Haploinsufficiency of RPS14 and Deregulation of Ribosomal- and Translation-Related Genes in MDS Patients with Del(5q)

Haploinsufficiency of RPS14 and Deregulation of Ribosomal- and Translation-Related Genes in MDS Patients with Del(5q)

Manylion Llyfryddiaeth
Prif Awduron:	Pellagati, A, Hellstroem-Lindberg, E, Giagounidis, A, Perry, J, Malcovati, L, Della Porta, M, Jaedersten, M, Killick, S, Sohal, D, Verma, A, Cazzola, M, Wainscoat, J, Boultwood, J
Fformat:	Conference item
Cyhoeddwyd:	2008

Eitemau Tebyg

Haploinsufficiency of RPS14 in 5q- syndrome is associated with deregulation of ribosomal- and translation-related genes.
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2008)

Haploinsufficiency of RPS14 in 5q- syndrome is associated with deregulation of ribosomal- and translation-related genes (British Journal of Haematology (2008) 142, (57-64))
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2009)

Frequent Mutation of the Polycomb-Associated Gene ASXL1 in the Myelodysplastic Syndromes and in Acute Myeloid Leukaemia
gan: Boultwood, J, et al.
Cyhoeddwyd: (2009)

Deregulated Gene Expression Pathways in Myelodysplastic Syndrome Hematopoietic Stem Cells
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2009)

Deregulated gene expression pathways in myelodysplastic syndrome hematopoietic stem cells.
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2010)

Gene Expression Profiling of CD34(+) Cells in Patients with Myelodysplastic Syndromes
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2008)

High-resolution genomic profiling of myelodysplasia (MDS) by microarray comparative genomic hybridization (CGH).
gan: Esoof, N, et al.
Cyhoeddwyd: (2006)

Downregulation of Ribosomal Proteins Is Seen in Non 5q-MDS
gan: Sohal, P, et al.
Cyhoeddwyd: (2008)

Haploinsufficiency of ribosomal proteins and p53 activation in anemia: Diamond-Blackfan anemia and the 5q- syndrome.
gan: Boultwood, J, et al.
Cyhoeddwyd: (2012)

The role of haploinsufficiency of RPS14 and p53 activation in the molecular pathogenesis of the 5q- syndrome.
gan: Boultwood, J
Cyhoeddwyd: (2011)

Identification of Prognostic Markers by Gene Expression Profiling In Myelodysplastic Syndrome Hematopoietic Stem Cells
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2010)

Identification of Prognostic Markers by Gene Expression Profiling In Myelodysplastic Syndrome Hematopoietic Stem Cells
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2010)

High-resolution genomic profiling of myelodysplasia (MDS) by microarray comparative genomic hybridisation (CGH)
gan: Esoof, N, et al.
Cyhoeddwyd: (2005)

Marked down-regulation of nucleophosmin-1 is associated with advanced del(5q) myelodysplastic syndrome.
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2011)

Identification of Prognostic Markers by Gene Expression Profiling In Myelodysplastic Syndrome Hematopoietic Stem Cells
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2010)

Marked down-regulation of nucleophosmin-1 is associated with advanced del(5q) myelodysplastic syndrome
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2011)

Genome-wide analysis of copy number change and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density SNP arrays
gan: Wang, L, et al.
Cyhoeddwyd: (2007)

Effects of L-leucine in 5q-syndrome and other RPS14-deficient erythroblasts
gan: Yip, B, et al.
Cyhoeddwyd: (2012)

Effects of L-leucine in 5q- syndrome and other RPS14-deficient erythroblasts.
gan: Yip, B, et al.
Cyhoeddwyd: (2012)

Expression profiling of CD34+cells in patients with myelodysplastic syndromes with and without a del(5q)
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2005)

Gene expression profiling of CD34+ cells in patients with the 5q- syndrome.
gan: Boultwood, J, et al.
Cyhoeddwyd: (2007)

Activation of the mTOR Signaling Pathway by L-Leucine in RPS14-Deficient Erythroid Cells
gan: Yip, B, et al.
Cyhoeddwyd: (2012)

Marked downregulation of the granulopoiesis regulator LEF1 is associated with disease progression in the myelodysplastic syndromes.
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2009)

Expression profiling of CD34+cells in patients with myelodysplastic syndromes: Involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype.
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2006)

Expression profiling of CD34+cells in patients with myelodysplastic syndromes: differences between early and advanced cases and analysis of apoptosis-related genes
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2007)

The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts
gan: Boultwood, J, et al.
Cyhoeddwyd: (2008)

Gene expression profiles of CD34+ cells in myelodysplastic syndromes: involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype.
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2006)

Identification of gene expression-based prognostic markers in the hematopoietic stem cells of patients with myelodysplastic syndromes.
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2013)

Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia.
gan: Boultwood, J, et al.
Cyhoeddwyd: (2010)

Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays.
gan: Wang, L, et al.
Cyhoeddwyd: (2008)

Lenalidomide selectively inhibits in vitro growth of the malignant clone in myelodysplastic syndrome (MDS) patients with 5q deletion.
gan: Jadersten, M, et al.
Cyhoeddwyd: (2005)

Activation of the mTOR signaling pathway by L-leucine in 5q- syndrome and other RPS14-deficient erythroblasts.
gan: Yip, B, et al.
Cyhoeddwyd: (2013)

Activation of the mTOR signaling pathway by L-leucine in 5q-syndrome and other RPS14-deficient erythroblasts
gan: Yip, B, et al.
Cyhoeddwyd: (2013)

Gene expression profiling of day 7 erythroblasts from RARS before and after treatment with G-CSF
gan: Nikpour, M, et al.
Cyhoeddwyd: (2007)

Differential expression of genes related to JAK-STAT pathway activation or megakaryocyte differentiation/maturation in CD34+cells from patients with refractory anemia with ringed sideroblasts and thrombocytosis (RARS-T)
gan: Malcovati, L, et al.
Cyhoeddwyd: (2007)

Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia
gan: Bolze, A, et al.
Cyhoeddwyd: (2013)

Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia.
gan: Bolze, A, et al.
Cyhoeddwyd: (2013)

Subfunctionalized expression drives evolutionary retention of ribosomal protein paralogs Rps27 and Rps27l in vertebrates
gan: Adele Francis Xu, et al.
Cyhoeddwyd: (2023-06-01)

COMPREHENSIVE ANALYSIS OF MUTATION STATUS, GENE EXPRESSION PROFILES, BLOOD AND BONE MARROW COUNTS AND OUTCOME IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES
gan: Pellagatti, A, et al.
Cyhoeddwyd: (2014)

Haploinsufficiency of the essential gene Rps12 causes defects in erythropoiesis and hematopoietic stem cell maintenance
gan: Virginia Folgado-Marco, et al.
Cyhoeddwyd: (2023-06-01)