| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A key role of toll-like receptor 3 in tissue factor activation through extracellular signal regulated kinase 1/2 pathway in a murine hypoxia model
|
Biswas, Indranil
|
|
2012
|
49 |
2 |
p. 92-101
10 p.
|
artikel
|
| 2 |
Clinical and molecular characterization of a rare 2.4kb deletion causing α+ thalassemia in a Chinese family
|
Lin, Min
|
|
2012
|
49 |
2 |
p. 83-84
2 p.
|
artikel
|
| 3 |
Comprehensive profile of cytogenetics in 2308 Chinese children and adults with de novo acute myeloid leukemia
|
Li, Xin
|
|
2012
|
49 |
2 |
p. 107-113
7 p.
|
artikel
|
| 4 |
Corrigendum to “The platelet P2 receptors in arterial thrombosis” [Blood Cells Mol. Dis. 36 (2006) 223–227]
|
Gachet, Christian
|
|
2012
|
49 |
2 |
p. 120-
1 p.
|
artikel
|
| 5 |
Editorial Board
|
|
|
2012
|
49 |
2 |
p. IFC-
1 p.
|
artikel
|
| 6 |
EPAS1 and EGLN1 associations with high altitude sickness in Han and Tibetan Chinese at the Qinghai–Tibetan Plateau
|
Buroker, Norman E.
|
|
2012
|
49 |
2 |
p. 67-73
7 p.
|
artikel
|
| 7 |
Iron metabolism in hepcidin1 knockout mice in response to phenylhydrazine-induced hemolysis
|
Masaratana, Patarabutr
|
|
2012
|
49 |
2 |
p. 85-91
7 p.
|
artikel
|
| 8 |
Phenotype heterogeneity of hyperbilirubinemia condition: The lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler–Najjar Syndrome type II in an Italian patient
|
Minucci, Angelo
|
|
2012
|
49 |
2 |
p. 118-119
2 p.
|
artikel
|
| 9 |
Preliminary characterization of the murine membrane reticulocyte proteome
|
Prenni, Jessica E.
|
|
2012
|
49 |
2 |
p. 74-82
9 p.
|
artikel
|
| 10 |
Recessive congenital methemoglobinemia caused by a rare mechanism: Maternal uniparental heterodisomy with segmental isodisomy of a chromosome 22
|
Huang, Yu-Hsiu
|
|
2012
|
49 |
2 |
p. 114-117
4 p.
|
artikel
|
| 11 |
Two isoforms of HOXA9 function differently but work synergistically in human MLL-rearranged leukemia
|
He, Miao
|
|
2012
|
49 |
2 |
p. 102-106
5 p.
|
artikel
|
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