ライフサイエンスコーパス: dyserythropoietic anemia

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1 yserythropoiesis similar to human congenital dyserythropoietic anemia.

2 leukemia, myelodysplastic syndrome (MDS) or dyserythropoietic anemia.

3 logical deficiency that is relevant to human dyserythropoietic anemia and likely other disease states

4 ofactor Friend of GATA-1 (FOG-1) suffer from dyserythropoietic anemia and thrombocytopenia.

5 acterized by recurrent osteomyelitis, fever, dyserythropoietic anemia, and cutaneous inflammation.

6 feature of megaloblastic anemias, congenital dyserythropoietic anemias, and myelodysplastic syndromes

7 The congenital dyserythropoietic anemias (CDAs) are an uncommon and het

8 The congenital dyserythropoietic anemias (CDAs) are hereditary disorder

9 acking a functional alphaM-II gene develop a dyserythropoietic anemia concurrent with loss of erythro

10 Congenital dyserythropoietic anemia type 1 (CDA-1), a rare inborn a

11 Congenital dyserythropoietic anemia type II (CDAII) and combined de

12 Congenital dyserythropoietic anemia type II (CDAII) is an autosomal

13 ion mutations in SEC23B result in Congenital Dyserythropoietic Anemia type II (CDAII), a disease limi

14 ions cause an unrelated disorder, congenital dyserythropoietic anemia type II, and SEC23B-deficient m

15 niolenticulosutural dysplasia and congenital dyserythropoietic anemia type II, respectively.

16 n mice that correlates with human congenital dyserythropoietic anemia type II.

17 ith an autosomal dominant form of congenital dyserythropoietic anemia type III (CDA III).

18 more severe than that present in congenital dyserythropoietic anemia type IV as a result of dominant

19 disorder, and a group of related congenital dyserythropoietic anemias with thrombocytopenia.

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