Protein microarrays and proteomics
G. Macbeath
págs. 526-532
Molecular portraits and the family tree of cancer
C. Chung, C. Perou, P. Bernard
págs. 533-540
págs. 541-546
Better therapeutics through microarrays
S. R. Gullans, R. V. Jensen, D. L. Gerhold
págs. 547-552
M. Bulger, M. Groudine
págs. 555-556
Pluripotency and tumorigenicity
J. M. Brickman, T. G. Burdon
págs. 557-558
M. N. Nitabach, J. Blau
pág. 559
Unfolding heterochromatin for replication
I. L. de la Serna, A. N. Imbalzano
págs. 560-561
J. N. Athanikar, J. V. Moran, T. A. Morrish
págs. 562-564
págs. 567-568
Biological and biomedical implications of the co-evolution of pathogens and their hosts
M. Woolhouse, E. Domingo, J. Webster
págs. 569-578
Mutations in two adjacent novel genes are associated with epidermodysplasia verruciformis
N. Ramoz, B. Bouadjar, L.-a. Rueda
pág. 579
A myogenic differentiation checkpoint activated by genotoxic stress
L. D. Wood, K. Bhakta, P. L. Puri
págs. 585-593
M. Rindapaa, C. Gaspar, M. F. Kielman
págs. 594-605
Acetylation inactivates the transcriptional repressor BCL6
R. Dalla-favera, O. R. Bereshchenko, W. Gu
págs. 606-613
Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia
H. Chen, S. O. Ang, K. Hirota
págs. 614-622
Long-range chromatin regulatory interactions in vivo
D. Carter, C.S. Osborne, L. Chakalova
págs. 623-626
An ACF1-ISWI chromatin-remodeling complex is required for DNA replication through heterochromatin
R. A. Poot, N. Collins, I. Kukimoto
págs. 627-632
Core-binding factor beta interacts with Runx2 and is required for skeletal development
Carolina Andrea Yoshida, T. Fujita, T. Furuichi
págs. 633-638
Cbfbeta interacts with Runx2 and has a critical role in bone development
A. Javed, J.-p. Jeon, M. Kundu
págs. 639-644
The core-binding factor beta subunit is required for bone formation and hematopoietic maturation
T. Stacy, A. Horner, J. Miller
págs. 645-649
K. Ozaki, A. Iida, Y. Ohnishi
págs. 650-654
A mouse model of human L1 retrotransposition
J. L. Goodier, R. J. Deberardinis, E. M. Ostertag
págs. 655-660
Mutations in PHF6 are associated with Borjeson-Forssman-Lehmann syndrome
K. M. Lower, B. A. Kerr, G. Turner
págs. 661-665
L. Prokunina, C. Castillejo-lopez, F. Oberg
págs. 666-669
Restoration of type VII collagen expression and function in dystrophic epidermolysis bullosa
M. Chen, D. R. Keene, N. Kasahara
págs. 670-675
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome
C. M. Robbins, J. D. Carpten, A. Villablanca
págs. 676-680
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