Zobrazeno 1 - 10
of 14
pro vyhledávání: '"David M. Stockley"'
Autor:
Fiona M. Ross, Laura Chiecchio, GianPaolo Dagrada, Rebecca K.M. Protheroe, David M. Stockley, Christine J. Harrison, Nicholas C.P. Cross, Alex J. Szubert, Mark T. Drayson, Gareth J. Morgan
Publikováno v:
Haematologica, Vol 95, Iss 7 (2010)
A large series of plasma cell dyscrasias (n=2207) was examined for translocations which deregulate the MAF genes, t(14;20)(q32;q12) and t(14;16)(q32;q23), and their disease behavior was compared to a group characterized by the t(4;14)(p16;q32) where
Externí odkaz:
https://doaj.org/article/2d1f91276fde424a95346b51dd4a947b
Autor:
Laura Chiecchio, Gian Paolo Dagrada, Ashraf H. Ibrahim, Elizabet Dachs Cabanas, Rebecca K.M. Protheroe, David M. Stockley, Kim H. Orchard, Nicholas C.P. Cross, Christine J. Harrison, Fiona M. Ross
Publikováno v:
Haematologica, Vol 94, Iss 12 (2009)
Background Multiple myeloma, monoclonal gammopathy of undetermined significance and smoldering multiple myeloma harbor common chromosomal abnormalities but the prevalence and relative association of aberrations in these diagnostic groups remains cont
Externí odkaz:
https://doaj.org/article/e9b3497140394e78bac7e16c57923a48
Autor:
Laura Chiecchio, Gian Paolo Dagrada, Rebecca K.M. Protheroe, David M. Stockley, Alastair G. Smith, Kim H. Orchard, Nicholas C.P. Cross, Christine J. Harrison, Fiona M. Ross
Publikováno v:
Haematologica, Vol 94, Iss 7 (2009)
We report serial genetic studies on a young female patient initially diagnosed with asymptomatic smouldering myeloma who progressed to symptomatic myeloma 4.5 years after presentation. An unbalanced translocation, der(14)t(4;14)(p16;q32), was initial
Externí odkaz:
https://doaj.org/article/aeb9beceb0af4767ad4210a825afded8
Autor:
Faith E. Davies, David M. Stockley, Gianpaolo Dagrada, Zoe J. Konn, Fiona M. Ross, Brian A Walker, Paola E. Leone, David W. Johnson, Walter M Gregory, Laura Chiecchio, Matthew W Jenner, Rebecca K.M. Protheroe, Gareth J. Morgan, David Gonzalez, Kevin Boyd, Nicholas J. Dickens
Publikováno v:
Blood. 116:e56-e65
To obtain a comprehensive genomic profile of presenting multiple myeloma cases we performed high-resolution single nucleotide polymorphism mapping array analysis in 114 samples alongside 258 samples analyzed by U133 Plus 2.0 expression array (Affymet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c846ed1b0f8da4ebe36f8ed0752dd5d7
https://doi.org/10.1182/blood-2010-04-279596
https://doi.org/10.1182/blood-2010-04-279596
Autor:
Nicholas C.P. Cross, Rebecca K.M. Protheroe, Gianpaolo Dagrada, Laura Chiecchio, Fiona M. Ross, David M. Stockley, Mark T. Drayson, Alex J Szubert, Gareth J. Morgan, Christine J. Harrison
Publikováno v:
Haematologica. 95:1221-1225
A large series of plasma cell dyscrasias (n=2207) was examined for translocations which deregulate the MAF genes, t(14;20)(q32;q12) and t(14;16)(q32;q23), and their disease behavior was compared to a group characterized by the t(4;14)(p16;q32) where
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7a9ede6f1915c4adf491349ce11a343
https://doi.org/10.3324/haematol.2009.016329
https://doi.org/10.3324/haematol.2009.016329
Autor:
Christine J. Harrison, Nicholas C.P. Cross, Gianpaolo Dagrada, Kim Orchard, David M. Stockley, Fiona M. Ross, Laura Chiecchio, Rebecca K.M. Protheroe, Ashraf H. Ibrahim, Elizabet Dachs Cabanas
Publikováno v:
Haematologica. 94:1708-1713
Background Multiple myeloma, monoclonal gammopathy of undetermined significance and smoldering multiple myeloma harbor common chromosomal abnormalities but the prevalence and relative association of aberrations in these diagnostic groups remains cont
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::775653979a639f9964ee5b84dd815c28
https://doi.org/10.3324/haematol.2009.011064
https://doi.org/10.3324/haematol.2009.011064
Autor:
J. Anthony Child, Walter M Gregory, Alex J Szubert, William J. Tapper, Graham Jackson, Fiona M. Ross, Zoe J. Konn, Sue E. Bell, Laura Chiecchio, David M. Stockley, Gianpaolo Dagrada, Gareth J. Morgan
Publikováno v:
Journal of Clinical Oncology. 29:e37-e39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be9a8621438d60a37b413306ac282a7c
https://doi.org/10.1200/jco.2010.31.0516
https://doi.org/10.1200/jco.2010.31.0516
Autor:
Fiona M. Ross, Alastair G. Smith, Kim Orchard, Laura Chiecchio, David M. Stockley, Rebecca K.M. Protheroe, Christine J. Harrison, Nicholas C.P. Cross, Gianpaolo Dagrada
We report serial genetic studies on a young female patient initially diagnosed with asymptomatic smouldering myeloma who progressed to symptomatic myeloma 4.5 years after presentation. An unbalanced translocation, der(14)t(4;14)(p16;q32), was initial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cc98bb754dabd546a7f980c147f03cd
https://europepmc.org/articles/PMC2704316/
https://europepmc.org/articles/PMC2704316/
Autor:
Kim Orchard, Kan Luk Cheung, Gianpaolo Dagrada, Rebecca K.M. Protheroe, Christine J. Harrison, Nicholas C.P. Cross, Laura Chiecchio, Helen E. White, David M. Stockley, Mark R. Towsend, Fiona M. Ross
Publikováno v:
Genes, chromosomescancer. 48(7)
Plasma cell leukemia (PCL) is a rare form of monoclonal gammopathy, which can originate de novo or evolve from multiple myeloma (MM) as a terminal leukemic phase. Previous cytogenetic studies of PCL have reported the presence of complex karyotypes wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a86e1bcee85e00068200da6d0d19acc6
https://pubmed.ncbi.nlm.nih.gov/19396865
https://pubmed.ncbi.nlm.nih.gov/19396865
Autor:
Faith E. Davies, Gianpaolo Dagrada, Laura Chiecchio, Brian A Walker, Matthew W Jenner, Nicholas J. Dickens, Mathew Nightingale, Elisabet Dachs Cabanas, Nicholas C.P. Cross, Monica Else, Rebecca K.M. Protheroe, Paola E. Leone, Gareth J. Morgan, David Gonzalez, Fiona M. Ross, David W. Johnson, David M. Stockley
Publikováno v:
Blood. 110(9)
We performed fluorescent in situ hybridization (FISH) for 16q23 abnormalities in 861 patients with newly diagnosed multiple myeloma and identified deletion of 16q [del(16q)] in 19.5%. In 467 cases in which demographic and survival data were available
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::935705d2af4dc6666bc04609e2bdcccd
https://pubmed.ncbi.nlm.nih.gov/17609426
https://pubmed.ncbi.nlm.nih.gov/17609426