Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Julie A. Lekstrom-Himes"'
Autor:
Angela Yen, Damiano Rondelli, la Fuente Josu de, Amanda M. Li, Jennifer Domm, Montalembert Mariane de, Tony W. Ho, Donna A. Wall, Brenda K. Eustace, Juergen Foell, Sujit Sheth, Haydar Frangoul, Rupert Handgretinger, Akshay Sharma, Sandeep Soni, Antonis Kattamis, Andrew Kernytsky, Franco Locatelli, Stephan A. Grupp, M. Domenica Cappellini, Julie A. Lekstrom-Himes, Selim Corbacioglu, David Altshuler, Markus Y. Mapara, Yi-Shan Chen, Martin H. Steinberg
Transfusion-dependent β-thalassemia (TDT) and sickle cell disease (SCD) are severe monogenic diseases with severe and potentially life-threatening manifestations. BCL11A is a transcription factor that represses γ-globin expression and fetal hemoglo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::294f2984b8848005c8f160412c9178cd
https://hdl.handle.net/10807/228473
https://hdl.handle.net/10807/228473
Autor:
Mary Louise Morris, Julie A. Lekstrom-Himes, Arthur M. Krieg, Heather L. Davis, Philip Leese, Chantal Laframboise, Alain Vicari, Mohammed J Al-Adhami, Susan M. Efler, Tess Schmalbach
Publikováno v:
Antiviral Therapy. 12:741-751
CPG 10101 (ACTILON™) is a novel potent and selective unmethylated cytidine-phosphate-guanosine (CpG)-containing oligodeoxynucleotide agonist of Toll-like receptor 9 (TLR9) being developed for the treatment of chronic infections such as HCV.Objectiv
Autor:
Vincent Idone, Theresa Zibello, Arati Khanna-Gupta, Julie A. Lekstrom-Himes, Hong Sun, Nancy Berliner
Publikováno v:
Experimental Hematology. 33:42-52
Objective Human neutrophil collagenase (HNC) is one of several secondary granule proteins (SGP) expressed late in the myeloid maturation pathway. SGPs are encoded by unlinked and functionally diverse genes that are hypothesized to be coordinately reg
Autor:
Pu Zhang, Koichi Akashi, Hirokazu Shigematsu, Elena Levantini, Julie A. Lekstrom-Himes, Hiromi Iwasaki, Daniel G. Tenen, Junko Iwasaki-Arai, Bronwyn M. Owens, Tajhal Dayaram, Maris Fenyus, Claudia S. Huettner
Publikováno v:
Immunity. 21:853-863
The transcription factor C/EBP alpha is required for granulopoiesis and frequently disrupted in human acute myeloid leukemia (AML). Here, we show disruption of C/EBP alpha blocks the transition from the common myeloid to the granulocyte/monocyte prog
Autor:
Monika J. Stankiewicz, Qing Xi, Jonathan E. Schmitz, Yang Liu, Julie A. Lekstrom-Himes, Steven J. Ackerman, Jian Du
Publikováno v:
Journal of Biological Chemistry. 277:43481-43494
GATA-1 and the ets factor PU.1 have been reported to functionally antagonize one another in the regulation of erythroid versus myeloid gene transcription and development. The CCAAT enhancer binding protein epsilon (C/EBPepsilon) is expressed as multi
Publikováno v:
Journal of Cellular Biochemistry. 80:606-616
The genomic locus of the mouse S100A9 (MRP14) gene, a myeloid expressed gene belonging to the S100 family, is split in three exons and two introns. Insertions of B1 like and LINE elements as well as several sequence repeat structures are scattered ov
Autor:
Julie A. Lekstrom-Himes, Matthew Godleski, Lesley Pesnicak, Sharon E. Straus, Rona A. LeBlanc
Publikováno v:
Journal of Virology. 74:6680-6683
Murine models of gamma interferon (IFN-γ) deficiency demonstrate the role of this cytokine in attenuating acute herpes simplex virus (HSV) disease; however, the effect of IFN-γ on the establishment and maintenance of neuronal latency and viral reac
Publikováno v:
Hematology. 2000:303-318
Recent advances in our understanding of the molecular basis of inherited neutrophil disorders and complementary studies in transgenic mouse models have provided new insights into the normal mechanisms regulating myelopoiesis and the functional respon
Publikováno v:
Hematology. 2000:303-318
Recent advances in our understanding of the molecular basis of inherited neutrophil disorders and complementary studies in transgenic mouse models have provided new insights into the normal mechanisms regulating myelopoiesis and the functional respon
Publikováno v:
The Journal of Experimental Medicine
Neutrophil-specific granule deficiency (SGD) is a rare disorder characterized by recurrent pyogenic infections, defective neutrophil chemotaxis and bactericidal activity, and lack of neutrophil secondary granule proteins. CCAAT/enhancer binding prote