Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Diana Linden"'
Autor:
Diana Linden
Publikováno v:
Panorama, Vol 4, Iss 2 (2018)
Externí odkaz:
https://doaj.org/article/7a721a8a72704a4abe7dfbbe466c145d
Autor:
Diana Linden
Publikováno v:
caa.reviews.
Autor:
Veronica Höiom, Sanela Kjellqvist, Daniel Edsgärd, Per Unneberg, Pär G. Engström, Muyi Yang, Johan Hansson, Diana Linden, Hildur Helgadottir, Rainer Tuominen, Hanna Eriksson
Publikováno v:
Genes, Chromosomes and Cancer. 55:601-611
We applied a targeted sequencing approach to identify germline mutations conferring a moderately to highly increased risk of cutaneous and uveal melanoma. Ninety-two high-risk melanoma patients were screened for inherited variation in 120 melanoma ca
Autor:
Pascal Wolter, Marianne Frostvik Stolt, Rosalyn Jewell, Johan Hansson, Carolina Johansson, Christer Lindholm, Joost van den Oord, Ulrika Stierner, Diana Linden, Christy Walker, Suzanne Egyhazi Brage, Rainer Tuominen, Helen Snowden, Julia Newton-Bishop, Hemming Johansson
Publikováno v:
International Journal of Cancer. 136:2844-2853
To investigate the predictive and prognostic value of O(6) -methylguanine DNA methyltransferase (MGMT) inactivation by analyses of promoter methylation in pretreatment tumor biopsies from patients with cutaneous melanoma treated with dacarbazine (DTI
Autor:
Rolf Kiessling, Giuseppe Masucci, Bo Nilsson, Isabel Poschke, Marianne Frostvik Stolt, Suzanne Egyhazi, C. Christian Johansson, Johan Hansson, Diana Linden, Dimitrios Mougiakakos, Rainer Tuominen, Liss Garberg, Helena Harlin
Publikováno v:
Cancer Immunology, Immunotherapy. 58:1085-1094
New prognostic markers are needed for malignant melanoma. Inducible nitric oxide synthase (iNOS) and cyclooxygenase type 2 (COX-2) have been described to correlate with progression of melanoma. Moreover, activating mutations in BRAF/NRAS oncogenes ar
Publikováno v:
Journal of Investigative Dermatology. 128(11):2696-2704
The aim of this study was to estimate the impact on survival of NRAS and BRAF mutations and activation of Akt and extracellular signal-regulated kinase (ERK) in primary melanomas. A cohort of 57 primary cutaneous T1-2 melanoma tumors was analyzed. Mu
Autor:
Johan Hansson, Diana Linden, Joakim Lundeberg, Veronica Höiom, Klas Sjöberg, Afshin Ahmadian, Suzanne Egyhazi, Max Käller, Eva Månsson-Brahme, Rainer Tuominen
Publikováno v:
Pigment cellmelanoma research. 22(2)
The genetic background of cutaneous malignant melanoma (CMM) includes both germ line aberrations in high-penetrance genes, like CDKN2A, and allelic variation in low-penetrance genes like the melanocortin-1 receptor gene, MC1R. Red-hair colour associa
Autor:
Harland, M, Goldstein, Am, Kukalizch, K, Taylor, C, Hogg, D, Puig, S, Badenas, C, Gruis, N, TER HUURNE, J, Bergman, W, Hayward, Nk, Stark, M, Tsao, H, Tucker, Ma, Landi, Mt, Bianchi, Giovanna, Ghiorzo, Paola, Kanetsky, Pa, Elder, D, Mann, Gj, Holland, Ea, Bishop, Dt, NEWTON BISHOP, J, Malvehy, J., Badenas, C., Cervera, R., Francisco, Cuellar, Rosa, Marti, JOAN BRUNET VIDAL, Guang, Yang, Nicholas, Martin, David, Whiteman, Adele, Green, Joanne, Aitken, Paola, Minghetti, Michela, Mantelli, Pastorino, Lorenza, Nasti, Sabina, Gargiulo, Sara, Sara, Gliori, Sushila, Mistry, JULIETTE RERSON MOOR, Wilma, Bergman, TER HUURNE, JEANET A. C., CLASINE VAN DER DRIFT, LENY VAN MOURIK, COBY OUT LUITING, FRANS VAN NIEUWPOORT, Valerie, Chaudru, Agnes, Chompret, Caroline, Kanengiesser, Michel, J. L., Grange, F., Sassolas, B., Limacher, J. M., Couillet, D., Truchetet, F., Cesarini, J. P., Boitier, F., CHEVRANT BRETON, J., Lasset, C., Longy, M., Joly, P., BASSET SEGUIN, N., Lesimple, T., Dugast, C., Michael, Ming, PATRICIA VAN BELLE, Anton, Platz, Suzanne, Egyhazi, Rainer, Tuominen, Diana, Linden, Helen, Schmid, Alon, Scope, Felix, Pavlotsky, Eitan, Friedman, Mark, Eliason
CDKN2A is the major melanoma susceptibility gene so far identified, but only 40% of three or more case families have identified mutations. A comparison of mutation detection rates was carried out by "blind" exchange of samples across GenoMEL, the Mel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e469e193a66e631a943aac0b0395b78
http://hdl.handle.net/11567/273207
http://hdl.handle.net/11567/273207
Autor:
Diana Linden
Publikováno v:
caa.reviews.
Autor:
Nicholas K. Hayward, Hensin Tsao, Mark J. Eliason, Suzanne Egyhazi, Paola Minghetti, Paola Ghiorzo, Alisa M. Goldstein, Julie Lang, Juliette Randerson-Moor, Nicole Basset-Seguin, Clasine van der Drift, D. Timothy Bishop, Nicholas G. Martin, Michel Longy, Guang Yang, Sabina Nasti, Adèle C. Green, Valérie Chaudru, Donato Calista, Sara Gargiulo, Florent Grange, Francisco Cuellar, Linda Whitaker, Joseph Malvehy, Esther Azizi, Richard F. Kefford, David E. Elder, Håkan Olsson, Nelleke A. Gruis, Joan Anton Puig-Butille, David W. Hogg, Margaret A. Tucker, Sushila Mistry, Wilma Bergman, Johan Westerdahl, Christian Ingvar, J. P. Cesarini, Jacqueline Chevrant-Breton, Leny van Mourik, Michela Mantelli, Arupa Ganguly, Jean -Marc Limacher, F. Truchetet, Maria Teresa Landi, Kristin B. Niendorf, Elizabeth A. Holland, Anna Måsbäck, Graham J. Mann, Agnès Chompret, Felix Pavlotsky, Veronica Magnusson, Anton Platz, Joanne F. Aitken, Brigitte Bressac-de Paillerets, Michael Ming, Marie-Françoise Avril, F. Boitier, J. L. Michel, May Chan, R. Cervera, Helen Schmid, Johan Hansson, Rosa M. Martí, Florence Demenais, Celia Badenas, Eitan Friedman, David C. Whiteman, Catherine Dugast, Rainer Tuominen, Lorenza Pastorino, D. Couillet, Emanuel Yakobson, T. Lesimple, Åke Borg, Pascal Joly, Julia A. Newton Bishop, Coby Out-Luiting, Peter A. Kanetsky, Caroline Kanengiesser, Sara Gliori, Diana Linden, Joan Brunet-Vidal, Christine Lasset, William Bruno, Susana Puig, Lisa A. Cannon Albright, Frans A. van Nieuwpoort, Alon Scope, Mitchell S. Stark, Giovanna Bianchi-Scarrà, B. Sassolas, Patricia Van Belle, Elizabeth M. Gillanders, Mark Harland, Jeanet A.C. ter Huurne, Rona M. MacKie, Femke A. de Snoo, Sancy A. Leachman, Jane M. Palmer
Publikováno v:
Cancer research. 66(20)
GenoMEL, comprising major familial melanoma research groups from North America, Europe, Asia, and Australia has created the largest familial melanoma sample yet available to characterize mutations in the high-risk melanoma susceptibility genes CDKN2A