Cytogenetic progression in MDS patients.

Figshare2015-12-02 更新2026-04-29 收录

骨髓增生异常综合征

细胞遗传学进展

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https://figshare.com/articles/dataset/_Cytogenetic_progression_in_MDS_patients_/415530 数据链接链接失效反馈

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9 non-responders with primary resistance showing abnormal cytogenetics, 6 patients showing cytogenetic progression from diagnosis to relapse.

创建时间：

2015-12-02

Supplementary Material for: Copper Deficiency Mimicking Myelodysplastic Syndrome: Zinc Supplementation in the Setting of COVID-19

铜缺乏症

骨髓增生异常综合征

While copper deficiency is rare, it can have serious consequences, including pancytopenia and neuropathy. This treatable vitamin deficiency can present very similarly to myelodysplastic syndrome (MDS)

DataCite Commons2023-07-22 更新80

The Bone marrow stroma in human myelodysplastic syndrome reveals alterations that regulate disease progression [CD34+CD38-_MDS]

骨髓增生异常综合征

骨髓微环境免疫调节

Myelodysplastic syndromes (MDS) are a heterogenous group of diseases affecting the hematopoietic stem cell that are curable only by stem cell transplantation. Both hematopoietic cell intrinsic changes

NIAID Data Ecosystem30

Functional Evidence Implicating Chromosome 7q22 Haploinsufficiency in Myelodysplastic Syndrome Pathogenesis

骨髓增生异常综合征

差异表达转录组分析

Purpose: 5A3+/del mice, which have a heterozygous germ line deletion of a 2-Mb interval of chromosome band 5A3 syntenic to a commonly deleted segment of human 7q22, exhibit hematopoietic stem cell (HS

Alliance of Genome Resources30

Synthetic lethal interactions and convergent biological effects underlie the mutual exclusivity of MDS-associated spliceosomal gene mutations

剪接体功能研究

骨髓增生异常综合征

RNA splicing factor mutations constitute the most common class of alterations in myelodysplastic syndromes (MDS). These occur as heterozygous mutations at restricted residues in SF3B1, SRSF2, and U2AF

NIAID Data Ecosystem40

Depletion of tet2 results in age-dependent changes in DNA methylation and gene expression in a zebrafish model of myelodysplastic syndrome [DNAmethylation]

骨髓增生异常综合征

DNA甲基化动态

Myelodysplastic Syndrome (MDS) is a heterogenous group of clonal hematopoietic disorders characterized by ineffective hematopoiesis, cytopenias and dysplasia. The gene encoding Ten-ele¬ven translocati

NIAID Data Ecosystem30

Cytogenetic progression in MDS patients.

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