نتایج جستجو برای: complex variant translocation

تعداد نتایج: 912747  

2014
RUI ZHANG YOUNG-MI KIM XIANFU WANG YAN LI HUI PANG JI-YUN LEE SHIBO LI

Acute promyelocytic leukemia (APL) is characterized by the t(15;17)(q22;q21), which results in the fusion of the promyelocytic leukemia (PML) gene at 15q22 with the retinoic acid α-receptor (RARA) gene at 17q21. The current study presents the case of a 54-year-old female with APL carrying the atypical PML/RARA fusion signal due to a novel complex variant translocation t(15;16;17)(q22;q24;q21), ...

2012
Abir Gmidène Hlima Sennana Rim Frikha Moez Elloumi Hatem Belaaj Ali Saad

A a Abstract. Variant forms of the classic translocation t(8;21) are uncommon and account approximately 3% of all t(8;21)(q22;q22) in acute myeloid leukemia (AML) patients. These forms involve chromosomes 8, 21, and other chromosomes. Here we report a Tunisian patient with a complex rearrangement t(21;8;1)(q22;q22;q32) revealed by conventional chromosomal study at diagnosis. Fluorescence in sit...

Journal: :Haematologica 1994
A Cantù-Rajnoldi A B Federici A Biondi A Cortelezzi L Romitti G Gornati G Gaipa G Gianotti P Mannucci

cute promyelocytic leukemia (APL) is a subtype of acute myeloid leukemia with unique morphologic, cytogenetic, molecular and clinical features. Besides the classical hypergranular variant, there is also a cytological microgranular variant with significant clinical implications in both children and adults. Moreover, a basophilic form and a hyperbasophilic microgranular variant have been describe...

Journal: :Journal of cell science 2014
Janine Berkholz Laura Michalick Barbara Munz

Skeletal and heart muscle-specific variant of the α subunit of nascent polypeptide associated complex (skNAC; encoded by NACA) is exclusively found in striated muscle cells. Its function, however, is largely unknown. Previous reports have demonstrated that skNAC binds to m-Bop/Smyd1, a multi-functional protein that regulates myogenesis both through the control of transcription and the modulatio...

2016
Muhammad Asif Mohammad Sarwar Jamal Abdul Rehman Khan Muhammad Imran Naseer Abrar Hussain Hani Choudhry Arif Malik Shahida Aziz Khan Maged Mostafa Mahmoud Ashraf Ali Saima Iram Kashif Kamran Asim Iqbal Zainularifeen Abduljaleel Peter Natesan Pushparaj Mahmood Rasool

Philadelphia (Ph) chromosome (9;22)(q34;q11) is well established in more than 90% of chronic myeloid leukemia (CML) patients, and the remaining 5-8% of CML patients show variant and complex translocations, with the involvement of third, fourth, or fifth chromosome other than 9;22. However, in very rare cases, the fourth chromosome is involved. Here, we found a novel case of four-way Ph+ chromos...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1984
B S Emanuel J R Selden R S Chaganti S Jhanwar P C Nowell C M Croce

The majority of chromosomal rearrangements observed in Burkitt lymphomas involve a translocation between 8q and 14q, while the remaining minority carry variant translocations between chromosome 8 and either 2 or 22. We have studied the JI Burkitt lymphoma cell line carrying the variant 2;8 chromosome translocation using a combination of high-resolution and molecular cytogenetic techniques. We h...

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