Search Results - (Author, Cooperation:P. J. Quesenberry)
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1W. Yang ; J. Wang ; D. C. Moore ; H. Liang ; M. Dooner ; Q. Wu ; R. Terek ; Q. Chen ; M. G. Ehrlich ; P. J. Quesenberry ; B. G. Neel
Nature Publishing Group (NPG)
Published 2013Staff ViewPublication Date: 2013-07-19Publisher: Nature Publishing Group (NPG)Print ISSN: 0028-0836Electronic ISSN: 1476-4687Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsKeywords: Animals ; Bone Neoplasms/drug therapy/genetics/*metabolism/*pathology ; Cartilage/metabolism/pathology ; Cathepsin K/deficiency/genetics/metabolism ; Cell Division ; Cell Lineage ; Chondromatosis/drug therapy/genetics/*metabolism/*pathology ; Exostoses, Multiple Hereditary/drug therapy/genetics/*metabolism/*pathology ; Fibroblast Growth Factors/metabolism ; Gene Deletion ; Gene Expression Regulation/drug effects ; Genes, Tumor Suppressor/physiology ; Hedgehog Proteins/antagonists & inhibitors/*metabolism ; MAP Kinase Signaling System ; Macrophages/metabolism ; Mesenchymal Stromal Cells/cytology/*metabolism ; Mice ; Mice, Knockout ; Mice, Transgenic ; Mitogen-Activated Protein Kinase Kinases/antagonists & inhibitors/metabolism ; Monocytes/metabolism ; Osteoclasts/metabolism ; Osteopetrosis/genetics/metabolism/pathology ; Parathyroid Hormone-Related Protein/metabolism ; Protein Tyrosine Phosphatase, Non-Receptor Type ; 11/*deficiency/genetics/metabolism ; *Signal Transduction/drug effectsPublished by: -
2Chorzalska, A., Morgan, J., Ahsan, N., Treaba, D. O., Olszewski, A. J., Petersen, M., Kingston, N., Cheng, Y., Lombardo, K., Schorl, C., Yu, X., Zini, R., Pacilli, A., Tepper, A., Coburn, J., Hryniewicz-Jankowska, A., Zhao, T. C., Oancea, E., Reagan, J. L., Liang, O., Kotula, L., Quesenberry, P. J., Gruppuso, P. A., Manfredini, R., Vannucchi, A. M., Dubielecka, P. M.
American Society of Hematology (ASH)
Published 2018Staff ViewPublication Date: 2018-11-09Publisher: American Society of Hematology (ASH)Print ISSN: 0006-4971Electronic ISSN: 1528-0020Topics: BiologyMedicineKeywords: Hematopoiesis and Stem Cells, Myeloid NeoplasiaPublished by: -
3Larcher, C. ; McQuain, C. ; Berger, C. ; Mitterer, M. ; Quesenberry, P. J. ; Huemer, H. P. ; Knecht, H.
Springer
Published 1997Staff ViewISSN: 1432-0584Keywords: Key words Lymphocytosis ; Epstein-Barr virus ; LMP-1 ; LMP-2A ; KindredSource: Springer Online Journal Archives 1860-2000Topics: MedicineNotes: Abstract Epstein-Barr virus (EBV) genomes have been detected in peripheral blood lymphocytes (PBL) of patients with persistent polyclonal B-cell lymphocytosis (PPBL). This is consistent with the hypothesis that latent EBV infection is involved in the pathogenesis of this disorder. Two EBV-encoded proteins expressed in viral latency are the latent membrane proteins 1 and 2A (LMP1 and LMP2A). We have studied the LMP1 oncogene and the LMP2A gene in a female patient with PPBL and her five siblings. A cell line derived from peripheral blood lymphocytes (PBL) of the patient was also analyzed. A distinct 69-base pair deletion was identified within the carboxy terminal NF-κB activation domain of the LMP1 oncogene in PBL of the patient and in the cell line, whereas none of the siblings harbored this deletion. The tyrosine-signaling motif and the HLA A2.1 epitope of the LMP2A gene were wild type in the patient and all siblings. The presence of a 69-base pair deletion variant of the LMP1 oncogene within the lymphocytes of a PPBL patient but absence of this deletion variant in the unaffected siblings suggests a direct implication of altered LMP1 oncoprotein-dependent function in the pathogenesis of PPBL.Type of Medium: Electronic ResourceURL: