Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Vicky Kartsogiannis"'
Autor:
Phillip Wong, Peter G. Kerr, Vicky Kartsogiannis, Matthew T. Gillespie, Donald K. Bowden, Eldho Paul, James C.G. Doery, Boyd Josef Gimnicher Strauss, Peter J. Fuller, Frances Milat
Publikováno v:
Journal of Bone and Mineral Research. 29:2468-2473
Thalassemia is an inherited disorder of alpha or beta globin chain synthesis leading to ineffective erythropoiesis requiring chronic transfusion therapy in its most severe form. This leads to iron overload, marrow expansion, and hormonal complication
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bbffa19ae549726f038bd64c341b157
https://doi.org/10.1002/jbmr.2266
https://doi.org/10.1002/jbmr.2266
Autor:
Boyd Josef Gimnicher Strauss, Phillip Wong, Peter J. Fuller, Matthew T. Gillespie, Donald K. Bowden, Vicky Kartsogiannis, Francis Milat
Publikováno v:
Osteoporosis International. 24:1965-1971
Thalassemia bone disease is well described, but the prevalence of nephrolithiasis has not been characterized. The association between nephrolithiasis, reduced bone density, and increased fractures has been demonstrated through this retrospective stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a001627afd835835ed41cea7655e2ba
https://doi.org/10.1007/s00198-012-2260-y
https://doi.org/10.1007/s00198-012-2260-y
Publikováno v:
Journal of Bone and Mineral Research. 13:1640-1643
Multiple myeloma frequently leads to complications, such as osteolytic lesions, hypercalcemia, and pathological fractures. Increased bone resorption in myeloma is due to osteoclast activation. The nature of the osteoclast activator(s) remains unclear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d721cc8c5678cb67ecfd950187b813d
https://doi.org/10.1359/jbmr.1998.13.10.1640
https://doi.org/10.1359/jbmr.1998.13.10.1640
Autor:
Vicky Kartsogiannis, Emma C. Walker, Matthew T. Gillespie, Mark J. Smyth, Morgan E. Wallace, Chi Ly, Hasnawati Saleh, Hong Zhou, Natalie A. Sims, Ingrid J Poulton, Mirijana Cipetic, T. John Martin, Kong Wah Ng, Narelle E. McGregor, J.M.W. Quinn
Publikováno v:
Journal of Biological Chemistry. 283:30850-30860
Osteoclast inhibitory lectin (OCIL or clrb) is a member of the natural killer cell C-type lectins that have a described role mostly in autoimmune cell function. OCIL was originally identified as an osteoblast-derived inhibitor of osteoclast formation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2f759c2b9ba727450302053cea5b82f
https://doi.org/10.1074/jbc.m801761200
https://doi.org/10.1074/jbc.m801761200
Autor:
Kong Wah Ng, S Bouralexis, Jessica L. Vieusseux, John T. Price, Chi Ly, Vicky Kartsogiannis, T. John Martin, Natalie A. Sims, Mirijana Cipetic, Matthew T. Gillespie, Akira Nakamura, Hong Zhou, Hasnawati Saleh, Julian M.W. Quinn
Publikováno v:
Bone. 40:305-315
Osteoclast inhibitory lectin (OCIL) is a type II C-type lectin and binds NK cell-associated receptor Nkrp1d and sulfated glycosaminoglycans. OCIL is expressed by several cell types found in bone and inhibits osteoclast differentiation. To determine w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfbb1d31bbfc25b65b1bdd11c9feaa32
https://doi.org/10.1016/j.bone.2006.09.001
https://doi.org/10.1016/j.bone.2006.09.001
Autor:
Qinzhang Zhu, Matthew T. Gillespie, Colin G. Brooks, Peter Chen, Ahmad Bakur Mahmoud, Midhun J. Thomas, Mir Munir A. Rahim, James R. Carlyle, Vicky Kartsogiannis, Andrew P. Makrigiannis, Amelia Mottashed
NKR-P1B is a homodimeric type II transmembrane C-type lectinlike receptor that inhibits natural killer (NK) cell function upon interaction with its cognate C-type lectin-related ligand, Clr-b. The NKR-P1B:Clr-b interaction represents a major histocom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c901a40c2074b86bf64142a96bd48076
https://europepmc.org/articles/PMC4383798/
https://europepmc.org/articles/PMC4383798/
Autor:
Jaehun Ma, Vicky Kartsogiannis, Oscar A. Aguilar, Andrew P. Makrigiannis, David S.J. Allan, Megan M. Tu, Peter Chen, Jason H. Fine, Miho Tanaka, Matthew T. Gillespie, Andrew Wight, Mir Munir A. Rahim, James R. Carlyle, Christina L. Kirkham
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 194(6)
MHC-I–specific receptors play a vital role in NK cell–mediated “missing-self” recognition, which contributes to NK cell activation. In contrast, MHC-independent NK recognition mechanisms are less well characterized. In this study, we investig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fb1a465fbed3e89ff106e782cac9eb7
https://pubmed.ncbi.nlm.nih.gov/25681346
https://pubmed.ncbi.nlm.nih.gov/25681346
Autor:
Christine Gange, Matthew T. Gillespie, Vicky Kartsogiannis, Julian M.W. Quinn, Kong Wah Ng, Hong Zhou
Publikováno v:
Journal of Biological Chemistry. 279:29043-29049
Osteoclast inhibitory lectin (OCIL) is a membrane-bound C-type lectin that blocks osteoclast differentiation and, via binding to its cognate receptor NKRP1D, inhibits natural killer cell-mediated cytotoxicity. OCIL is a member of the natural killer c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fefb38b33dc27b0551e46b8fa6128d26
https://doi.org/10.1074/jbc.m312518200
https://doi.org/10.1074/jbc.m312518200
Autor:
Hong Zhou, Christine Gange, Matthew T. Gillespie, Julian M.W. Quinn, Chi Ly, J Elliott, Kong Wah Ng, Vicky Kartsogiannis
Publikováno v:
Journal of Biological Chemistry. 277:48808-48815
We have identified two novel type II membrane-bound C-lectins, designated mOCILrP1 and mOCILrP2, of 218 and 217 amino acids, respectively, that share substantial identity with the murine osteoclast inhibitory lectin (OCIL). The extracellular domains
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1108c77e1ed766be8f889f74170bd6e
https://doi.org/10.1074/jbc.m209059200
https://doi.org/10.1074/jbc.m209059200
Autor:
Phillip, Wong, Peter J, Fuller, Matthew T, Gillespie, Vicky, Kartsogiannis, Peter G, Kerr, James Cg, Doery, Eldho, Paul, Donald K, Bowden, Boyd J, Strauss, Frances, Milat
Publikováno v:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 29(11)
Thalassemia is an inherited disorder of alpha or beta globin chain synthesis leading to ineffective erythropoiesis requiring chronic transfusion therapy in its most severe form. This leads to iron overload, marrow expansion, and hormonal complication
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::96a9070a8ccffcd32c6fee725a84620f
https://pubmed.ncbi.nlm.nih.gov/24764138
https://pubmed.ncbi.nlm.nih.gov/24764138