Unknown

Dataset Information

0

Molecular pathophysiology of myelodysplastic syndromes.


ABSTRACT: The clinicopathologic heterogeneity of myelodysplastic syndromes (MDS) is driven by diverse, somatically acquired genetic abnormalities. Recent technological advances have enabled the identification of many new mutations, which have implicated novel pathways in MDS pathogenesis, including RNA splicing and epigenetic regulation of gene expression. Molecular abnormalities, either somatic point mutations or chromosomal lesions, can be identified in the vast majority of MDS cases and underlie specific disease phenotypes. As the full array of molecular abnormalities is characterized, genetic variables are likely to complement standard morphologic evaluation in future MDS classification schemes and risk models.

SUBMITTER: Lindsley RC 

PROVIDER: S-EPMC3514602 | biostudies-literature | 2013 Jan

REPOSITORIES: biostudies-literature

altmetric image

Publications

Molecular pathophysiology of myelodysplastic syndromes.

Lindsley R Coleman RC   Ebert Benjamin L BL  

Annual review of pathology 20120828


The clinicopathologic heterogeneity of myelodysplastic syndromes (MDS) is driven by diverse, somatically acquired genetic abnormalities. Recent technological advances have enabled the identification of many new mutations, which have implicated novel pathways in MDS pathogenesis, including RNA splicing and epigenetic regulation of gene expression. Molecular abnormalities, either somatic point mutations or chromosomal lesions, can be identified in the vast majority of MDS cases and underlie specif  ...[more]

Similar Datasets

| S-EPMC6199665 | biostudies-literature
| S-EPMC6347085 | biostudies-literature
| S-EPMC4340482 | biostudies-literature
| S-EPMC8791166 | biostudies-literature
2019-10-30 | PXD013609 | Pride
| S-EPMC2413090 | biostudies-other
| S-EPMC3487546 | biostudies-literature
| S-EPMC8541058 | biostudies-literature
| S-EPMC8582368 | biostudies-literature
| S-EPMC7917605 | biostudies-literature