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au.\*:("WINQVIST, R")

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Improved carrier testing for multiple endocrine neoplasia, type 1, using new microsatellite-type DNA markersKYTÖLÄ, S; LEISTI, J; WINQVIST, R et al.Human genetics. 1995, Vol 96, Num 4, pp 449-453, issn 0340-6717Article

myc oncogenes: activation and amplificationALITALO, K; KOSKINEN, P; MAKELA, T. P et al.Biochimica et biophysica acta. 1987, Vol 907, Num 1, pp 1-32, issn 0006-3002Article

Aberrant expression of an amplified c-myb oncogene in two cell lines from a colon carcinomaALITALO, K; WINQVIST, R; LIN, C. C et al.Proceedings of the National Academy of Sciences of the United States of America. Biological sciences. 1984, Vol 81, Num 14, pp 4534-4538, issn 0273-1134Article

A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5BESNARD-GUERIN, C; NEWSHAM, I; WINQVIST, R et al.Human genetics. 1996, Vol 97, Num 2, pp 163-170, issn 0340-6717Article

Mapping of the human spermidine synthase gene (SRM) to 1p36 and a probable pseudogene (SRML2) to region 3p14→q21WINQVIST, R; ALHONEN, L; GRZESCHIK, K.-H et al.Cytogenetics and cell genetics. 1993, Vol 64, Num 1, pp 64-68, issn 0301-0171Article

Refinement of regional loss of heterozygosity for chromosome 11p15.5 in human breast tumorsWINQVIST, R; MANNERMAA, A; ALAVAIKLO, M et al.Cancer research (Baltimore). 1993, Vol 53, Num 19, pp 4486-4488, issn 0008-5472Article

Mapping of amplified c-myb oncogene, sister chromatid exchanges, and karyotypic analysis of the COLO 205 colon carcinoma cell lineWINQVIST, R; KNUUTILA, S; LEPRINCE, D et al.Cancer genetics and cytogenetics. 1985, Vol 18, Num 3, pp 251-264, issn 0165-4608Article

PREDICT Plus: development and validation of a prognostic model for early breast cancer that includes HER2WISHART, G. C; BAJDIK, C. D; OLSON, J. E et al.British journal of cancer. 2012, Vol 107, Num 5, pp 800-807, issn 0007-0920, 8 p.Article

Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer : enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignanciesKARPPINEN, S.-M; BARKARDOTTIR, R. B; JOHANNESDOTTIR, G et al.Journal of medical genetics. 2006, Vol 43, Num 11, pp 856-862, issn 0022-2593, 7 p.Article

Chromosome 11q22.3-q25 LOH in ovarian cancer : Association with a more aggressive disease course and involved subregionsLAUNONEN, V; STENBÄCK, F; PUISTOLA, U et al.Gynecologic oncology (Print). 1998, Vol 71, Num 2, pp 299-304, issn 0090-8258Article

Human familial and sporadic breast cancer : analysis of the coding regions of the 17β-hydroxysteroid dehydrogenase 2 gene (EDH17B2) using a single-strand conformation polymorphism assayMANNERMAA, A; PELTOKETO, H; WINQVIST, R et al.Human genetics. 1994, Vol 93, Num 3, pp 319-324, issn 0340-6717Article

Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the finnish populationNOKELAINEN, P; ALANEN-KURKI, L; WINQVIST, R et al.Human genetics. 1990, Vol 85, Num 5, pp 541-545, issn 0340-6717, 5 p.Article

Acute myelogenous leukaemia with C-myc amplification and double minute chromosomesALITALO, K; SAKSELA, K; WINQVIST, R et al.Lancet (British edition). 1985, Num 8463, pp 1035-1039, issn 0140-6736Article

Breast-Cancer Risk in Families with Mutations in PALB2ANTONIOU, A. C; CASADEI, S; TOMIAK, E et al.The New England journal of medicine. 2014, Vol 371, Num 6, pp 497-506, issn 0028-4793, 10 p.Article

Familial breast cancer screening reveals an alteration in the RAP80 UIM domain that impairs DNA damage response functionNIKKILÄ, J; COLEMAN, K. A; MORRISSEY, D et al.Oncogene (Basingstoke). 2009, Vol 28, Num 16, pp 1843-1852, issn 0950-9232, 10 p.Article

Mutation analysis of aryl hydrocarbon receptor interacting protein (AIP) gene in colorectal, breast, and prostate cancersGEORGITSI, M; KARHU, A; WINQVIST, R et al.British journal of cancer. 2007, Vol 96, Num 2, pp 352-356, issn 0007-0920, 5 p.Article

ATM mutations in finnish breast cancer patientsALLINEN, M; LAUNONEN, V; LAAKE, K et al.Journal of medical genetics. 2002, Vol 39, Num 3, pp 192-196, issn 0022-2593Article

Mutation analysis of BRCA1 and BRCA2 in Turkish cancer families : a novel mutation BRCA2 3414de14 found in male breast cancerBALCI, A; HUUSKO, P; PÄÄKKÖNEN, K et al.European journal of cancer (1990). 1999, Vol 35, Num 5, pp 707-710, issn 0959-8049Article

Population variation at the polymorphic ApaLI restriction enzyme site in intron 5 of the WT1 geneBESNARD-GUERIN, C; WINQVIST, R; NEWSHAM, I et al.Clinical genetics. 1996, Vol 50, Num 6, pp 555-557, issn 0009-9163Article

Chromosomal localization to 3q21→qter and two TaqI RFLPs of human prostate-specific acid phosphatase gene (ACPP)WINQVIST, R; VIRKKUNEN, P; GRZESCHIK, K.-H et al.Cytogenetics and cell genetics. 1989, Vol 52, Num 1-2, pp 68-71, issn 0301-0171Article

Mouse and human ornithine decarboxylase genes: methylation polymorphism and amplificationALHONEN-HONGISTO, L; LEINONEN, P; SINERVIRTA, R et al.Biochemical journal (London. 1906). 1987, Vol 242, Num 1, pp 205-210, issn 0006-2936Article

No evidence of involvement of germline BACH1 mutations in Finnish breast and ovarian cancer familiesKARPPINEN, S.-M; VUOSKU, J; HEIKKINEN, K et al.European journal of cancer (1990). 2003, Vol 39, Num 3, pp 366-371, issn 0959-8049, 6 p.Article

Germ-line TP53 mutations in Finnish cancer families exhibiting features of the Li-Fraumeni syndrome and negative for BRCA1 and BRCA2HUUSKO, P; CASTREN, K; LAUNONEN, V et al.Cancer genetics and cytogenetics. 1999, Vol 112, Num 1, pp 9-14, issn 0165-4608Conference Paper

Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotypeSHELBOURNE, P; WINQVIST, R; KUNERT, E et al.Human molecular genetics (Print). 1992, Vol 1, Num 7, pp 467-473, issn 0964-6906Article

Intrachromosomal rearrangements fusing L-myc and rlf in small-cell lung cancerMAKELA, T. P; KERE, J; WINQVIST, R et al.Molecular and cellular biology (Print). 1991, Vol 11, Num 8, pp 4015-4021, issn 0270-7306Article

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