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Showing 1 to 7 of 7 for “"Brjóstakrabbamein"”.

  1. Aurora A nuclear expression and telomere length in BRCA2 related breast cancer

    Brjóstakrabbamein er algengasta gerð krabbameina meðal kvenna í hinum vestræna heimi. Arfgengar stökkbreytingar í BRCA2 geninu tengjast aukinni brjóstakrabbameinsáhættu og arfberar eru almennt að greinast yngri. Í þessari rannsókn voru skoðuð annars vegar Aurora A yfirtjáning í brjóstaæxlissýnum og …

    u-iceland Repository record for Aurora A nuclear expression and telomere length in BRCA2 related breast cancer (opens in a new tab)

  2. Sviperfðabreytingar í Eggjastokkakrabbameinum

    … höfðu >60% fengið fleiri krabbamein (þar af 56% brjóstakrabbamein), m.v. <40% hinna . Lifun kvenna með kímlínustökkbreytingu í BRCA1/2 var marktækt betri, en leiðrétt var fyrir greiningaraldri, greiningarári, stigi og æxlisvexti til staðar eftir aðgerð. BRCA-arfberar sem fengu platínulyf urðu …

    u-iceland Repository record for Sviperfðabreytingar í Eggjastokkakrabbameinum (opens in a new tab)

  3. FANCD2 in relation to BRCA2 mutated breast cancer

    Breast cancer (BC) is the most common cancer among women in the world. Around 5-10% of BC is considered hereditary and caused by mutations in the BRCA1 and BRCA2 genes. BRCA1 and BRCA2 proteins have been shown to be involved in a multitude of pivotal cellular processes and are required for …

    u-iceland Repository record for FANCD2 in relation to BRCA2 mutated breast cancer (opens in a new tab)

  4. Áhrif sértæks Aurora-A kínasahindra á brjóstaþekjufrumulínur með stökkbreytingu í BRCA2 geninu

    Brjóstakrabbamein er algengasta krabbameinið hjá konum á Íslandi og má áætla að ein af hverjum tíu konum muni greinast með brjóstakrabbamein á lífsleiðinni. Meiri hluti brjóstakrabbameina eru tilkomin vegja tilviljanakenndra sómatískra stökkbreytinga en þó má rekja næstum fjórðung …

    u-iceland Repository record for Áhrif sértæks Aurora-A kínasahindra á brjóstaþekjufrumulínur með stökkbreytingu í BRCA2 geninu (opens in a new tab)

  5. ALKBH3 and FTO: New Epitranscriptomic Regulators of DNA Double-Strand Break Response

    … á að ALKBH3 er metýlerað á stýrilsvæði í ~20% brjóstakrabbameina og að sterk fylgni sé milli aukins hlutfalls metýleringa og verri lífslíkum. Einnig hafa frumgögn hópsins bent til þess að ALKBH3 og FTO spili hlutverk í að viðhalda próteintjáningu RNF168 með sviperfðastjórnun, en slíkt er …

    u-iceland Repository record for ALKBH3 and FTO: New Epitranscriptomic Regulators of DNA Double-Strand Break Response (opens in a new tab)

  6. Monitoring the Effects of the Oncogenic S250F Mutation on the Intrinsically Disordered C-terminal of FoxA1

    Forkhead box protein A1 (FoxA1) belongs to the class of pioneer transcription factors (pTFs) that have the ability to bind and open condensed chromatin and thus establish tissue-specific gene expression. FoxA1 plays a pivotal role for the correct development of various mesoderm derived tissues …

    u-iceland Repository record for Monitoring the Effects of the Oncogenic S250F Mutation on the Intrinsically Disordered C-terminal of FoxA1 (opens in a new tab)

  7. Clinical evaluation of an Icelandic adaptation of Moving Forward : a post-treatment course offered to women who have completed treatment for breast cancer

    With higher survival rates due to better screening and treatment options for breast cancer, the research into practical and suitable aftercare treatments for breast cancer survivors (BCS) has increased in recent decades. Many BCS feel insecure when their treatment finishes as they are not in …

    reykjavik Repository record for Clinical evaluation of an Icelandic adaptation of Moving Forward : a post-treatment course offered to women who have completed treatment for breast cancer (opens in a new tab)