نتایج جستجو برای: igvh mutation

تعداد نتایج: 291497  

2016
Matthias Pauthner Jenny Yeung Chris Ullman Joost Bakker Thierry Wurch Janice M. Reichert Fridtjof Lund-Johansen Andrew R.M. Bradbury Paul J. Carter Joost P.M. Melis

The 26th Antibody Engineering & Therapeutics meeting, the annual meeting of The Antibody Society united over 800 participants from all over the world in San Diego from 6-10 December 2015. The latest innovations and advances in antibody research and development were discussed, covering a myriad of antibody-related topics by more than 100 speakers, who were carefully selected by The Antibody Soci...

Journal: :Blood 2014
Steven Marionneaux Larry Smith

A 77-year-old woman presented with cervical adenopathy. A complete blood count was performed: white 1 , and ZAP70 1. Cytogenetics/molecular analysis revealed trisomy 12 and unmutated immunoglobulin heavy chain variable region (IgVH). Positron emission tomography computed tomography showed splenomegaly and widespread adenopathy. WBC differential by digital microscopy (Cellavision) revealed 9% ne...

Journal: :British journal of haematology 2003
Gordon W Dewald Stephanie R Brockman Sarah F Paternoster Nancy D Bone Judith R O'Fallon Cristine Allmer Charles D James Diane F Jelinek Renee C Tschumper Curtis A Hanson Rajiv K Pruthi Thomas E Witzig Timothy G Call Neil E Kay

Fluorescence in situ hybridization (FISH) was used to detect 6q-, 11q-, +12, 13q-, 17p- and translocations involving 14q32 in interphase nuclei from blood and/or bone marrow from 113 patients with B-cell chronic lymphocytic leukaemia (B-CLL). A total of 87 patients (77%) had a FISH anomaly: 13q- x 1 was most frequent (64%) followed by 13q- x 2 (28%), +12 (25%), 11q- (15%), 17p- (8%) and 6q- (0%...

Journal: :Cancer research 2010
Verònica Fernàndez Olga Salamero Blanca Espinet Francesc Solé Cristina Royo Alba Navarro Francisca Camacho Sílvia Beà Elena Hartmann Virginia Amador Luis Hernández Claudio Agostinelli Rachel L Sargent Maria Rozman Marta Aymerich Dolors Colomer Neus Villamor Steven H Swerdlow Stefano A Pileri Francesc Bosch Miguel A Piris Emili Montserrat German Ott Andreas Rosenwald Armando López-Guillermo Pedro Jares Sergi Serrano Elías Campo

Mantle cell lymphoma (MCL) is typically a very aggressive disease with poor outcomes, but some cases display an indolent behavior that might not necessitate treatment at diagnosis. To define molecular criteria that might permit recognition of such cases, we compared the clinicopathologic features, gene expression, and genomic profile of patients who had indolent or conventional disease (iMCL or...

Journal: :Blood 2009
Constantine S Tam Tait D Shanafelt William G Wierda Lynne V Abruzzo Daniel L Van Dyke Susan O'Brien Alessandra Ferrajoli Susan A Lerner Alice Lynn Neil E Kay Michael J Keating

To determine the clinical fate of patients with de novo deletion 17p13.1 (17p-) chronic lymphocytic leukemia (CLL), we retrospectively studied the outcome of 99 treatment-naive 17p- CLL patients from the M. D. Anderson Cancer Center (n = 64) and the Mayo Clinic (n = 35). Among 67 asymptomatic patients followed for progression, 53% developed CLL requiring treatment over 3 years. Patients who had...

Journal: :Current molecular medicine 2006
Alexey V Danilov Olga V Danilova Andreas K Klein Brigitte T Huber

Chronic lymphocytic leukemia (CLL) is unique among malignancies since it represents an accumulation of B-lymphocytes resistant to apoptosis. Several factors are thought to confer this unusual feature to a CLL B-cell. Misbalance between cytoplasmic pro-survival and pro-death molecules, such as Bcl-2, Mcl-1 and alike, appears to be one of the key factors defining B-cell longevity. Autocrine pathw...

2012
Maher Hanoun Lewin Eisele Masako Suzuki John M. Greally Andreas Hüttmann Semra Aydin René Scholtysik Ludger Klein-Hitpass Ulrich Dührsen Jan Dürig

Disruption of circadian rhythm is believed to play a critical role in cancer development. Cryptochrome 1 (CRY1) is a core component of the mammalian circadian clock and we have previously shown its deregulated expression in a subgroup of patients with chronic lymphocytic leukemia (CLL). Using real-time RT-PCR in a cohort of 76 CLL patients and 35 normal blood donors we now demonstrate that diff...

Journal: :Journal of immunology 1999
J Spencer M Dunn D K Dunn-Walters

Somatic hypermutation affects Ig genes during T-dependent B cell responses and is characterized by a high frequency of single base substitutions. Hypermutation is not a completely random process; a study of mutations in different systems has revealed the presence of sequence motifs that target mutation. In a recent analysis of the sequences surrounding individual mutated bases in out-of-frame h...

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