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pro vyhledávání: '"Nicolás Schnake"'
Publikováno v:
Human Genomics, Vol 13, Iss 1, Pp 1-9 (2019)
Abstract Background RUNX1 gene, a master regulator of the hematopoietic process, participates in pathological conditions as a partner for several genes in chromosomal translocations. One of the most frequent chromosomal translocations found in acute
Externí odkaz:
https://doaj.org/article/ac1b68fd6cf1490992ed862c477f8339
Autor:
Nicolás Schnake, Soraya Gutiérrez
Publikováno v:
Leukemia Research Reports, Vol 12, Iss , Pp - (2019)
In this work, we analyzed the association between RUNX1 gene expression and the accessibility of BCR3, one of RUNX1 gene breakpoint regions involved in the chromosomal translocation (8;21), a frequent translocation in treatment-related acute myeloid
Externí odkaz:
https://doaj.org/article/1534a9da86574dd8a65acdcc69a78857
Publikováno v:
Human Genomics
Human Genomics, Vol 13, Iss 1, Pp 1-9 (2019)
Human Genomics, Vol 13, Iss 1, Pp 1-9 (2019)
Background RUNX1 gene, a master regulator of the hematopoietic process, participates in pathological conditions as a partner for several genes in chromosomal translocations. One of the most frequent chromosomal translocations found in acute myeloid l
Autor:
Soraya E. Gutierrez, Nicolás Schnake
Publikováno v:
Leukemia Research Reports, Vol 12, Iss, Pp-(2019)
In this work, we analyzed the association between RUNX1 gene expression and the accessibility of BCR3, one of RUNX1 gene breakpoint regions involved in the chromosomal translocation (8;21), a frequent translocation in treatment-related acute myeloid