Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Beata Piovesan"'
Autor:
Nadia L. Prigoda-Leea, Diane Rushlowa, Beata Piovesan, Katherine Zhang, Helen Dimaras, Sanja Pajovic, Brenda L. Galliea
Publikováno v:
Cellular Oncology, Vol 31, Iss 3, Pp 249-250 (2009)
Externí odkaz:
https://doaj.org/article/7fb8111d9b7f43b786650ae25d55624f
Autor:
Donco Matevski, Timothy W. Corson, Sameh E. Soliman, Diane Rushlow, Bob Argiropoulos, Hilary Racher, Heather MacDonald, Renee Perrier, Helen S. L. Chan, Beata Piovesan, Furqan Shaikh, Brenda L. Gallie
Publikováno v:
Cancer genetics. 209(7-8)
The pediatric ocular tumor retinoblastoma readily metastasizes, but these lesions can masquerade as histologically similar pediatric small round blue cell tumors. Since 98% of retinoblastomas have RB1 mutations and a characteristic genomic copy numbe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13ad0b29e97cf095db7e93b04b4941b6
https://pubmed.ncbi.nlm.nih.gov/27318443
https://pubmed.ncbi.nlm.nih.gov/27318443
Autor:
Helen Dimaras, Jeremy A. Squire, Ralph C. Eagle, Vikas Khetan, Paula Marrano, Marija Orlic, William Halliday, Nadia L. Prigoda, Brenda L. Gallie, Beata Piovesan, Timothy W. Corson
Publikováno v:
Human Molecular Genetics. 17:1363-1372
Retinoblastoma clinical observations revealed the role of tumor suppressor genes in human cancer, Knudson's 'two-hit' model of cancer induction. We now demonstrate that loss of both RB1 tumor suppressor gene alleles initiates quiescent RB1(-/-) retin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::328e0095a06431b15b0c5faf4e8ac145
https://doi.org/10.1093/hmg/ddn024
https://doi.org/10.1093/hmg/ddn024
Autor:
N L Prigoda, E Zhang, Hilmi Ozcelik, Kirk Vandezande, Sevtap Savas, Beata Piovesan, S A Abdalla, Diane Rushlow, Michelle Letarte, Brenda L. Gallie
Publikováno v:
Journal of Medical Genetics. 43:722-728
Background: Hereditary haemorrhagic telangiectasia (HHT) is a genetic disorder present in 1 in 8000 people and associated with arteriovenous malformations. Genetic testing can identify individuals at risk of developing the disease and is a useful dia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe5cdce1214f818a84ee8a5b72484833
https://doi.org/10.1136/jmg.2006.042606
https://doi.org/10.1136/jmg.2006.042606
Autor:
Daniela Dumitru, Donco Matevski, Brenda L. Gallie, Nadia Prigoda Lee, Diane Rushlow, Beata Piovesan
Publikováno v:
Journal of medical genetics. 48(5)
Background Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant genetic disorder affecting the vascular system, characterised by epistaxis, arteriovenous malformations and mucocutaneous and gastrointestinal telangiectases. Mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8649fd5abdaae65283be234c1521108
https://pubmed.ncbi.nlm.nih.gov/21415079
https://pubmed.ncbi.nlm.nih.gov/21415079
Autor:
Brenda L. Gallie, Robin D. Clark, Nadia L. Prigoda-Lee, Beata Piovesan, Mellone N. Marchong, Diane Rushlow, Katherine Zhang
Publikováno v:
Human mutation. 30(5)
The RB1 gene mutation detection rate in 1,020 retinoblastoma families was increased by the use of highly sensitive allele specific-PCR (AS-PCR) to detect low-level mosaicism for 11 recurrent RB1 CGA>TGA nonsense mutations. For bilaterally affected pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3619ad7c8896f713553002a4b5d59216
https://pubmed.ncbi.nlm.nih.gov/19280657
https://pubmed.ncbi.nlm.nih.gov/19280657
Publikováno v:
Oncogene. 17(18)
Human lymphoblastoid cells were transfected with expression vectors containing p53 cDNA mutated at either codon 135 or 246. The cells were subjected to cisplatin treatment or gamma-radiation and observed for changes in the cell cycle arrest and apopt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05b069e359f8ad05ce9ab7a97bd7b9c8
https://pubmed.ncbi.nlm.nih.gov/9811465
https://pubmed.ncbi.nlm.nih.gov/9811465