Gene expression profiles of CD34+ cells in myelodysplastic syndromes: involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype.

Gene expression profiles of CD34+ cells in myelodysplastic syndromes: involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype.

To gain insight into the poorly understood pathophysiology of the myelodysplastic syndromes (MDSs), we have determined the gene expression profiles of the CD34+ cells of 55 patients with MDS by using a comprehensive array platform. These profiles showed many similarities to reported interferon-gamma...

وصف كامل

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Pellagatti, A, Cazzola, M, Giagounidis, A, Malcovati, L, Porta, MG, Killick, S, Campbell, L, Wang, L, Langford, C, Fidler, C, Oscier, D, Aul, C, Wainscoat, J, Boultwood, J
التنسيق:	Journal article
اللغة:	English
منشور في:	2006

مواد مشابهة

Expression profiling of CD34+cells in patients with myelodysplastic syndromes: Involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype.
حسب: Pellagatti, A, وآخرون
منشور في: (2006)

Expression profiling of CD34+cells in patients with myelodysplastic syndromes with and without a del(5q)
حسب: Pellagatti, A, وآخرون
منشور في: (2005)

Expression profiling of CD34+cells in patients with myelodysplastic syndromes with and without a del(5q).
حسب: Pellagatti, A, وآخرون
منشور في: (2004)

Expression profiling of CD34+cells in patients with myelodysplastic syndromes: differences between early and advanced cases and analysis of apoptosis-related genes
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Genome-wide analysis of copy number change and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density SNP arrays
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Frequent Mutation of the Polycomb-Associated Gene ASXL1 in the Myelodysplastic Syndromes and in Acute Myeloid Leukaemia
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Deregulated Gene Expression Pathways in Myelodysplastic Syndrome Hematopoietic Stem Cells
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Gene Expression Profiling of CD34(+) Cells in Patients with Myelodysplastic Syndromes
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Identification of Prognostic Markers by Gene Expression Profiling In Myelodysplastic Syndrome Hematopoietic Stem Cells
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Identification of Prognostic Markers by Gene Expression Profiling In Myelodysplastic Syndrome Hematopoietic Stem Cells
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Deregulated gene expression pathways in myelodysplastic syndrome hematopoietic stem cells.
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High-resolution genomic profiling of myelodysplasia (MDS) by microarray comparative genomic hybridization (CGH).
حسب: Esoof, N, وآخرون
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Identification of Prognostic Markers by Gene Expression Profiling In Myelodysplastic Syndrome Hematopoietic Stem Cells
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Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays.
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منشور في: (2005)

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Marked down-regulation of nucleophosmin-1 is associated with advanced del(5q) myelodysplastic syndrome.
حسب: Pellagatti, A, وآخرون
منشور في: (2011)

Marked down-regulation of nucleophosmin-1 is associated with advanced del(5q) myelodysplastic syndrome
حسب: Pellagatti, A, وآخرون
منشور في: (2011)

Gene expression profiling of CD34+ cells in patients with the 5q- syndrome.
حسب: Boultwood, J, وآخرون
منشور في: (2007)

Haploinsufficiency of RPS14 in 5q- syndrome is associated with deregulation of ribosomal- and translation-related genes (British Journal of Haematology (2008) 142, (57-64))
حسب: Pellagatti, A, وآخرون
منشور في: (2009)

Identification of gene expression-based prognostic markers in the hematopoietic stem cells of patients with myelodysplastic syndromes.
حسب: Pellagatti, A, وآخرون
منشور في: (2013)

Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia.
حسب: Boultwood, J, وآخرون
منشور في: (2010)

Marked downregulation of the granulopoiesis regulator LEF1 is associated with disease progression in the myelodysplastic syndromes.
حسب: Pellagatti, A, وآخرون
منشور في: (2009)

Targeted re-sequencing analysis of 25 genes commonly mutated in myeloid disorders in del(5q) myelodysplastic syndromes.
حسب: Fernandez-Mercado, M, وآخرون
منشور في: (2013)

High-resolution genomic profiling of myelodysplasia (MDS) by microarray comparative genomic hybridisation (CGH)
حسب: Esoof, N, وآخرون
منشور في: (2005)

Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays
حسب: Li Wang, وآخرون
منشور في: (2008-07-01)

Targeted re-sequencing analysis of 25 genes commonly mutated in myeloid disorders in del(5q) myelodysplastic syndromes
حسب: Marta Fernandez-Mercado, وآخرون
منشور في: (2013-12-01)

COMPREHENSIVE ANALYSIS OF MUTATION STATUS, GENE EXPRESSION PROFILES, BLOOD AND BONE MARROW COUNTS AND OUTCOME IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES
حسب: Pellagatti, A, وآخرون
منشور في: (2014)

Neutrophil PRV-1 gene expression in myeloproliferative, myelodysplastic and reactive blood disorders
حسب: Zhang, J, وآخرون
منشور في: (2004)

Gene expression profiling in 5q-syndrome and myelodysplastic syndromes.
حسب: Pellagatti, A, وآخرون
منشور في: (2003)

Identification of aberrant splicing events in myelodysplastic syndrome patients with splicing factor gene mutations
حسب: Pellagatti, A, وآخرون
منشور في: (2017)

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حسب: Boultwood, J, وآخرون
منشور في: (1995)

Gene expression profiling in the myelodysplastic syndromes using cDNA microarray technology.
حسب: Pellagatti, A, وآخرون
منشور في: (2004)

The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts
حسب: Boultwood, J, وآخرون
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Low expression of the putative tumour suppressor gene gravin in chronic myeloid leukaemia, myelodysplastic syndromes and acute myeloid leukaemia.
حسب: Boultwood, J, وآخرون
منشور في: (2004)

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حسب: Boultwood, J, وآخرون
منشور في: (1990)

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حسب: Boultwood, J, وآخرون
منشور في: (1997)

Haploinsufficiency of RPS14 and Deregulation of Ribosomal- and Translation-Related Genes in MDS Patients with Del(5q)
حسب: Pellagati, A, وآخرون
منشور في: (2008)

GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR GENE IN MYELODYSPLASTIC SYNDROMES - REPLY
حسب: Boultwood, J, وآخرون
منشور في: (1991)

Frequent Mutation of the Polycomb-Associated Gene ASXL1 In Acute Myeloid Leukemia Secondary to Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia
حسب: Fernandez-Mercado, M, وآخرون
منشور في: (2010)