Zobrazeno 1 - 10
of 241
pro vyhledávání: '"oncogenetics"'
Autor:
Radoi Viorica-Elena, Pop Lucian-Gheorghe, Maioru Ovidiu-Virgil I., Sabau Delia, Dan Andra, Riza Maria, Bohiltea Laurentiu-Camil
Publikováno v:
Romanian Journal of Laboratory Medicine, Vol 31, Iss 3, Pp 163-174 (2023)
Introduction: Cancer is the leading cause of death and an important impediment to increasing life expectancy in every country of the world. During the process of oncogenesis, genetic and epigenetic changes lead to abnormal expression of genes associa
Externí odkaz:
https://doaj.org/article/68888742832e4b25bede4962dae9422d
Autor:
Luana Conte, Emanuele Rizzo, Tiziana Grassi, Francesco Bagordo, Elisabetta De Matteis, Giorgio De Nunzio
Publikováno v:
Computation, Vol 12, Iss 3, p 47 (2024)
Pedigree charts remain essential in oncological genetic counseling for identifying individuals with an increased risk of developing hereditary tumors. However, this valuable data source often remains confined to paper files, going unused. We propose
Externí odkaz:
https://doaj.org/article/03b2876e418f40228e04be0e356f11be
Akademický článek
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Autor:
O. P. Dribnokhodova, E. A. Dunaeva, G. V. Leshkina, E. A. Yarygina, A. Yu. Bukharina, Ya. A. Voiciehovskaya, E. V. Borisova, S. K. Bormotova, A. I. Daoud, V. N. Khlavich, K. O. Mironov
Publikováno v:
Сибирский онкологический журнал, Vol 20, Iss 5, Pp 75-83 (2021)
Introduction. Detection of somatic mutations in the BRAF gene can be used in clinical oncology to clarify the diagnosis, select therapy and assess the prognosis of the disease. Pyrosequencing technology makes it possible to identify both already know
Externí odkaz:
https://doaj.org/article/c9a2a247394241b89a9ae6d39e726c46
Publikováno v:
Dermatopathology, Vol 8, Iss 3, Pp 301-314 (2021)
Cutaneous melanomas are exceptional in children and represent a variety of clinical situations, each with a different prognosis. In congenital nevi, the risk of transformation is correlated with the size of the nevus. The most frequent type is latera
Externí odkaz:
https://doaj.org/article/bd41641b670d4d96a426ef9b036e3ef2
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
M.-C. Villy, J. Masliah-Planchon, S. Melaabi, O. Trabelsi Grati, E. Girard, G. Bataillon, A. Vincent-Salomon, J. Le Gall, L. Golmard, D. Stoppa-Lyonnet, I. Bieche, C. Colas
Publikováno v:
Gynecologic Oncology Reports, Vol 37, Iss , Pp 100855- (2021)
Objective: Tumors harboring a POLE pathogenic variant, associated with high tumor mutational burden, are good candidates for immunotherapy. However, POLE pathogenic variants are not currently screened in routine clinical practice. Can these tumors be
Externí odkaz:
https://doaj.org/article/b7167e1ceefb447b850e2daf637b6876
Autor:
Fabrice Kwiatkowski, Mathilde Gay-Bellile, Pascal Dessenne, Claire Laquet, Véronique Boussion, Marie Béguinot, Marie-Françoise Petit, Anne-Sophie Grémeau, Céline Verlet, Charlotte Chaptal, Marilyn Broult, Sylvie Jouvency, Martine Duclos, Yves-Jean Bignon
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 17, Iss 1, Pp 1-9 (2019)
Abstract Background In families with high risk of hereditary breast/ovarian cancer (HBOC), women before age 30 do not yet undergo clinical screening, but they are exposed to contradictory information from diverse sources. They may be presented with s
Externí odkaz:
https://doaj.org/article/59e5953435484fc6a190314a37ec1036
Autor:
Nerea Vega-García, Sara Perez-Jaume, Elena Esperanza-Cebollada, Clara Vicente-Garcés, Montserrat Torrebadell, Antonio Jiménez-Velasco, Margarita Ortega, Marta Llop, Lorea Abad, José Manuel Vagace, Alfredo Minguela, Marta Pratcorona, Joaquín Sánchez-Garcia, Clara B. García-Calderón, María Teresa Gómez-Casares, Estela Martín-Clavero, Adela Escudero, Marta Riñón Martinez-Gallo, Luz Muñoz, María Rosario Velasco, Marina García-Morin, Albert Català, Antonia Pascual, Pablo Velasco, José Mª. Fernández, Alvaro Lassaletta, José Luis Fuster, Isabel Badell, Águeda Molinos-Quintana, Antonio Molinés, Pilar Guerra-García, Antonio Pérez-Martínez, Miriam García-Abós, Reyes Robles Ortiz, Sandra Pisa, Rosa Adán, Cristina Díaz de Heredia, José Luis Dapena, Susana Rives, Manuel Ramírez-Orellana, Mireia Camós
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2021)
Robust and applicable risk-stratifying genetic factors at diagnosis in pediatric T-cell acute lymphoblastic leukemia (T-ALL) are still lacking, and most protocols rely on measurable residual disease (MRD) assessment. In our study, we aimed to analyze
Externí odkaz:
https://doaj.org/article/76d44086f8a049c3816cf6758487be24