTERACT WITH CRK AND NCK, Oncogene, 15(19), 1997, pp. 2257-2265
IDENTIFICATION OF SHC DOCKING SITE ON RET TYROSINE KINASE
Authors: ARIGHI E ALBERTI L TORRITI F GHIZZONI S RIZZETTI MG PELICCI G PASINI B BONGARZONE I PIUTTI C PIEROTTI MA BORRELLO MG
Citation: E. Arighi et al., IDENTIFICATION OF SHC DOCKING SITE ON RET TYROSINE KINASE, Oncogene, 14(7), 1997, pp. 773-782
SOMATIC IN FRAME DELETIONS NOT INVOLVING JUXTAMEMBRANOUS CYSTEINE RESIDUES STRONGLY ACTIVATE THE RET PROTOONCOGENE
Authors: CECCHERINI I PASINI B PACINI F GULLO M BONGARZONE I ROMEI C SANTAMASIA G MATERA I MONDELLINI P SCOPSI L PINCHERA A PIEROTTI MA ROMEO G
Citation: I. Ceccherini et al., SOMATIC IN FRAME DELETIONS NOT INVOLVING JUXTAMEMBRANOUS CYSTEINE RESIDUES STRONGLY ACTIVATE THE RET PROTOONCOGENE, Oncogene, 14(21), 1997, pp. 2609-2612
MALIGNANT PHEOCHROMOCYTOMA IN MULTIPLE ENDOCRINE NEOPLASIA TYPE 2B SYNDROME - CASE-REPORT AND REVIEW OF THE LITERATURE
Authors: SCOPSI L CASTELLANI MR GULLO M CUSUMANO F CAMERINI E PASINI B OREFICE S
Citation: L. Scopsi et al., MALIGNANT PHEOCHROMOCYTOMA IN MULTIPLE ENDOCRINE NEOPLASIA TYPE 2B SYNDROME - CASE-REPORT AND REVIEW OF THE LITERATURE, Tumori, 82(5), 1996, pp. 480-484
THE FULL ONCOGENIC ACTIVITY OF RET PTC2 DEPENDS ON TYROSINE-539, A DOCKING SITE FOR PHOSPHOLIPASE-C-GAMMA/
Authors: BORRELLO MG ALBERTI L ARIGHI E BONGARZONE I BATTISINI C BARDELLI A PASINI B PIUTTI C RIZZETTI MG MONDELLINI P RADICE MT PIEROTTI MA
Citation: Mg. Borrello et al., THE FULL ONCOGENIC ACTIVITY OF RET PTC2 DEPENDS ON TYROSINE-539, A DOCKING SITE FOR PHOSPHOLIPASE-C-GAMMA/, Molecular and cellular biology, 16(5), 1996, pp. 2151-2163
RET MUTATIONS IN HUMAN-DISEASE
Authors: PASINI B CECCHERINI I ROMEO G
Citation: B. Pasini et al., RET MUTATIONS IN HUMAN-DISEASE, Trends in genetics, 12(4), 1996, pp. 138-144
LOSS OF FUNCTION EFFECT OF RET MUTATIONS CAUSING HIRSCHSPRUNG DISEASE
Authors: PASINI B BORRELLO MG GRECO A BONGARZONE I LUO Y MONDELLINI P ALBERTI L MIRANDA C ARIGHI E BOCCIARDI R SERI M BARONE V RADICE MT ROMEO G PIEROTTI MA
Citation: B. Pasini et al., LOSS OF FUNCTION EFFECT OF RET MUTATIONS CAUSING HIRSCHSPRUNG DISEASE, Nature genetics, 10(1), 1995, pp. 35-40
THE PHYSICAL MAP OF THE HUMAN RET PROTOONCOGENE
Authors: PASINI B HOFSTRA RMW YIN L BOCCIARDI R SANTAMARIA G GROOTSCHOLTEN PM CECCHERINI I PATRONE G PRIOLO M BUYS CHCM ROMEO G
Citation: B. Pasini et al., THE PHYSICAL MAP OF THE HUMAN RET PROTOONCOGENE, Oncogene, 11(9), 1995, pp. 1737-1743
RET ACTIVATION BY GERMLINE MEN2A AND MEN2B MUTATIONS
Authors: BORRELLO MG SMITH DP PASINI B BONGARZONE I GRECO A LORENZO MJ ARIGHI E MIRANDA C ENG C ALBERTI L BOCCIARDI R MONDELLINI P SCOPSI L ROMEO G PONDER BAJ PIEROTTI MA
Citation: Mg. Borrello et al., RET ACTIVATION BY GERMLINE MEN2A AND MEN2B MUTATIONS, Oncogene, 11(11), 1995, pp. 2419-2427
ORDERING OF MARKERS IN THE PERICENTROMERIC REGION OF CHROMOSOME-10
Authors: HOFSTRA RMW STELWAGEN T PASINI B VANDERVEEN AY PONDER BAJ NAKAMURA Y ROMEO G BUYS CHCM
Citation: Rmw. Hofstra et al., ORDERING OF MARKERS IN THE PERICENTROMERIC REGION OF CHROMOSOME-10, Human genetics, 96(1), 1995, pp. 116-118
DNA POLYMORPHISMS AND CONDITIONS FOR SSCP ANALYSIS OF THE 20 EXONS OFTHE RET PROTOONCOGENE
Authors: CECCHERINI I HOFSTRA RMW LUO Y STULP RP BARONE V STELWAGEN T BOCCIARDI R NIJVEEN H BOLINO A SERI M RONCHETTO P PASINI B BOZZANO M BUYS CHCM ROMEO G
Citation: I. Ceccherini et al., DNA POLYMORPHISMS AND CONDITIONS FOR SSCP ANALYSIS OF THE 20 EXONS OFTHE RET PROTOONCOGENE, Oncogene, 9(10), 1994, pp. 3025-3029
THE GENETICS OF HIRSCHSPRUNG DISEASE AND THE CONCEPT OF PHENOTYPIC DIVERSITY DUE TO ALLELIC SERIES
Authors: ROMEO G LERONE M PASINI B YIN L CECCHERINI I BARONE V BOLINO A SERI M MARTUCCIELLO G
Citation: G. Romeo et al., THE GENETICS OF HIRSCHSPRUNG DISEASE AND THE CONCEPT OF PHENOTYPIC DIVERSITY DUE TO ALLELIC SERIES, Rivista italiana di pediatria, 20(4), 1994, pp. 441-445
A MUTATION IN THE RET PROTOONCOGENE ASSOCIATED WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-2B AND SPORADIC MEDULLARY-THYROID CARCINOMA
Authors: HOFSTRA RMW LANDSVATER RM CECCHERINI I STULP RP STELWAGEN T LUO Y PASINI B HOPPENER JWM VANAMSTEL HKP ROMEO G LIPS CJM BUYS CHCM
Citation: Rmw. Hofstra et al., A MUTATION IN THE RET PROTOONCOGENE ASSOCIATED WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-2B AND SPORADIC MEDULLARY-THYROID CARCINOMA, Nature, 367(6461), 1994, pp. 375-376
POINT MUTATIONS AFFECTING THE TYROSINE KINASE DOMAIN OF THE RET PROTOONCOGENE IN HIRSCHPRUNGS DISEASE
Authors: ROMEO G RONCHETTO P LUO Y BARONE V SERI M CECCHERINI I PASINI B BOCCIARDI R LERONE M KAARIAINEN H MARTUCCIELLO G
Citation: G. Romeo et al., POINT MUTATIONS AFFECTING THE TYROSINE KINASE DOMAIN OF THE RET PROTOONCOGENE IN HIRSCHPRUNGS DISEASE, Nature, 367(6461), 1994, pp. 377-378
CLOSE LINKAGE WITH THE RET PROTOONCOGENE AND BOUNDARIES OF DELETION MUTATIONS IN AUTOSOMAL-DOMINANT HIRSCHSPRUNG DISEASE
Authors: LUO Y CECCHERINI I PASINI B MATERA I BICOCCHI MP BARONE V BOCCIARDI R KAARIAINEN H WEBER D DEVOTO M ROMEO G
Citation: Y. Luo et al., CLOSE LINKAGE WITH THE RET PROTOONCOGENE AND BOUNDARIES OF DELETION MUTATIONS IN AUTOSOMAL-DOMINANT HIRSCHSPRUNG DISEASE, Human molecular genetics, 2(11), 1993, pp. 1803-1808
EXON STRUCTURE AND FLANKING INTRONIC SEQUENCES OF THE HUMAN RET PROTOONCOGENE
Authors: CECCHERINI I BOCCIARDI R LUO Y PASINI B HOFSTRA R TAKAHASHI M ROMEO G
Citation: I. Ceccherini et al., EXON STRUCTURE AND FLANKING INTRONIC SEQUENCES OF THE HUMAN RET PROTOONCOGENE, Biochemical and biophysical research communications, 196(3), 1993, pp. 1288-1295
AUTOSOMAL-DOMINANT HIRSCHSPRUNG DISEASE - CLOSE LINKAGE WITH THE RET PROTOONCOGENE AND DELETION MAPPING OF THE REGION
Authors: ROMEO G YIN L CECCHERINI I PASINI B MATERA I BARONE V TOCCO T KAARIAINEN H WEBER D DEVOTO M
Citation: G. Romeo et al., AUTOSOMAL-DOMINANT HIRSCHSPRUNG DISEASE - CLOSE LINKAGE WITH THE RET PROTOONCOGENE AND DELETION MAPPING OF THE REGION, American journal of human genetics, 53(3), 1993, pp. 133-133
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