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Advances in the 5q− syndrome

Blood, 2010-12, Vol.116 (26), p.5803-5811

2010

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Microrna expression distinguishes between germinal center B cell‐like and activated B cell‐like subtypes of diffuse large B cell lymphoma

International journal of cancer, 2007-09, Vol.121 (5), p.1156-1161

2007

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Lenalidomide inhibits the malignant clone and up-regulates the SPARC gene mapping to the commonly deleted region in 5q- syndrome patients

Proceedings of the National Academy of Sciences - PNAS, 2007-07, Vol.104 (27), p.11406-11411

2007

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MicroRNA expression in Sézary syndrome: identification, function, and diagnostic potential

Blood, 2010-08, Vol.116 (7), p.1105-1113

2010

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Mutation patterns of 16 genes in primary and secondary acute myeloid leukemia (AML) with normal cytogenetics

PloS one, 2012-08, Vol.7 (8), p.e42334-e42334

2012

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Clonal heterogeneity in the 5q- syndrome: p53 expressing progenitors prevail during lenalidomide treatment and expand at disease progression

Haematologica (Roma), 2009-12, Vol.94 (12), p.1762

2009

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The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts

PloS one, 2008-04, Vol.3 (4), p.e1970-e1970

2008

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MicroRNA expression in multiple myeloma is associated with genetic subtype, isotype and survival

Biology direct, 2011-05, Vol.6 (1), p.23-23, Article 23

2011

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Induction of p53 and up-regulation of the p53 pathway in the human 5q− syndrome

Blood, 2010-04, Vol.115 (13), p.2721-2723

2010

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5q- syndrome

Current pharmaceutical design, 2012, Vol.18 (22), p.3180

2012

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Targeted re-sequencing analysis of 25 genes commonly mutated in myeloid disorders in del(5q) myelodysplastic syndromes

Haematologica (Roma), 2013-12, Vol.98 (12), p.1856

2013

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Presence of fetal DNA in maternal plasma and serum

The Lancet (British edition), 1997-08, Vol.350 (9076), p.485-487

1997

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Silencing of ASXL1 impairs the granulomonocytic lineage potential of human CD34+ progenitor cells

British journal of haematology, 2013-03, Vol.160 (6), p.842-850

2013

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Narrowing and genomic annotation of the commonly deleted region of the 5q− syndrome

Blood, 2002-06, Vol.99 (12), p.4638-4641

2002

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Prenatal Diagnosis of Fetal RhD Status by Molecular Analysis of Maternal Plasma

The New England journal of medicine, 1998-12, Vol.339 (24), p.1734-1738

1998

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Gene silencing by DNA methylation in haematological malignancies

British journal of haematology, 2007-07, Vol.138 (1), p.3-11

2007

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Detection of elevated levels of tumour‐associated microRNAs in serum of patients with diffuse large B‐cell lymphoma

British journal of haematology, 2008-06, Vol.141 (5), p.672-675

2008

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A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q- syndrome

Nature medicine, 2010-01, Vol.16 (1), p.59-66

2010

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Gene expression profiling in the myelodysplastic syndromes using cDNA microarray technology

British journal of haematology, 2004-06, Vol.125 (5), p.576-583

2004

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Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotype

PloS one, 2011-06, Vol.6 (6), p.e20607-e20607

2011

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Expression of microRNAs in diffuse large B cell lymphoma is associated with immunophenotype, survival and transformation from follicular lymphoma

Journal of cellular and molecular medicine, 2009-07, Vol.13 (7), p.1248-1260

2009

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Molecular and clinical features of refractory anemia with ringed sideroblasts associated with marked thrombocytosis

Blood, 2009-10, Vol.114 (17), p.3538-3545

2009

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Delineation of the minimal commonly deleted segment and identification of candidate tumor-suppressor genes in del(9q) acute myeloid leukemia

Genes chromosomes & cancer, 2005-11, Vol.44 (3), p.279-291

2005

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Advances in the 5q− syndrome

Microrna expression distinguishes between germinal center B cell‐like and activated B cell‐like subtypes of diffuse large B cell lymphoma

Lenalidomide inhibits the malignant clone and up-regulates the SPARC gene mapping to the commonly deleted region in 5q- syndrome patients

MicroRNA expression in Sézary syndrome: identification, function, and diagnostic potential

Mutation patterns of 16 genes in primary and secondary acute myeloid leukemia (AML) with normal cytogenetics

TET2 mutations are associated with specific 5-methylcytosine and 5-hydroxymethylcytosine profiles in patients with chronic myelomonocytic leukemia

Clonal heterogeneity in the 5q- syndrome: p53 expressing progenitors prevail during lenalidomide treatment and expand at disease progression

The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts

MicroRNA expression in multiple myeloma is associated with genetic subtype, isotype and survival

Induction of p53 and up-regulation of the p53 pathway in the human 5q− syndrome

5q- syndrome

Targeted re-sequencing analysis of 25 genes commonly mutated in myeloid disorders in del(5q) myelodysplastic syndromes

Presence of fetal DNA in maternal plasma and serum

Silencing of ASXL1 impairs the granulomonocytic lineage potential of human CD34+ progenitor cells

Narrowing and genomic annotation of the commonly deleted region of the 5q− syndrome

Prenatal Diagnosis of Fetal RhD Status by Molecular Analysis of Maternal Plasma

Gene silencing by DNA methylation in haematological malignancies

Detection of elevated levels of tumour‐associated microRNAs in serum of patients with diffuse large B‐cell lymphoma

A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q- syndrome

Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms

Gene expression profiling in the myelodysplastic syndromes using cDNA microarray technology

Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotype

Expression of microRNAs in diffuse large B cell lymphoma is associated with immunophenotype, survival and transformation from follicular lymphoma

Molecular and clinical features of refractory anemia with ringed sideroblasts associated with marked thrombocytosis

Delineation of the minimal commonly deleted segment and identification of candidate tumor-suppressor genes in del(9q) acute myeloid leukemia

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