骨髓纤维化
表观遗传学
疾病
医学
生物
生物信息学
计算生物学
病理
免疫学
遗传学
骨髓
基因
作者
Muftah Mahmud,Swati Vasireddy,Krisstina Gowin,Akshay Amaraneni
标识
DOI:10.3390/ijms242417383
摘要
Myelofibrosis (MF), Myeloproliferative neoplasms (MPNs), and MDS/MPN overlap syndromes have a broad range of clinical presentations and molecular abnormalities, making their diagnosis and classification complex. This paper reviews molecular aberration, epigenetic modifications, chromosomal anomalies, and their interactions with cellular and other immune mechanisms in the manifestations of these disease spectra, clinical features, classification, and treatment modalities. The advent of new-generation sequencing has broadened the understanding of the genetic factors involved. However, while great strides have been made in the pharmacological treatment of these diseases, treatment of advanced disease remains hematopoietic stem cell transplant.
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