Digitale Bibliotheek
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                             19 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome Curran, Mark E
1995
80 5 p. 795-803
9 p.
artikel
2 Amyotrophic lateral sclerosis: Recent insights from genetics and transgenic mice Brown Jr., Robert H
1995
80 5 p. 687-692
6 p.
artikel
3 An amino-terminal domain of Mxi1 mediates anti-myc oncogenic activity and interacts with a homolog of the Yeast Transcriptional Repressor SIN3 Schreiber-Agus, Nicole
1995
80 5 p. 777-786
10 p.
artikel
4 A phosphotyrosine interaction domain Bork, Peer
1995
80 5 p. 693-694
2 p.
artikel
5 B7-1 and B7-2 costimulatory molecules activate differentially the Th1/Th2 developmental pathways: Application to autoimmune disease therapy Kuchroo, Vijay K
1995
80 5 p. 707-718
12 p.
artikel
6 Binding of pumilio to maternal hunchback mRNA is required for posterior patterning in drosophila embryos Murata, Yoshihiko
1995
80 5 p. 747-756
10 p.
artikel
7 Branch migration during homologous recombination: assembly of a RuvAB-holliday junction complex in vitro Hiom, Kevin
1995
80 5 p. 787-793
7 p.
artikel
8 Defective DNA-dependent protein kinase activity is linked to V(D)J recombination and DNA repair defects associated with the murine scid mutation Blunt, Tracy
1995
80 5 p. 813-823
11 p.
artikel
9 Fibroblast growth factors induce additional limb development from the flank of chick embryos Cohn, Martin J
1995
80 5 p. 739-746
8 p.
artikel
10 Increased neutrophil respiratory burst in bcr-null mutants Voncken, Jan Willem
1995
80 5 p. 719-728
10 p.
artikel
11 Mad-max transcriptional repression is mediated by ternary complex formation with mammalian homologs of yeast repressor Sin3 Ayer, Donald E
1995
80 5 p. 767-776
10 p.
artikel
12 Molecular mimicry in T cell-mediated autoimmunity: Viral peptides activate human T cell clones specific for myelin basic protein Wucherpfennig, Kai W
1995
80 5 p. 695-705
11 p.
artikel
13 Overexcited or inactive: Ion channels in muscle disease Hoffman, Eric P
1995
80 5 p. 681-686
6 p.
artikel
14 Positions available 1995
80 5 p. i-xiv
nvt p.
artikel
15 SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome Wang, Qing
1995
80 5 p. 805-811
7 p.
artikel
16 Specific deficit of the ON response in visual transmission by targeted disruption of the mGIuR6 gene Masu, Masayuki
1995
80 5 p. 757-765
9 p.
artikel
17 Specific recruitment of SH-PTP1 to the erythropoietin receptor causes inactivation of JAK2 and termination of proliferative signals Klingmüller, Ursula
1995
80 5 p. 729-738
10 p.
artikel
18 The initiation of the limb bud: Growth factors, Hox genes, and retinoids Tabin, Cliff
1995
80 5 p. 671-674
4 p.
artikel
19 Three muscular dystrophies: Loss of cytoskeleton-extracellular matrix linkage Campbell, Kevin P
1995
80 5 p. 675-679
5 p.
artikel
                             19 gevonden resultaten
 
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