Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Marketta Kähkönen"'
Autor:
Satu Mustjoki, Sari Hernesniemi, Auvo Rauhala, Marketta Kähkönen, Anders Almqvist, Tuija Lundán, Kimmo Porkka
Publikováno v:
Haematologica, Vol 94, Iss 10 (2009)
Externí odkaz:
https://doaj.org/article/970a97f9b65b44438694ca231c1e2830
Autor:
Roger A. Greenberg, Jukka S. Moilanen, Lisa A. Moreau, Kym M. Boycott, A. Micheil Innes, David A. Dyment, Jacek Majewski, Martin Kircher, Jeremy Schwartzentruber, Marketta Kähkönen, Lei Tian, Sarah L. Sawyer
Supplementary Figure 3. BRCA1 mutations result in compromised DNA damage repair.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40f20d1c057843a50a7b64621f017be9
https://doi.org/10.1158/2159-8290.22530594.v1
https://doi.org/10.1158/2159-8290.22530594.v1
Autor:
Roger A. Greenberg, Jukka S. Moilanen, Lisa A. Moreau, Kym M. Boycott, A. Micheil Innes, David A. Dyment, Jacek Majewski, Martin Kircher, Jeremy Schwartzentruber, Marketta Kähkönen, Lei Tian, Sarah L. Sawyer
Supplementary Figure 1. BRCA1 mutations lead to impaired MMC induced DNA damage signaling.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0532760bd962cbf7fc57649914de88e2
https://doi.org/10.1158/2159-8290.22530600.v1
https://doi.org/10.1158/2159-8290.22530600.v1
Autor:
Roger A. Greenberg, Jukka S. Moilanen, Lisa A. Moreau, Kym M. Boycott, A. Micheil Innes, David A. Dyment, Jacek Majewski, Martin Kircher, Jeremy Schwartzentruber, Marketta Kähkönen, Lei Tian, Sarah L. Sawyer
Supplementary Figure 2. Functional analysis of the BRCA1 (p.Arg1699Trp) mutation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebbbb4ebee3c4a85595c8bb0dede092d
https://doi.org/10.1158/2159-8290.22530597
https://doi.org/10.1158/2159-8290.22530597
Autor:
Annamari Ranki, Tapio Visakorpi, Pärt Peterson, Kalle Saksela, Jadwiga Roszkiewicz, Annemarie Poustka, Inge Krebs, Harri Sihto, Nina Nupponen, Hanna Nevala, Maria Pesonen, Vesna Blazevic, Ying Zhou, Soili Kytölä, Boguslaw Nedoszytko, Marketta Kähkönen, Sanna Syrjä, Ritva Karhu, Suvi Päivinen, Sonja Hahtola, Leena Karenko
Tables S2 & S3, Legends, and Supplementary Methods from Primary Cutaneous T-Cell Lymphomas Show a Deletion or Translocation Affecting NAV3, the Human UNC-53 Homologue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::603e9d1aec376c61bc73a7eaa2eead97
https://doi.org/10.1158/0008-5472.22363524.v1
https://doi.org/10.1158/0008-5472.22363524.v1
Autor:
Annamari Ranki, Tapio Visakorpi, Pärt Peterson, Kalle Saksela, Jadwiga Roszkiewicz, Annemarie Poustka, Inge Krebs, Harri Sihto, Nina Nupponen, Hanna Nevala, Maria Pesonen, Vesna Blazevic, Ying Zhou, Soili Kytölä, Boguslaw Nedoszytko, Marketta Kähkönen, Sanna Syrjä, Ritva Karhu, Suvi Päivinen, Sonja Hahtola, Leena Karenko
Supplementary Figure S7 from Primary Cutaneous T-Cell Lymphomas Show a Deletion or Translocation Affecting NAV3, the Human UNC-53 Homologue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::176d42a9ccec76984f2f113c1a9440ca
https://doi.org/10.1158/0008-5472.22363530.v1
https://doi.org/10.1158/0008-5472.22363530.v1
Autor:
Annamari Ranki, Tapio Visakorpi, Pärt Peterson, Kalle Saksela, Jadwiga Roszkiewicz, Annemarie Poustka, Inge Krebs, Harri Sihto, Nina Nupponen, Hanna Nevala, Maria Pesonen, Vesna Blazevic, Ying Zhou, Soili Kytölä, Boguslaw Nedoszytko, Marketta Kähkönen, Sanna Syrjä, Ritva Karhu, Suvi Päivinen, Sonja Hahtola, Leena Karenko
Multicolor fluorescent in situ hybridization (FISH) was used to identify acquired chromosomal aberrations in 12 patients with mycosis fungoides or Sézary syndrome, the most common forms of primary cutaneous T-cell lymphoma (CTCL). The most frequent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::336bb019874cb147e377766a03f82cf8
https://doi.org/10.1158/0008-5472.c.6493752.v1
https://doi.org/10.1158/0008-5472.c.6493752.v1
Autor:
Annamari Ranki, Tapio Visakorpi, Pärt Peterson, Kalle Saksela, Jadwiga Roszkiewicz, Annemarie Poustka, Inge Krebs, Harri Sihto, Nina Nupponen, Hanna Nevala, Maria Pesonen, Vesna Blazevic, Ying Zhou, Soili Kytölä, Boguslaw Nedoszytko, Marketta Kähkönen, Sanna Syrjä, Ritva Karhu, Suvi Päivinen, Sonja Hahtola, Leena Karenko
Supplementary Figures S8 & S9 from Primary Cutaneous T-Cell Lymphomas Show a Deletion or Translocation Affecting NAV3, the Human UNC-53 Homologue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4183da8dd944d133f150a0dae1da04ab
https://doi.org/10.1158/0008-5472.22363527
https://doi.org/10.1158/0008-5472.22363527
Autor:
Kym M. Boycott, Jukka S. Moilanen, Lisa A. Moreau, A. Micheil Innes, Sarah L. Sawyer, Jeremy Schwartzentruber, Marketta Kähkönen, Martin Kircher, David A. Dyment, Lei Tian, Roger A. Greenberg, Jacek Majewski
Publikováno v:
Cancer Discovery. 5:135-142
Deficiency in BRCA-dependent DNA interstrand crosslink (ICL) repair is intimately connected to breast cancer susceptibility and to the rare developmental syndrome Fanconi anemia. Bona fide Fanconi anemia proteins, BRCA2 (FANCD1), PALB2 (FANCN), and B
Autor:
Johanna Schleutker, K. Parto, Robert Winqvist, Veli-Matti Kosma, Anne Kallioniemi, Marketta Kähkönen, Arto Mannermaa, Kristiina Avela, Katri Pylkäs, Satu-Leena Laasanen, Tuomo Mantere, Maria Haanpää, H. Hanenberg, Kristiina Aittomäki, Jaana M. Hartikainen, H. Von Koskull
Publikováno v:
Clinical Genetics. 88:68-73
Mutations in downstream Fanconi anemia (FA) pathway genes, BRCA2, PALB2, BRIP1 and RAD51C, explain part of the hereditary breast cancer susceptibility, but the contribution of other FA genes has remained questionable. Due to FA's rarity, the finding