| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Activation of a cryptic splice site in a potentially lethal coagulation defect accounts for a functional protein variant
|
Cavallari, Nicola
|
|
2012
|
1822 |
7 |
p. 1109-1113
5 p.
|
artikel
|
| 2 |
Adaptation of respiratory chain biogenesis to cytochrome c oxidase deficiency caused by SURF1 gene mutations
|
Kovářová, Nikola
|
|
2012
|
1822 |
7 |
p. 1114-1124
11 p.
|
artikel
|
| 3 |
A relation between TGF-β and mast cell tryptase in experimental emphysema models
|
Mortaz, Esmaeil
|
|
2012
|
1822 |
7 |
p. 1154-1160
7 p.
|
artikel
|
| 4 |
Controlling a master switch of adipocyte development and insulin sensitivity: Covalent modifications of PPARγ
|
Floyd, Z. Elizabeth
|
|
2012
|
1822 |
7 |
p. 1090-1095
6 p.
|
artikel
|
| 5 |
Editorial Board
|
|
|
2012
|
1822 |
7 |
p. i-
1 p.
|
artikel
|
| 6 |
Increased cone sensitivity to ABCA4 deficiency provides insight into macular vision loss in Stargardt's dystrophy
|
Conley, Shannon M.
|
|
2012
|
1822 |
7 |
p. 1169-1179
11 p.
|
artikel
|
| 7 |
β2 long-acting and anticholinergic drugs control TGF-β1-mediated neutrophilic inflammation in COPD
|
Profita, Mirella
|
|
2012
|
1822 |
7 |
p. 1079-1089
11 p.
|
artikel
|
| 8 |
Lysosomal di-N-acetylchitobiase-deficient mouse tissues accumulate Man2GlcNAc2 and Man3GlcNAc2
|
Persichetti, Emanuele
|
|
2012
|
1822 |
7 |
p. 1137-1146
10 p.
|
artikel
|
| 9 |
Overexpression of VMAT-2 and DT-diaphorase protects substantia nigra-derived cells against aminochrome neurotoxicity
|
Muñoz, Patricia
|
|
2012
|
1822 |
7 |
p. 1125-1136
12 p.
|
artikel
|
| 10 |
Quantitative magnetic analysis reveals ferritin-like iron as the most predominant iron-containing species in the murine Hfe-haemochromatosis
|
Gutiérrez, Lucía
|
|
2012
|
1822 |
7 |
p. 1147-1153
7 p.
|
artikel
|
| 11 |
Transcriptional changes in OXPHOS complex I deficiency are related to anti-oxidant pathways and could explain the disturbed calcium homeostasis
|
Voets, A.M.
|
|
2012
|
1822 |
7 |
p. 1161-1168
8 p.
|
artikel
|
| 12 |
ß-Ureidopropionase deficiency: Phenotype, genotype and protein structural consequences in 16 patients
|
van Kuilenburg, André B.P.
|
|
2012
|
1822 |
7 |
p. 1096-1108
13 p.
|
artikel
|
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