Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Annika Rökman"'
Autor:
Caroline E. Mohai, Ethan M. Lange, Derek Gildea, Erica Riedesel, Bao Li Chang, William B. Isaacs, Kathleen E. Wiley, S. Lilly Zheng, Mary Pat Jones, Johanna Schleutker, John D. Carpten, Jeffrey M. Trent, Kathleen A. Cooney, Teuvo L.J. Tammela, Joan E. Bailey-Wilson, Fredrik Wiklund, Deborah A. Meyers, Agnes Baffoe-Bonnie, Julie Albertus, W. Mark Brown, Annika Rökman, Henrik Grönberg, Sarah D. Isaacs, Mika P. Matikainen, Jianfeng Xu, Patrick C. Walsh, Elizabeth M. Gillanders
Publikováno v:
JNCI Journal of the National Cancer Institute. 96:1240-1247
Background: Prostate cancer represents a substantial public health burden worldwide. It is the second leading cause of cancer death among men in the United States. A family history of the disease is among the most well-established risk factors for pr
Autor:
Tarja Ikonen, Annika Rökman, Olli Kallioniemi, Nina Mononen, Pasi A. Koivisto, Teuvo L.J. Tammela, Eija H. Seppälä, Mika P. Matikainen, John D. Carpten, Jeffrey M. Trent, Nina N. Nupponen, Ville Autio, Joan E. Bailey-Wilson, Johanna Schleutker
Publikováno v:
The American Journal of Human Genetics. 70:1299-1304
The RNASEL gene (2',5'-oligoisoadenylate-synthetase dependent) encodes a ribonuclease that mediates the antiviral and apoptotic activities of interferons. The RNASEL gene maps to the hereditary-prostate-cancer (HPC)-predisposition locus at 1q24-q25 (
Autor:
Johanna Schleutker, Mika P. Matikainen, Tuula Kuukasjärvi, Annika Rökman, Heikki Helin, Marita Poutiainen, Ritva Karhu, Pasi A. Koivisto, Olli-P. Kallioniemi
Publikováno v:
The Prostate. 46:233-239
Background Germline mutations in recessive cancer predisposition genes are uncovered by somatic genetic deletions during tumor development. Analysis of genetic changes in tumor tissues from patients with an inherited predisposition may therefore high
Autor:
Paula Kujala, Jorma Isola, Synnöve Staff, Saara Kares, Joanna Ilvesaro, Ritva Karhu, Annika Rökman
Publikováno v:
Journal of clinical pathology. 66(9)
Formalin fixation preserves tissue morphology at the expense of macromolecule integrity. Freshly frozen samples are the golden standard for DNA and RNA analyses but require laborious deep-freezing and frozen sectioning for morphological studies. Alte
Autor:
Henna Fredriksson, Johanna Schleutker, Kenneth D. Gibbs, Elizabeth M. Gillanders, Diane Freas-Lutz, Carol Markey, Mary Pat Jones, Agnes Baffoe-Bonnie, Tarja Ikonen, Jeffrey M. Trent, Teuvo L.J. Tammela, Olli Kallioniemi, Annika Rökman, Joan E. Bailey-Wilson, Mika P. Matikainen, Ville Autio, Pasi A. Koivisto, Derek Gildea
Publikováno v:
Rökman, A, Baffoe-Bonnie, A B, Gillanders, E, Fredriksson, H, Autio, V, Ikonen, T, Gibbs Jr, K D, Jones, M, Gildea, D, Freas-Lutz, D, Markey, C, Matikainen, M P, Koivisto, P A, Tammela, T L J, Kallioniemi, O, Trent, J, Bailey-Wilson, J E & Schleutker, J 2005, ' Hereditary prostate cancer in Finland : Fine-mapping validates 3p26 as a major predisposition locus ', Human Genetics, vol. 116, no. 1-2, pp. 43-50 . https://doi.org/10.1007/s00439-004-1214-7
In a recent genome-wide linkage (GWL) analysis of Finnish families at high risk for prostate cancer, we found two novel putative susceptibility loci at 3p25-p26 and 11q14. Here, we report the fine-mapping of these two critical regions at high resolut
Autor:
Eija H, Seppälä, Tarja, Ikonen, Ville, Autio, Annika, Rökman, Nina, Mononen, Mika P, Matikainen, Teuvo L J, Tammela, Johanna, Schleutker
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 9(14)
The MSR1 gene maps to 8p22-23, a novel susceptibility locus for hereditary prostate cancer (HPC). Mutations in MSR1 have been reported to associate with prostate cancer (PRCA) risk. Here we report a follow-up study from Finland to evaluate the associ
Autor:
Johanna Schleutker, Julie M. Cunningham, Annika Rökman, Tarja Ikonen, D J Schaid, Mika P. Matikainen, Rainer Lehtonen, S. N. Thibodeau, Nina N. Nupponen, Auli Karhu, Lauri A. Aaltonen, O. P. Kallioniemi, Maija Ht Kiuru
Mutations in fumarate hydratase (fumarase, FH ), a nuclear gene encoding a mitochondrial tricarboxylic acid cycle or Krebs cycle protein also present in the cytosol, have recently been shown to predispose to hereditary leiomyomatosis and renal cell c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b507640998fc8b77c178fa7e39a577a1
https://europepmc.org/articles/PMC1735396/
https://europepmc.org/articles/PMC1735396/
Autor:
Johanna Schleutker, Olli-P. Kallioniemi, Ville Autio, Annika Rökman, Pasi A. Koivisto, Tarja Ikonen, Mika P. Matikainen, Teuvo L.J. Tammela, Nina Mononen
Publikováno v:
Human genetics. 111(2)
Recent studies have suggested that polymorphisms of the androgen receptor gene ( AR) may influence the risk of prostate cancer (PC) development and progression. Here, we analyzed the length of the CAG repeat of the AR gene in 1363 individuals, includ
Autor:
Pasi A. Koivisto, Teuvo L.J. Tammela, C. Palmberg, Marita Laurila, Kyllikki Haapala, E. Hyytinen, Annika Rökman
Publikováno v:
Cancer genetics and cytogenetics. 131(1)
The genetic mechanisms of prostate cancer recurrence during hormonal therapy are largely unknown. So far, data from conventional karyotype analysis on hormone-refractory prostate carcinomas have not been published, mainly because of the difficulties
Autor:
Johanna Schleutker, Eija H. Seppälä, Teuvo L.J. Tammela, Annika Rökman, Nina Mononen, Ville Autio, Tarja Ikonen, Mika P. Matikainen
Publikováno v:
Journal of Urology. 171:108-108