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                             20 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A European allele map of the C282Y mutation of hemochromatosis: Celtic versus Viking origin of the mutation? Lucotte, Gérard
2003
31 2 p. 262-267
6 p.
artikel
2 Author index for volume 31, number 2 2003
31 2 p. 298-
1 p.
artikel
3 Commentary on “The 1604A (R496H) mutation in Gaucher disease: genotype/phenotype correlation,” by Brautbar et al. Allitto, Bernice A.
2003
31 2 p. 190-191
2 p.
artikel
4 Donor cell replacement in mice transplanted in utero is limited by immune-independent mechanisms Barker, J.E
2003
31 2 p. 291-297
7 p.
artikel
5 Expression of ferroportin in hemochromatosis liver Adams, Paul C
2003
31 2 p. 256-261
6 p.
artikel
6 Glucose-6-phosphate dehydrogenase (G6PD) mutations and UDP-glucuronosyltransferase promoter polymorphism among G6PD deficient Kuwaitis Samilchuk, Elena
2003
31 2 p. 201-205
5 p.
artikel
7 HFE mutations in the elderly Willis, Gavin
2003
31 2 p. 240-246
7 p.
artikel
8 Inhibition of sickling in vitro by three purine-based antiviral agents: DeBellis, Robert H
2003
31 2 p. 286-290
5 p.
artikel
9 Multilineage gene expression in human bone marrow stromal cells as evidenced by single-cell microarray analysis☆ Seshi, Beerelli
2003
31 2 p. 268-285
18 p.
artikel
10 Myb protein specificity: evidence of a context-specific transcription factor code Ness, Scott A
2003
31 2 p. 192-200
9 p.
artikel
11 Myeloid differentiation (MyD) primary response genes in hematopoiesis Liebermann, Dan A
2003
31 2 p. 213-228
16 p.
artikel
12 [No title] Rochette, Prof.J.
2003
31 2 p. 174-
1 p.
artikel
13 Phenotypic expression of the C282Y/Q283P compound heterozygosity in HFE and molecular modeling of the Q283P mutation effect Oberkanins, Dr.Christian
2003
31 2 p. 173-
1 p.
artikel
14 Search for genetic determinants of individual variability of the erythropoietin response to high altitude Jedlickova, Katerina
2003
31 2 p. 175-182
8 p.
artikel
15 Short insertion in a hemoglobin chain: Hb Esch, an unstable α1 variant with duplication of the sequence Ala65-Leu-Thr-Asn68 Préhu, C
2003
31 2 p. 234-239
6 p.
artikel
16 The 1604A (R496H) mutation in Gaucher disease: genotype/phenotype correlation Brautbar, Ariel
2003
31 2 p. 187-189
3 p.
artikel
17 The importance of PU.1 concentration in hematopoietic lineage commitment and maturation Dahl, Richard
2003
31 2 p. 229-233
5 p.
artikel
18 The role of endogenous heme synthesis and degradation domain cysteines in cellular iron-dependent degradation of IRP2 Bourdon, Emmanuel
2003
31 2 p. 247-255
9 p.
artikel
19 The role of EVI1 in normal and leukemic cells Buonamici, Silvia
2003
31 2 p. 206-212
7 p.
artikel
20 Unsuccessful chimeraplast strategy for the correction of a mutation causing Gaucher disease Diaz-Font, Anna
2003
31 2 p. 183-186
4 p.
artikel
                             20 gevonden resultaten
 
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