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Results: 1-7 |
Results: 7
Generation of HIV latency during thymopoiesis
Authors: Brooks, DG Kitchen, SG Kitchen, CMR Scripture-Adams, DD Zack, JA
Citation: Dg. Brooks et al., Generation of HIV latency during thymopoiesis, NAT MED, 7(4), 2001, pp. 459-464
Mutant K-ras enhances apoptosis in embryonic stem cells in combination with DNA damage and is associated with increased levels of p19(ARF)
Authors: Brooks, DG James, RM Patek, CE Williamson, J Arends, MJ
Citation: Dg. Brooks et al., Mutant K-ras enhances apoptosis in embryonic stem cells in combination with DNA damage and is associated with increased levels of p19(ARF), ONCOGENE, 20(17), 2001, pp. 2144-2152
In vivo evidence of brain galactitol accumulation in an infant with galactosemia and encephalopathy
Authors: Berry, GT Hunter, JV Wang, ZY Dreha, S Mazur, A Brooks, DG Ning, C Zimmerman, RA Segal, S
Citation: Gt. Berry et al., In vivo evidence of brain galactitol accumulation in an infant with galactosemia and encephalopathy, J PEDIAT, 138(2), 2001, pp. 260-262
Reversible subacute combined degeneration of the spinal cord in a 14-year-old due to a strict vegan diet
Authors: Licht, DJ Berry, GT Brooks, DG Younkin, DP
Citation: Dj. Licht et al., Reversible subacute combined degeneration of the spinal cord in a 14-year-old due to a strict vegan diet, CLIN PEDIAT, 40(7), 2001, pp. 413-415
Increased serum transferrin receptor concentrations in Friedreich ataxia
Authors: Wilson, RB Lynch, DR Farmer, JM Brooks, DG Fischbeck, KH
Citation: Rb. Wilson et al., Increased serum transferrin receptor concentrations in Friedreich ataxia, ANN NEUROL, 47(5), 2000, pp. 659-661
Human immunodeficiency virus type 1-induced hematopoietic inhibition is independent of productive infection of progenitor cells in vivo
Authors: Koka, PS Jamieson, BD Brooks, DG Zack, JA
Citation: Ps. Koka et al., Human immunodeficiency virus type 1-induced hematopoietic inhibition is independent of productive infection of progenitor cells in vivo, J VIROLOGY, 73(11), 1999, pp. 9089-9097
Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes
Authors: Annunen, S Korkko, J Czarny, M Warman, ML Brunner, HG Kaariainen, H Mulliken, JB Tranebjaerg, L Brooks, DG Cox, GF Cruysberg, JR Curtis, MA Davenport, SLH Friedrich, CA Kaitila, I Krawczynski, MR Latos-Bielenska, A Mukai, S Olsen, BR Shinno, N Somer, M Vikkula, M Zlotogora, J Prockop, DJ Ala-Kokko, L
Citation: S. Annunen et al., Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes, AM J HU GEN, 65(4), 1999, pp. 974-983
Risultati: 1-7 |