Authors:
SALOMON R
ATTIE T
PELET A
BIDAUD C
ENG C
AMIEL J
SARNACKI S
GOULET O
RICOUR C
NIHOULFEKETE C
MUNNICH A
LYONNET S
Citation: R. Salomon et al., GERMLINE MUTATIONS OF THE RET LIGAND GDNF ARE NOT SUFFICIENT TO CAUSEHIRSCHSPRUNG DISEASE, Nature genetics, 14(3), 1996, pp. 345-347
Authors:
NELEN MR
PADBERG GW
PEETERS EAJ
LIN AY
VANDENHELM B
FRANTS RR
COULON V
GOLDSTEIN AM
VANREEN MMM
EASTON DF
EELES RA
HODGSON S
MULVIHILL JJ
MURDAY VA
TUCKER MA
MARIMAN ECM
STARINK TM
PONDER BAJ
ROPERS HH
KREMER H
LONGY M
ENG C
Citation: Mr. Nelen et al., LOCALIZATION OF THE GENE FOR COWDEN DISEASE TO CHROMOSOME 10Q22-23, Nature genetics, 13(1), 1996, pp. 114-116
Authors:
EDERY P
ATTIE T
AMIEL J
PELET A
ENG C
HOFSTRA RMW
MARTELLI H
BIDAUD C
MUNNICH A
LYONNET S
Citation: P. Edery et al., MUTATION OF THE ENDOTHELIN-3 GENE IN THE WAARDENBURG-HIRSCHSPRUNG DISEASE (SHAH-WAARDENBURG SYNDROME), Nature genetics, 12(4), 1996, pp. 442-444
Authors:
LLOYD S
WATSON M
DAVIDSON J
EBBS S
EELES R
ENG C
MURDAY V
PONDER B
SACKS N
Citation: S. Lloyd et al., RISK PERCEPTION, MENTAL-HEALTH AND HEALTH BEHAVIORS IN WOMEN WITH A FAMILY HISTORY OF BREAST-CANCER PRESENTING FOR GENETIC-COUNSELING, Psycho-oncology, 5(4), 1996, pp. 355-356
Citation: Sm. Ivanchuk et al., DE-NOVO MUTATION OF GDNF, LIGAND FOR THE RET GDNFR-ALPHA RECEPTOR COMPLEX, IN HIRSCHSPRUNG DISEASE/, Human molecular genetics, 5(12), 1996, pp. 2023-2026
Authors:
MARSH DJ
LEAROYD DL
ANDREW SD
KRISHNAN L
POJER R
RICHARDSON AL
DELBRIDGE L
ENG C
ROBINSON BG
Citation: Dj. Marsh et al., SOMATIC MUTATIONS IN THE RET PROTOONCOGENE IN SPORADIC MEDULLARY-THYROID CARCINOMA, Clinical endocrinology, 44(3), 1996, pp. 249-257
Authors:
ENG C
CLAYTON D
SCHUFFENECKER I
LENOIR G
COTE G
GAGEL RF
VANAMSTEL HKP
LIPS CJM
NISHISHO I
TAKAI SI
MARSH DJ
ROBINSON BG
FRANKRAUE K
RAUE F
XUE FY
NOLL WW
ROMEI C
PACINI F
FINK M
NIEDERLE B
ZEDENIUS J
NORDENSKJOLD M
KOMMINOTH P
HENDY GN
GHARIB H
THIBODEAU SN
LACROIX A
FRILLING A
PONDER BAJ
MULLIGAN LM
Citation: C. Eng et al., THE RELATIONSHIP BETWEEN SPECIFIC RET PROTOONCOGENE MUTATIONS AND DISEASE PHENOTYPE IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-2 - INTERNATIONAL RET MUTATION CONSORTIUM ANALYSIS, JAMA, the journal of the American Medical Association, 276(19), 1996, pp. 1575-1579
Citation: Hph. Neumann et al., VON HIPPEL-LINDAU DISEASE AND PHEOCHROMOCYTOMA - REPLY, JAMA, the journal of the American Medical Association, 275(11), 1996, pp. 840-840
Citation: C. Eng, SEMINARS IN MEDICINE OF THE BETH-ISRAEL-HOSPITAL, BOSTON - THE RET PROTOONCOGENE IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-2 AND HIRSCHSPRUNGS-DISEASE, The New England journal of medicine, 335(13), 1996, pp. 943-951
Citation: M. Campbell et al., THE SIMIAN FOAMY VIRUS TYPE-1 TRANSCRIPTIONAL TRANSACTIVATOR (TAS) BINDS AND ACTIVATES AN ENHANCER ELEMENT IN THE GAG GENE, Journal of virology, 70(10), 1996, pp. 6847-6855
Authors:
BARUCH L
ODWYER P
PATACSIL P
STERN EH
CHOCKALINGAM S
ENG C
JAVED MT
Citation: L. Baruch et al., THROMBOGENIC MILIEU OF ATRIAL-FLUTTER AND ATRIAL-FIBRILLATION - SIMILAR OR DIFFERENT - A TRANSESOPHAGEAL ECHOCARDIOGRAPHIC STUDY BEFORE ANDAFTER CARDIOVERSION, Circulation, 94(8), 1996, pp. 2662-2662
Authors:
ENG C
MULLIGAN LM
HEALEY CS
HOUGHTON C
FRILLING A
RAUE F
THOMAS GA
PONDER BAJ
Citation: C. Eng et al., HETEROGENEOUS MUTATION OF THE RET PROTOONCOGENE IN SUBPOPULATIONS OF MEDULLARY-THYROID CARCINOMA, Cancer research, 56(9), 1996, pp. 2167-2170
Authors:
MARSH DJ
ANDREW SD
ENG C
LEAROYD DL
CAPES AG
POJER R
RICHARDSON AL
HOUGHTON C
MULLIGAN LM
PONDER BAJ
ROBINSON BG
Citation: Dj. Marsh et al., GERMLINE AND SOMATIC MUTATIONS IN AN ONCOGENE - RET MUTATIONS IN INHERITED MEDULLARY-THYROID CARCINOMA, Cancer research, 56(6), 1996, pp. 1241-1243
Authors:
ENG C
FOSTER KA
HEALEY CS
HOUGHTON C
GAYTHER SA
MULLIGAN LM
PONDER BAJ
Citation: C. Eng et al., MUTATION ANALYSIS OF THE C-MOS PROTOONCOGENE AND THE ENDOTHELIN-B RECEPTOR GENE IN MEDULLARY-THYROID CARCINOMA AND PHEOCHROMOCYTOMA, British Journal of Cancer, 74(3), 1996, pp. 339-341
Authors:
ELEAZER GP
HORNUNG CA
EGBERT CB
EGBERT JR
ENG C
HEDGEPETH J
MCCANN R
STROTHERS H
SAPIR M
WEI M
WILSON M
Citation: Gp. Eleazer et al., THE RELATIONSHIP BETWEEN ETHNICITY AND ADVANCE DIRECTIVES IN A FRAIL OLDER POPULATION, Journal of the American Geriatrics Society, 44(8), 1996, pp. 938-943
Authors:
ENG C
MULLIGAN LM
SMITH DP
HEALEY CS
FRILLING A
RAUE F
NEUMANN HPH
PFRAGNER R
BEHMEL A
LORENZO MJ
STONEHOUSE TJ
PONDER MA
PONDER BAJ
Citation: C. Eng et al., MUTATION OF THE RET PROTOONCOGENE IN SPORADIC MEDULLARY-THYROID CARCINOMA, Genes, chromosomes & cancer, 12(3), 1995, pp. 209-212
Authors:
ATTIE T
PELET A
EDERY P
ENG C
MULLIGAN LM
AMIEL J
BOUTRAND L
BELDJORD C
NIHOULFEKETE C
MUNNICH A
PONDER BAJ
LYONNET S
Citation: T. Attie et al., DIVERSITY OF RET PROTOONCOGENE MUTATIONS IN FAMILIAL AND SPORADIC HIRSCHSPRUNG DISEASE, Human molecular genetics, 4(8), 1995, pp. 1381-1386
Authors:
MULLIGAN LM
MARSH DJ
ROBINSON BG
SCHUFFENECKER L
ZEDENIUS J
LIPS CJM
GAGEL RF
TAKAI SL
NOLL WW
FINK M
RAUE F
LACROIX A
THIBODEAU SN
FRILLING A
PONDER BAJ
ENG C
Citation: Lm. Mulligan et al., GENOTYPE-PHENOTYPE CORRELATION IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-2- REPORT OF THE INTERNATIONAL-RET-MUTATION-CONSORTIUM, Journal of internal medicine, 238(4), 1995, pp. 343-346
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
Citation: Sm. Myers et al., CHARACTERIZATION OF RET PROTOONCOGENE 3'-SPLICING VARIANTS AND POLYADENYLATION SITES - A NOVEL C-TERMINUS FOR RET, Oncogene, 11(10), 1995, pp. 2039-2045
Authors:
LORENZO MJ
ENG C
MULLIGAN LM
STONEHOUSE TJ
HEALEY CS
PONDER BAJ
SMITH DP
Citation: Mj. Lorenzo et al., MULTIPLE MESSENGER-RNA ISOFORMS OF THE HUMAN RET PROTOONCOGENE GENERATED BY ALTERNATE SPLICING, Oncogene, 10(7), 1995, pp. 1377-1383
Authors:
ENG C
SMITH DP
MULLIGAN LM
HEALEY CS
ZVELEBIL MJ
STONEHOUSE TJ
PONDER MA
JACKSON CE
WATERFIELD MD
PONDER BAJ
Citation: C. Eng et al., A NOVEL POINT MUTATION IN THE TYROSINE KINASE DOMAIN OF THE RET PROTOONCOGENE IN SPORADIC MEDULLARY-THYROID CARCINOMA AND IN A FAMILY WITH FMTC, Oncogene, 10(3), 1995, pp. 509-513
Authors:
FRILLING A
HOPPNER W
ENG C
MULLIGAN L
RAUE F
BROELSCH CE
Citation: A. Frilling et al., PRESYMPTOMATIC GENETIC SCREENING IN FAMILIES WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-2, Journal of molecular medicine, 73(5), 1995, pp. 229-233
Authors:
TOOGOOD AA
ENG C
SMITH DP
PONDER BAJ
SHALET SM
Citation: Aa. Toogood et al., NO MUTATION AT CODON-918 OF THE RET GENE IN A FAMILY WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE 2B, Clinical endocrinology, 43(6), 1995, pp. 759-762