AAAAAA

   
Results: 1-14 |
Results: 14
Mining the genome for causes and cures of neurological disease
Authors: Lieberman, AP Puls, I Fischbeck, KH
Citation: Ap. Lieberman et al., Mining the genome for causes and cures of neurological disease, TRENDS PHAR, 22(4), 2001, pp. 161-162
Polyglutamine and CBP: Fatal attraction?
Authors: McCampbell, A Fischbeck, KH
Citation: A. Mccampbell et Kh. Fischbeck, Polyglutamine and CBP: Fatal attraction?, NAT MED, 7(5), 2001, pp. 528-530
Gentamicin treatment of Duchenne and Becker muscular dystrophy due to nonsense mutations
Authors: Wagner, KR Hamed, S Hadley, DW Gropman, AL Burstein, AH Escolar, DM Hoffman, EP Fischbeck, KH
Citation: Kr. Wagner et al., Gentamicin treatment of Duchenne and Becker muscular dystrophy due to nonsense mutations, ANN NEUROL, 49(6), 2001, pp. 706-711
Polyglutamine expansion neurodegenerative disease
Authors: Fischbeck, KH
Citation: Kh. Fischbeck, Polyglutamine expansion neurodegenerative disease, BRAIN RES B, 56(3-4), 2001, pp. 161-163
Androgens regulate the mammalian homologues of invertebrate sex determination genes tra-2 and fox-1
Authors: Lieberman, AP Friedlich, DL Harmison, G Howell, BW Jordan, CL Breedlove, SM Fischbeck, KH
Citation: Ap. Lieberman et al., Androgens regulate the mammalian homologues of invertebrate sex determination genes tra-2 and fox-1, BIOC BIOP R, 282(2), 2001, pp. 499-506
Impact of the human genome sequence on neurology and neuroscience
Authors: Puls, I Lieberman, AP Fischbeck, KH
Citation: I. Puls et al., Impact of the human genome sequence on neurology and neuroscience, ARCH NEUROL, 58(11), 2001, pp. 1750-1751
CREB-binding protein sequestration by expanded polyglutamine
Authors: McCampbell, A Taylor, JP Taye, AA Robitschek, J Li, M Walcott, J Merry, D Chai, YH Paulson, H Sobue, G Fischbeck, KH
Citation: A. Mccampbell et al., CREB-binding protein sequestration by expanded polyglutamine, HUM MOL GEN, 9(14), 2000, pp. 2197-2202
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
Triplet repeat expansion in neuromuscular disease
Authors: Lieberman, AP Fischbeck, KH
Citation: Ap. Lieberman et Kh. Fischbeck, Triplet repeat expansion in neuromuscular disease, MUSCLE NERV, 23(6), 2000, pp. 843-850
Androgen receptor mutation in Kennedy's disease
Authors: Fischbeck, KH Lieberman, A Bailey, CK Abel, A Merry, DE
Citation: Kh. Fischbeck et al., Androgen receptor mutation in Kennedy's disease, PHI T ROY B, 354(1386), 1999, pp. 1075-1078
Ataxin 1 and ataxin 3 in neuronal intranuclear inclusion disease
Authors: Lieberman, AP Trojanowski, JQ Leonard, DGB Chen, KL Barnett, JL Leverenz, JB Bird, TD Robitaille, Y Malandrini, A Fischbeck, KH
Citation: Ap. Lieberman et al., Ataxin 1 and ataxin 3 in neuronal intranuclear inclusion disease, ANN NEUROL, 46(2), 1999, pp. 271-273
Is CMTX an axonopathy?
Authors: Scherer, SS Fischbeck, KH
Citation: Ss. Scherer et Kh. Fischbeck, Is CMTX an axonopathy?, NEUROLOGY, 52(2), 1999, pp. 432-433
A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathy
Authors: Hadjigeorgiou, GM Kim, SH Fischbeck, KH Andreu, AL Berry, GT Bingham, P Shanske, S Bonilla, E DiMauro, S
Citation: Gm. Hadjigeorgiou et al., A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathy, J NEUR SCI, 164(2), 1999, pp. 153-157
Studies in transgenic mice indicate a loss of connexin32 function in X-linked Charcot-Marie-tooth disease
Authors: Abel, A Bone, LJ Messing, A Scherer, SS Fischbeck, KH
Citation: A. Abel et al., Studies in transgenic mice indicate a loss of connexin32 function in X-linked Charcot-Marie-tooth disease, J NE EXP NE, 58(7), 1999, pp. 702-710
Risultati: 1-14 |