Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Marianne, Tiainen"'
Autor:
Niklas Ekman, Marianne Tiainen, Tea Vallenius, Pekka Katajisto, Tomi P. Mäkelä, Kari Vaahtomeri, Anou Londesborough
Publikováno v:
Development. 135:2331-2338
Inactivation of the tumor suppressor kinase Lkb1 in mice leads to vascular defects and midgestational lethality at embryonic day 9-11 (E9-E11). Here, we have used conditional targeting to investigate the defects underlying the Lkb1(-/-) phenotype. En
Autor:
Tea Vallenius, Lina Udd, Kari Vaahtomeri, Tomi P. Mäkelä, Marianne Tiainen, Pekka Katajisto, Niklas Ekman
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Reviews on Cancer. 1775:63-75
Inactivating germline mutations in the LKB1 gene underlie Peutz-Jeghers syndrome characterized by hamartomatous polyps and an elevated risk for cancer. Recent studies suggest the involvement of LKB1 also in more common human disorders including diabe
Autor:
Alessandra Sacco, Angelina Felici, Marco Crescenzi, Ada Sacchi, Lucia Latella, Daniela Macera, Deborah Pajalunga, Marianne Tiainen, Marco D'Angelo
Publikováno v:
Molecular and Cellular Biology. 21:5631-5643
Terminal cell differentiation entails definitive withdrawal from the cell cycle. Although most of the cells of an adult mammal are terminally differentiated, the molecular mechanisms preserving the postmitotic state are insufficiently understood. Ter
Publikováno v:
Proceedings of the National Academy of Sciences. 96:9248-9251
Germ-line mutations of LKB1 ( STK11 ) lead to Peutz–Jeghers syndrome characterized by gastrointestinal polyps and cancer of different organ systems. The mutations lead to loss or severe impairment of Lkb1 serine/threonine kinase activity. Therefore
Autor:
Marianne Tiainen, O. Moesker, A. Laasonen, L. Tammilehto, Sakari Knuutila, Frans C. S. Ramaekers, Seppo Pyrhönen, Karin Mattson, Anton H. N. Hopman, Maija Wessman
Publikováno v:
Cancer Genetics and Cytogenetics. 62:171-179
We performed in situ hybridization (ISH) studies of malignant pleural mesotheliomas to detect numerical aberrations of chromosomes 1 and 7 in interphase nuclei of paraffin sections of 13 cases that had been analyzed previously by conventional karyoty
Autor:
P. A. Miescher, Sakari Knuutila, Ph. Beris, M. Jotterand Bellomo, Marianne Tiainen, V. Parlier
Publikováno v:
British Journal of Haematology. 81:296-304
Paroxysmal nocturnal haemoglobinuria (PNH) was diagnosed in a 20-year-old male patient who suffered from anaemia since the age of 11. Eighteen years after diagnosis, PNH transformed into refractory anaemia with ringed sideroblasts (RARS). Trisomy 8 w
Autor:
J. Rautonen, L. Tammilehto, Marianne Tiainen, Seppo Pyrhönen, Karin Mattson, A. Laasonen, Sakari Knuutila
Publikováno v:
Cancer Genetics and Cytogenetics. 60:8-13
The correlation between flow cytometric analysis and classical karyotyping was examined in malignant mesothelioma. Flow cytometry was used to determine the DNA ploidy mainly from paraffin blocks of 31 mesotheliomas, of which the S-phase fraction (SPF
Autor:
J. Rautonen, Timo Tuomi, Marianne Tiainen, Seppo Pyrhönen, Karin Mattson, Sakari Knuutila, L. Tammilehto
Publikováno v:
European Journal of Cancer. 28:1373-1379
The clinical characteristics and the results of mineral fibre and cytogenetic analyses were coordinated prospectively for 41 patients with confirmed malignant pleural mesothelioma. A correlation was found between high total fibre concentration, and p
Autor:
AP Losada, Woessner S, Sakari Knuutila, HF Willard, AH Hopman, Francesc Solé, Caballin, Maija Wessman, Marianne Tiainen
Publikováno v:
ResearcherID
Interphase cytogenetics by means of in situ hybridization with the chromosome 12-specific biotinylated alpha satellite DNA probe pSP 12–1 was used for the study of trisomy 12, the most common chromosomal abnormality in chronic lymphocytic leukemia.
Publikováno v:
Duodecim; laaketieteellinen aikakauskirja. 120(11)