Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Angelina Miloloza"'
Autor:
Angelina Miloloza, Regina Kroiss, Katja Hofer, Marion Kubista, Margit Rosner, Markus Hengstschläger, Erika Marton, Andrea-Romana Prusa
Publikováno v:
Mutation Research/Reviews in Mutation Research. 512:165-172
Breast cancer is one of the most frequent malignancies affecting women. The human breast cancer gene 1 (BRCA1) gene is mutated in a distinct proportion of hereditary breast and ovarian cancers. Tumourigenesis in individuals with germline BRCA1 mutati
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 61:154-163
Tuberous sclerosis is an autosomal dominant disease affecting approximately 1 in 6,000 individuals. It is caused by mutations in either TSC1 on chromosome 9q34, which encodes hamartin, or TSC2 on chromosome 16p13.3, which encodes tuberin. The growths
Autor:
Katja Braun, Thomas Soucek, Angelina Miloloza, Elke Hengstschläger-Ottnad, Markus Hengstschläger
Publikováno v:
Mutation Research/Reviews in Mutation Research. 436:1-9
In the mammalian cell cycle, the transition from the G1 phase to S phase, in which DNA replication occurs, is dependent on tight cell size control and has been shown to be regulated by the cyclin-dependent kinases (Cdks) 2, 3, 4 and 6. Activities of
Autor:
Angelina Miloloza, Irena Linhartova, Heike Stroissnigg, Friedrich Propst, Hartmut Beug, Marion Repitz, Gerhard Wiche
Publikováno v:
Experimental cell research. 278(2)
Using an antiserum directed against marginal band associated proteins of chicken erythrocytes we isolated clones encoding the chicken homolog of 14.7K-interacting protein 2 (FIP-2), a protein potentially involved in tumor necrosis factor-alpha/nuclea
Autor:
Markus Hengstschläger, Marion Kubista, David M. Rodman, Margit Rosner, Angelina Miloloza, Elke Hengstschläger-Ottnad
Publikováno v:
Mutation research. 488(3)
Two genes, TSC1 and TSC2, have been shown to be responsible for tuberous sclerosis (TSC). The detection of loss of heterozygosity of TSC1 or TSC2 in hamartomas, the growths characteristically occurring in TSC patients, suggested a tumor suppressor fu
Autor:
Angelina Miloloza, Margit Rosner, Thomas Soucek, Markus Hengstschläger, Julian R. Sampson, Marion Kubista, Jeremy Peter Cheadle
Publikováno v:
Oncogene. 20(35)
The autosomal dominant disease tuberous sclerosis (TSC) is caused by mutations in either TSC1 on chromosome 9q34, encoding hamartin, or TSC2 on chromosome 16p13.3, encoding tuberin. TSC is characterized by hamartomas that occur in many organs of affe
Autor:
Gerhard Bernaschek, Dicky J. J. Halley, Margit Rosner, Markus Hengstschläger, Mark Nellist, Angelina Miloloza
Publikováno v:
Human Molecular Genetics, 9(12), 1721-1727. Oxford University Press
Tuberous sclerosis is an autosomal dominant hereditary disease caused by mutations in either the TSC1 or the TSC2 tumor suppressor gene. The TSC1 gene on chromosome 9q34 encodes a 130 kDa protein named hamartin, and the TSC2 gene on chromosome 16p13.