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Seminars in Hematology
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October 8, 2005
Chromosomal abnormalities and molecular markers in myeloproliferative disorders
Anthony J Bench, Heike L Pahl
Methods in Molecular Biology (Clifton, N.J.)
|
January 9, 2013
Methods for detecting mutations in the human JAK2 gene
Anthony J Bench, E Joanna Baxter, Anthony R Green
British Journal of Haematology
|
October 4, 2007
Prevalance of JAK2 V617F and exon 12 mutations in polycythaemia vera
Linda M Scott, Philip A Beer, Anthony J Bench, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 5, 2004
Imprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in human myeloid malignancies
Juan Li, Anthony J Bench, George S Vassiliou, et al.
Methods in Molecular Medicine
|
March 1, 2006
Methods for the detection of the JAK2 V617F mutation in human myeloproliferative disorders
Peter J Campbell, Linda M Scott, E Joanna Baxter, et al.
Genomics
|
August 6, 2005
L3mbtl, the mouse orthologue of the imprinted L3MBTL, displays a complex pattern of alternative splicing and escapes genomic imprinting
Juan Li, Anthony J Bench, Sandie Piltz, et al.
Haematologica
|
July 5, 2006
Size matters: the prognostic implications of large and small deletions of the derivative 9 chromosome in chronic myeloid leukemia
Nasios Fourouclas, Peter J Campbell, Anthony J Bench, et al.
Genome Research
|
May 9, 2002
Analyses of the extent of shared synteny and conserved gene orders between the genome of Fugu rubripes and human 20q
Sarah F Smith, Philip Snell, Frank Gruetzner, et al.
British Journal of Haematology
|
November 30, 2004
Characterization of the imprinted polycomb gene L3MBTL, a candidate 20q tumour suppressor gene, in patients with myeloid malignancies
Anthony J Bench, Juan Li, Brian J P Huntly, et al.
British Journal of Haematology
|
September 14, 2011
High resolution melting analysis for detection of BRAF exon 15 mutations in hairy cell leukaemia and other lymphoid malignancies
Elaine M Boyd, Anthony J Bench, Mars B van 't Veer, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 3
Seminars in Hematology
|
October 8, 2005
Chromosomal abnormalities and molecular markers in myeloproliferative disorders
Anthony J Bench, Heike L Pahl
Methods in Molecular Biology (Clifton, N.J.)
|
January 9, 2013
Methods for detecting mutations in the human JAK2 gene
Anthony J Bench, E Joanna Baxter, Anthony R Green
British Journal of Haematology
|
October 4, 2007
Prevalance of JAK2 V617F and exon 12 mutations in polycythaemia vera
Linda M Scott, Philip A Beer, Anthony J Bench, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 5, 2004
Imprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in human myeloid malignancies
Juan Li, Anthony J Bench, George S Vassiliou, et al.
Methods in Molecular Medicine
|
March 1, 2006
Methods for the detection of the JAK2 V617F mutation in human myeloproliferative disorders
Peter J Campbell, Linda M Scott, E Joanna Baxter, et al.
Genomics
|
August 6, 2005
L3mbtl, the mouse orthologue of the imprinted L3MBTL, displays a complex pattern of alternative splicing and escapes genomic imprinting
Juan Li, Anthony J Bench, Sandie Piltz, et al.
Haematologica
|
July 5, 2006
Size matters: the prognostic implications of large and small deletions of the derivative 9 chromosome in chronic myeloid leukemia
Nasios Fourouclas, Peter J Campbell, Anthony J Bench, et al.
Genome Research
|
May 9, 2002
Analyses of the extent of shared synteny and conserved gene orders between the genome of Fugu rubripes and human 20q
Sarah F Smith, Philip Snell, Frank Gruetzner, et al.
British Journal of Haematology
|
November 30, 2004
Characterization of the imprinted polycomb gene L3MBTL, a candidate 20q tumour suppressor gene, in patients with myeloid malignancies
Anthony J Bench, Juan Li, Brian J P Huntly, et al.
British Journal of Haematology
|
September 14, 2011
High resolution melting analysis for detection of BRAF exon 15 mutations in hairy cell leukaemia and other lymphoid malignancies
Elaine M Boyd, Anthony J Bench, Mars B van 't Veer, et al.
Page
of 3