pág. 391
J. S. Mattick
pág. 393
Explaining the biological activity of transactivation-deficient p53 variants
M. Tang, G. M. Wahl
págs. 395-396
Reply to Explaining the biological activity of transactivation-deficient p53 variants
T. M. Johnson, L. D. Attardi
págs. 396-397
Enrichment of regulatory motifs upstream of predicted DAF-16 targets
C. Kenyon, C. T. Murphy
págs. 397-398
Reply to Enrichment of regulatory motifs upstream of predicted DAF-16 targets
S. W. Oh, A. Mukhopadhyay
pág. 398
Skin barrier function and allergic risk
T. J. Hudson
págs. 399-400
A sweet link between TGFß and vascular disease?
R. J. Akhurst
págs. 400-401
Clonal diversity in tumor progression
D. Shibata
págs. 402-403
págs. 403-404
A simple recipe for drug interaction networks earns its stars
S. Friend, D. Schmatz
págs. 405-406
pág. 407
pág. 409
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis
M. J. Greenway, P. M. Andersen
págs. 411-413
Mutations in different components of FGF signaling in LADD syndrome
H. G. Brunner, E. Rohmann
págs. 414-417
Epistasis and the release of genetic variation during long-term selection
L. Jacobsson, O. Carlborg
págs. 418-420
págs. 421-430
The Oct4 and Nanog transcription network regulates pluripotency in mouse embryonic stem cells
Y. H. Loh
págs. 431-440
C. N. Palmer, A. D. Irvine, A. Terron-Kwiatkowski
págs. 441-446
M. F. Waters, N. A. Minassian
págs. 447-451
B. Callewaert, M. W. Wessels, P. J. Coucke, A. Willaert
págs. 452-457
B. Gold, J. E. Merriam
págs. 458-462
High mutation rates have driven extensive structural polymorphism among human Y chromosomes
S. Repping, S. K. van Daalen
págs. 463-467
Genetic clonal diversity predicts progression to esophageal adenocarcinoma
P. C. Galipeau, C. C. Maley
págs. 468-473
Calcium oxalate urolithiasis in mice lacking anion transporter Slc26a6
J. R. Asplin, Z. Jiang
págs. 474-478
págs. 479-483
T. Bataillon, R. Kassen
págs. 484-488
Functional classification of drugs by properties of their pairwise interactions
A. I. Tschumi, P. Yeh
págs. 489-494
Erratum: Mutations in different components of FGF signaling in LADD syndrome
H. G. Brunner, E. Rohmann
pág. 495
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