| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A comprehensive molecular characterization of beta thalassemia in a highly heterogeneous population
|
Akhavan-Niaki, Haleh
|
|
2011
|
47 |
1 |
p. 29-32
4 p.
|
artikel
|
| 2 |
A founder mutation in the MPL gene causes congenital amegakaryocytic thrombocytopenia (CAMT) in the Ashkenazi Jewish population
|
Jalas, Chaim
|
|
2011
|
47 |
1 |
p. 79-83
5 p.
|
artikel
|
| 3 |
Ancestry of African Americans with sickle cell disease
|
Solovieff, Nadia
|
|
2011
|
47 |
1 |
p. 41-45
5 p.
|
artikel
|
| 4 |
Cytokines and culture medium have a major impact on human in vitro T-cell differentiation
|
Six, Emmanuelle M.
|
|
2011
|
47 |
1 |
p. 72-78
7 p.
|
artikel
|
| 5 |
Detection of MPL exon10 mutations in 103 Chinese patients with JAK2V617F-negative myeloproliferative neoplasms
|
Chen, Xiuhua
|
|
2011
|
47 |
1 |
p. 67-71
5 p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
2011
|
47 |
1 |
p. IFC-
1 p.
|
artikel
|
| 7 |
Expression of the H-subunit and L-subunit of ferritin in bone marrow macrophages and cells of the erythron during cellular immune activation
|
Koorts, A.M.
|
|
2011
|
47 |
1 |
p. 50-55
6 p.
|
artikel
|
| 8 |
Krüppel-like factor 2 regulated gene expression in mouse embryonic yolk sac erythroid cells
|
Redmond, Latasha C.
|
|
2011
|
47 |
1 |
p. 1-11
11 p.
|
artikel
|
| 9 |
Lack of iron-related phenotype in Sp6 intestinal knockout mice
|
Matak, Pavle
|
|
2011
|
47 |
1 |
p. 46-49
4 p.
|
artikel
|
| 10 |
Oral chelators in transfusion-dependent thalassemia major patients may prevent or reverse iron overload complications
|
Farmaki, Kallistheni
|
|
2011
|
47 |
1 |
p. 33-40
8 p.
|
artikel
|
| 11 |
PAX5 deletion is common and concurrently occurs with CDKN2A deletion in B-lineage acute lymphoblastic leukemia
|
Kim, Miyoung
|
|
2011
|
47 |
1 |
p. 62-66
5 p.
|
artikel
|
| 12 |
Regulation of γ-globin gene expression involves signaling through the p38 MAPK/CREB1 pathway
|
Ramakrishnan, Valya
|
|
2011
|
47 |
1 |
p. 12-22
11 p.
|
artikel
|
| 13 |
Relationship between oxidative stress, glutathione S-transferase polymorphisms and hydroxyurea treatment in sickle cell anemia
|
Silva, Danilo Grünig Humberto
|
|
2011
|
47 |
1 |
p. 23-28
6 p.
|
artikel
|
| 14 |
Significant and continuous improvement in bone mineral density among type 1 Gaucher disease patients treated with velaglucerase alfa: 69-month experience, including dose reduction
|
Elstein, Deborah
|
|
2011
|
47 |
1 |
p. 56-61
6 p.
|
artikel
|
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