منابع مشابه
Special Section on Smart Multimedia & Communication Systems
The IEICE Transactions on Fundamentals of Electronics, Communications and Computer Sciences announces a forthcoming Special Section on Smart Multimedia & Communication Systems to be published in November 2018. The IEICE TC SIS conducted the 2017 International Workshop on Smart Info-Media Systems in Asia (SISA 2017) in order to enhance research activities on smart multimedia & communication fiel...
متن کاملLeukaemia Section Short Communication
Clinics and pathology Disease De novo ANLL; (one case of blast crisis CML). Phenotype / cell stem origin Mainly M2 or M4, but also M1, M5a, M5b, or M7 ANLL; may be preceded by MDS. Epidemiology About 30 reported cases, mainly found in young adults; children cases are described; median age is about 30 yrs; balanced sex ratio. Clinics Blood data: anemia, thrombocytopenia, mild hyperleucocytosis; ...
متن کاملLeukaemia Section Short Communication
Although the underlying mechanism for these chromosomal alterations is unclear, it is possible that chromosomes with large constitutive heterochromatin bands such as chromosome 1 may be at risk of centromeric instability and be predisposed to centromeric fusion with other chromosomes. This possibility is supported by observations that unbalanced chromosome rearrangements frequently involve the ...
متن کاملLeukaemia Section Short Communication
Disease Myelodysplastic syndrome (21 cases), Acute Myeloid Leukemia (5 cases), Chronic Myelomonocytic Leukemia (1 case). Phenotype/cell stem origin Thrombopenia (90%) with anemia (60%). Dysplastic changes in bone marrow: dyserythropoeisis associated with dysgranulopoieisis and/or dysmegakaryocytopoeisis. Epidemiology The frequency of ider(20q) is estimated at 0.49% in myelodysplastic syndrome a...
متن کاملLeukaemia Section Short Communication
The breakpoint on chromosome 20 is not constant; 20qis frequently associated with other cytogenetic abnormalities as del(5q), trisomy 8, trisomy 21, deletions or translocations involving the long arm of chromosome 13; a newly described translocation t(11;20)(p15;q11) resulting in a NUP98TOP1 fusion gene was described in therapy-related myelodysplastic syndrome (RAEB); t(11;20)(p15;q11) is a rar...
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ژورنال
عنوان ژورنال: Science
سال: 1962
ISSN: 0036-8075,1095-9203
DOI: 10.1126/science.135.3503.535