نتایج جستجو برای: q27

تعداد نتایج: 214  

Journal: :Cancer research 2000
A Jackson P Carrara V Duke P Sinclair M Papaioannou C J Harrison L Foroni

Two distinct regions of minimal deletion (RMD) have been identified at 6q25-q27 in non-Hodgkin's lymphoma (RMD-1), and at 6q21-q23 in acute lymphoblastic leukemia (ALL; RMD-2) by loss of heterozygosity and fluorescence in situ hybridization studies. In this study, 30 overlapping yeast artificial chromosomes (YACs), 1 expressed sequence tag, and 11 novel YAC ends were identified using bidirectio...

Journal: :Human molecular genetics 2001
S Cichon J Schumacher D J Müller M Hürter C Windemuth K Strauch S Hemmer T G Schulze G Schmidt-Wolf M Albus M Borrmann-Hassenbach E Franzek M Lanczik J Fritze R Kreiner U Reuner B Weigelt J Minges D Lichtermann B Lerer K Kanyas M P Baur T F Wienker W Maier M Rietschel P Propping M M Nöthen

Bipolar affective disorder (BPAD), also known as manic depressive illness, is a severe psychiatric disorder characterized by episodes of mania and depression. It has a lifetime prevalence of approximately 1% in all human populations. In order to identify chromosomal regions containing genes that play a role in determining susceptibility to this psychiatric condition, we have conducted a complet...

Journal: :Molecular vision 2007
Qingjiong Zhang Xueshan Xiao Shiqiang Li Xiangming Guo

PURPOSE To identify mutations causing X-linked congenital motor nystagmus (XL-CMN) in Chinese families. METHODS Genomic DNA was prepared from peripheral blood leukocytes. Cycle sequencing was used to detect the sequence variation of the FERM domain containing 7 (FRMD7) gene, where mutations have been identified recently to associate with XL-CMN. RESULTS Sequencing of the coding and the adja...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1990
J D Rowley M O Diaz R Espinosa Y D Patel E van Melle S Ziemin P Taillon-Miller P Lichter G A Evans J H Kersey

Translocations involving chromosome 11, band q23, are frequent recurring abnormalities in human acute lymphoblastic and acute myeloid leukemia. We used 19 biotin-labeled probes derived from genes and anonymous cosmids for hybridization to metaphase chromosomes from leukemia cells that contained four translocations involving band 11q23: t(4;11)(q21;q23), t(6;11)(q27;q23), t(9;11)(p22;q23), and t...

Journal: :Human molecular genetics 2005
Mario Falchi Toby Andrew Harold Snieder Ramasamyiyer Swaminathan Gabriela L Surdulescu Tim D Spector

Using a novel approach for a two-locus model that provides a greatly increased power to detect multiple quantitative trait loci (QTLs) in simulated data, we identified in a sample of 961 female sib-pairs, three genome-wide significant QTLs for apolipoprotein A1 on chromosomes 8p21.1-q13.1 (LOD score 3.71), 9q21.32-33.1 (LOD score 3.28) and 10p15.1-p13 (LOD score 5.51), two for lipoprotein (a) o...

Journal: :The Journal of Experimental Medicine 2000
Aaron J. Marshall Hiroaki Niiro Cara G. Lerner Theodore J. Yun Sushma Thomas Christine M. Disteche Edward A. Clark

We have identified and characterized a novel src homology 2 (SH2) and pleckstrin homology (PH) domain-containing adaptor protein, designated Bam32 (for B cell adaptor molecule of 32 kD). cDNAs encoding the human and mouse Bam32 coding sequences were isolated and the human bam32 gene was mapped to chromosome 4q25-q27. Bam32 is expressed by B lymphocytes, but not T lymphocytes or nonhematopoietic...

Journal: :The EMBO journal 1995
B H Ye S Chaganti C C Chang H Niu P Corradini R S Chaganti R Dalla-Favera

The BCL6 gene codes for a zinc-finger transcription factor and is involved in chromosomal rearrangements in 30-40% of diffuse large-cell lymphoma (DLCL). These rearrangements cluster within the 5' regulatory region of BCL6 spanning its first non-coding exon. To determine the functional consequences of these alterations, we have analyzed the structure of the rearranged BCL6 alleles and their cor...

Journal: :Cancer research 1993
B H Ye P H Rao R S Chaganti R Dalla-Favera

Chromosomal translocations involving band 3q27 and various chromosomal sites, including the sites of the immunoglobulin (Ig) loci (14q32, 2p12, 22q11), represent recurrent aberrations in non-Hodgkin's lymphoma (NHL). In order to identify the putative protooncogene involved in these translocations, we have cloned the breakpoints from two B-cell NHL cases carrying t(3;14)(q27;q32) translocations ...

2006
Bihui H. Ye P. H. Rao R. S. K. Chaganti Riccardo Dalla-Favera

Chromosomal translocations involving band 3q27 and various chromo somal sites, including the sites of the immunoglobulin (Ig) loci (14q32, 2pl2, 22qll), represent recurrent aberrations in non-Hodgkin's lymphoma (NHL). In order to identify the putative protooncogene involved in these translocations, we have cloned the breakpoints from two B-cell NHL cases carrying t(3;14)(q27;q32) translocations...

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