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Deregulated gene expression pathways in myelodysplastic syndrome hematopoietic stem cells

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

2010

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

MicroRNA expression in lymphocyte development and malignancy

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

2008

Volltextzugriff (PDF)

Quantitation of circulating DNA in the serum of breast cancer patients by real-time PCR

British journal of cancer, 2004-03, Vol.90 (6), p.1211-1215

2004

Volltextzugriff (PDF)

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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Quantitative Analysis of Fetal DNA in Maternal Plasma and Serum: Implications for Noninvasive Prenatal Diagnosis

American journal of human genetics, 1998-04, Vol.62 (4), p.768-775

1998

Volltextzugriff (PDF)

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

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

2012

Volltextzugriff (PDF)

hTERT, the catalytic component of telomerase, is downregulated in the haematopoietic stem cells of patients with chronic myeloid leukaemia

Leukemia, 2006-04, Vol.20 (4), p.671-679

2006

Volltextzugriff (PDF)

Somatic SF3B1 Mutation in Myelodysplasia with Ring Sideroblasts

The New England journal of medicine, 2011-10, Vol.365 (15), p.1384-1395

2011

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Two-way cell traffic between mother and fetus : Biologic and clinical implications

Blood, 1996-12, Vol.88 (11), p.4390-4395

1996

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

The 5q– Syndrome

Blood, 1994-11, Vol.84 (10), p.3253-3260

1994

Volltextzugriff (PDF)

Clinical Characteristics of Subjects with a Missense Mutation in Glucokinase

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

1995

Volltextzugriff (PDF)

Linkage of type 2 diabetes to the glucokinase gene

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

1992

Volltextzugriff (PDF)

Determination of RhD Zygosity: Comparison of a Double Amplification Refractory Mutation System Approach and a Multiplex Real-Time Quantitative PCR Approach

Clinical chemistry (Baltimore, Md.), 2001-04, Vol.47 (4), p.667-672

2001

Volltextzugriff (PDF)

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.1762-1766

2009

Volltextzugriff (PDF)

High-mobility group A (HMGA) genes: from solid to liquid tumours?

Leukemia, 2005-02, Vol.19 (2), p.195-196

2005

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Telomere length in myelodysplastic syndromes

American journal of hematology, 1997-12, Vol.56 (4), p.266-271

1997

Volltextzugriff (PDF)

A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia

Blood, 2001-08, Vol.98 (4), p.1264-1267

2001

Volltextzugriff (PDF)

Assessment of clonality in human tumors: a review

Cancer research (Chicago, Ill.), 1990-03, Vol.50 (5), p.1355-1360

1990

Volltextzugriff (PDF)

Amplification of mitochondrial DNA in acute myeloid leukaemia

British journal of haematology, 1996-11, Vol.95 (2), p.426-431

1996

Volltextzugriff (PDF)

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)

Nature genetics, 2003-08, Vol.34 (4), p.446-449

2003

Volltextzugriff (PDF)

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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

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

MicroRNA expression in lymphocyte development and malignancy

Quantitation of circulating DNA in the serum of breast cancer patients by real-time PCR

Presence of fetal DNA in maternal plasma and serum

Quantitative Analysis of Fetal DNA in Maternal Plasma and Serum: Implications for Noninvasive Prenatal Diagnosis

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

hTERT, the catalytic component of telomerase, is downregulated in the haematopoietic stem cells of patients with chronic myeloid leukaemia

Somatic SF3B1 Mutation in Myelodysplasia with Ring Sideroblasts

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

Two-way cell traffic between mother and fetus : Biologic and clinical implications

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

The 5q– Syndrome

Clinical Characteristics of Subjects with a Missense Mutation in Glucokinase

Linkage of type 2 diabetes to the glucokinase gene

Determination of RhD Zygosity: Comparison of a Double Amplification Refractory Mutation System Approach and a Multiplex Real-Time Quantitative PCR Approach

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

High-mobility group A (HMGA) genes: from solid to liquid tumours?

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

Telomere length in myelodysplastic syndromes

A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia

Assessment of clonality in human tumors: a review

Amplification of mitochondrial DNA in acute myeloid leukaemia

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)

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