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Results: 1-13 |
Results: 13
EVIDENCE OF FOUNDER MUTATIONS IN FINNISH BRCA1 AND BRCA2 FAMILIES
Authors: HUUSKO P PAAKKONEN K LAUNONEN V POYHONEN M BLANCO G KAUPPILA A PUISTOLA U KIVINIEMI H KUJALA M LEISTI J WINQVIST R
Citation: P. Huusko et al., EVIDENCE OF FOUNDER MUTATIONS IN FINNISH BRCA1 AND BRCA2 FAMILIES, American journal of human genetics, 62(6), 1998, pp. 1544-1548
MOLECULAR-CLONING, EXPRESSION AND CHROMOSOMAL LOCALIZATION OF A HUMANGENE ENCODING A 33 KDA PUTATIVE METALLOPEPTIDASE (PRSM1)
Authors: SCOTT IC HALILA R JENKINS JM MEHAN S APOSTOLOU S WINQVIST R CALLEN DF PROCKOP DJ PELTONEN L KADLER KE
Citation: Ic. Scott et al., MOLECULAR-CLONING, EXPRESSION AND CHROMOSOMAL LOCALIZATION OF A HUMANGENE ENCODING A 33 KDA PUTATIVE METALLOPEPTIDASE (PRSM1), Gene, 174(1), 1996, pp. 135-143
A COMMON REGION OF LOSS OF HETEROZYGOSITY IN WILMS-TUMOR AND EMBRYONAL RHABDOMYOSARCOMA DISTAL TO THE D11S988 LOCUS ON CHROMOSOME 11P15.5
Authors: BESNARDGUERIN C NEWSHAM I WINQVIST R CAVENEE WK
Citation: C. Besnardguerin et al., A COMMON REGION OF LOSS OF HETEROZYGOSITY IN WILMS-TUMOR AND EMBRYONAL RHABDOMYOSARCOMA DISTAL TO THE D11S988 LOCUS ON CHROMOSOME 11P15.5, Human genetics, 97(2), 1996, pp. 163-170
POPULATION VARIATION AT THE POLYMORPHIC APALI RESTRICTION ENZYME SITEIN INTRON-5 OF THE WT1 GENE
Authors: BESNARDGUERIN C WINQVIST R NEWSHAM I CAVENEE WK
Citation: C. Besnardguerin et al., POPULATION VARIATION AT THE POLYMORPHIC APALI RESTRICTION ENZYME SITEIN INTRON-5 OF THE WT1 GENE, Clinical genetics, 50(6), 1996, pp. 555-557
IMPROVED CARRIER TESTING FOR MULTIPLE ENDOCRINE NEOPLASIA, TYPE-1, USING NEW MICROSATELLITE-TYPE DNA MARKERS
Authors: KYTOLA S LEISTI J WINQVIST R SALMELA P
Citation: S. Kytola et al., IMPROVED CARRIER TESTING FOR MULTIPLE ENDOCRINE NEOPLASIA, TYPE-1, USING NEW MICROSATELLITE-TYPE DNA MARKERS, Human genetics, 96(4), 1995, pp. 449-453
LOSS OF HETEROZYGOSITY FOR CHROMOSOME-11 IN PRIMARY HUMAN BREAST-TUMORS IS ASSOCIATED WITH POOR SURVIVAL AFTER METASTASIS
Authors: WINQVIST R HAMPTON GM MANNERMAA A BLANCO G AIAVAIKKO M KIVINIEMI H TASKINEN PJ EVANS GA WRIGHT FA NEWSHAM I CAVENEE WK
Citation: R. Winqvist et al., LOSS OF HETEROZYGOSITY FOR CHROMOSOME-11 IN PRIMARY HUMAN BREAST-TUMORS IS ASSOCIATED WITH POOR SURVIVAL AFTER METASTASIS, Cancer research, 55(12), 1995, pp. 2660-2664
CHROMOSOMAL SUBLOCALLIZATION AND CLINICAL CONSEQUENCES OF LOSS OF HETEROZYGOSITY FOR CHROMOSOME-11 IN HUMAN BREAST-TUMORS
Authors: WINQVIST R HAMPTON G MANNERMAA A LAUNONEN V BLANCO G ALAVAIKKO M KIVINIEMI H TASKINEN PJ EVANS G WRIGHT PA NEWSHAM I CAVENEE W
Citation: R. Winqvist et al., CHROMOSOMAL SUBLOCALLIZATION AND CLINICAL CONSEQUENCES OF LOSS OF HETEROZYGOSITY FOR CHROMOSOME-11 IN HUMAN BREAST-TUMORS, American journal of human genetics, 57(4), 1995, pp. 431-431
CELL LINEAGE INVOLVEMENT OF RECURRENT CHROMOSOMAL-ABNORMALITIES IN HEMATOLOGIC NEOPLASMS
Authors: KNUUTILA S TEERENHOVI L LARRAMENDY ML ELONEN E FRANSSILA KO NYLUND SJ TIMONEN T HEINONEN K MAHLAMAKI E WINQVIST R RUUTU T
Citation: S. Knuutila et al., CELL LINEAGE INVOLVEMENT OF RECURRENT CHROMOSOMAL-ABNORMALITIES IN HEMATOLOGIC NEOPLASMS, Genes, chromosomes & cancer, 10(2), 1994, pp. 95-102
A POINT MUTATION IN THE PUTATIVE TATA BOX, DETECTED IN NONDISEASED INDIVIDUALS AND PATIENTS WITH HEREDITARY BREAST-CANCER, DECREASES PROMOTER ACTIVITY OF THE 17-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE-1 GENE-2 (EDH17B2) IN-VITRO
Authors: PELTOKETO H PIAO YS MANNERMAA A PONDER BAJ ISOMAA V POUTANEN M WINQVIST R VIHKO R
Citation: H. Peltoketo et al., A POINT MUTATION IN THE PUTATIVE TATA BOX, DETECTED IN NONDISEASED INDIVIDUALS AND PATIENTS WITH HEREDITARY BREAST-CANCER, DECREASES PROMOTER ACTIVITY OF THE 17-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE-1 GENE-2 (EDH17B2) IN-VITRO, Genomics, 23(1), 1994, pp. 250-252
HUMAN FAMILIAL AND SPORADIC BREAST-CANCER - ANALYSIS OF THE CODING REGIONS OF THE 17-BETA-HYDROXYSTEROID DEHYDROGENASE 2 GENE (EDH17B2) USING A SINGLE-STRAND CONFORMATION POLYMORPHISM ASSAY
Authors: MANNERMAA A PELTOKETO H WINQVIST R PONDER BAJ KIVINIEMI H EASTON DF POUTANEN M ISOMAA V VIHKO R
Citation: A. Mannermaa et al., HUMAN FAMILIAL AND SPORADIC BREAST-CANCER - ANALYSIS OF THE CODING REGIONS OF THE 17-BETA-HYDROXYSTEROID DEHYDROGENASE 2 GENE (EDH17B2) USING A SINGLE-STRAND CONFORMATION POLYMORPHISM ASSAY, Human genetics, 93(3), 1994, pp. 319-324
APPLICATION OF FINE-NEEDLE ASPIRATION TO THE DEMONSTRATION OF ERBB2 AND MYC EXPRESSION BY IN-SITU HYBRIDIZATION IN BREAST-CARCINOMA
Authors: SOINI Y MANNERMAA A WINQVIST R KAMEL D POIKONEN K KIVINIEMI H PAAKKO P
Citation: Y. Soini et al., APPLICATION OF FINE-NEEDLE ASPIRATION TO THE DEMONSTRATION OF ERBB2 AND MYC EXPRESSION BY IN-SITU HYBRIDIZATION IN BREAST-CARCINOMA, The Journal of histochemistry and cytochemistry, 42(6), 1994, pp. 795-803
MAPPING OF THE HUMAN SPERMIDINE SYNTHASE GENE (SRM) TO 1P36 AND A PROBABLE PSEUDOGENE (SRML2) TO REGION 3P14-]Q21
Authors: WINQVIST R ALHONEN L GRZESCHIK KH JANNE J ELORANTA TO
Citation: R. Winqvist et al., MAPPING OF THE HUMAN SPERMIDINE SYNTHASE GENE (SRM) TO 1P36 AND A PROBABLE PSEUDOGENE (SRML2) TO REGION 3P14-]Q21, Cytogenetics and cell genetics, 64(1), 1993, pp. 64-68
REFINEMENT OF REGIONAL LOSS OF HETEROZYGOSITY FOR CHROMOSOME-11P15.5 IN HUMAN BREAST-TUMORS
Authors: WINQVIST R MANNERMAA A ALAVAIKKO M BLANCO G TASKINEN PJ KIVINIEMI H NEWSHAM I CAVENEE W
Citation: R. Winqvist et al., REFINEMENT OF REGIONAL LOSS OF HETEROZYGOSITY FOR CHROMOSOME-11P15.5 IN HUMAN BREAST-TUMORS, Cancer research, 53(19), 1993, pp. 4486-4488
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