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Multipaint FISH: a rapid and reliable way to define cryptic and complex abnormalities.
Published in:
Clinical Genetics, 1999, v. 56, n. 3, p. 192, doi. 10.1034/j.1399-0004.1999.560303.x
By:
- Joyce, Christine A;
- Ross, Fiona M;
- Dennis, Nicholas R;
- Wyre, Nicholas D;
- Barber, John Ck
Publication type:
Article
Adenosine monophosphate as a mediator of ATP effects at P1 purinoceptors.
Published in:
British Journal of Pharmacology, 1998, v. 124, n. 4, p. 818, doi. 10.1038/sj.bjp.0701890
By:
- Ross, Fiona M;
- Brodie, Martin J;
- Stone, Trevor W
Publication type:
Article
RESEARCH PAPER The context, measures and outcomes of psychosocial care interventions in long-term health care for older people.
Published in:
International Journal of Nursing Practice (Wiley-Blackwell), 2004, v. 10, n. 1, p. 39, doi. 10.1111/j.1440-172X.2003.00456.x
By:
- Mackenzie, Ann E;
- Lee, Diana TF;
- Ross, Fiona M
Publication type:
Article
Standardized assessment for elderly people (SAFE)--a feasibility study in district nursing.
Published in:
Journal of Clinical Nursing (Wiley-Blackwell), 1995, v. 4, n. 5, p. 303, doi. 10.1111/j.1365-2702.1995.tb00028.x
By:
- Ross, Fiona M.;
- Bower, Peter
Publication type:
Article
Osteonecrosis of the jaw and renal safety in patients with newly diagnosed multiple myeloma: Medical Research Council Myeloma IX Study results.
Published in:
British Journal of Haematology, 2014, v. 166, n. 1, p. 109, doi. 10.1111/bjh.12861
By:
- Jackson, Graham H.;
- Morgan, Gareth J.;
- Davies, Faith E.;
- Wu, Ping;
- Gregory, Walter M.;
- Bell, Sue E.;
- Szubert, Alexander J.;
- Navarro Coy, Nuria;
- Drayson, Mark T.;
- Owen, Roger G.;
- Feyler, Sylvia;
- Ashcroft, Andrew J.;
- Ross, Fiona M.;
- Byrne, Jennifer;
- Roddie, Huw;
- Rudin, Claudius;
- Boyd, Kevin D.;
- Osborne, Wendy L.;
- Cook, Gordon;
- Child, J. Anthony
Publication type:
Article
Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.
Published in:
Nature Genetics, 2012, v. 44, n. 1, p. 58, doi. 10.1038/ng.993
By:
- Broderick, Peter;
- Chubb, Daniel;
- Johnson, David C;
- Weinhold, Niels;
- Försti, Asta;
- Lloyd, Amy;
- Olver, Bianca;
- Ma, Yussanne P;
- Dobbins, Sara E;
- Walker, Brian A;
- Davies, Faith E;
- Gregory, Walter A;
- Child, J Anthony;
- Ross, Fiona M;
- Jackson, Graham H;
- Neben, Kai;
- Jauch, Anna;
- Hoffmann, Per;
- Mühleisen, Thomas W;
- Nöthen, Markus M
Publication type:
Article
Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders.
Published in:
Nature Genetics, 2010, v. 42, n. 8, p. 722, doi. 10.1038/ng.621
By:
- Ernst, Thomas;
- Chase, Andrew J.;
- Score, Joannah;
- Hidalgo-Curtis, Claire E.;
- Bryant, Catherine;
- Jones, Amy V.;
- Waghorn, Katherine;
- Zoi, Katerina;
- Ross, Fiona M;
- Reiter, Andreas;
- Hochhaus, Andreas;
- Drexler, Hans G.;
- Duncombe, Andrew;
- Cervantes, Francisco;
- Oscier, David;
- Boultwood, Jacqueline;
- Grand, Francis H.;
- Cross, Nicholas C. P.
Publication type:
Article
Permutation characters.
Published in:
Journal of the Australian Mathematical Society, 1972, v. 13, n. 1, p. 76, doi. 10.1017/S1446788700010624
By:
- Ross, Fiona M.
Publication type:
Article
A molecular diagnostic approach able to detect the recurrent genetic prognostic factors typical of presenting myeloma.
Published in:
Genes, Chromosomes & Cancer, 2015, v. 54, n. 2, p. 91, doi. 10.1002/gcc.22222
By:
- Boyle, Eileen M.;
- Proszek, Paula Z.;
- Kaiser, Martin F.;
- Begum, Dil;
- Dahir, Nasrin;
- Savola, Suvi;
- Wardell, Christopher P.;
- Leleu, Xavier;
- Ross, Fiona M.;
- Chiecchio, Laura;
- Cook, Gordon;
- Drayson, Mark T.;
- Owen, Richard G.;
- Ashcroft, John M.;
- Jackson, Graham H.;
- Anthony Child, James;
- Davies, Faith E.;
- Walker, Brian A.;
- Morgan, Gareth J.
Publication type:
Article
Identification of a novel t(7;14) translocation in multiple myeloma resulting in overexpression of EGFR.
Published in:
Genes, Chromosomes & Cancer, 2013, v. 52, n. 9, p. 817, doi. 10.1002/gcc.22077
By:
- Walker, Brian A.;
- Wardell, Christopher P.;
- Ross, Fiona M.;
- Morgan, Gareth J.
Publication type:
Article
The clinical impact and molecular biology of del(17p) in multiple myeloma treated with conventional or thalidomide-based therapy.
Published in:
Genes, Chromosomes & Cancer, 2011, v. 50, n. 10, p. 765, doi. 10.1002/gcc.20899
By:
- Boyd, Kevin D.;
- Ross, Fiona M.;
- Tapper, William J.;
- Chiecchio, Laura;
- Dagrada, GianPaolo;
- Konn, Zoe J.;
- Gonzalez, David;
- Walker, Brian A.;
- Hockley, Sarah L.;
- Wardell, Christopher P.;
- Gregory, Walter M.;
- Anthony Child, J.;
- Jackson, Graham H.;
- Davies, Faith E.;
- Morgan, Gareth J.
Publication type:
Article
Frequent upregulation of MYC in plasma cell leukemia.
Published in:
Genes, Chromosomes & Cancer, 2009, v. 48, n. 7, p. 624, doi. 10.1002/gcc.20670
By:
- Chiecchio, Laura;
- Dagrada, Gian Paolo;
- White, Helen E.;
- Towsend, Mark R.;
- Protheroe, Rebecca K. M.;
- Cheung, Kan Luk;
- Stockley, David M.;
- Orchard, Kim H.;
- Cross, Nicholas C. P.;
- Harrison, Christine J.;
- Ross, Fiona M.
Publication type:
Article
The complex genomic profile of ETV6-RUNX1 positive acute lymphoblastic leukemia highlights a recurrent deletion of TBL1XR1.
Published in:
Genes, Chromosomes & Cancer, 2008, v. 47, n. 12, p. 1118, doi. 10.1002/gcc.20613
By:
- Parker, Helen;
- An, Qian;
- Barber, Kerry;
- Case, Marian;
- Davies, Teresa;
- Konn, Zoë;
- Stewart, Adam;
- Wright, Sarah;
- Griffiths, Mike;
- Ross, Fiona M.;
- Moorman, Anthony V.;
- Hall, Andy G.;
- Irving, Julie A.;
- Harrison, Christine J.;
- Strefford, Jon C.
Publication type:
Article
Comparative expressed sequence hybridization studies of high‐hyperdiploid childhood acute lymphoblastic leukemia.
Published in:
Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 191
By:
- Alicja M. Gruszka‐Westwood;
- Sharon W. Horsley;
- Angel Martinez‐Ramirez;
- Christine J. Harrison;
- Helena Kempski;
- Anthony V. Moorman;
- Fiona M. Ross;
- Michael Griffiths;
- Mel F. Greaves;
- Lyndal Kearney
Publication type:
Article
Identification of a novel gene, FGFR1OP2, fused to FGFR1 in 8p11 myeloproliferative syndrome.
Published in:
Genes, Chromosomes & Cancer, 2004, v. 40, n. 1, p. 78, doi. 10.1002/gcc.20023
By:
- Effie K. Grand;
- Francis H. Grand;
- Andrew J. Chase;
- Fiona M. Ross;
- Martin M Corcoran;
- David G. Oscier
Publication type:
Article
Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia.
Published in:
Nature, 2014, v. 508, n. 7494, p. 98, doi. 10.1038/nature13115
By:
- Li, Yilong;
- Schwab, Claire;
- Ryan, Sarra L.;
- Papaemmanuil, Elli;
- Robinson, Hazel M.;
- Jacobs, Patricia;
- Moorman, Anthony V.;
- Dyer, Sara;
- Borrow, Julian;
- Griffiths, Mike;
- Heerema, Nyla A.;
- Carroll, Andrew J.;
- Talley, Polly;
- Bown, Nick;
- Telford, Nick;
- Ross, Fiona M.;
- Gaunt, Lorraine;
- McNally, Richard J. Q.;
- Young, Bryan D.;
- Sinclair, Paul
Publication type:
Article
Response and biological subtype of myeloma are independent prognostic factors and combine to define outcome after high-dose therapy.
Published in:
British Journal of Haematology, 2013, v. 161, n. 2, p. 291, doi. 10.1111/bjh.12218
By:
- Brioli, Annamaria;
- Boyd, Kevin D.;
- Kaiser, Martin F.;
- Pawlyn, Charlotte;
- Wu, Ping;
- Gregory, Walter M.;
- Owen, Roger;
- Ross, Fiona M.;
- Jackson, Graham H.;
- Cavo, Michele;
- Davies, Faith E.;
- Morgan, Gareth J.
Publication type:
Article
Methylation of tumour suppressor gene promoters in the presence and absence of transcriptional silencing in high hyperdiploid acute lymphoblastic leukaemia.
Published in:
British Journal of Haematology, 2009, v. 144, n. 6, p. 838, doi. 10.1111/j.1365-2141.2008.07523.x
By:
- Paulsson, Kajsa;
- Qian An;
- Moorman, Anthony V.;
- Parker, Helen;
- Molloy, Gael;
- Davies, Teresa;
- Griffiths, Mike;
- Ross, Fiona M.;
- Irving, Julie;
- Harrison, Christine J.;
- Young, Bryan D.;
- Strefford, Jon C.
Publication type:
Article
IgM myeloma: a rare entity characterized by a CD20−CD56−CD117− immunophenotype and the t(11;14).
Published in:
British Journal of Haematology, 2008, v. 140, n. 5, p. 547, doi. 10.1111/j.1365-2141.2007.06969.x
By:
- Feyler, Sylvia;
- O'Connor, Sheila J. M.;
- Rawstron, Andy C.;
- Subash, Chezhian;
- Ross, Fiona M.;
- Pratt, Guy;
- Drayson, Mark T.;
- Ashcroft, John;
- Cook, Gordon;
- Owen, Roger G.
Publication type:
Article
Der(6)t(1;6)(q21–23;p21.3): a specific cytogenetic abnormality in myelofibrosis with myeloid metaplasia.
Published in:
British Journal of Haematology, 2005, v. 130, n. 2, p. 229, doi. 10.1111/j.1365-2141.2005.05593.x
By:
- Dingli, David;
- Grand, Francis H.;
- Mahaffey, Victor;
- Spurbeck, Jack;
- Ross, Fiona M.;
- Watmore, Ann E.;
- Reilly, John T.;
- Cross, Nicholas C. P.;
- Dewald, Gordon W.;
- Tefferi, Ayalew
Publication type:
Article
Interphase molecular cytogenetic screening for chromosomal abnormalities of prognostic significance in childhood acute lymphoblastic leukaemia: a UK Cancer Cytogenetics Group Study.
Published in:
British Journal of Haematology, 2005, v. 129, n. 4, p. 520, doi. 10.1111/j.1365-2141.2005.05497.x
By:
- Harrison, Christine J.;
- Moorman, Anthony V.;
- Barber, Kerry E.;
- Broadfield, Zoë J.;
- Cheung, Kan L.;
- Harris, Rachel L.;
- Jalali, G. Reza;
- Robinson, Hazel M.;
- Strefford, Jonathan C.;
- Stewart, Adam;
- Wright, Sarah;
- Griffiths, Mike;
- Ross, Fiona M.;
- Harewood, Louise;
- Martineau, Mary
Publication type:
Article
Translocations of 14q32 and deletions of 13q14 are common chromosomal abnormalities in systemic amyloidosis.
Published in:
British Journal of Haematology, 2002, v. 117, n. 2, p. 427, doi. 10.1046/j.1365-2141.2002.03438.x
By:
- Harrison, Christine J;
- Mazzullo, Helen;
- Ross, Fiona M;
- Cheung, Kan L;
- Gerrard, Gareth;
- Harewood, Louise;
- Mehta, Atul;
- Lachmann, Helen J;
- Hawkins, Philip N;
- Orchard, Kim H
Publication type:
Article
Detection of minimal residual disease in childhood acute lymphoblastic leukaemia using fluorescence in-situ hybridization.
Published in:
British Journal of Haematology, 1995, v. 91, n. 4, p. 1019, doi. 10.1111/j.1365-2141.1995.tb05428.x
By:
- White, Denise M.;
- Crolla, John A.;
- Ross, Fiona M.
Publication type:
Article
Detection of t(14;18) in British follicular lymphoma using cytogenetics, Southern blotting and the polymerase chain reaction.
Published in:
British Journal of Haematology, 1995, v. 89, n. 1, p. 223, doi. 10.1111/j.1365-2141.1995.tb08938.x
By:
- Turner, Gillian E.;
- Ross, Fiona M.;
- Krajewski, Andrew S.
Publication type:
Article

Found: 24

Multipaint FISH: a rapid and reliable way to define cryptic and complex abnormalities.

Adenosine monophosphate as a mediator of ATP effects at P1 purinoceptors.

RESEARCH PAPER The context, measures and outcomes of psychosocial care interventions in long-term health care for older people.

Standardized assessment for elderly people (SAFE)--a feasibility study in district nursing.

Osteonecrosis of the jaw and renal safety in patients with newly diagnosed multiple myeloma: Medical Research Council Myeloma IX Study results.

Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders.

Permutation characters.

A molecular diagnostic approach able to detect the recurrent genetic prognostic factors typical of presenting myeloma.

Identification of a novel t(7;14) translocation in multiple myeloma resulting in overexpression of EGFR.

The clinical impact and molecular biology of del(17p) in multiple myeloma treated with conventional or thalidomide-based therapy.

Frequent upregulation of MYC in plasma cell leukemia.

The complex genomic profile of ETV6-RUNX1 positive acute lymphoblastic leukemia highlights a recurrent deletion of TBL1XR1.

Comparative expressed sequence hybridization studies of high‐hyperdiploid childhood acute lymphoblastic leukemia.

Identification of a novel gene, FGFR1OP2, fused to FGFR1 in 8p11 myeloproliferative syndrome.

Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia.

Response and biological subtype of myeloma are independent prognostic factors and combine to define outcome after high-dose therapy.

Methylation of tumour suppressor gene promoters in the presence and absence of transcriptional silencing in high hyperdiploid acute lymphoblastic leukaemia.

IgM myeloma: a rare entity characterized by a CD20<sup>−</sup>CD56<sup>−</sup>CD117<sup>−</sup> immunophenotype and the t(11;14).

Der(6)t(1;6)(q21–23;p21.3): a specific cytogenetic abnormality in myelofibrosis with myeloid metaplasia.

Interphase molecular cytogenetic screening for chromosomal abnormalities of prognostic significance in childhood acute lymphoblastic leukaemia: a UK Cancer Cytogenetics Group Study.

Translocations of 14q32 and deletions of 13q14 are common chromosomal abnormalities in systemic amyloidosis.

Detection of minimal residual disease in childhood acute lymphoblastic leukaemia using fluorescence in-situ hybridization.

Detection of t(14;18) in British follicular lymphoma using cytogenetics, Southern blotting and the polymerase chain reaction.