Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ilaria, Scarpelli"'
Autor:
Alexander C. Leeksma, Panagiotis Baliakas, Theodoros Moysiadis, Anna Puiggros, Karla Plevova, Anne-Marie van der Kevie-Kersemaekers, Hidde Posthuma, Ana E. Rodriguez-Vicente, Anh Nhi Tran, Gisela Barbany, Larry Mansouri, Rebeqa Gunnarsson, Helen Parker, Eva van den Berg, Mar Bellido, Zadie Davis, Meaghan Wall, Ilaria Scarpelli, Anders Österborg, Lotta Hansson, Marie Jarosova, Paolo Ghia, Pino Poddighe, Blanca Espinet, Sarka Pospisilova, Constantine Tam, Loïc Ysebaert, Florence Nguyen-Khac, David Oscier, Claudia Haferlach, Jacqueline Schoumans, Marian Stevens-Kroef, Eric Eldering, Kostas Stamatopoulos, Richard Rosenquist, Jonathan C. Strefford, Clemens Mellink, Arnon P. Kater
Publikováno v:
Haematologica, Vol 106, Iss 1 (2020)
Complex karyotype (CK) identified by chromosome-banding analysis (CBA) has shown prognostic value in chronic lymphocytic leukemia (CLL). Genomic arrays offer high-resolution genome-wide detection of copy-number alterations (CNAs) and could therefore
Externí odkaz:
https://doaj.org/article/b0edf60d944d4c6fab629017cf3cd09c
Publikováno v:
Acta Haematologica.
The gene encoding for transcription factor ETV6 presents recurrent lesions in hematologic neoplasms, most notably the ETV6-RUNX1 rearrangement in childhood B-ALL. The role of ETV6 for normal hematopoiesis is unknown, but loss of its function probably
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f6ae279586f4583d0b1c2aff548550a
https://doi.org/10.1159/000529844
https://doi.org/10.1159/000529844
Autor:
Guido MARCHI, Domenico RIZZO, Francesco RANALDI, Luisa GHELARDINI, Massimo RICCIOLINI, Ilaria SCARPELLI, Lorenzo DROSERA, Emanuele GOTI, Paolo CAPRETTI, Giuseppe SURICO
Publikováno v:
Phytopathologia Mediterranea, Vol 57, Iss 3 (2018)
Externí odkaz:
https://doaj.org/article/1fbecb2dcbab4ea2aa478922b20bb4de
Autor:
Elisabetta Gargani, Anita Nencioni, Agostino Strangi, Ilaria Cutino, Claudia Benvenuti, Patrizia Sacchetti, Ilaria Scarpelli, Immacolata Iovinella, Massimo Ricciolini, Domenico Rizzo, Pio Federico Roversi, Leonardo Marianelli
Publikováno v:
Redia. 104:75-88
The vector‐borne bacterium Xylella fastidiosa(Wells and Raju) causes several serious diseases to plants. Recently, different subspecies of X. fastidiosa were reported in some European countries. The risk of the bacterium’s spread on the entire Eu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::441bb0827a8945773d34f28b3a965f04
https://doi.org/10.19263/redia-104.21.09
https://doi.org/10.19263/redia-104.21.09
Autor:
Jacqueline Schoumans, Sabine Blum, Michael Lübbert, Olivier Spertini, Ilaria Scarpelli, Filipe Martins, Michael Kruszewski
Publikováno v:
Annals of Hematology. 100:63-78
Myelodysplastic syndromes (MDS) are a heterogeneous group of diseases, with a variable probability of transformation into acute leukemia, which is, in the vast majority of cases, of myeloid lineage. Nevertheless, rare cases of acute lymphoblastic leu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0348cbc3b65aa234b137d3193194fd6d
https://doi.org/10.1007/s00277-020-04114-2
https://doi.org/10.1007/s00277-020-04114-2
Autor:
Filipe, Martins, Michael, Kruszewski, Ilaria, Scarpelli, Jacqueline, Schoumans, Olivier, Spertini, Michael, Lübbert, Sabine, Blum
Publikováno v:
Annals of hematology. 100(1)
Myelodysplastic syndromes (MDS) are a heterogeneous group of diseases, with a variable probability of transformation into acute leukemia, which is, in the vast majority of cases, of myeloid lineage. Nevertheless, rare cases of acute lymphoblastic leu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::139ed0e0deea1b9821c99b3099426480
https://pubmed.ncbi.nlm.nih.gov/32556451
https://pubmed.ncbi.nlm.nih.gov/32556451
Autor:
Clemens Mellink, Šárka Pospíšilová, Paolo Ghia, Constantine S. Tam, Mar Bellido, Marie Jarošová, Richard Rosenquist, Eva van den Berg, Jacqueline Schoumans, Claudia Haferlach, Lotta Hansson, Zadie Davis, Blanca Espinet, Anna Puiggros, David Oscier, Eric Eldering, Marian Stevens-Kroef, Jonathan C. Strefford, Panagiotis Baliakas, Karla Plevová, Ana E. Rodríguez-Vicente, Alexander C. Leeksma, Kostas Stamatopoulos, Rebeqa Gunnarsson, Pino J Poddighe, Anne Marie van der Kevie-Kersemaekers, Arnon P. Kater, Meaghan Wall, Florence Nguyen-Khac, Theodoros Moysiadis, Anders Österborg, Anh Nhi Tran, Larry Mansouri, Ilaria Scarpelli, Hidde Posthuma, Gisela Barbany, Loic Ysebaert, Helen Parker
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Haematologica, 105(5). Ferrata Storti Foundation
Haematologica, 106, 87-97
Haematologica, vol. 106, no. 1, pp. 87-97
Haematologica, 106(1), 87-97. FERRATA STORTI FOUNDATION
Haematologica, 106, 1, pp. 87-97
Leeksma, A C, Baliakas, P, Moysiadis, T, Puiggros, A, Plevova, K, van der Kevie-Kersemaekers, A M, Posthuma, H, Rodriguez-Vicente, A E, Tran, A N, Barbany, G, Mansouri, L, Gunnarsson, R, Parker, H, van den Berg, E, Bellido, M, Davis, Z, Wall, M, Scarpelli, I, Österborg, A, Hansson, L, Jarosova, M, Ghia, P, Poddighe, P, Espinet, B, Pospisilova, S, Tam, C, Ysebaert, L, Nguyen-Khac, F, Oscier, D, Haferlach, C, Schoumans, J, Stevens-Kroef, M, Eldering, E, Stamatopoulos, K, Rosenquist, R, Strefford, J C, Mellink, C, Kater, A P & ERIC, the European Research Initiative on CLL 2020, ' Genomic arrays identify high-risk chronic lymphocytic leukemia with genomic complexity : A multi-center study ', Haematologica, vol. 105, no. 5 . https://doi.org/10.3324/HAEMATOL.2019.239947
Haematologica
instname
Haematologica, 105(5). Ferrata Storti Foundation
Haematologica, 106, 87-97
Haematologica, vol. 106, no. 1, pp. 87-97
Haematologica, 106(1), 87-97. FERRATA STORTI FOUNDATION
Haematologica, 106, 1, pp. 87-97
Leeksma, A C, Baliakas, P, Moysiadis, T, Puiggros, A, Plevova, K, van der Kevie-Kersemaekers, A M, Posthuma, H, Rodriguez-Vicente, A E, Tran, A N, Barbany, G, Mansouri, L, Gunnarsson, R, Parker, H, van den Berg, E, Bellido, M, Davis, Z, Wall, M, Scarpelli, I, Österborg, A, Hansson, L, Jarosova, M, Ghia, P, Poddighe, P, Espinet, B, Pospisilova, S, Tam, C, Ysebaert, L, Nguyen-Khac, F, Oscier, D, Haferlach, C, Schoumans, J, Stevens-Kroef, M, Eldering, E, Stamatopoulos, K, Rosenquist, R, Strefford, J C, Mellink, C, Kater, A P & ERIC, the European Research Initiative on CLL 2020, ' Genomic arrays identify high-risk chronic lymphocytic leukemia with genomic complexity : A multi-center study ', Haematologica, vol. 105, no. 5 . https://doi.org/10.3324/HAEMATOL.2019.239947
Haematologica
Complex karyotype (CK) identified by chromosome-banding analysis (CBA) has shown prognostic value in chronic lymphocytic leukemia (CLL). Genomic arrays offer high-resolution genome-wide detection of copy-number alterations (CNAs) and could therefore
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3075b2a6908d0109aebb0114832e447c
http://hdl.handle.net/10261/222849
http://hdl.handle.net/10261/222849
Autor:
Naomi Porret, Ekkehard Hewer, Ulrike Bacher, Johanna Flach, Myriam Legros, Jacqueline Schoumans, Joelle Tchinda, Urban Novak, Evgenii Shumilov, Thomas Pabst, Ilaria Scarpelli, Raphael Joncourt
Publikováno v:
Genes, chromosomescancerREFERENCES. 59(4)
Reciprocal RUNX1 fusions are traditionally found in up to 10% of acute myeloid leukemia (AML) patients, usually associated with a translocation (8;21)(q22;q22) corresponding to the RUNX1-RUNX1T1 fusion gene. So far, alternative RUNX1 rearrangements h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::794dfbe995da7554b1fdfacf88ab060e
https://pubmed.ncbi.nlm.nih.gov/31756777
https://pubmed.ncbi.nlm.nih.gov/31756777
Autor:
Marchi, Guido, Domenico, Rizzo, Ranaldi, Francesco, Ghelardini, Luisa, Massimo, Ricciolini, Ilaria, Scarpelli, Lorenzo, Drosera, Goti, Emanuele, Capretti, Paolo, Surico, Giuseppe
Publikováno v:
Phytopathologia Mediterranea, Vol 57, Iss 3 (2018)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b8f72c9b87e8da73fad91fb411741329
https://oajournals.fupress.net/index.php/pm/article/view/5775
https://oajournals.fupress.net/index.php/pm/article/view/5775
Publikováno v:
OBM Genetics. 3:1-1
With the advent of next generation sequencing (NGS), genomic profiling of tumors has gradually been introduced into the clinical setting and become a standard in cancer care. NGS allows easier, faster and cheaper sequencing and commercially available
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57924855baf947671ed6b99033c63ab3
https://doi.org/10.21926/obm.genet.1903088
https://doi.org/10.21926/obm.genet.1903088