
Inv (11) (q21q23) fuses MLL to the Notch co-activator ... - Nature
2008年3月13日 · Here, we describe the development of secondary T-cell acute lymphoblastic leukemia (T-ALL) in two adolescent leukemia patients. Therapy-related ALL (t-ALL) was …
The inv(11)(p15q22) Chromosome Translocation of De Novo and …
1997年6月1日 · The inv (11) (p15q22) is a recurrent chromosomal abnormality associated with de novo and therapy-related myeloid malignancies. Here we report the molecular definition of this …
The inv(11)(p15q22) chromosome translocation of de novo and
1997年6月1日 · The inv(11)(p15q22) is a recurrent chromosomal abnormality associated with de novo and therapy-related myeloid malignancies. Here we report the molecular definition of this …
The inv(11)(p15q22) chromosome translocation of therapy-related ...
Our case confirms that the inv(11) is a rare chromosomal translocation that is associated with therapy-related or de novo myeloid malignancy and involves NUP98 and DDX10 but not MLL. …
Inversion of chromosome 11 inv (11) (p15q22), as a recurring
We identified a yeast artificial chromosome (YAC) clone that spanned the inv (11) breakpoints on 11q. From this YAC, we identified a P1 clone, which included the breakpoints in at least three …
inv(11)(q21q23) KMT2A/MAML2 in therapy related leukemias
2007年6月1日 · Inv (11) (q21q23); KMT2A-MAML2, a Recurrent Genetic Abnormality in T-Cell Therapy-related Acute Lymphoblastic Leukemia. Molecular pathology of thymomas: …
inv (11) (p15q23) - My Cancer Genome
Significance of inv(11)(p15q23) in Diseases Acute Myeloid Leukemia + inv(11)(p15q23) is an inclusion criterion in 87 clinical trials for acute myeloid leukemia, of which 39 are open and 48 …
inv(11)(p15q22) NUP98/DDX10 t(11;11)(p15;q22) NUP98/DDX10
The inv(11)(p15q22) chromosome translocation of de novo and therapy-related myeloid malignancies results in fusion of the nucleoporin gene, NUP98, with the putative RNA helicase …
Homozygous inv(11)(q21q23) and MLL gene rearrangement in …
2014年5月15日 · In vast majority of cases with MLL gene rearrangements, only one chromosome 11 or a single MLL allele got involved. We report two very unusual cases of myeloid …
Two pericentric inversions of human chromosome 11. - PMC
In another family studied by several banding methods in search of chromosomal markers, a pericentric inv(11) (p11q11) was found. It was detectable only by C-banding, the darkly …