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 …

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 …

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. …

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 …

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 …

Band p12 represented the most common breakpoint on chro-mosome 10. The t(10;11) subgroup defined a subset of younger 11q23 patients, the majority of whom achieve a first complete …

2007年10月1日 · 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 …

Here we report T-t-ALL with inv(11) (q21q23), which involves KMT2A and MAML2, a transcriptional coactivator of NOTCH proteins, that occurred after chemotherapy for …

2018年3月23日 · 说白了就是:inv[i]=-(mod/i)*inv[mod%i] 然后边界是inv[1]=1 这不仅为我们提供了一个线性求逆元的方法，也提供了一种O(logmod)求逆元的方法

急性髓细胞白血病 (acute myeloid leukemia，AML)是一组高度异质性血液系统恶性肿瘤，具有分子细胞遗传学上特异性基因突变及染色体畸变，这些遗传学异常可以引起原始细胞克隆性增殖及 …