Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Jose M, De Campos"'
Autor:
Miguel Torres-Martin, Luis Lassaletta, Jose M de Campos, Alberto Isla, Javier Gavilan, Giovanny R Pinto, Rommel R Burbano, Farida Latif, Barbara Melendez, Javier S Castresana, Juan A Rey
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e65868 (2013)
BACKGROUND: Vestibular schwannomas are benign tumors that arise from Schwann cells in the VIII cranial pair and usually present NF2 gene mutations and/or loss of heterozygosity on chromosome 22q. Deregulation has also been found in several genes, suc
Externí odkaz:
https://doaj.org/article/6f66e52d5e954454837d9f4113979c8b
Autor:
Elisabetta Zanoletti, Patrice Tran Ba Huy, Claudio Letizia, Mathieu Peyre, Olivier Sterkers, Giuseppe Opocher, Gabriela Sanso, Stéphane Richard, Carlos Suárez, Ulrich F. Wellner, Charis Eng, Carsten Christof Boedeker, Jose M. de Campos, Hartmut P. H. Neumann, Marta Barontini, Birke Bausch, Mariagiulia Anglani, Sophie Giraud, Francesca Schiavi, Christian Offergeld, Angelica Malinoc, Tobias Krauss, Eamonn R. Maher, Hiroshi Kanno, S. Bobin, Claudia Hader, Sven Gläsker, Frederik J. Hes, Thera P. Links, Stefan Zschiedrich
Publikováno v:
Head & Neck. 38:E673-E679
Hartmut P.H. Neumann is supported by grants from the Deutsche Krebshilfe (Grant 107995 to H.P.H.N.). Stephane Richard is supported by grants from the Direction Generale de l’Organisation des Soins (French Department of Health), the Institut Nationa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98eeaac9d7c61d426238af8731f71d41
https://doi.org/10.1002/hed.24067
https://doi.org/10.1002/hed.24067
Autor:
Luis Lassaletta, Giovanny R. Pinto, Juan A. Rey, Bárbara Meléndez, Miguel Torres-Martín, Rommel Rodríguez Burbano, Alberto Isla, Javier S. Castresana, Jose M. de Campos
Publikováno v:
Genes, Chromosomes and Cancer. 54:197-209
Schwannomas are tumors that develop from Schwann cells in the peripheral nerves and commonly arise from the vestibular nerve. Vestibular schwannomas can present unilaterally and sporadically or bilaterally when the tumor is associated with neurofibro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d235850b0ac1a4b14a49094d86ca610c
https://doi.org/10.1002/gcc.22232
https://doi.org/10.1002/gcc.22232
Autor:
Luis Lassaletta, Juan A. Rey, Rommel Rodríguez Burbano, Giovanny R. Pinto, Bárbara Meléndez, Jose M. de Campos, Miguel Torres-Martín, Alberto Isla, Javier S. Castresana
Publikováno v:
Oncology Reports
Schwannomas and grade I meningiomas are non-metastatic neoplasms that share the common mutation of gene NF2. They usually appear in neurofibromatosis type 2 patients. Currently, there is no drug treatment available for both tumors, thus the use of wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9236ff6d15bca5728bd8692566313045
http://europepmc.org/articles/PMC4240498
http://europepmc.org/articles/PMC4240498
Autor:
Birke, Bausch, Ulrich, Wellner, Mathieu, Peyre, Carsten C, Boedeker, Frederik J, Hes, Mariagiulia, Anglani, Jose M, de Campos, Hiroshi, Kanno, Eamonn R, Maher, Tobias, Krauss, Gabriela, Sansó, Marta, Barontini, Claudio, Letizia, Claudia, Hader, Francesca, Schiavi, Elisabetta, Zanoletti, Carlos, Suárez, Christian, Offergeld, Angelica, Malinoc, Stefan, Zschiedrich, Sven, Glasker, Serge, Bobin, Olivier, Sterkers, Patrice Tran, Ba Huy, Sophie, Giraud, Thera, Links, Charis, Eng, Giuseppe, Opocher, Stephane, Richard, Hartmut P H, Neumann
Publikováno v:
Head and Neck: Journal of the Sciences and Specialties of the Head and Neck, 38(S1), E673-E679. Wiley
Background. Endolymphatic sac tumors (ELSTs) are, with a prevalence of up to 16%, a component of von Hippel-Lindau (VHL) disease. Data from international registries regarding heritable fraction and characteristics, germline VHL mutation frequency, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::123c4f77f839f5ecdc26d3454de11231
https://research.rug.nl/en/publications/12b97d25-3280-49cb-b588-54e666f60d5f
https://research.rug.nl/en/publications/12b97d25-3280-49cb-b588-54e666f60d5f
Autor:
Jesús Vaquero, Juan A. Rey, Manuel Gutierrez, Alberto Isla, Carmen Franco-Hernandez, Dolores Arjona, Victor Martinez-Glez, Jose M. de Campos
Publikováno v:
Cancer Genetics and Cytogenetics. 173:63-67
Clinical response to Gefitinib (Iressa, ZD1839) has been found to be associated with somatic mutations, primarily of exons 18-21, of the epidermal growth factor receptor gene (EGFR) in non-small cell lung cancer (NSCLC). Evidence of a positive respon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c018f92ce33ea1a7120397c3efec5356
https://doi.org/10.1016/j.cancergencyto.2006.09.023
https://doi.org/10.1016/j.cancergencyto.2006.09.023
Autor:
Marcos Malumbres, Cristina Montero-Conde, Fátima Mercadillo, Javier Benitez, Alberto Cascón, Cristina Rodríguez-Antona, Ana Osorio, Mercedes Robledo, Rocío Letón, Sergio Ruiz-Llorente, Jose M. de Campos, Beatriz Escobar, José M. García-Sagredo
Publikováno v:
Human Mutation. 28:613-621
Clear cell renal cell carcinoma (ccRCC) is the most common malignant neoplasm of the kidney. The majority of hereditary and sporadic ccRCC cases are associated with germline and somatic mutations in the Von Hippel-Lindau gene (VHL), respectively. Gro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d904edb34d739de1dd41beaa29ed0e97
https://doi.org/10.1002/humu.20496
https://doi.org/10.1002/humu.20496
Autor:
M. Eva Alonso, M. Josefa Bello, Dolores Arjona, Victor Martinez-Glez, Jose M. de Campos, Alberto Isla, M. Elena Kusak, Jesús Vaquero, Manuel Gutierrez, Jose L. Sarasa, Juan A. Rey
Publikováno v:
American Journal of Clinical Pathology. 123:900-906
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1b7dae1c52ef8c58a98301248162aae
https://doi.org/10.1309/448yrwnc43te32kq
https://doi.org/10.1309/448yrwnc43te32kq
Autor:
M. Josefa Bello, M. Eva Alonso, Jesús Vaquero, Juan A. Rey, Jose M. de Campos, Jesus Lomas, Alberto Isla, Isabel Lopez-Marin, Cinthia Amiñoso, Dolores Arjona, Victor Martinez-Glez
Publikováno v:
Genes, Chromosomes and Cancer. 42:314-319
The role of the NF2 gene in the development of meningiomas has recently been documented; inactivating mutations plus allelic loss at 22q, the site of this gene (at 22q12), have been identified in both sporadic and neurofibromatosis type 2-associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::568aac7d25b96cfd04dd76b10e682884
https://doi.org/10.1002/gcc.20141
https://doi.org/10.1002/gcc.20141
Autor:
Alberto Isla, Dolores Arjona, M. Eva Alonso, Pilar Gonzalez-Gomez, Jose M. de Campos, Cinthia Amiñoso, Cacilda Casartelli, Jose L. Sarasa, Jesús Vaquero, Juan A. Rey, Manuel Gutierrez, Isabel Lopez-Marin, Nilson Praia Anselmo, M.Elena Kusak, Luis Lassaletta, M. Josefa Bello
Publikováno v:
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 554:23-32
O6-methylguanine-DNA methyltransferase (MGMT) plays a major role in repairing DNA damage from alkylating agents. By removing alkyl groups from the O6-position in guanine, MGMT can prevent G:C to A:T transition mutations, a type of variation frequentl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df4abfa293a83a152c5136283c7bce66
https://doi.org/10.1016/j.mrfmmm.2004.02.011
https://doi.org/10.1016/j.mrfmmm.2004.02.011