Zobrazeno 1 - 10
of 74
pro vyhledávání: '"CHROMOSOMAL BREAKPOINTS"'
Autor:
Bonaglia, M. C., Bertuzzo, S., Ciaschini, A. M., Discepoli, G., Castiglia, L., Romaniello, R., Zuffardi, O., Fichera, M.
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-8 (2020)
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-8 (2020)
Background It has been known for more than 30 years that balanced translocations, especially if de novo, can associate with congenital malformations and / or neurodevelopmental disorders, following the disruption of a disease gene or its cis-regulato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d84b2cef31bb1679b0d38450fe24a3f0
http://hdl.handle.net/20.500.11769/499059
http://hdl.handle.net/20.500.11769/499059
As alterações cromossômicas estruturais associadas a fenótipos clínicos oferecem a oportunidade de identificação de genes cujas mutações possam estar determinando essas patologias, tendo em vista a possibilidade de que esses genes podem ter
Akademický článek
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Publikováno v:
International journal of oncology. 28(4):891-897
Routine cytogenetic analysis provides important information on diagnostic and prognostic relevance for hematological malignancies. However, it is often difficult to obtain good karyotypes, especially of cells from cases with acute lymphoblastic leuke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dris___01423::843a940b4c0085d7dd34050d860b6da6
https://research.rug.nl/en/publications/10b1dbc7-9486-4341-8bfa-9102a2fcd378
https://research.rug.nl/en/publications/10b1dbc7-9486-4341-8bfa-9102a2fcd378
Publikováno v:
Cellular Oncology, Vol 28, Iss 1-2, Pp 31-35 (2006)
Cellular Oncology : the Official Journal of the International Society for Cellular Oncology
Cellular Oncology : the Official Journal of the International Society for Cellular Oncology
Background: Chromosomal translocations are causally related to the development of many tumors. In Burkitt's lymphoma, abnormalities involving the c-myc gene are essential. The CT-element of the c-myc promoter adopts non-B-conformation in vivo and in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b07987309c256a7166283240fc586860
https://doaj.org/article/1b64a5763e3347d3ae43f60b05df9871
https://doaj.org/article/1b64a5763e3347d3ae43f60b05df9871
Publikováno v:
GENES CHROMOSOMES & CANCER. 40(1):10-18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dris___00893::03d1fe646c3848d1209225083b3124ad
https://doi.org/10.1002/gcc.20009
https://doi.org/10.1002/gcc.20009
Akademický článek
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Autor:
Luiz Carlos Zangrande Vieira
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USPUniversidade de São PauloUSP.
As alterações cromossômicas estruturais associadas a fenótipos clínicos oferecem a oportunidade de identificação de genes cujas mutações possam estar determinando essas patologias, tendo em vista a possibilidade de que esses genes podem ter
Autor:
Ulrich Wedding, Hasmik Mkrtchyan, Detlef Haase, Klaus Höffken, Madeleine Gross, Thomas Liehr, Constanze Karst
Publikováno v:
International journal of oncology, 28(4), 891-897. SPANDIDOS PUBL LTD
Routine cytogenetic analysis provides important information on diagnostic and prognostic relevance for hematological malignancies. However, it is often difficult to obtain good karyotypes, especially of cells from cases with acute lymphoblastic leuke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a7773ff2c94850b8f80744c6c68b298
https://research.rug.nl/en/publications/10b1dbc7-9486-4341-8bfa-9102a2fcd378
https://research.rug.nl/en/publications/10b1dbc7-9486-4341-8bfa-9102a2fcd378