نتائج البحث - "Young, B.D."

Relation: Archibald, K.M. et al. (2012) Sequential genetic change at the TP53 and chemokine receptor CXCR4 locus during transformation of human ovarian surface epithelium. Oncogene , 31(48), pp. 4987-4995. (doi:10.1038/onc.2011.653 )

الاتاحة: http://eprints.gla.ac.uk/76038/

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16

Academic Journal

Depletion of RUNX1/ETO in t(8;21) AML cells leads to genome-wide changes in chromatin structure and transcription factor binding

المؤلفون: Ptasinska, A., Assi, S.A., Mannari, D., James, S.R., Williamson, D., Dunne, J., Hoogenkamp, M., Wu, M., Care, M., McNeill, H., Cauchy, P., Cullen, M., Tooze, R.M., Tenen, D.G., Young, B.D., Cockerill, P.N., Westhead, D.R., Heidenreich, O., Bonifer, C.

المساهمون: CANCER SCIENCE INSTITUTE OF SINGAPORE

المصدر: Scopus

مصطلحات موضوعية: acute myeloid leukemia, chromatin, epigenetic regulation, integrated analysis of high-throughput data, RUNX1/ETO

Relation: Ptasinska, A., Assi, S.A., Mannari, D., James, S.R., Williamson, D., Dunne, J., Hoogenkamp, M., Wu, M., Care, M., McNeill, H., Cauchy, P., Cullen, M., Tooze, R.M., Tenen, D.G., Young, B.D., Cockerill, P.N., Westhead, D.R., Heidenreich, O., Bonifer, C. (2012-08). Depletion of RUNX1/ETO in t(8;21) AML cells leads to genome-wide changes in chromatin structure and transcription factor binding. Leukemia 26 (8) : 1829-1841. ScholarBank@NUS Repository. https://doi.org/10.1038/leu.2012.49; http://scholarbank.nus.edu.sg/handle/10635/116971; 000307650000011

الاتاحة: http://scholarbank.nus.edu.sg/handle/10635/116971

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17

Academic Journal

13q deletion anatomy and disease progression in patients with chronic lymphocytic leukemia

المؤلفون: Parker, H., Rose-Zerilli, M.J.J., Parker, A., Chaplin, T., Wade, R., Gardiner, A., Griffiths, M., Collins, A., Young, B.D., Oscier, D.G., Strefford, J.C.

Relation: Parker, H., Rose-Zerilli, M.J.J., Parker, A., Chaplin, T., Wade, R., Gardiner, A., Griffiths, M., Collins, A., Young, B.D., Oscier, D.G. and Strefford, J.C. (2011) 13q deletion anatomy and disease progression in patients with chronic lymphocytic leukemia. Leukemia, 25 (3), 489-497. (doi:10.1038/leu.2010.288 ). (PMID:21151023 )

الاتاحة: https://eprints.soton.ac.uk/179417/

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18

Academic Journal

The Interlaboratory RObustness of Next-generation sequencing (IRON) study: a deep sequencing investigation of TET2, CBL and KRAS mutations by an international consortium involving 10 laboratories.

المصدر: Leukemia, 25, 12, pp. 1840-8

مصطلحات موضوعية: NCMLS 2: Immune Regulation ONCOL 3: Translational research

Relation: http://hdl.handle.net/2066/98406

الاتاحة: http://hdl.handle.net/2066/98406
https://doi.org/10.1038/leu.2011.155

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19

Academic Journal

1.15 The Genome-Wide Analysis of Copy Number Alterations and Acquired UPD Events in CLL

المؤلفون: Strefford, J.C., Rose-Zerilli, M.J.J., Parker, H., Parker, A., Rodriguez, A., Chaplin, T., Gardiner, A., Collins, A., Young, B.D., Oscier, D.G.

المصدر: Clinical Lymphoma Myeloma and Leukemia ; volume 11, page S150-S151 ; ISSN 2152-2650

الاتاحة: http://dx.doi.org/10.1016/j.clml.2011.09.016
https://api.elsevier.com/content/article/PII:S2152265011002862?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S2152265011002862?httpAccept=text/plain

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20

Academic Journal

Specific JAK2 mutation (JAK2R683) and multiple gene deletions in Down syndrome acute lymphoblastic leukemia

المؤلفون: Kearney, L., De Castro, D.G., Yeung, J., Procter, J., Horsley, S.W., Eguchi-Ishimae, M., Bateman, C.M., Anderson, K., Chaplin, T., Young, B.D., Harrison, C.J., Kempski, H., So, C.W.E., Ford, A.M., Greaves, M.

المصدر: Kearney , L , De Castro , D G , Yeung , J , Procter , J , Horsley , S W , Eguchi-Ishimae , M , Bateman , C M , Anderson , K , Chaplin , T , Young , B D , Harrison , C J , Kempski , H , So , C W E , Ford , A M & Greaves , M 2009 , ' Specific JAK2 mutation (JAK2R683) and multiple gene deletions in Down syndrome acute lymphoblastic leukemia ' , Blood , vol. 113 , no. 3 , pp. 646-648 . https://doi.org/10.1182/blood-2008-08-170928

مصطلحات موضوعية: MYELOPROLIFERATIVE DISORDERS, MEGAKARYOBLASTIC LEUKEMIA, CHILDHOOD, GATA1, DIFFERENTIATION, CHILDREN, DISEASE, LESIONS, FLT3

الاتاحة: https://pure.qub.ac.uk/en/publications/dd8987dc-5490-4d57-b59b-b7d96ff2bde4
https://doi.org/10.1182/blood-2008-08-170928

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