Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Edwin Haghnazari"'
Autor:
Amit Verma, Li Zhou, Tony A. Navas, Simrit Parmar, Perry Pahanish, Linda S. Higgins, Jing Ying Ma, Yin Xu, Myka Estes, Lubomir Sokol, Aaron N. Nguyen, A. List, Leonidas C. Platanias, Mani Mohindru, Edwin Haghnazari, Irene Kerr, Robert H. Collins
Publikováno v:
Blood. 108:4170-4177
The myelodysplastic syndromes (MDSs) are collections of heterogeneous hematologic diseases characterized by refractory cytopenias as a result of ineffective hematopoiesis. Development of effective treatments has been impeded by limited insights into
Autor:
Edwin Haghnazari, Wolf Dietrich Heyer
Publikováno v:
Nucleic Acids Research. 32:4257-4268
A DNA gap repair assay was used to determine the effect of mutations in the DNA damage checkpoint system on the efficiency and outcome (crossover/non-crossover) of recombinational DNA repair. In Saccharomyces cerevisiae gap repair is largely achieved
Autor:
Wolf Dietrich Heyer, Edwin Haghnazari
Publikováno v:
DNA Repair. 3:769-776
The DNA damage checkpoint pathway and the MAP kinase pathway respond to various forms of environmental as well as endogenous stresses through signal transduction mechanisms involving protein kinases. Both pathways are intertwined in mammalian cells,
Autor:
John R. Yates, Scott Anderson, Kristina Herzberg, Wolf Dietrich Heyer, Vladimir I. Bashkirov, W. Hayes McDonald, Elena V. Bashkirova, Edwin Haghnazari, Michael Rolfsmeier
DNA damage checkpoints coordinate the cellular response to genotoxic stress and arrest the cell cycle in response to DNA damage and replication fork stalling. Homologous recombination is a ubiquitous pathway for the repair of DNA double-stranded brea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d3f7b70f8401eebba9877b1cabbca92
https://europepmc.org/articles/PMC1636779/
https://europepmc.org/articles/PMC1636779/
Autor:
Wolf Dietrich Heyer, Vladimir I. Bashkirov, Edwin Haghnazari, Alexey S. Vlasenko, Kristina Herzberg
Rad55 protein is one of two Rad51 paralogs in the budding yeast Saccharomyces cerevisiae and forms a stable heterodimer with Rad57, the other Rad51 paralog. The Rad55-Rad57 heterodimer functions in homologous recombination during the assembly of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab015bae263e571e292a337f0a75e6f6
https://doi.org/10.1016/s0076-6879(05)09010-5
https://doi.org/10.1016/s0076-6879(05)09010-5
Autor:
Andy Protter, Sun J. Choi, Jing Y. Ma, Satyanarayana Medicherla, George F. Schreiner, Edwin Haghnazari, Linda S. Higgins, Tony A. Navas, G. David Roodman, Ann M. Kapoun, Mamatha Reddy, Diana Quon, Margaret Henson, Noriyoshi Kurihara, Gilbert O'Young, Debby Damm, Aaron N. Nguyen, Elizabeth G. Stebbins, Judy Anderson
Publikováno v:
Experimental cell research. 312(10)
The multiple myeloma (MM) bone marrow (BM) microenvironment plays a critical role in supporting tumor growth and survival as well as in promoting formation of osteolytic lesions. Recent results suggest that the p38 mitogen-activated protein kinase (M
Autor:
Leonidas C. Platanias, Linda S. Higgins, T. Cao, Yongkai Mo, Mani Mohindru, Li Zhou, Myka Estes, Tony Navas, Amit Verma, A. List, Perry Pahanish, Aaron N. Nguyen, Edwin Haghnazari
Publikováno v:
Leukemia & Lymphoma. 50:1554-1554
Autor:
Linda S. Higgins, Aaron N. Nguyen, Margaret Henson, Satya Medicherla, Edwin Haghnazari, Elizabeth G. Stebbins, Jing Y. Ma, Andy Protter, Tony A. Navas, Mamatha M. Reddy, Ann M. Kapoun, Gilbert O'Young
Publikováno v:
Blood. 104:1501-1501
Despite recent advances in the treatment of multiple myeloma (MM), this disease remains incurable. Accumulating evidence suggest that the bone marrow (BM) microenvironment of MM plays a critical role in tumor growth, survival, and drug resistance. A
Autor:
Aaron N. Nguyen, Tony A. Navas, Edwin Haghnazari, Elizabeth G. Stebbins, Alan F. List, Ruth Heaton, Linda S. Higgins, Jing Y. Ma
Publikováno v:
Blood. 104:3424-3424
Progress in the development of more effective therapeutics for myelodysplastic syndrome (MDS) has been limited by the lack of targets critical to the pathobiology of the disease. Ineffective hematopoiesis in MDS is characterized by accelerated prolif