Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Ulf Kressner"'
Autor:
Kristina K. Lagerstedt, Erik Kristiansson, Christina Lönnroth, Marianne Andersson, Britt-Marie Iresjö, Annika Gustafsson, Elisabeth Hansson, Ulf Kressner, Svante Nordgren, Fredrik Enlund, Kent Lundholm
Publikováno v:
Cancer Informatics, Vol 2010, Iss 9, Pp 79-91 (2010)
Background: Genetic and epigenetic alterations in colorectal cancer are numerous. However, it is difficult to judge whether such changes are primary or secondary to the appearance and progression of tumors. Therefore, the aim of the present study was
Externí odkaz:
https://doaj.org/article/e2cbca899756430b80ad2cd49d1f115d
Autor:
Åke Borg, Kent Lundholm, Svante Nordgren, Lars Lindström, Christina Lönnroth, Ulf Kressner, Göran Jönsson, Elisabeth Hansson, Johan Staaf, Kristina K. Lagerstedt
Publikováno v:
Cancer Informatics, Vol 3, Pp 341-355 (2007)
Genome wide DNA alterations were evaluated by array CGH in addition to RNA expression profiling in colorectal cancer from patients with excellent and poor survival following primary operations.DNA was used for CGH in BAC and cDNA arrays. Global RNA e
Externí odkaz:
https://doaj.org/article/6286c70f870140e39b9e189d235f28b3
Autor:
Kristina K. Lagerstedt, Johan Staaf, Göran Jönsson, Elisabeth Hansson, Christina Lönnroth, Ulf Kressner, Lars Lindström, Svante Nordgren, Åke Borg, Kent Lundholm
Publikováno v:
Cancer Informatics, Vol 3 (2007)
Genome wide DNA alterations were evaluated by array CGH in addition to RNA expression profiling in colorectal cancer from patients with excellent and poor survival following primary operations. DNA was used for CGH in BAC and cDNA arrays. Global RNA
Externí odkaz:
https://doaj.org/article/d11692d247aa4a05a0a16a0dc2f60a8e
Autor:
Elham Rekabdar, Fredrik Enlund, Marianne Andersson, Elisabeth Hansson, Ulf Kressner, Christina Lönnroth, Kent Lundholm, Kristina Lagerstedt, Erik Kristiansson, Annika Gustafsson Asting
Publikováno v:
Journal of Cancer Therapy. :1354-1361
Background: Sporadic colorectal tumors probably carry genetic alterations that may be related to familiar clusters according to risk loci visualized by SNP arrays on normal tissues. The aim of the present study was therefore to search for DNA regions
Autor:
Stefan Skullman, Ulf Kressner, Gunnar Edlund, Martin Janson, Bo Anderberg, Eva Haglind, Elisabet Lindholm, Lars Påhlman
Publikováno v:
Surgical Endoscopy. 23:1764-1769
The colon cancer laparoscopic or open resection (COLOR) trial is an international, randomised controlled trial comparing outcomes of open and laparoscopic surgery for colon cancer. The main purpose of this study was to determine representability by c
Autor:
Christina Lönnroth, Elisabeth Hansson, Kent Lundholm, Ulf Kressner, Wenhua Wang, Svante Nordgren, Annika Gustafsson, Marianne Andersson
Publikováno v:
International Journal of Cancer. 121:232-240
The importance of prostaglandins in tumor growth and progression is well recognized, including antineoplastic activities by cyclooxygenase (COX) inhibitors. Variation in treatment response to COX inhibition has questioned differences in expression of
Autor:
Ulf Kressner, Annika Lindblom, Xiao-Feng Sun, Barbro Werelius, Ulrika K. Eriksson, Xiao-Lei Zhou
Publikováno v:
International Journal of Cancer. 110:550-557
Many families experience an apparently inherited increased risk of colorectal cancer (CRC) similar to the known syndromes familial adenomatous polyposis (FAP) and hereditary nonpolyposis colorectal cancer (HNPCC). Besides these high-risk syndromes, a
Publikováno v:
Diseases of the Colon & Rectum. 45:316-321
PURPOSE: The influence of septic complications on long-term prognosis after surgery for rectal cancer is controversial. This study was performed to investigate whether an abdominal or perineal septic complication was associated with rectal cancer rec
Autor:
Annika Lindblom, Lars Påhlman, Sima Salahshor, Ulf Kressner, Helene Fischer, Gudrun Lindmark, Bengt Glimelius
Publikováno v:
British Journal of Cancer
Hereditary non-polyposis colorectal cancer (HNPCC) is linked to an inherited defect in the DNA mismatch repair system. DNA from HNPCC tumours shows microsatellite instability (MSI). It has been reported that HNPCC patients have a better prognosis tha
Autor:
Ulf Kressner, Sigrid Lystad, Anne Lise Børresen-Dale, Jens Bjørheim, Gustav Gaudernack, Annika Lindblom, Janne Røe, William G. Thilly, Sophia Westring, Per Olaf Ekstrøm, Gudrun Lindmark, Siobhan Wahlberg
Publikováno v:
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 403:103-112
Mutations in the KRAS gene is a key event in the carcinogenesis of many human cancers and may serve as a diagnostic marker and a target for therapeutic intervention. In this study we have applied three different techniques for mutation detection of K