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Basic sciences of the myeloproliferative diseases: pathogenic mechanisms of ET and PV.
- Published in:
- 2002
- By:
- Publication type:
- journal article
Insertional mutagenesis combined with acquired somatic mutations causes leukemogenesis following gene therapy of SCID-X1 patients.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Therapy for isocitrate dehydrogenase 2 (IDH2)<sup>R172</sup>‐mutant acute myeloid leukaemia.
- Published in:
- British Journal of Haematology, 2022, v. 196, n. 6, p. 1348, doi. 10.1111/bjh.17981
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- Publication type:
- Article
The clinical impact of mutant DNMT3A R882 variant allele frequency in acute myeloid leukaemia.
- Published in:
- British Journal of Haematology, 2020, v. 189, n. 3, p. e81, doi. 10.1111/bjh.16486
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- Publication type:
- Article
Analysis of the clinical impact of NPM1 mutant allele burden in a large cohort of younger adult patients with acute myeloid leukaemia.
- Published in:
- British Journal of Haematology, 2020, v. 188, n. 6, p. 852, doi. 10.1111/bjh.16239
- By:
- Publication type:
- Article
In trans early mosaic mutational escape and novel phenotypic features of germline SAMD9 mutation.
- Published in:
- British Journal of Haematology, 2020, v. 188, n. 4, p. e53, doi. 10.1111/bjh.16322
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- Publication type:
- Article
Immunophenotypic analysis of cell cycle status in acute myeloid leukaemia: relationship to cytogenetics, genotype and clinical outcome.
- Published in:
- British Journal of Haematology, 2018, v. 181, n. 4, p. 486, doi. 10.1111/bjh.15211
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- Publication type:
- Article
Cell cycle status in AML blast cells from peripheral blood, bone marrow aspirates and trephines and implications for biological studies and treatment.
- Published in:
- British Journal of Haematology, 2016, v. 174, n. 2, p. 275, doi. 10.1111/bjh.14055
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- Publication type:
- Article
The value of molecular stratification for CEBPA<sup>DM</sup> and NPM1<sup>MUT</sup> FLT3<sup>WT</sup> genotypes in older patients with acute myeloid leukaemia.
- Published in:
- British Journal of Haematology, 2016, v. 172, n. 4, p. 573, doi. 10.1111/bjh.13873
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- Publication type:
- Article
PIM and AKT kinase inhibitors show synergistic cytotoxicity in acute myeloid leukaemia that is associated with convergence on mTOR and MCL1 pathways.
- Published in:
- British Journal of Haematology, 2014, v. 167, n. 1, p. 69, doi. 10.1111/bjh.13013
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- Publication type:
- Article
GATA2 mutations in sporadic and familial acute myeloid leukaemia patients with CEBPA mutations.
- Published in:
- British Journal of Haematology, 2013, v. 161, n. 5, p. 701, doi. 10.1111/bjh.12317
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- Publication type:
- Article
Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1262, doi. 10.1038/ng.994
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- Publication type:
- Article
Frequency of NPM1 Mutations in Pakistani Acute Myeloid Leukemia Patients.
- Published in:
- Pakistan Journal of Zoology, 2013, v. 45, n. 5, p. 1429
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- Publication type:
- Article
An activating mutation in the transmembrane domain of the granulocyte colony-stimulating factor receptor in patients with acute myeloid leukemia .
- Published in:
- Oncogene, 2002, v. 21, n. 39, p. 5981, doi. 10.1038/sj.onc.1205767
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- Publication type:
- Article
Lack of pathogenic mutations in the 5′-untranslated region of the thrombopoietin gene in patients with non-familial essential thrombocythaemia.
- Published in:
- European Journal of Haematology, 2001, v. 67, n. 4, p. 232, doi. 10.1034/j.1600-0609.2001.00550.x
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- Publication type:
- Article
Detection of FLT3/TKD and IDH1 Mutations in Pakistani Acute Myeloid Leukemia Patients by Denaturing HPLC.
- Published in:
- Journal of Cellular Biochemistry, 2017, v. 118, n. 5, p. 1174, doi. 10.1002/jcb.25761
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- Publication type:
- Article
Novel regions of acquired uniparental disomy discovered in acute myeloid leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 2008, v. 47, n. 9, p. 729, doi. 10.1002/gcc.20573
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- Publication type:
- Article
Mutations of the AML1 gene in acute myeloid leukemia of FAB types M0 and M7.
- Published in:
- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 24, doi. 10.1002/gcc.10031
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- Publication type:
- Article
Does BCR/ ABL1 positive Acute Myeloid Leukaemia Exist?
- Published in:
- British Journal of Haematology, 2013, v. 161, n. 4, p. 541, doi. 10.1111/bjh.12301
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- Publication type:
- Article
Phenotypic heterogeneity and evidence of a founder effect associated with G6 PC3 mutations in patients with severe congenital neutropenia.
- Published in:
- British Journal of Haematology, 2012, v. 158, n. 1, p. 146, doi. 10.1111/j.1365-2141.2012.09110.x
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- Publication type:
- Article
The production of JAK2 wild-type platelets is not downregulated in patients with JAK2 V617F mutant-positive essential thrombocythaemia.
- Published in:
- British Journal of Haematology, 2009, v. 145, n. 1, p. 128, doi. 10.1111/j.1365-2141.2009.07597.x
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- Publication type:
- Article
Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindreds.
- Published in:
- British Journal of Haematology, 2009, v. 144, n. 5, p. 762, doi. 10.1111/j.1365-2141.2008.07493.x
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- Publication type:
- Article
Most acute myeloid leukaemia patients with intermediate mutant FLT3/ITD levels do not have detectable bi-allelic disease, indicating that heterozygous disease alone is associated with an adverse outcome.
- Published in:
- British Journal of Haematology, 2008, v. 142, n. 3, p. 423, doi. 10.1111/j.1365-2141.2008.07196.x
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- Publication type:
- Article
Acute myeloid leukaemia blast cells with a tyrosine kinase domain mutation of FLT3 are less sensitive to lestaurtinib than those with a FLT3 internal tandem duplication.
- Published in:
- British Journal of Haematology, 2008, v. 141, n. 4, p. 454, doi. 10.1111/j.1365-2141.2008.07025.x
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- Publication type:
- Article
Flt3 mutations and leukaemia.
- Published in:
- British Journal of Haematology, 2003, v. 122, n. 4, p. 523, doi. 10.1046/j.1365-2141.2003.04500.x
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- Publication type:
- Article
Long-term follow-up of granulocyte colony-stimulating factor receptor mutations in patients with severe congenital neutropenia: implications for leukaemogenesis and therapy.
- Published in:
- British Journal of Haematology, 2003, v. 120, n. 4, p. 685, doi. 10.1046/j.1365-2141.2003.04160.x
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- Publication type:
- Article
Dynamics of telomere shortening in neutrophils and T lymphocytes during ageing and the relationship to skewed X chromosome inactivation patterns.
- Published in:
- British Journal of Haematology, 2000, v. 109, n. 2, p. 272, doi. 10.1046/j.1365-2141.2000.01970.x
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- Publication type:
- Article
G6PC3 mutations are associated with a major defect of glycosylation: a novel mechanism for neutrophil dysfunction.
- Published in:
- Glycobiology, 2011, v. 21, n. 7, p. 914, doi. 10.1093/glycob/cwr023
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- Publication type:
- Article
Platelet c-mpl expression is dysregulated in patients with essential thrombocythaemia but this is not of diagnostic value.
- Published in:
- British Journal of Haematology, 1999, v. 107, n. 1, p. 139, doi. 10.1046/j.1365-2141.1999.01667.x
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- Publication type:
- Article
Activating point mutations in the β[sub C] chain of the GM-CSF, IL-3 and IL-5 receptors are not a major contributory factor in the pathogenesis of acute myeloid leukaemia.
- Published in:
- British Journal of Haematology, 1998, v. 103, n. 1, p. 66
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- Publication type:
- Article
The activating splice mutation in intron 3 of the thrombopoietin gene is not found in patients with non-familial essential thrombocythaemia.
- Published in:
- British Journal of Haematology, 1998, v. 102, n. 5, p. 00, doi. 10.1046/j.1365-2141.1998.00921.x
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- Publication type:
- Article
Mutations of the granulocyte-colony stimulating factor receptor in patients with severe congenital neutropenia are not required for transformation to acute myeloid leukaemia and may be a bystander phenomenon.
- Published in:
- British Journal of Haematology, 1998, v. 101, n. 1, p. 141, doi. 10.1046/j.1365-2141.1998.00652.x
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- Publication type:
- Article
Acquired skewing of X-chromosome inactivation patterns in myeloid cells of the elderly suggests stochastic clonal loss with age.
- Published in:
- British Journal of Haematology, 1997, v. 98, n. 3, p. 512, doi. 10.1046/j.1365-2141.1997.2573078.x
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- Publication type:
- Article
THE RETINOBLASTOMA GENE ( RB1) IN ACUTE MYELOID LEUKAEMIA: ANALYSIS OF GENE REARRANGEMENTS, PROTEIN EXPRESSION AND COMPARISON OF DISEASE OUTCOME.
- Published in:
- British Journal of Haematology, 1996, v. 94, n. 2, p. 342, doi. 10.1046/j.1365-2141.1996.d01-1804.x
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- Publication type:
- Article
Analysis of granulocyte colony stimulating factor receptor isoforms, polymorphisms and mutations in normal haemopoietic cells and acute myeloid leukaemia blasts.
- Published in:
- British Journal of Haematology, 1996, v. 93, n. 3, p. 527, doi. 10.1046/j.1365-2141.1996.d01-1696.x
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- Publication type:
- Article
LINEAGE INVOLVEMENT ON CHRONIC MYELOPROLIFERATIVE DISORDERS.
- Published in:
- British Journal of Haematology, 1994, v. 87, n. 4, p. 882, doi. 10.1111/j.1365-2141.1994.tb06763.x
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- Publication type:
- Article
CLONAL ANALYSIS USING X-LINKED DNA POLYMORPHISMS.
- Published in:
- British Journal of Haematology, 1993, v. 85, n. 1, p. 2, doi. 10.1111/j.1365-2141.1993.tb08637.x
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- Publication type:
- Article
X-chromosome inactivation patterns using HPRT and PGK polymorphisms in haematologically normal and post-chemotherapy females.
- Published in:
- British Journal of Haematology, 1991, v. 79, n. 2, p. 193, doi. 10.1111/j.1365-2141.1991.tb04521.x
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- Publication type:
- Article