Search Results - "Banas, R A"

Wave-guided optical waveguides by Palima, D, Bañas, A R, Vizsnyiczai, G, Kelemen, L, Ormos, P, Glückstad, J

“…This work primarily aims to fabricate and use two photon polymerization (2PP) microstructures capable of being optically manipulated into any arbitrary…”
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Amnion‐Derived Multipotent Progenitor Cells Support Allograft Tolerance Induction by Anam, K., Lazdun, Y., Davis, P. M., Banas, R. A., Elster, E. A., Davis, T. A.

“…Donor‐specific immunological tolerance using high doses of bone marrow cells (BMCs) has been demonstrated in mixed chimerism‐based tolerance induction…”
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DNA microarray technology for neonatal screening by Dobrowolski, SF, Banas, RA, Naylor, EW, Powdrill, T, Thakkar, D

“…Modern molecular biology, owing much to the Human Genome Initiative, has elucidated many of the genetic mechanisms underlying heritable metabolic disease…”
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Effect of human amnion-derived multipotent progenitor cells on hematopoietic recovery after total body irradiation in C57BL/6 mice by Du, Y, Banas, R A, McCart, E A, George, J, Oakley, K, Han, Y, Landauer, M R, Day, R M

“…Background: The hematopoietic system is sensitive to the adverse effects of ionizing radiation. Cellular therapies utilizing mesenchymal stem cells or vascular…”
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Immunogenicity and immunomodulatory effects of amnion-derived multipotent progenitor cells by Banas, Richard Allan, Trumpower, Catherine, Bentlejewski, Carol, Marshall, Vivienne, Sing, George, Zeevi, Adriana

“…Summary This is the first study on the immunologic properties of a clinically relevant population of cells derived from the amnion of human placenta. Unlike…”
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Real time PCR assays to detect common mutations in the biotinidase gene and application of mutational analysis to newborn screening for biotinidase deficiency by Dobrowolski, Steven F, Angeletti, Janine, Banas, Richard A, Naylor, Edwin W

“…Biotinidase deficiency is an autosomal recessive disorder of biotin metabolism caused by defects in the biotinidase gene. Symptoms of biotinidase deficiency…”
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Analysis of Common Mutations in the Galactose-1-Phosphate Uridyl Transferase Gene: New Assays to Increase the Sensitivity and Specificity of Newborn Screening for Galactosemia by Dobrowolski, Steven F, Banas, Richard A, Suzow, Joseph G, Berkley, Michelle, Naylor, Edwin W

“…Classical galactosemia is a genetic disease caused by mutations in the galactose-1-phosphate uridyl transferase (GALT) gene. Prospective newborn screening for…”
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TGF-beta 1 pretreatment impairs the allostimulatory function of human bone marrow-derived antigen-presenting cells for both naive and primed T cells by Bonham, C A, Lu, L, Banas, R A, Fontes, P, Rao, A S, Starzl, T E, Zeevi, A, Thomson, A W

“…Transforming growth factor-beta (TGF-beta) exhibits strong antiproliferative effects upon lymphocytes and inhibits many of the effector functions of activated…”
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