نتایج جستجو برای: q11

تعداد نتایج: 696  

Journal: :Journal of medical genetics 1993
N Morichon-Delvallez A L Delezoide M Vekemans

We describe here a fetus with holoprosencephaly and signs of caudal deficiency sequence. Chromosome examination showed a de novo balanced reciprocal translocation (7;22) (q36;q11) with loss of the derivative chromosome 22 in 50% of the cells examined. The present report and available published data indicate that the terminal region of the long arm of chromosome 7 contains genes implicated in th...

2017

According to the Gα subunit amino acid sequence homology, G proteins divide into four families that can couple to different GPCRs. To investigate the combination of interaction between G proteins (Gs, Gi/Go, q11 and 12/13) and A2A, D2R, or A2A/D2 respectively, Föster resonance energy transfer (FRET) and bimolecular fluorescence complementation (BiFC) assays, with the advantage to analyze protei...

2017

According to the Gα subunit amino acid sequence homology, G proteins divide into four families that can couple to different GPCRs. To investigate the combination of interaction between G proteins (Gs, Gi/Go, q11 and 12/13) and A2A, D2R, or A2A/D2 respectively, Föster resonance energy transfer (FRET) and bimolecular fluorescence complementation (BiFC) assays, with the advantage to analyze protei...

Journal: :Electronic Colloquium on Computational Complexity (ECCC) 2014
Ankit Gupta

We present an algebraic-geometric approach for devising a deterministic polynomial time blackbox identity testing (PIT) algorithm for depth-4 circuits with bounded top fanin. Using our approach, we devise such an algorithm for the case when such circuits have bounded bottom fanin and satisfy a certain non-degeneracy condition. In particular, we present an algorithm that, given blackboxes to P1 ...

Journal: :Haematologica 2009
Daniel Nowak Emilie Le Toriellec Marc-Henri Stern Norihiko Kawamata Tadayuki Akagi Martin J Dyer Wolf-Karsten Hofmann Seishi Ogawa H Phillip Koeffler

BACKGROUND T-cell prolymphocytic leukemia is a rare aggressive lymphoproliferative disease with a mature T-cell phenotype and characteristic genomic lesions such as inv(14)(q11q34), t(14;14)(q11;q32) or t(X;14)(q28;q11), mutation of the ATM gene on chromosome 11 and secondary alterations such as deletions of chromosome 8p and duplications of 8q. DESIGN AND METHODS We analyzed malignant cells ...

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

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