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22 Myelodysplastic syndromes: molecular markers

Leukemia research, 2007, Vol.31, p.S13-S13

Wainscoat, J.S

2007

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Deregulated gene expression pathways in myelodysplastic syndrome hematopoietic stem cells

Leukemia, 2010-04, Vol.24 (4), p.756-764

2010

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Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia

Leukemia, 2010-05, Vol.24 (5), p.1062-1065

2010

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1 A mouse model highlights a role for p53 in 5q− syndrome

Leukemia research, 2011, Vol.35, p.S1-S1

2011

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High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression

Leukemia, 2010-06, Vol.24 (6), p.1139-1145

2010

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YI1 Gene expression profiling of day 7 erythroblasts from refractory anemia with ringed sideroblasts (RARS) and microarray-based identification of erythroid granulocyte-CSF (G-CSF) targets

Leukemia research, 2009-05, Vol.33, p.S55-S55

2009

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MicroRNA expression in lymphocyte development and malignancy

Leukemia, 2008-07, Vol.22 (7), p.1440-1446

2008

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C019 Genome-wide analysis of copy number change and loss of heterozygosity in myelodysplastic syndrome with del (5q) using high-density SNP arrays

Leukemia research, 2007, Vol.31, p.S33-S33

2007

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Missense glucokinase mutation in maturity-onset diabetes of the young and mutation screening in late-onset diabetes

Nature genetics, 1992-10, Vol.2 (2), p.153-156

1992

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C023 Expression profiling of CD34+ cells in patients with myelodysplastic syndromes: differences between early and advanced cases and analysis of apoptosis-related genes

Leukemia research, 2007, Vol.31, p.S35-S35

2007

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Effects of L-leucine in 5q- syndrome and other RPS14-deficient erythroblasts

Leukemia, 2012-09, Vol.26 (9), p.2154-2158

2012

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Activation of the mTOR signaling pathway by L-leucine in 5q- syndrome and other RPS14-deficient erythroblasts

Leukemia, 2013-08, Vol.27 (8), p.1760-1763

2013

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Direct haplotype determination by double ARMS : specificity, sensitivity and genetic applications

Nucleic acids research, 1991-07, Vol.19 (13), p.3561-3567

1991

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Expression profiling of persistent polyclonal B-cell lymphocytosis suggests constitutive expression of the AP-1 transcription complex and downregulation of Fas-apoptotic and TGFβ signalling pathways

Leukemia, 2009-03, Vol.23 (3), p.581-583

2009

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PRENATAL SEX DETERMINATION BY DNA AMPLIFICATION FROM MATERNAL PERIPHERAL BLOOD

The Lancet (British edition), 1989-12, Vol.334 (8676), p.1363-1365

1989

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Genotypic analysis of large cell lymphomas which express the Ki-1 antigen

Histopathology, 1987-07, Vol.11 (7), p.733-740

1987

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Clinical Characteristics of Subjects with a Missense Mutation in Glucokinase

Diabetic medicine, 1995-03, Vol.12 (3), p.209-217

1995

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Linkage of type 2 diabetes to the glucokinase gene

The Lancet (British edition), 1992-05, Vol.339 (8805), p.1307-1310

1992

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An incidental case of thrombus formation in a patient with a portacath inserted for regular blood transfusions

British heart journal, 2003-03, Vol.89 (3), p.244-244

2003

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Prenatal determination of fetal RhD status by analysis of peripheral blood of rhesus negative mothers

The Lancet (British edition), 1993-05, Vol.341 (8853), p.1147-1148

1993

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Molecular Mapping of Uncharacteristically Small 5q Deletions in Two Patients with the 5q- Syndrome: Delineation of the Critical Region on 5q and Identification of a 5q- Breakpoint

Genomics (San Diego, Calif.), 1994-02, Vol.19 (3), p.425-432

1994

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Hematological Malignancies

Hematology (Luxembourg), 2004-08, Vol.9 (4), p.271-277

2004

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Detection of single-copy fetal DNA sequence from maternal blood

The Lancet (British edition), 1990-06, Vol.335 (8703), p.1463-1464

1990

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Culture of fetal erythroid cells from maternal peripheral blood

The Lancet (British edition), 1994-07, Vol.344 (8917), p.264-265

1994

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MALIGNANT HISTIOCYTOSIS OF THE INTESTINE: A T-CELL LYMPHOMA

The Lancet (British edition), 1985, Vol.326 (8457), p.688-691

1985

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22 Myelodysplastic syndromes: molecular markers

Deregulated gene expression pathways in myelodysplastic syndrome hematopoietic stem cells

Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia

1 A mouse model highlights a role for p53 in 5q− syndrome

High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression

YI1 Gene expression profiling of day 7 erythroblasts from refractory anemia with ringed sideroblasts (RARS) and microarray-based identification of erythroid granulocyte-CSF (G-CSF) targets

MicroRNA expression in lymphocyte development and malignancy

C019 Genome-wide analysis of copy number change and loss of heterozygosity in myelodysplastic syndrome with del (5q) using high-density SNP arrays

Missense glucokinase mutation in maturity-onset diabetes of the young and mutation screening in late-onset diabetes

C023 Expression profiling of CD34+ cells in patients with myelodysplastic syndromes: differences between early and advanced cases and analysis of apoptosis-related genes

Effects of L-leucine in 5q- syndrome and other RPS14-deficient erythroblasts

Activation of the mTOR signaling pathway by L-leucine in 5q- syndrome and other RPS14-deficient erythroblasts

Direct haplotype determination by double ARMS : specificity, sensitivity and genetic applications

Expression profiling of persistent polyclonal B-cell lymphocytosis suggests constitutive expression of the AP-1 transcription complex and downregulation of Fas-apoptotic and TGFβ signalling pathways

PRENATAL SEX DETERMINATION BY DNA AMPLIFICATION FROM MATERNAL PERIPHERAL BLOOD

Genotypic analysis of large cell lymphomas which express the Ki-1 antigen

Clinical Characteristics of Subjects with a Missense Mutation in Glucokinase

Linkage of type 2 diabetes to the glucokinase gene

An incidental case of thrombus formation in a patient with a portacath inserted for regular blood transfusions

Prenatal determination of fetal RhD status by analysis of peripheral blood of rhesus negative mothers

Molecular Mapping of Uncharacteristically Small 5q Deletions in Two Patients with the 5q- Syndrome: Delineation of the Critical Region on 5q and Identification of a 5q- Breakpoint

Hematological Malignancies

Detection of single-copy fetal DNA sequence from maternal blood

Culture of fetal erythroid cells from maternal peripheral blood

MALIGNANT HISTIOCYTOSIS OF THE INTESTINE: A T-CELL LYMPHOMA

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