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Results: 1-25 | 26-26
Results: 1-25/26
CHARACTERIZATION OF THE MOUSE MEN1 GENE AND ITS EXPRESSION DURING DEVELOPMENT
Authors: STEWART C PARENTE F PIEHL F FARNEBO F QUINCEY D SILINS G BERGMAN L CARLE GF LEMMENS I GRIMMOND S XIAN CZ KHODEI S TEH BT LAGERCRANTZ J SIGGERS P CALENDER A VANDEVEM V KAS K WEBER G HAYWARD N GAUDRAY P LARSSON C
Citation: C. Stewart et al., CHARACTERIZATION OF THE MOUSE MEN1 GENE AND ITS EXPRESSION DURING DEVELOPMENT, Oncogene, 17(19), 1998, pp. 2485-2493
NO EVIDENCE FOR THE H133Y MUTATION IN SONIC HEDGEHOG IN A COLLECTION OF COMMON TUMOR TYPES
Authors: WICKING C EVANS T HENK B HAYWARD N SIMMS LA CHENEVIXTRENCH G PIETSCH T WAINWRIGHT B
Citation: C. Wicking et al., NO EVIDENCE FOR THE H133Y MUTATION IN SONIC HEDGEHOG IN A COLLECTION OF COMMON TUMOR TYPES, Oncogene, 16(8), 1998, pp. 1091-1093
ASSOCIATION OF MISSENSE AND 5'-SPLICE-SITE MUTATIONS IN TAU WITH THE INHERITED DEMENTIA FTDP-17
Authors: HUTTON M LENDON CL RIZZU P BAKER M FROELICH S HOULDEN H PICKERINGBROWN S CHAKRAVERTY S ISAACS A GROVER A HACKETT J ADAMSON J LINCOLN S DICKSON D DAVIES P PETERSEN RC STEVENS M DEGRAAFF E WAUTERS E VANBAREN J HILLEBRAND M JOOSSE M KWON JM NOWOTNY P CHE LK NORTON J MORRIS JC REED LA TROJANOWSKI J BASUN H LANNFELT L NEYSTAT M FAHN S DARK F TANNENBERG T DODD PR HAYWARD N KWOK JBJ SCHOFIELD PR ANDREADIS A SNOWDEN J CRAUFURD D NEARY D OWEN F OOSTRA BA HARDY J GOATE A VANSWIETEN J MANN D LYNCH T HEUTINK P
Citation: M. Hutton et al., ASSOCIATION OF MISSENSE AND 5'-SPLICE-SITE MUTATIONS IN TAU WITH THE INHERITED DEMENTIA FTDP-17, Nature, 393(6686), 1998, pp. 702-705
MUTATION ANALYSIS OF THE MEN1 GENE IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-1, FAMILIAL ACROMEGALY AND FAMILIAL ISOLATED HYPERPARATHYROIDISM
Authors: TEH BT KYTOLA S FARNEBO F BERGMAN L WONG FK WEBER G HAYWARD N LARSSON C SKOGSEID B BECKERS A PHELAN C EDWARDS M EPSTEIN M ALFORD F HURLEY D GRIMMOND S SILINS G WALTERS M STEWART C CARDINAL J KHODAEI S PARENTE F TRANEBJAERG L JORDE R MENON J KHIR A TAN TT CHAN SP ZAINI A KHALID BAK SANDELIN K THOMPSON N BRANDI ML WARTH M STOCK J LEISTI J CAMERON D SHEPHERD JJ OBERG K NORDENSKJOLD M SALMELA P
Citation: Bt. Teh et al., MUTATION ANALYSIS OF THE MEN1 GENE IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-1, FAMILIAL ACROMEGALY AND FAMILIAL ISOLATED HYPERPARATHYROIDISM, The Journal of clinical endocrinology and metabolism, 83(8), 1998, pp. 2621-2626
CHARACTERIZATION OF A NEW HUMAN AND MURINE MEMBER OF THE DNAJ FAMILY OF PROTEINS
Authors: SILINS G GRIMMOND S HAYWARD N
Citation: G. Silins et al., CHARACTERIZATION OF A NEW HUMAN AND MURINE MEMBER OF THE DNAJ FAMILY OF PROTEINS, Biochemical and biophysical research communications, 243(1), 1998, pp. 273-276
LOSS OF HETEROZYGOSITY OF CHROMOSOME-13 IN MERKEL CELL-CARCINOMA
Authors: LEONARD JH HAYWARD N
Citation: Jh. Leonard et N. Hayward, LOSS OF HETEROZYGOSITY OF CHROMOSOME-13 IN MERKEL CELL-CARCINOMA, Genes, chromosomes & cancer, 20(1), 1997, pp. 93-97
IDENTIFICATION OF THE MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 (MEN1) GENE
Authors: LEMMENS I VANDEVEN WJM KAS K ZHANG CX GIRAUD S WAUTOT V BUISSON N DEWITTE K SALANDRE J LENOIR G PUGEAT M CALENDER A PARENTE F QUINCEY D GAUDRAY P DEWIT MJ LIPS CJM HOPPENER JWM KHODAEI S GRANT AL WEBER G KYTOLA S TEH BT FARNEBO F PHELAN C HAYWARD N LARSSON C PANNETT AAJ FORBES SA BASSETT JHD THAKKER RV
Citation: I. Lemmens et al., IDENTIFICATION OF THE MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 (MEN1) GENE, Human molecular genetics, 6(7), 1997, pp. 1177-1183
LOCALIZATION OF FRONTOTEMPORAL DEMENTIA WITH PARKINSONISM IN AN AUSTRALIAN KINDRED TO CHROMOSOME 17Q21-22
Authors: BAKER M KWOK JBJ KUCERA S CROOK R FARRER M HOULDEN H ISAACS A LINCOLN S ONSTEAD L HARDY J WITTENBERG L DODD P WEBB S HAYWARD N TANNENBERG T ANDREADIS A HALLUPP M SCHOFIELD P DARK F HUTTON M
Citation: M. Baker et al., LOCALIZATION OF FRONTOTEMPORAL DEMENTIA WITH PARKINSONISM IN AN AUSTRALIAN KINDRED TO CHROMOSOME 17Q21-22, Annals of neurology, 42(5), 1997, pp. 794-798
EXCLUSION OF THE PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE C-BETA-3 (PLCB3) GENE AS A CANDIDATE FOR MULTIPLE ENDOCRINE NEOPLASIA TYPE-1
Authors: WEBER G GRIMMOND S LAGERCRANTZ J FRIEDMAN E PHELAN C CARSON E HAYWARD N JACOBOVITZ O NORDENSKJOLD M LARSSON C
Citation: G. Weber et al., EXCLUSION OF THE PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE C-BETA-3 (PLCB3) GENE AS A CANDIDATE FOR MULTIPLE ENDOCRINE NEOPLASIA TYPE-1, Human genetics, 99(1), 1997, pp. 130-132
EVIDENCE FOR ASYMMETRIC ACCRETION AND LOW-ANGLE, PLANAR FAULTS IN SLOW-SPREADING OCEANIC-CRUST
Authors: COLLIER JS DANOBEITIA JJ CANALES JP DALWOOD R GADD S HAYWARD N HENSTOCK T KRASTEL S PEIRCE C WATTS A
Citation: Js. Collier et al., EVIDENCE FOR ASYMMETRIC ACCRETION AND LOW-ANGLE, PLANAR FAULTS IN SLOW-SPREADING OCEANIC-CRUST, Geology, 25(12), 1997, pp. 1075-1078
ANALYSIS OF THE PROMOTER REGION OF THE HUMAN VEGF-RELATED FACTOR GENE
Authors: SILINS G GRIMMOND S EGERTON M HAYWARD N
Citation: G. Silins et al., ANALYSIS OF THE PROMOTER REGION OF THE HUMAN VEGF-RELATED FACTOR GENE, Biochemical and biophysical research communications, 230(2), 1997, pp. 413-418
GERMLINE MUTATIONS IN THE P16(INK4A) BINDING DOMAIN OF CDK4 IN FAMILIAL MELANOMA
Authors: ZUO L WEGER J YANG QB GOLDSTEIN AM TUCKER MA WALKER GJ HAYWARD N DRACOPOLI NC
Citation: L. Zuo et al., GERMLINE MUTATIONS IN THE P16(INK4A) BINDING DOMAIN OF CDK4 IN FAMILIAL MELANOMA, Nature genetics, 12(1), 1996, pp. 97-99
CLONING AND CHARACTERIZATION OF A NOVEL HUMAN GENE-RELATED TO VASCULAR ENDOTHELIAL GROWTH-FACTOR
Authors: GRIMMOND S LAGERCRANTZ J DRINKWATER C SILINS G TOWNSON S POLLOCK P GOTLEY D CARSON E RAKAR S NORDENSKJOLD M WARD L HAYWARD N WEBER G
Citation: S. Grimmond et al., CLONING AND CHARACTERIZATION OF A NOVEL HUMAN GENE-RELATED TO VASCULAR ENDOTHELIAL GROWTH-FACTOR, PCR methods and applications, 6(2), 1996, pp. 124-131
PERMEABILITY OF THE BLOOD-BRAIN-BARRIER BY THE BRADYKININ AGONIST, RMP-7 - EVIDENCE FOR A SENSITIVE, AUTO-REGULATED, RECEPTOR-MEDIATED SYSTEM
Authors: BARTUS RT ELLIOTT P HAYWARD N DEAN R MCEWEN EL FISHER SK
Citation: Rt. Bartus et al., PERMEABILITY OF THE BLOOD-BRAIN-BARRIER BY THE BRADYKININ AGONIST, RMP-7 - EVIDENCE FOR A SENSITIVE, AUTO-REGULATED, RECEPTOR-MEDIATED SYSTEM, Immunopharmacology, 33(1-3), 1996, pp. 270-278
CLUSTERED INACTIVATING MUTATIONS AND BENIGN POLYMORPHISMS OF THE CALCIUM RECEPTOR GENE IN FAMILIAL BENIGN HYPOCALCIURIC HYPERCALCEMIA SUGGEST RECEPTOR FUNCTIONAL DOMAINS
Authors: HEATH H ODELBERG S JACKSON CE TEH BT HAYWARD N LARSSON C BUIST NRM KRAPCHO KJ HUNG BC CAPUANO IV GARRETT JE LEPPERT MF
Citation: H. Heath et al., CLUSTERED INACTIVATING MUTATIONS AND BENIGN POLYMORPHISMS OF THE CALCIUM RECEPTOR GENE IN FAMILIAL BENIGN HYPOCALCIURIC HYPERCALCEMIA SUGGEST RECEPTOR FUNCTIONAL DOMAINS, The Journal of clinical endocrinology and metabolism, 81(4), 1996, pp. 1312-1317
CHARACTERIZATION OF THE MURINE VEGF-RELATED FACTOR GENE
Authors: TOWNSON S LAGERCRANTZ J GRIMMOND S SILINS G NORDENSKJOLD M WEBER G HAYWARD N
Citation: S. Townson et al., CHARACTERIZATION OF THE MURINE VEGF-RELATED FACTOR GENE, Biochemical and biophysical research communications, 220(3), 1996, pp. 922-928
ALLELIC LOSSES ON CHROMOSOME BAND 11Q13 IN ALDOSTERONE-PRODUCING ADRENAL-TUMORS
Authors: LIDA A BLAKE K TUNNY T KLEMM S STOWASSER M HAYWARD N GORDON R NAKAMURA Y IMAI T
Citation: A. Lida et al., ALLELIC LOSSES ON CHROMOSOME BAND 11Q13 IN ALDOSTERONE-PRODUCING ADRENAL-TUMORS, Genes, chromosomes & cancer, 12(1), 1995, pp. 73-75
EXCLUSION OF THE 13-KDA RAPAMYCIN BINDING-PROTEIN GENE (FKBP2) AS A CANDIDATE GENE FOR MULTIPLE ENDOCRINE NEOPLASIA TYPE-1
Authors: GRIMMOND S WEBER G LARSSON C WALTERS M TEH B SHEPHERD J NORDENSKJOLD M HAYWARD N
Citation: S. Grimmond et al., EXCLUSION OF THE 13-KDA RAPAMYCIN BINDING-PROTEIN GENE (FKBP2) AS A CANDIDATE GENE FOR MULTIPLE ENDOCRINE NEOPLASIA TYPE-1, Human genetics, 95(4), 1995, pp. 455-458
GLUTATHIONE-S-TRANSFERASE GSTM1 NULL GENOTYPE IS NOT OVERREPRESENTED IN AUSTRALIAN PATIENTS WITH NEVOID BASAL-CELL CARCINOMA SYNDROME OR SPORADIC MELANOMA
Authors: SHANLEY SM CHENEVIXTRENCH G PALMER J HAYWARD N
Citation: Sm. Shanley et al., GLUTATHIONE-S-TRANSFERASE GSTM1 NULL GENOTYPE IS NOT OVERREPRESENTED IN AUSTRALIAN PATIENTS WITH NEVOID BASAL-CELL CARCINOMA SYNDROME OR SPORADIC MELANOMA, Carcinogenesis, 16(8), 1995, pp. 2003-2004
FREQUENCY OF FAMILIAL MELANOMA AND MLM2 GENE - REPLY
Authors: HAYWARD N
Citation: N. Hayward, FREQUENCY OF FAMILIAL MELANOMA AND MLM2 GENE - REPLY, Lancet, 345(8949), 1995, pp. 582-582
MULTIPLE ENDOCRINE NEOPLASIA TYPE-I - CLINICAL SYNDROME TO MOLECULAR-GENETICS
Authors: TEH BT GRIMMOND S SHEPHERD J LARSSON C HAYWARD N
Citation: Bt. Teh et al., MULTIPLE ENDOCRINE NEOPLASIA TYPE-I - CLINICAL SYNDROME TO MOLECULAR-GENETICS, Australian and New Zealand journal of surgery, 65(10), 1995, pp. 708-713
CANDIDATE GENES FOR MULTIPLE ENDOCRINE NEOPLASIA TYPE-1
Authors: LAGERCRANTZ J WEBER G FRIEDMAN E GRIMMOND S HAYWARD N NORDENSKJOLD M LARSSON C
Citation: J. Lagercrantz et al., CANDIDATE GENES FOR MULTIPLE ENDOCRINE NEOPLASIA TYPE-1, Journal of cellular biochemistry, 1994, pp. 207-207
INCIDENCE OF FAMILIAL MELANOMA AND MLM2 GENE
Authors: BATTISTUTTA D PALMER J WALTERS M WALKER G NANCARROW D HAYWARD N
Citation: D. Battistutta et al., INCIDENCE OF FAMILIAL MELANOMA AND MLM2 GENE, Lancet, 344(8937), 1994, pp. 1607-1608
DIRECT EVIDENCE FOR THE DISTRIBUTION AND OCCURRENCE OF HYDROTHERMAL ACTIVITY BETWEEN 27-DEGREES-N-30-DEGREES-N ON THE MID-ATLANTIC RIDGE
Authors: MURTON BJ KLINKHAMMER G BECKER K BRIAIS A EDGE D HAYWARD N MILLARD N MITCHELL I ROUSE I RUDNICKI M SAYANAGI K SLOAN H PARSON L
Citation: Bj. Murton et al., DIRECT EVIDENCE FOR THE DISTRIBUTION AND OCCURRENCE OF HYDROTHERMAL ACTIVITY BETWEEN 27-DEGREES-N-30-DEGREES-N ON THE MID-ATLANTIC RIDGE, Earth and planetary science letters, 125(1-4), 1994, pp. 119-128
DO SMOOTHLY CURVING, SPIRAL-SHAPED INCLUSION TRAILS SIGNIFY PORPHYROBLAST ROTATION - REPLY
Authors: BELL TH FORDE A HAYWARD N
Citation: Th. Bell et al., DO SMOOTHLY CURVING, SPIRAL-SHAPED INCLUSION TRAILS SIGNIFY PORPHYROBLAST ROTATION - REPLY, Geology, 21(5), 1993, pp. 480-480
Risultati: 1-25 | 26-26