首页/数据集/Homozygous alpha+ thalassaemia in Zimbabwe: an unrecognized cause of hypochromia and microcytosis

Homozygous alpha+ thalassaemia in Zimbabwe: an unrecognized cause of hypochromia and microcytosis

Global Health Data Exchange ()2024-06-26 收录

数据链接：

https://ghdx.healthdata.org/record/homozygous-alpha-thalassaemia-zimbabwe-unrecognized-cause-hypochromia-and-microcytosis 数据链接链接失效反馈

官方服务：

资源简介：

Homozygous alpha+ thalassaemia in Zimbabwe: an unrecognized cause of hypochromia and microcytosis

应用场景：

相关数据集

KiViDrag/bloodmnist_55

医学图像分析

血液学

该数据集包含图像和对应的标签，标签代表不同类型的白细胞。具体来说，标签包括嗜碱性粒细胞、嗜酸性粒细胞、成红细胞、未成熟粒细胞（包括髓细胞、晚幼粒细胞和早幼粒细胞）、淋巴细胞、单核细胞、中性粒细胞和血小板。数据集被分割为训练集，包含107,631个样本，总大小为261,057,727.125字节。

Hugging Face2024-11-08 更新130

Increased BM plasma level of soluble CD30 in AA

血液学

免疫学

BM CD3+ T cells from healthy individuals and SAA patients were co-cultured with mitomycin C treated allogenetic mononuclear cells for a total of 7 days, kinetics of cell surface expression of CD30 by

DataCite Commons2020-09-04 更新60

Comprehensive screening for coexisting heterozygous α 0 -thalassemia in hemoglobin E trait

地中海贫血

血红蛋白E

Objectives: A sensitive screening for the coexistence of α 0 -thalassemia and the hemoglobin E (Hb E) trait is important to identify at-risk couples for hydrops fetalis. However, previ

DataCite Commons2021-05-18 更新60

Hematological analysis of bloods obtained from mice administrated with 50/kg or 100 mg/kg of AE-BCT.

血液学

药物效果评估

Data are presented as mean ± SD. Each group of mice (n = 3) were orally administrated with 50 or 100 mg/kg daily, sacrificed at 15 days, and analyzed hematologic parameters. CBC, complete blood cell c

NIAID Data Ecosystem60

Enhanced binding of GP1BA variant to VWF multimer:collagen

分子生物学

血液学

The Reactome event describes gain-of-function variants of glycoprotein Ib α (GPIbα, encoded by GP1BA) that cause macrothrombocytopenia and mucocutaneous bleeding in patients with platelet-type von Wil

reactome.org60