Zobrazeno 1 - 10
of 147
pro vyhledávání: '"ANTECKA, EMILIA"'
Autor:
Souza Filho, João Pessoa, Martins, Maria C., Correa, Zelia Maria S., Odashiro, Alexandre N., Antecka, Emilia, Coutinho, Anamaria B., Macedo, Carla R., Vianna, Raul N.G., Burnier, Miguel N., Jr
Publikováno v:
In American Journal of Ophthalmology 2006 142(4):625-631
Autor:
Odashiro Alexandre N, Antecka Emilia, Marshall Jean-Claude, Martins Claudia, Fernandes Bruno F, Maloney Shawn, Di Cesare Sebastian, Dawson William W, Burnier Miguel N
Publikováno v:
Journal of Experimental & Clinical Cancer Research, Vol 28, Iss 1, p 48 (2009)
Abstract Background Uveal melanoma (UM) cell lines, when exposed to blue light in vitro, show a significant increase in proliferation. In order to determine if similar effects could be seen in vivo, we investigated the effect of blue light exposure i
Externí odkaz:
https://doaj.org/article/788a89da418e4fbd91ac1366aefb1830
Autor:
Antecka Emilia, Logan Patrick, Fernandes Bruno F, Marshall Jean-Claude, Di Cesare Sebastian, Filho Vasco, Burnier Miguel N
Publikováno v:
Cancer Cell International, Vol 7, Iss 1, p 17 (2007)
Abstract Purpose The CXCR4/CXCL12 chemokine axis may play a critical role in guiding CXCR4+ circulating malignant cells to organ specific locations that actively secrete its ligand CXCL12 (SDF-1) such as bone, brain, liver, and lungs. We sought to ch
Externí odkaz:
https://doaj.org/article/06b41d3b0e3b46208f3b316a601caf9a
Autor:
Odashiro Alexandre N, Odashiro Danilo N, Pereira Patrícia R, Godeiro Katyanne, Antecka Emilia, Di Cesare Sebastian, Burnier Miguel N
Publikováno v:
Cancer Cell International, Vol 6, Iss 1, p 26 (2006)
Abstract Background Uveal melanoma (UM) is the most common primary intraocular malignant tumor in adults, and nearly 40% of UM will develop metastasis that will ultimately lead to death. The Epithelial Cell Adhesion Molecule (EpCAM) is a type I trans
Externí odkaz:
https://doaj.org/article/68d362c72ac14b1d87a844601c451fea
Autor:
Maloney, Shawn C.1 shawn.maloney@mail.mcgill.ca, Antecka, Emilia1, Odashiro, Alexandre N.1, Fernandes, Bruno F.1, Doyle, Madeline1, Lim, Li-Anne1, Katib, Yousef1, Burnier, Miguel N.1
Publikováno v:
Stem Cells International. 2012, p1-8. 8p. 3 Color Photographs, 1 Graph.
Autor:
Özdal, Pinar Ç.1 (AUTHOR), Antecka, Emilia2 (AUTHOR), Baines, Malcolm G.3 (AUTHOR), Vianna, Raul N. G.1 (AUTHOR), Rudzinski, Marcello1 (AUTHOR), Deschênes, Jean1 (AUTHOR)
Publikováno v:
Ocular Immunology & Inflammation. Dec2005, Vol. 13 Issue 6, p435-438. 4p. 1 Chart.
Publikováno v:
Arquivos Brasileiros de Oftalmologia, Volume: 79, Issue: 6, Pages: 395-399, Published: DEC 2016
Purpose: The cellular origin of retinoblastoma is uncertain as constituent tumor cells heterogeneously express markers of both immature and mature retinal cells. An immunohistochemical analysis of cellular origin may yield valuable insights into dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______608::8e0c7f2cfa66789f125d9512b7d431df
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27492016000600395&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27492016000600395&lng=en&tlng=en
Autor:
Cools-Lartigue, Jonathan J., McCauley, Cristin S., Marshall, Jean-Claude A., Di Cesare, Sebastian, Gregoire, Francois, Antecka, Emilia, Logan, Patrick, Burnier, Miguel N.
Publikováno v:
Molecular Vision
Purpose Uveal melanoma (UM) is the most common intra-ocular tumor in adults. Despite advances in diagnosis and treatment, the survival rate of UM has not increased in the last several decades. Approximately 50% of patients will die as a consequence o
Autor:
Solari, Helena Parente, Ventura, Marcelo Palis, Antecka, Emilia, Belfort Junior, Rubens, Burnier Jr, Miguel Noel
Publikováno v:
Arquivos Brasileiros de Oftalmologia, Volume: 74, Issue: 4, Pages: 286-288, Published: AUG 2011
Familial amyloidosis of the Finnish type (FAF) is an autosomal dominant form of systemic amyloidosis showing marked geographic clustering in Finland. The disease is caused by a point mutation, 654G-A, in the gelsolin gene. The Danish-subtype of FAF h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______608::f1f003f6d0b2d9d7e5d432c5c8eb96c8
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27492011000400012&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27492011000400012&lng=en&tlng=en
Autor:
Solari,Helena Parente, Ventura,Marcelo Palis, Antecka,Emilia, Belfort Junior,Rubens, Burnier Jr,Miguel Noel
Publikováno v:
Arquivos Brasileiros de Oftalmologia v.74 n.4 2011
Arquivos brasileiros de oftalmologia
Conselho Brasileiro de Oftalmologia (CBO)
instacron:CBO
Arquivos brasileiros de oftalmologia
Conselho Brasileiro de Oftalmologia (CBO)
instacron:CBO
Familial amyloidosis of the Finnish type (FAF) is an autosomal dominant form of systemic amyloidosis showing marked geographic clustering in Finland. The disease is caused by a point mutation, 654G-A, in the gelsolin gene. The Danish-subtype of FAF h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::f1f003f6d0b2d9d7e5d432c5c8eb96c8
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27492011000400012
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27492011000400012