نتایج جستجو برای: bcl11a

تعداد نتایج: 301  

2016
Gift Dineo Pule Shaheen Mowla Nicolas Novitzky Ambroise Wonkam

BACKGROUND The major therapeutic benefit of hydroxyurea, the only FDA-approved pharmacologic treatment for sickle cell disease (SCD), is directly related to fetal hemoglobin (HbF) production that leads to significant reduction of morbidity and mortality. However, potential adverse effects such as infertility, susceptibility to infections, or teratogenic effect have been subject of concerns. The...

2014
Anna Kwiecinska Koichi Ichimura Mattias Berglund Andrii Dinets Luqman Sulaiman V Peter Collins Catharina Larsson Anna Porwit Svetlana Bajalica Lagercrantz

To outline further genetic mechanisms of transformation from follicular lymphoma (FL) to diffuse large B-cell lymphoma (DLBCL), we have performed whole genome array-CGH in 81 tumors from 60 patients [29 de novo DLBCL (dnDLBCL), 31 transformed DLBCL (tDLBCL), and 21 antecedent FL]. In 15 patients, paired tumor samples (primary FL and a subsequent tDLBCL) were available, among which three possess...

2017
Hiroko Shimbo Takayuki Yokoi Noriko Aida Seiji Mizuno Hiroshi Suzumura Junichi Nagai Kazumi Ida Yumi Enomoto Chihiro Hatano Kenji Kurosawa

BACKGROUND Chromosome 2p15p16.1 deletion syndrome is a rare genetic disorder characterized by intellectual disability (ID), neurodevelopmental delay, language delay, growth retardation, microcephaly, structural brain abnormalities, and dysmorphic features. More than 30 patients with 2p15p16.1 microdeletion syndrome have been reported in the literature. METHODS Molecular analysis was performed...

2012
Sara B. Estruch Víctor Buzón Laia R. Carbó Lenka Schorova Jens Lüders Eva Estébanez-Perpiñá

Nuclear orphan receptor TLX (NR2E1) functions primarily as a transcriptional repressor and its pivotal role in brain development, glioblastoma, mental retardation and retinopathologies make it an attractive drug target. TLX is expressed in the neural stem cells (NSCs) of the subventricular zone and the hippocampus subgranular zone, regions with persistent neurogenesis in the adult brain, and fu...

Journal: :American journal of clinical pathology 2007
Beverly P Nelson Rohit Gupta Gordon W Dewald Sarah F Paternoster Steven T Rosen LoAnn C Peterson

Interphase fluorescence in situ hybridization (FISH) is an alternative to conventional chromosome analysis of chronic lymphocytic leukemia (CLL) cells. We analyzed 172 samples from 136 possible CLL cases using a FISH panel. Reflex testing with probes to CCND1, BCL2, BCL3, BCL11A, c-MYC, MALT1, and a break-apart immunoglobulin heavy chain (IGH) probe was done if more than 2 signals for 14q32 occ...

ژورنال: :پژوهش در پزشکی 0
زهرا شمسی zahra shamsi دانشگاه تربیت مدرس امیر آتشی amir atashi دانشگاه تربیت مدرس سعید آبرون saied abroun دانشگاه تربیت مدرس کاوه طاری kaveh tari دانشگاه تربیت مدرس مهشید اخوان رهنما mahshid akhavanrahnama دانشگاه تربیت مدرس آزاده انبارلو azadeh anbarlou دانشگاه تربیت مدرس مسعود سلیمانی

زمینه و هدف: القا هموگلوبین جنینی (hb-f) در بیماران مبتلا به هموگلوبینوپاتی علائم بیماری را بهبود می بخشد. عوامل متعددی می سابقه و هدف: القا هموگلوبین جنینی در بیماران مبتلا به هموگلوبینوپاتی علائم بیماری را بهبود می بخشد. عوامل متعددی می توانند بیان ژن گاما گلوبین را القاء نموده و سبب افزایش میزان هموگلوبین جنینی در بیماران شوند. از آنجایی که امروزه یکی از بهترین رویکردهای درمانی برای بیماران ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2008
Manuela Uda Renzo Galanello Serena Sanna Guillaume Lettre Vijay G Sankaran Weimin Chen Gianluca Usala Fabio Busonero Andrea Maschio Giuseppe Albai Maria Grazia Piras Natascia Sestu Sandra Lai Mariano Dei Antonella Mulas Laura Crisponi Silvia Naitza Isadora Asunis Manila Deiana Ramaiah Nagaraja Lucia Perseu Stefania Satta Maria Dolores Cipollina Carla Sollaino Paolo Moi Joel N Hirschhorn Stuart H Orkin Gonçalo R Abecasis David Schlessinger Antonio Cao

beta-Thalassemia and sickle cell disease both display a great deal of phenotypic heterogeneity, despite being generally thought of as simple Mendelian diseases. The reasons for this are not well understood, although the level of fetal hemoglobin (HbF) is one well characterized ameliorating factor in both of these conditions. To better understand the genetic basis of this heterogeneity, we carri...

Journal: :FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2014
Mark Roosjen Bradley McColl Betty Kao Linden J Gearing Marnie E Blewitt Jim Vadolas

The clinical symptoms of hemoglobin disorders such as β-thalassemia and sickle cell anemia are significantly ameliorated by the persistent expression of γ-globin after birth. This knowledge has driven the discovery of important regulators that silence γ-globin postnatally. Improved understanding of the γ- to β-globin switching mechanism holds the key to devising targeted therapies for β-hemoglo...

Journal: :Thalassemia Reports 2023

Genetic polymorphisms in Quantitative Trait Loci (QTL) genes such as BCL11A, HBS1L-MYB and KLF1 have been reported to influence fetal hemoglobin (HbF) levels. This prospective study was planned evaluate the role of genetic QTL determinant HbF levels beta thalassemia major patients. The carried out on 100 Blood samples were collected EDTA plain vials for biochemical molecular evaluation. genotyp...

2015
Amanda J. Grieco Henny H. Billett Nancy S. Green M. Catherine Driscoll Eric E. Bouhassira Andrew C. Wilber

The molecular mechanisms governing γ-globin expression in a subset of fetal hemoglobin (α2γ2: HbF) expressing red blood cells (F-cells) and the mechanisms underlying the variability of response to hydroxyurea induced γ-globin expression in the treatment of sickle cell disease are not completely understood. Here we analyzed intra-person clonal populations of basophilic erythroblasts (baso-Es) de...

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