Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Esteban, Mocetti"'
Autor:
Andrés Guercovich, Luciano Piazzoni, Zenon Beguelín, Juan Paez, Jorgelina B. Ibañez, Esteban Mocetti
Publikováno v:
Oncología Clínica. 21
La mutación del receptor del factor de crecimiento epidérmico (EGFR) en los tumores de pulmón puede observarse en un 10-47% de pacientes. El 90% de las mutaciones son deleciones del exón 19 o mutaciones puntuales del L858R del exón 21, y se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab1b07198cb567e6c4761e8bde6ed2ee
https://doi.org/10.56969/oc.v21i3.86
https://doi.org/10.56969/oc.v21i3.86
Publikováno v:
Oncología Clínica. 21
El gen de fusión EML4-ALK es producto de la inversión dentro del brazo corto del cromosoma 2 que da lugar a una proteína quimérica con actividad tirosinquinasa y oncogénica. EML4-ALK está presente en una pequeña proporción de paciente
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2237f192bc243a24e903a141c872395
https://doi.org/10.56969/oc.v21i2.88
https://doi.org/10.56969/oc.v21i2.88
Autor:
Wael M. Abdel-Rahman, Henry T. Lynch, Esteban Mocetti, Karin E. Lönnqvist, Päivi Peltomäki, Tiina E. Raevaara, Carlos A. Vaccaro, Shashi Bala, Reetta Kariola, Minna Nystrom-Lahti
Publikováno v:
Gastroenterology. 125:501-509
Background & Aims: Hereditary nonpolyposis colorectal cancer is associated with mismatch repair deficiency. Most predisposing mutations prevent the production of functional mismatch repair protein. Thus, when the wild-type copy is also inactivated, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36c2eb7942796b34f768587cfaa31ba5
https://doi.org/10.1016/s0016-5085(03)00905-3
https://doi.org/10.1016/s0016-5085(03)00905-3
Autor:
Francisco Piccaluga, Esteban Mocetti, Ana Morandi, Alejandro Gonzalez Della Valle, Laura Pineiro, Martin Buttaro
Publikováno v:
Acta Orthopaedica Scandinavica. 74:505-513
We compared the incorporation of bone allografts with or without vancomycin in tibial defects of 18 pigs. High-quality radiographs, histological examination, immunological expression of metalloproteinase-13 (MMP-13) and transforming growth factor-bet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36b60747271190055a7b9eadd6a1dbc1
https://doi.org/10.1080/00016470310017884
https://doi.org/10.1080/00016470310017884
Autor:
Alejandra Hidalgo, Oscar Campetella, Juan Mucci, Esteban Mocetti, Pablo Argibay, M. Susana Leguizamón
Publikováno v:
Proceedings of the National Academy of Sciences. 99:3896-3901
Trypanosoma cruzi , the causative agent of Chagas' disease, induces transient thymic aplasia early after infection—a phenomenon that stills lacks a molecular explanation. The parasite sheds an enzyme known as trans -sialidase (TS), which is able to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b96fa3a6fc326b6c09bd4ae763790b29
https://doi.org/10.1073/pnas.052496399
https://doi.org/10.1073/pnas.052496399
Autor:
Pablo Argibay, M. Susana Leguizamón, Oscar Campetella, Esteban Mocetti, Hernán García Rivello
Publikováno v:
The Journal of Infectious Diseases. 180:1398-1402
Trypanosoma cruzi, the etiologic agent of Chagas' disease, expresses trans-sialidase, an enzyme able to direct transfer of sialyl residues among macromolecules. The enzyme is shed and can be detected in blood during the acute phase of the disease. Se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4b01eca3bb4c7d0053b05d53b2b55f8
https://doi.org/10.1086/315001
https://doi.org/10.1086/315001
Autor:
Pablo Argibay, H. Garcia Rivello, A. Escalada, Esteban Mocetti, P. Ruybal, Silvia Christiansen, C. Mongini
Publikováno v:
Transplantation Proceedings. 30:2673-2676
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c2c86391147d7ca93f4bb2453d57887
https://doi.org/10.1016/s0041-1345(98)00785-4
https://doi.org/10.1016/s0041-1345(98)00785-4
Autor:
L. Lupinacci, Esteban Mocetti, Maria J. Labanca, José Lastiri, Mercedes Dalurzo, J.N. Minatta
Publikováno v:
Journal of Thoracic Oncology. 12:S1232
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54437e916cc530c4b5dd4087d224f991
https://doi.org/10.1016/j.jtho.2016.11.1737
https://doi.org/10.1016/j.jtho.2016.11.1737
Autor:
Carlos A. Vaccaro, Päivi Peltomäki, Maria Ana Redal, M. B. Clark, Esteban Mocetti, Shashi Bala, Eduardo Mullen, Hernán García Rivello, Jane F. Lynch, Fernando Bonadeo, Henry T. Lynch, Analía V. Roverano, Guillermo Ojea-Quintana, Mario L Benati, Renkonen E
Publikováno v:
Diseases of the colon and rectum. 50(10)
The first Argentine experience with epidemiologic, molecular, and genetic counseling data is reported. We analyzed 43 families fulfilling Amsterdam criteria identified from a prospective database with data from 779 relatives. Eleven families (25.6 pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6953b1b3e4230176a5165dcd4654cb2
https://pubmed.ncbi.nlm.nih.gov/17846840
https://pubmed.ncbi.nlm.nih.gov/17846840
Autor:
Carlos A, Vaccaro, Jorge E, Carrozzo, Esteban, Mocetti, Mariana, Berho, Paula, Valdemoros, Eduardo, Mullen, Myriam, Oviedo, Maria A, Redal
Publikováno v:
Medicina. 67(3)
Mutation of the mismatch repair genes MLH1 and MSH2 account for the majority of the genetic abnormalities in Lynch syndrome. Immunohistochemical detection of their protein products is becoming an increasingly common method to detect these mutations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9e2efadee88a31e6295dbd6e495b4fbd
https://pubmed.ncbi.nlm.nih.gov/17628916
https://pubmed.ncbi.nlm.nih.gov/17628916