AAAAAA

   
Results: 1-25 | 26-50 | 51-75 | 76-100 | >>
Results: 51-75/136
RET PROTOONCOGENE MUTATIONS IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-2 AND MEDULLARY-THYROID CARCINOMA
Authors: MARSH DJ MULLIGAN LM ENG C
Citation: Dj. Marsh et al., RET PROTOONCOGENE MUTATIONS IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-2 AND MEDULLARY-THYROID CARCINOMA, Hormone research, 47(4-6), 1997, pp. 168-178
RET IN HUMAN-DEVELOPMENT AND ONCOGENESIS
Authors: EDERY P ENG C MUNNICH A LYONNET S
Citation: P. Edery et al., RET IN HUMAN-DEVELOPMENT AND ONCOGENESIS, BioEssays, 19(5), 1997, pp. 389-395
P-TEN, THE TUMOR-SUPPRESSOR FROM HUMAN-CHROMOSOME-10Q23, IS A DUAL-SPECIFICITY PHOSPHATASE
Authors: MYERS MP STOLAROV JP ENG C LI J WANG SI WIGLER MH PARSONS R TONKS NK
Citation: Mp. Myers et al., P-TEN, THE TUMOR-SUPPRESSOR FROM HUMAN-CHROMOSOME-10Q23, IS A DUAL-SPECIFICITY PHOSPHATASE, Proceedings of the National Academy of Sciences of the United Statesof America, 94(17), 1997, pp. 9052-9057
GLIAL-CELL LINE-DERIVED NEUROTROPHIC FACTOR (GDNF) EXPRESSION IN NORMAL AND NEOPLASTIC TISSUES - AN IMMUNOHISTOCHEMICAL STUDY
Authors: KILGALLEN C DIAZCANO S ENG C WOLFE HJ
Citation: C. Kilgallen et al., GLIAL-CELL LINE-DERIVED NEUROTROPHIC FACTOR (GDNF) EXPRESSION IN NORMAL AND NEOPLASTIC TISSUES - AN IMMUNOHISTOCHEMICAL STUDY, Laboratory investigation, 76(1), 1997, pp. 879-879
LONG-CHAIN PCR ON ARCHIVAL MATERIAL FOR RAPID DETECTION OF POINT MUTATIONS AND MOLECULAR SCREENING FOR PROGNOSTIC FACTORS IN NEOPLASTIC PROGRESSION
Authors: KILGALLEN C SMITH W SHAPIRO S DIAZCANO S VIJG J ENG C WOLFE HJ
Citation: C. Kilgallen et al., LONG-CHAIN PCR ON ARCHIVAL MATERIAL FOR RAPID DETECTION OF POINT MUTATIONS AND MOLECULAR SCREENING FOR PROGNOSTIC FACTORS IN NEOPLASTIC PROGRESSION, Laboratory investigation, 76(1), 1997, pp. 1072-1072
THE MOLECULAR-BASIS OF COWDENS-SYNDROME
Authors: TSOU HC PING X XIE X YAO Y SCHRAGER C GRUENER A CHRISTIANO AM LIAW D PARSONS R ENG C PEACOCKE M
Citation: Hc. Tsou et al., THE MOLECULAR-BASIS OF COWDENS-SYNDROME, Journal of investigative dermatology, 109(1), 1997, pp. 5-5
MUTATION ANALYSIS OF GLIAL-CELL LINE-DERIVED NEUROTROPHIC FACTOR, A LIGAND FOR AN RET CORECEPTOR COMPLEX, IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-2 AND SPORADIC NEUROENDOCRINE TUMORS/
Authors: MARSH DJ ZHENG ZM ARNOLD A ANDREW SD LEAROYD D FRILLING A KOMMINOTH P NEUMANN HPH PONDER BAJ ROLLINS BJ SHAPIRO GI ROBINSON BG MULLIGAN LM ENG C
Citation: Dj. Marsh et al., MUTATION ANALYSIS OF GLIAL-CELL LINE-DERIVED NEUROTROPHIC FACTOR, A LIGAND FOR AN RET CORECEPTOR COMPLEX, IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-2 AND SPORADIC NEUROENDOCRINE TUMORS/, The Journal of clinical endocrinology and metabolism, 82(9), 1997, pp. 3025-3028
GERMLINE DINUCLEOTIDE MUTATION IN CODON-883 OF THE RET PROTOONCOGENE IN MULTIPLE-ENDOCRINE-NEOPLASIA TYPE-2B WITHOUT CODON-918 MUTATION
Authors: GIMM O MARSH DJ ANDREW SD FRILLING A DAHIA PLM MULLIGAN LM ZAJAC JD ROBINSON BG ENG C
Citation: O. Gimm et al., GERMLINE DINUCLEOTIDE MUTATION IN CODON-883 OF THE RET PROTOONCOGENE IN MULTIPLE-ENDOCRINE-NEOPLASIA TYPE-2B WITHOUT CODON-918 MUTATION, The Journal of clinical endocrinology and metabolism, 82(11), 1997, pp. 3902-3904
PRESENCE OF MORE THAN ONE HMSH2 OR HMLHI MUTATION IN 4 HEREDITARY NONPOLYPOSIS COLON-CANCER (HNPCC) KINDREDS
Authors: SYNGAL S FOX E ENG C GARBER JE KOLODNER RD
Citation: S. Syngal et al., PRESENCE OF MORE THAN ONE HMSH2 OR HMLHI MUTATION IN 4 HEREDITARY NONPOLYPOSIS COLON-CANCER (HNPCC) KINDREDS, Gastroenterology, 112(4), 1997, pp. 664-664
MUTATION OF RET CODON-768 IS ASSOCIATED WITH THE FMTC PHENOTYPE
Authors: BOCCIA LM GREEN JS JOYCE C ENG C TAYLOR SAM MULLIGAN LM
Citation: Lm. Boccia et al., MUTATION OF RET CODON-768 IS ASSOCIATED WITH THE FMTC PHENOTYPE, Clinical genetics, 51(2), 1997, pp. 81-85
DIFFERENTIAL LOSS OF HETEROZYGOSITY IN THE REGION OF THE COWDEN LOCUSWITHIN 10Q22-23 IN FOLLICULAR THYROID ADENOMAS AND CARCINOMAS
Authors: MARSH DJ ZHENG ZM ZEDENIUS J KREMER H PADBERG GW LARSSON C LONGY M ENG C
Citation: Dj. Marsh et al., DIFFERENTIAL LOSS OF HETEROZYGOSITY IN THE REGION OF THE COWDEN LOCUSWITHIN 10Q22-23 IN FOLLICULAR THYROID ADENOMAS AND CARCINOMAS, Cancer research, 57(3), 1997, pp. 500-503
EXCLUSION OF PTEN AND 10Q22-24 AS THE SUSCEPTIBILITY LOCUS FOR JUVENILE POLYPOSIS SYNDROME
Authors: MARSH DJ ROTH S LUNETTA KL HEMMINKI A DAHIA PLM SISTONEN P ZHENG ZM CARON S VANORSOUW NJ BODMER WF COTTRELL SE DUNLOP MG ECCLES D HODGSON SV JARVINEN H KELLOKUMPU I MARKIE D NEALE K PHILLIPS R ROZEN P SYNGAL S VIJG J TOMLINSON IPM AALTONEN LA ENG C
Citation: Dj. Marsh et al., EXCLUSION OF PTEN AND 10Q22-24 AS THE SUSCEPTIBILITY LOCUS FOR JUVENILE POLYPOSIS SYNDROME, Cancer research, 57(22), 1997, pp. 5017-5021
SOMATIC DELETIONS AND MUTATIONS IN THE COWDEN-DISEASE GENE, PTEN, IN SPORADIC THYROID-TUMORS
Authors: DAHIA PLM MARSH DJ ZHENG ZM ZEDENIUS J KOMMINOTH P FRISK T WALLIN G PARSONS R LONGY M LARSSON C ENG C
Citation: Plm. Dahia et al., SOMATIC DELETIONS AND MUTATIONS IN THE COWDEN-DISEASE GENE, PTEN, IN SPORADIC THYROID-TUMORS, Cancer research, 57(21), 1997, pp. 4710-4713
MUTATION ANALYSIS OF GLIAL-CELL LINE-DERIVED NEUROTROPHIC FACTOR (GDNF), A LIGAND FOR THE RET GDNF RECEPTOR-ALPHA COMPLEX, IN SPORADIC PHEOCHROMOCYTOMAS/
Authors: DAHIA PLM TOLEDO SPA MULLIGAN LM MAHER ER GROSSMAN AB ENG C
Citation: Plm. Dahia et al., MUTATION ANALYSIS OF GLIAL-CELL LINE-DERIVED NEUROTROPHIC FACTOR (GDNF), A LIGAND FOR THE RET GDNF RECEPTOR-ALPHA COMPLEX, IN SPORADIC PHEOCHROMOCYTOMAS/, Cancer research, 57(2), 1997, pp. 310-313
THE ROLE OF MMAC1 MUTATIONS IN EARLY-ONSET BREAST-CANCER - CAUSATIVE IN ASSOCIATION WITH COWDEN-SYNDROME AND EXCLUDED IN BRCA1-NEGATIVE CASES
Authors: TSOU HC TENG DHF PING XL BRANCOLINI V DAVIS T HU R XIE XX GRUENER AC SCHRAGER CA CHRISTIANO AM ENG C STECK P OTT J TAVTIGIAN SV PEACOCKE M
Citation: Hc. Tsou et al., THE ROLE OF MMAC1 MUTATIONS IN EARLY-ONSET BREAST-CANCER - CAUSATIVE IN ASSOCIATION WITH COWDEN-SYNDROME AND EXCLUDED IN BRCA1-NEGATIVE CASES, American journal of human genetics, 61(5), 1997, pp. 1036-1043
GERMLINE MUTATIONS OF THE PTEN GENE IN COWDEN-DISEASE AND BANNAYAN-ZONANA-SYNDROME
Authors: ENG C MARSH D LIAW D DAHIA P LI J ZHENG Z TSOU H PEACOCKE M GORLIN R PARSONS R
Citation: C. Eng et al., GERMLINE MUTATIONS OF THE PTEN GENE IN COWDEN-DISEASE AND BANNAYAN-ZONANA-SYNDROME, American journal of human genetics, 61(4), 1997, pp. 69-69
LOSS OF HETEROZYGOSITY OF CHROMOSOMAL REGION 10Q23 IN HUMAN SPORADIC BREAST-CARCINOMA
Authors: COULON V FEILOTTER HE BOAG AH DORIONBONNET F DUBOUE B LATHAM WCW ENG C LONGY M MULLIGAN LM
Citation: V. Coulon et al., LOSS OF HETEROZYGOSITY OF CHROMOSOMAL REGION 10Q23 IN HUMAN SPORADIC BREAST-CARCINOMA, American journal of human genetics, 61(4), 1997, pp. 335-335
MUTATION AND DELETION ANALYSIS OF THE COWDEN-DISEASE GENE, PTEN, IN SPORADIC NONMEDULLARY THYROID-TUMORS
Authors: DAHLA PLM MARSH DJ ZHENG Z ZEDENIUS J KOMMINOTH P PARSONS R LONGY M LARSSON C ENG C
Citation: Plm. Dahla et al., MUTATION AND DELETION ANALYSIS OF THE COWDEN-DISEASE GENE, PTEN, IN SPORADIC NONMEDULLARY THYROID-TUMORS, American journal of human genetics, 61(4), 1997, pp. 338-338
ANALYSIS OF THE PTEN CODING REGION IN PRIMARY PROSTATE CARCINOMAS
Authors: FEILOTTER HE NAGAL MA BOAG AH ENG C MULLIGAN LM
Citation: He. Feilotter et al., ANALYSIS OF THE PTEN CODING REGION IN PRIMARY PROSTATE CARCINOMAS, American journal of human genetics, 61(4), 1997, pp. 348-348
ROLE OF MMAC1 MUTATIONS IN EARLY-ONSET BREAST-CANCER - CAUSATIVE IN ASSOCIATION WITH COWDENS-SYNDROME AND EXCLUDED IN BRCA1-NEGATIVE CASES
Authors: TSOU HC TENG D PING XL BRONCOLINI V DAVIS T HU R XIE XX GRUENER AC SCHRAGER AC CHRISTIANO AC ENG C STECK P OTT J TAVITIGIAN S PEACOCKE M
Citation: Hc. Tsou et al., ROLE OF MMAC1 MUTATIONS IN EARLY-ONSET BREAST-CANCER - CAUSATIVE IN ASSOCIATION WITH COWDENS-SYNDROME AND EXCLUDED IN BRCA1-NEGATIVE CASES, American journal of human genetics, 61(4), 1997, pp. 468-468
THE PHYSICAL STRUCTURES OF GDNFR-ALPHA AND NDNR-ALPHA
Authors: MYERS SM ENG C HESSION C CATE R KOGON MD MULLIGAN LM
Citation: Sm. Myers et al., THE PHYSICAL STRUCTURES OF GDNFR-ALPHA AND NDNR-ALPHA, American journal of human genetics, 61(4), 1997, pp. 2231-2231
CASE-REPORT - 3 FMR-1 ALLELES DETECTED IN A DEVELOPMENTALLY DELAYED FEMALE CHILD WITH A 46,XX KARYOTYPE
Authors: KORNREICH R KRAIZA K DEBAUCHE D STEVENS C ENG C MCINTOSH N GERSEN S
Citation: R. Kornreich et al., CASE-REPORT - 3 FMR-1 ALLELES DETECTED IN A DEVELOPMENTALLY DELAYED FEMALE CHILD WITH A 46,XX KARYOTYPE, American journal of human genetics, 61(4), 1997, pp. 2374-2374
PREVALENCE AND PARENTAL ORIGIN OF DE-NOVO RET MUTATIONS IN MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A AND FAMILIAL MEDULLARY-THYROID CARCINOMA
Authors: SCHUFFENECKER I GINET N GOLDGAR D ENG C CHAMBE B BONEU A HOUDENT C PALLO D SCHLUMBERGER M THIVOLET C LENOIR GM
Citation: I. Schuffenecker et al., PREVALENCE AND PARENTAL ORIGIN OF DE-NOVO RET MUTATIONS IN MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A AND FAMILIAL MEDULLARY-THYROID CARCINOMA, American journal of human genetics, 60(1), 1997, pp. 233-237
PROGRAM OF ALL-INCLUSIVE CARE FOR THE ELDERLY (PACE) - AN INNOVATIVE MODEL OF INTEGRATED GERIATRIC CARE AND FINANCING
Authors: ENG C PEDULLA J ELEAZER P MCCANN R FOX N
Citation: C. Eng et al., PROGRAM OF ALL-INCLUSIVE CARE FOR THE ELDERLY (PACE) - AN INNOVATIVE MODEL OF INTEGRATED GERIATRIC CARE AND FINANCING, Journal of the American Geriatrics Society, 45(2), 1997, pp. 223-232
THE PACE PROGRAM - REPLY
Authors: ENG C PEDULLA J ELEAZER GP MCCANN R FOX N
Citation: C. Eng et al., THE PACE PROGRAM - REPLY, Journal of the American Geriatrics Society, 45(10), 1997, pp. 1280-1281
Risultati: 1-25 | 26-50 | 51-75 | 76-100 | >>