Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Amanda P. Cline"'
Autor:
Robert I. Liem, Nancy E. Seidel, David M. Bodine, Laurie A. Steiner, Patrick G. Gallagher, Ashley N. Owen, Lisa Garrett, Amanda P. Cline
Publikováno v:
Journal of Clinical Investigation. 120:4453-4465
Defects of the ankyrin-1 gene are the most common cause in humans of hereditary spherocytosis, an inherited anemia that affects patients of all ethnic groups. In some kindreds, linked -108/-153 nucleotide substitutions have been found in the upstream
Autor:
Philip S. Low, Erin M. Parry, Lisa Garrett-Beal, Amanda P. Cline, Nicholas O. Markham, Patrick G. Gallagher, Marko Stefanovic, David M. Bodine
Publikováno v:
Proceedings of the National Academy of Sciences. 104:13972-13977
The best-studied cytoskeletal system is the inner surface of the erythrocyte membrane, which provides an erythrocyte with the structural support needed to be stable yet flexible as it passes through the circulation. Current structural models predict
Autor:
Denise E. Sabatino, Patrick G. Gallagher, Stacie M. Anderson, David M. Bodine, Amanda P. Cline, Nancy E. Seidel
Publikováno v:
Annals of the New York Academy of Sciences. 938:246-261
Gene therapy for patients with hemoglobin disorders such has been hampered by the inability of retrovirus vectors to transfer globin genes and the locus control region (LCR) into hematopoietic stem cells without rearrangement. In addition, the expres
Autor:
Nancy E. Seidel, David J. Curtis, David M. Bodine, Michael J. Nemeth, Martha Kirby, Amanda P. Cline, Lisa Garrett-Beal
Publikováno v:
Blood. 102:1298-1306
Hmgb3 is a member of a family of chromatin-binding proteins that can alter DNA structure to facilitate transcription factor binding. We identified the Hmgb3 cDNA in a subtractive hybridization screen for transcripts that are preferentially expressed
Autor:
Douglas M. Nilson, Amanda P. Cline, David M. Bodine, Patrick G. Gallagher, Clara Wong, Lisa Garrett, Daniela S. Basseres, Denise E. Sabatino
Publikováno v:
Journal of Biological Chemistry. 276:41683-41689
Ankyrin defects are the most common cause of hereditary spherocytosis (HS). In several kindreds with recessive, ankyrin-deficient HS, mutations have been identified in the ankyrin promoter that have been proposed to decrease ankyrin synthesis. We ana
Publikováno v:
Annals of the New York Academy of Sciences. 872:243-255
We have begun to isolate gene sequences that are specifically expressed in hematopoietic stem cells (HSCs). There are at least three fundamental requirements for the isolation of HSC-specific transcripts. First, highly enriched populations of HSCs, a
Autor:
Denise E. Sabatino, Amanda P. Cline, Bernard G. Forget, Patrick G. Gallagher, David M. Bodine, Marc Romana, Lisa Garrett
Publikováno v:
Journal of Biological Chemistry. 274:6062-6073
beta-Spectrin is an erythrocyte membrane protein that is defective in many patients with abnormalities of red blood cell shape including hereditary spherocytosis and elliptocytosis. It is expressed not only in erythroid tissues but also in muscle and
Autor:
Nancy E. Seidel, Sandra Doren, David M. Bodine, Stephanie L. Sellers, Amanda P. Cline, Mark E. Metzger, Brian A. Agricola, Cynthia E. Dunbar, Robert E. Donahue
Publikováno v:
Proceedings of the National Academy of Sciences. 93:11871-11876
In previous studies we showed that 5 days of treatment with granulocyte colony-stimulating factor (G-CSF) and stem cell factor (SCF) mobilized murine repopulating cells to the peripheral blood (PB) and that these cells could be efficiently transduced
Autor:
Amanda P. Cline, Laurie J. Girard, Donald Orlic, David M. Bodine, Stacie M. Anderson, Craig T. Jordan
Publikováno v:
Proceedings of the National Academy of Sciences. 93:11097-11102
The low level of amphotropic retrovirus-mediated gene transfer into human hematopoietic stem cells (HSC) has been a major impediment to gene therapy for hematopoietic diseases. In the present study, we have examined amphotropic retrovirus receptor (a
Autor:
Clara Wong, Emily D. Rout, Jolinta Y. Lin, David M. Bodine, Laurie A. Steiner, Patrick G. Gallagher, Lisa Garrett, Ashley O. Yocum, Nancy E. Seidel, Amanda P. Cline
Publikováno v:
Blood. 120(17)
The human ankyrin-1 gene (ANK1) contains 3 tissue-specific alternative promoters. We have shown previously that the erythroid-specific ankyrin 1 (ANK1E) core promoter contains a 5′ DNase I hypersensitive site (HS) with barrier insulator function th