Familial Cancer, 1389-9600

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  1. Absence of the common IGF1 19 CA-repeat allele is more common among BRCA1 mutation carriers than among non-carriers from BRCA1 families.

    Maria Henningson, Erika Bågeman, Therese Törngren, Åke Borg, Håkan Olsson & Helena Jernström, 2007, I : Familial Cancer. 6, 4, s. 445-452

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  2. BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population.

    Henriette Roed Nielsen, Mef Nilbert, Janne Petersen, Steen Ladelund, Mads Thomassen, Inge Søkilde Pedersen, Thomas V O Hansen, Anne-Bine Skytte, Åke Borg & Christina Therkildsen, 2016, I : Familial Cancer. 15, 4, s. 507-512

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  3. Can a phenotype for recessive inheritance in breast cancer be defined?

    Carolina Ellberg, Göran B Jönsson & Håkan Olsson, 2010, I : Familial Cancer. 9, 4, s. 525-530

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  4. Cancer risks and immunohistochemical profiles linked to the Danish MLH1 Lynch syndrome founder mutation

    Christina Therkildsen, Anna Isinger-Ekstrand, Steen Ladelund, Anja Nissen, Eva Rambech, Inge Bernstein & Mef Nilbert, 2012, I : Familial Cancer. 11, 4, s. 579-585

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  5. Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individuals

    Mev Dominguez, Felipe Carneiro da Silva, Erika Maria Monteiro dos Santos, Bianca Garcia Lisboa, Ligia Petrolini de Oliveira, Fabio de Oliveira Ferreira, Israel Gomy, Wilson Toshihiko Nakagawa, Samuel Aguiar Junior, Mariana Redal, Carlos Vaccaro, Adriana Della Valle, Carlos Sarroca, Dirce Maria Carraro & Benedito Mauro Rossi, 2011, I : Familial Cancer. 10, 4, s. 641-647

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  6. Deranged Wnt signaling is frequent in hereditary nonpolyposis colorectal cancer.

    Anna Isinger Ekstrand, Christina Therkildsen, Inge Bernstein & Mef Nilbert, 2011, I : Familial Cancer. 10, s. 239-243

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  7. Distinct gene expression profiles in ovarian cancer linked to Lynch syndrome.

    Jenny-Maria Jönsson, Katarina Bartuma, Mev Dominguez, Katja Harbst, Zohreh Ketabi, Susanne Malander, Mats Jönsson, Ana Carneiro, Anna Måsbäck, Göran B Jönsson & Mef Nilbert, 2014, I : Familial Cancer. 13, 4, s. 537-545 9 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  8. Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing

    Anna Rohlin, Eva Rambech, Anders Kvist, Therese Törngren, Frida Eiengård, Ulf Lundstam, Theofanis Zagoras, Samuel Gebre-Medhin, Åke Borg, Jan Björk, Mef Nilbert & Margareta Nordling, 2017 apr, I : Familial Cancer. 16, 2, s. 195-203

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  9. Frequent alterations of the PI3K/AKT/mTOR pathways in hereditary nonpolyposis colorectal cancer.

    Anna Isinger Ekstrand, Mats Jönsson, Annika Lindblom, Åke Borg & Mef Nilbert, 2010, I : Familial Cancer. 9, s. 125-129

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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