نتایج جستجو برای: q21

تعداد نتایج: 1024  

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2012

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

Journal: :Cancer genetics and cytogenetics 1995
J C Cigudosa M J Calasanz M D Odero J Marin E Bengoechea A Gullón

We report two cases of acute myeloid leukemia (M1 and M5B subtypes) with a similar translocation, t(3;11)(q21;q13). We discuss the involvement of these breakpoints in acute leukemia and their putative clinical implications.

Journal: :Blood 2000
N Mochizuki S Shimizu T Nagasawa H Tanaka M Taniwaki J Yokota K Morishita

The reciprocal translocation t(1;3)(p36;q21) occurs in a subset of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML), which is frequently characterized by trilineage dysplasia, in particular dysmegakaryocytopoiesis, and poor prognosis. Previously, the breakpoint cluster region (BCR) at 3q21 was identified within a 60-kilobase (kb) region centromeric to the BCR of 3q21q26 syndrome ...

1998
István Szapudi

The first non-trivial cumulant correlator of the galaxy density fieldQ21 is examined from the point of view of biasing. It is shown that to leading order it depends on two biasing parameters b, and b2, and on q21, the underlying cumulant correlator of the mass. As the skewness Q3 has analogous properties, the slope of the correlation function −γ, Q3, and Q21 uniquely determine the bias paramete...

Journal: :Blood 2005
Liza Ho R Eric Davis Béatrice Conne Richard Chappuis Margaret Berczy Paulette Mhawech Louis M Staudt Juerg Schwaller

The most frequently recurring translocations in mucosa-associated lymphoid tissue (MALT) B-cell non-Hodgkin lymphoma, t(11;18)(q21;q21) and t(14;18)(q32; q21), lead to formation of an API2-MALT1 fusion or IgH-mediated MALT1 overexpression. Various approaches have implicated these proteins in nuclear factor kappaB (NF-kappa B) signaling, but this has not been shown experimentally in human B cell...

2013
A Pazarbasi O Demirhan D Alptekin FT Ozgunen L Ozpak MB Yilmaz E Nazlican N Tanriverdi U Luleyap D Gümürdülü

The majority of chromosome rearrangements are balanced reciprocal and Robertsonian translocations. It is now known that such abnormalities cause no phenotypic effect on the carrier but lead to increased risk of producing unbalanced gametes. Here, we report the inheritance of a translocation between chromosomes 3 and 21 in a family with one of two fetuses with Down Syndrome carrying the same tra...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید