Lan-Lan Smith

发表

Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia.

T. Lister, T. A. Lister, J. Fitzgibbon, 2008, Blood.

CEBPA (CCAAT enhancer binding protein alpha)

Lan-Lan Smith, Lan‐Lan Smith, 2011 .

Development of a quantitative real‐time polymerase chain reaction method for monitoring CEBPA mutations in normal karyotype acute myeloid leukaemia

J. Fitzgibbon, D. Bonnet, D. Pearce, 2006, British journal of haematology.

2013 ASCO Annual Meeting

Lan-Lan Smith, Lan‐Lan Smith, 2013 .

Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias.

T. A. Lister, J. Fitzgibbon, M. Raghavan, 2005, Cancer research.

Functional crosstalk between Bmi1 and MLL/Hoxa9 axis in establishment of normal hematopoietic and leukemic stem cells.

Amanda J. Wilson, I. Huijbers, E. Taskesen, 2011, Cell stem cell.

Development of a human acute myeloid leukaemia screening panel and consequent identification of novel gene mutation in FLT3 and CCND3

J. Fitzgibbon, J. Cavenagh, C. Taylor, 2005, British journal of haematology.

AML engraftment in the NOD/SCID assay reflects the outcome of AML: implications for our understanding of the heterogeneity of AML.

T. Lister, A. Rohatiner, C. Preudhomme, 2006, Blood.

relapsed acute myeloid leukemia Segmental uniparental disomy is a commonly acquired genetic event in

T. Lister, J. Fitzgibbon, J. Cavenagh, 2013 .

NCRI Cancer Conference

Lan-Lan Smith, 2013 .

58th American Society of Hematology Annual Meeting.

Lan-Lan Smith, 2017, The Lancet. Oncology.