Výsledky vyhledávání - "Belén Canet"

Gene expression analysis identifies two groups of ovarian high-grade serous carcinomas with different prognosis

Autor: Belén Canet, Josefina Muñoz, Lluis Catasus, Emanuela D'Angelo, Inigo Espinosa, Jaime Prat

Publikováno v: MODERN PATHOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname

Gene expression profiling is an important tool to evaluate genetic heterogeneity in carcinomas and is useful to develop expression-based classifications for many types of cancer, as well as markers of disease outcome. In this study, we have investiga

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3b7e3ceb69e10938954a5780ca9fb1b
https://doi.org/10.1038/modpathol.2011.12

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Role of tumor-associated macrophages and angiogenesis in desmoid-type fibromatosis

Autor: Belén Canet, Stefhanie Romero, Eliovel Cabrera, Ana I. Peiró, Allan Gonzalez, Jaume Llauger, Inigo Espinosa, Jaime Prat, Justyna Szafranska, Silvia Bagué, Luis Ortega

Publikováno v: Virchows Archiv : an international journal of pathology. 461(2)

Desmoid-type fibromatosis (DTF) is a rare soft tissue tumor with fibroblastic features affecting two to four individuals per million population per year. Despite its bland microscopic appearance, the tumor behaves aggressively. Although unable to met

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a3ea3c285426a485d62801268c0427e
https://pubmed.ncbi.nlm.nih.gov/22744289

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CDC42-positive macrophages may prevent malignant transformation of ovarian endometriosis

Autor: Belén Canet, Jaime Prat, Inigo Espinosa, Cristina Pons

Publikováno v: HUMAN PATHOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Instituto de Salud Carlos III (ISCIII)

It is currently thought that most clear cell and endometrioid carcinomas arise from ovarian endometriosis. We recently suggested that, besides their origin in the ovary, reduction of CDC42 messenger RNA (a member of the RHO GTPase family) may contrib

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39cffe560aab97f3c8f3df8dcf8036bf
https://pubmed.ncbi.nlm.nih.gov/21944080

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Ovarian clear cell carcinomas: RHO GTPases may contribute to explain their singular biologic behavior

Autor: Inigo Espinosa, Belén Canet, Jaime Prat, Cristina Pons

Publikováno v: HUMAN PATHOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname

Ovarian clear cell carcinoma is found more often confined to the ovary (stage 1) than high-grade serous carcinoma. The RHO GTPase family of proteins is involved in tumor invasion and metastasis through regulation of the cytoskeleton. The expression o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa8e58ce13deccf243fd16984324f429
https://pubmed.ncbi.nlm.nih.gov/21208644

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Myometrial Invasion and Lymph Node Metastasis in Endometrioid Carcinomas: Tumor-associated Macrophages, Microvessel Density, and HIF1A Have a Crucial Role

Autor: Belén Canet, Maria José Carnicer, Inigo Espinosa, Emanuela D'Angelo, Lluis Catasus, Gian Franco Zannoni, Jaime Prat

Publikováno v: AMERICAN JOURNAL OF SURGICAL PATHOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname

Myometrial invasion is an independent prognostic parameter of the endometrioid carcinomas which correlates with the risk of metastasis to pelvic and/or paraaortic lymph nodes. Recognition of myometrial invasion is sometimes difficult. In fact, myoinv

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a62aed6ae64beb8b59b3098898bfa0ba
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=12477

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Antisense therapeutics for neurofibromatosis type 1 caused by deep intronic mutations

Autor: Eduard Serra, Aurora Sánchez, María Asunción López-Ariztegui, Feliciano J. Ramos, Gabriel Capellá, Juana Fernández-Rodríguez, Belén Canet, Ignacio Blanco, Ana Benavides, Llúcia Benito, Eva Pros, Conxi Lázaro

Publikováno v: Human mutation. 30(3)

Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder affecting 1:3,500 individuals. Disease expression is highly variable and complications are diverse. However, currently there is no specific treatment for the disease. NF1 is caused by m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18995c7d7b034a32c9e970e46126a072
https://pubmed.ncbi.nlm.nih.gov/19241459

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