5 results match your criteria: "The U.T.M.D. Anderson Cancer Center[Affiliation]"
EMBO J
July 2010
Department of Genetics Unit 1010, The U.T.M.D. Anderson Cancer Center, Houston, TX, USA.
Progressive telomere attrition or deficiency of the protective shelterin complex elicits a DNA damage response as a result of a cell's inability to distinguish dysfunctional telomeric ends from DNA double-strand breaks. SNMIB/Apollo is a shelterin-associated protein and a member of the SMN1/PSO2 nuclease family that localizes to telomeres through its interaction with TRF2. Here, we generated SNMIB/Apollo knockout mouse embryo fibroblasts (MEFs) to probe the function of SNMIB/Apollo at mammalian telomeres.
View Article and Find Full Text PDFHaematologica
February 2008
The U.T. M.D. Anderson Cancer Center, Department of Stem Cell Transplantation and Cellular Therapy 1515 Holcombe Boulevard, Unit 423, Houston, TX 77030 USA.
Background: The role of reduced-intensity conditioning allogeneic stem cell transplantation in relapsed/refractory Hodgkin's lymphoma remains poorly defined. We here present an update of our single-center experience with fludarabine-melphalan as a preparative regimen.
Design And Methods: Fifty-eight patients with relapsed/refractory Hodgkin's lymphoma underwent RIC and allogeneic stem cell transplantation from a matched related donor (MRD; n=25) or a matched unrelated donor (MUD; n=33).
The purpose of this study was to determine if the first-pass of FDG can be used to measure regional blood flow in tumors in the absence of perfusion imaging with a known blood flow tracer.PET scans were obtained in patients being evaluated for tumor perfusion and metabolism in a Phase I dose escalating protocol for Endostatin, a novel antiangiogenic agent. A two minutes perfusion scan was done with a bolus injection of 60 mCi of O-15 labeled water followed by a 10 mCi dose of FDG and four sequential scans consisting of a first pass two minutes scan and three 15 minutes scans.
View Article and Find Full Text PDFRadiat Res
April 2000
Department of Experimental Radiation Oncology and Neurosurgery, The U.T.M.D Anderson Cancer Center, Houston, Texas 77030, USA.
Radiation continues to be a major treatment modality for tumors located within and close to the central nervous system (CNS). Consequently, alleviating or protecting against radiation-induced CNS injury would be of benefit in cancer treatment. However, the rational development of such interventional strategies will depend on a more complete understand-ing of the mechanisms responsible for the development of this form of normal tissue injury.
View Article and Find Full Text PDFCurr Biol
January 1992
Department of Biochemistry and Molecular Biology, The U.T. M.D. Anderson Cancer Center at Houston, 1515 Holcombe Boulevard, Box 117, Houston, Texas 77030, USA.