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Results:
1-21
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Results: 21
Authors:
HULSHOF MM
VANHAERINGEN A
GRUIS NA
SNELS DCGTM
BERGMAN W
Citation: Mm. Hulshof et al., MULTIPLE AGMINATE SPITZ NEVI, Melanoma research, 8(2), 1998, pp. 156-160
Authors:
HILLE ETM
VANDUIJN E
GRUIS NA
ROSENDAAL FR
BERGMAN W
VANDENBROUCKE JP
Citation: Etm. Hille et al., EXCESS CANCER MORTALITY IN 6 DUTCH PEDIGREES WITH THE FAMILIAL ATYPICAL MULTIPLE MOLE-MELANOMA SYNDROME FROM 1830 TO 1994, Journal of investigative dermatology, 110(5), 1998, pp. 788-792
Authors:
GRUIS NA
VANDERVELDEN PA
BERGMAN W
FRANTS RR
Citation: Na. Gruis et al., GENETICS OF FAMILIAL ATYPICAL MULTIPLE MOLE-MELANOMA (FAMMM) SYNDROMEIN THE NETHERLANDS - HOW FAR HAVE WE COME, Bulletin du cancer, 85(7), 1998, pp. 627-630
Authors:
LIU L
GOLDSTEIN AM
TUCKER MA
BRILL H
GRUIS NA
HOGG D
LASSAM NJ
Citation: L. Liu et al., AFFECTED MEMBERS OF MELANOMA-PRONE FAMILIES WITH LINKAGE TO 9P21 BUT LACKING MUTATIONS IN CDKN2A DO NOT HARBOR MUTATIONS IN THE CODING REGIONS OF EITHER CDKN2B OR P19(ARF), Genes, chromosomes & cancer, 19(1), 1997, pp. 52-54
Authors:
GRUIS NA
VANDERVELDEN PA
SANDKUIJL LA
BERGMAN W
FRANTS RR
Citation: Na. Gruis et al., MELANOCORTIN-1 RECEPTOR (MC1R) VARIANT ARG151CYS IS GENERALLY ASSOCIATED WITH FAIR SKIN AND MODIFIES MELANOMA RISK IN DUTCH FAMILIAR ATYPICAL MULTIPLE MOLE MELANOMA (FAMMM), American journal of human genetics, 61(4), 1997, pp. 1153-1153
Authors:
SNELS DGCTM
BERGMAN W
GRUIS NA
Citation: Dgctm. Snels et al., RISK OF CUTANEOUS MALIGNANT-MELANOMA IN PATIENTS WITH NONFAMILIAL DYSPLASTIC NEVI, Journal of investigative dermatology, 107(3), 1996, pp. 72-72
Authors:
GRUIS NA
VANDERVELDEN PA
SANDKUIJL LA
PRINS DE
WEAVERFELDHAUS J
KAMB A
BERGMAN W
FRANTS RR
Citation: Na. Gruis et al., HOMOZYGOTES FOR CDKN2 (P16) GERMLINE MUTATION IN DUTCH FAMILIAL MELANOMA KINDREDS, Nature genetics, 10(3), 1995, pp. 351-353
Authors:
GRUIS NA
SANDKUIJL LA
VANDERVELDEN PA
BERGMAN W
FRANTS RR
Citation: Na. Gruis et al., CDKN2 EXPLAINS PART OF THE CLINICAL PHENOTYPE IN DUTCH FAMILIAL ATYPICAL MULTIPLE-MOLE MELANOMA (FAMMM) SYNDROME FAMILIES, Melanoma research, 5(3), 1995, pp. 169-177
Authors:
LIU Q
NEUHAUSEN S
MCCLURE M
FRYE C
WEAVERFELDHAUS J
GRUIS NA
EDDINGTON K
ALLALUNISTURNER MJ
SKOLNICK MH
FUJIMURA FK
KAMB A
Citation: Q. Liu et al., CDKN2 (MTS1) TUMOR-SUPPRESSOR GENE-MUTATIONS IN HUMAN TUMOR-CELL LINES, Oncogene, 10(6), 1995, pp. 1061-1067
INVESTIGATING THE CELL-CYCLE REGULATORS P15 AND P16 IN EXTENSIVE AND RECURRENT BASAL-CELL CARCINOMAS
Authors:
KREKELS GAM
GRUIS NA
BERKHOUT R
PRINS DE
NEUMANN HAM
Citation: Gam. Krekels et al., INVESTIGATING THE CELL-CYCLE REGULATORS P15 AND P16 IN EXTENSIVE AND RECURRENT BASAL-CELL CARCINOMAS, Journal of investigative dermatology, 105(3), 1995, pp. 480-480
Authors:
GRUIS NA
VANDERVELDEN PA
SANDKUIJL LA
PRINS DE
BERGMAN W
FRANTS RR
VERMEER BJ
Citation: Na. Gruis et al., HOMOZYGOTES FOR CDKN2 P16 GERMLINE MUTATION IN DUTCH FAMILIAL ATYPICAL MULTIPLE MOLE MELANOMA (FAMMM) SYNDROME FAMILIES ARE VIABLE/, Journal of investigative dermatology, 104(4), 1995, pp. 584-584
Authors:
BERNS EMJJ
KLIJN JGM
SMID M
VANSTAVEREN IL
GRUIS NA
FOEKENS JA
Citation: Emjj. Berns et al., INFREQUENT CDKN2 (MTS1 P16) GENE ALTERATIONS IN HUMAN PRIMARY BREAST-CANCER/, British Journal of Cancer, 72(4), 1995, pp. 964-967
Authors:
GRUIS NA
WEAVERFELDHAUS J
LIU QY
FRYE C
EELES R
ORLOW I
LACOMBE L
PONCECASTANEDA V
LIANES P
LATRES E
SKOLNICK M
CORDONCARDO C
KAMB A
Citation: Na. Gruis et al., GENETIC-EVIDENCE IN MELANOMA AND BLADDER CANCERS THAT P16 AND P53 FUNCTION IN SEPARATE PATHWAYS OF TUMOR SUPPRESSION, The American journal of pathology, 146(5), 1995, pp. 1199-1206
Authors:
FRANTS RR
VANDERVELDEN PA
SANDKUIJL LA
PRINS DE
BERGMAN W
GRUIS NA
Citation: Rr. Frants et al., VIABILITY OF HOMOZYGOTES FOR A GERMLINE DELETION OF 19 BP IN THE CODING REGION OF THE CDKN2 P16 GENE IN DUTCH MELANOMA FAMILIES/, American journal of human genetics, 57(4), 1995, pp. 338-338
Authors:
KAMB A
SHATTUCKEIDENS D
EELES R
LIU Q
GRUIS NA
DING W
HUSSEY C
TRAN T
MIKI Y
WEAVERFELDHAUS J
MCCLURE M
AITKEN JF
ANDERSON DE
BERGMAN W
FRANTS R
GOLDGAR DE
GREEN A
MACLENNAN R
MARTIN NG
MEYER LJ
YOUL P
ZONE JJ
SKOLNICK MH
CANNONALBRIGHT LA
Citation: A. Kamb et al., ANALYSIS OF THE P16 GENE (CDKN2) AS A CANDIDATE FOR THE CHROMOSOME 9PMELANOMA SUSCEPTIBILITY LOCUS, Nature genetics, 8(1), 1994, pp. 22-26
Authors:
CANNONALBRIGHT LA
GOLDGAR DE
NEUHAUSEN S
GRUIS NA
ANDERSON DE
LEWIS CM
JOST M
TRAN TD
NYGUEN K
KAMB A
WEAVERFELDHAUS J
MEYER LJ
ZONE JJ
SKOLNICK MH
Citation: La. Cannonalbright et al., LOCALIZATION OF THE 9P MELANOMA SUSCEPTIBILITY LOCUS (MLM) TO A 2-CM REGION BETWEEN D9S736 AND D9S171, Genomics, 23(1), 1994, pp. 265-268
Authors:
KAMB A
GRUIS NA
WEAVERFELDHAUS J
LIU QY
HARSHMAN K
TAVTIGIAN SV
STOCKERT E
DAY RS
JOHNSON BE
SKOLNICK MH
Citation: A. Kamb et al., A CELL-CYCLE REGULATOR POTENTIALLY INVOLVED IN GENESIS OF MANY TUMOR TYPES, Science, 264(5157), 1994, pp. 436-440
Authors:
WEAVERFELDHAUS J
GRUIS NA
NEUHAUSEN S
LEPASLIER D
STOCKERT E
SKOLNICK MH
KAMB A
Citation: J. Weaverfeldhaus et al., LOCALIZATION OF A PUTATIVE TUMOR-SUPPRESSOR GENE BY USING HOMOZYGOUS DELETIONS IN MELANOMAS, Proceedings of the National Academy of Sciences of the United Statesof America, 91(16), 1994, pp. 7563-7567
Authors:
BERGMAN W
GRUIS NA
SANDKUIJL LA
FRANTS RR
Citation: W. Bergman et al., GENETICS OF 7 DUTCH FAMILIAL ATYPICAL MULTIPLE MOLE MELANOMA SYNDROMEFAMILIES - A REVIEW OF LINKAGE RESULTS INCLUDING CHROMOSOME-1 AND CHROMOSOME-9, Journal of investigative dermatology, 103(5), 1994, pp. 190000122-190000125
Authors:
GRUIS NA
SANDKUIJL LA
WEBER JL
VANDERZEE A
BORGSTEIN AM
BERGMAN W
FRANTS RR
Citation: Na. Gruis et al., LINKAGE ANALYSIS IN DUTCH FAMILIAL ATYPICAL MULTIPLE MOLE MELANOMA (FAMMM) SYNDROME FAMILIES - EFFECT OF NEVUS COUNT, Melanoma research, 3(4), 1993, pp. 271-277
Authors:
GRUIS NA
ABELN ECA
BARDOEL AFJ
DEVILEE P
FRANTS RR
CORNELISSE CJ
Citation: Na. Gruis et al., PCR-BASED MICROSATELLITE POLYMORPHISMS IN THE DETECTION OF LOSS OF HETEROZYGOSITY IN FRESH AND ARCHIVAL TUMOR-TISSUE, British Journal of Cancer, 68(2), 1993, pp. 308-313
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1-21
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