Congenital dyserythropoietic anemia (CDA) type IV is caused by a heterozygous mutation, Glu325Lys (E325K), in the KLF1 transcription factor. A molecular understanding of this disease is absent, partly

NIAID Data Ecosystem50

Additional file 8 of MAPK14 over-expression is a transcriptomic feature of polycythemia vera and correlates with adverse clinical outcomes

基因表达分析

血液病分子机制

Additional file 8: Table S1. The list of hub genes in the ‘tan’ module.

Figshare2024-02-06 更新40

Small ncRNA expression-profiling of blood from Hemophilia A patients identifies miR-1246 as a potential regulator of Factor 8 gene

血液病分子机制

lncRNA表达调控

Hemophilia A (HA) is a bleeding disorder caused by deficiency of functional plasma clotting factor VIII (FVIII). In addition to genetic mutations in the gene encoding FVIII (F8), there is evidence tha

NIAID Data Ecosystem50

Combined GWAS and homozygosity for HG.

血液病分子机制

遗传病基因定位

Pelger-Huët anomaly (PHA) in humans is an autosomal dominant hematological phenotype without major clinical consequences. PHA involves a characteristic hyposegmentation of granulocytes (HG). Human PHA

NIAID Data Ecosystem50

4abe3499-fd48-418b-8aa9-86f792152839 - samples

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