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                             36 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Analysis of heat shock transcription factor for suppression of polyglutamine toxicity Rimoldi, Monica
 2001
 56 3-4 p. 353-362
10 p.
 artikel
2 Anterior cingulate cortical transplantation in transgenic Huntington’s disease mice van Dellen, Anton
 2001
 56 3-4 p. 313-318
6 p.
 artikel
3 Are there CAG repeat expansion-related disorders outside the central nervous system? Ferro, Paola
 2001
 56 3-4 p. 259-264
6 p.
 artikel
4 A structural approach to trinucleotide expansion diseases Masino, Laura
 2001
 56 3-4 p. 183-189
7 p.
 artikel
5 A survey of trinucleotide/tandem repeat-containing transcripts (TNRTs) isolated from human spinal cord to identify genes containing unstable DNA regions as candidates for disorders of motor function Malaspina, Andrea
 2001
 56 3-4 p. 299-306
8 p.
 artikel
6 Brain-derived neurotrophic factor inhibits apoptosis and dopamine-induced free radical production in striatal neurons but does not prevent cell death Petersén, Å
 2001
 56 3-4 p. 331-335
5 p.
 artikel
7 Calcium homeostasis and spinocerebellar ataxia-1 (SCA-1) Vig, P.J.S
 2001
 56 3-4 p. 221-225
5 p.
 artikel
8 Clinical and genetic analysis of hereditary and sporadic ataxia in central Italy Cellini, E.
 2001
 56 3-4 p. 363-366
4 p.
 artikel
9 Coenzyme Q10, exercise lactate and CTG trinucleotide expansion in myotonic dystrophy Siciliano, G
 2001
 56 3-4 p. 405-410
6 p.
 artikel
10 Cytochrome c oxidase subunit Vb interacts with human androgen receptor: a potential mechanism for neurotoxicity in spinobulbar muscular atrophy Beauchemin, Annie M.J.
 2001
 56 3-4 p. 285-297
13 p.
 artikel
11 Differential susceptibility of cultured cell lines to aggregate formation and cell death produced by the truncated Machado-Joseph disease gene product with an expanded polyglutamine stretch Yoshizawa, Toshihiro
 2001
 56 3-4 p. 349-352
4 p.
 artikel
12 Expression of the Huntington’s disease transgene in neural stem cell cultures from R6/2 transgenic mice Chu-LaGraff, Quynh
 2001
 56 3-4 p. 307-312
6 p.
 artikel
13 Familial hemiplegic migraine: a ion channel disorder Carrera, Paola
 2001
 56 3-4 p. 239-241
3 p.
 artikel
14 Fragile X syndrome and Friedreich’s ataxia: two different paradigms for repeat induced transcript insufficiency Grabczyk, Ed
 2001
 56 3-4 p. 367-373
7 p.
 artikel
15 Kennedy’s disease: a triplet repeat disorder or a motor neuron disease? Gallo, Jean-Marc
 2001
 56 3-4 p. 209-214
6 p.
 artikel
16 Localization of ataxin-2 within the cerebellar cortex of the rat Fusco, Francesca Romana
 2001
 56 3-4 p. 343-347
5 p.
 artikel
17 Molecular pathogenesis of spinal and bulbar muscular atrophy Merry, Diane E.
 2001
 56 3-4 p. 203-207
5 p.
 artikel
18 Myotonic dystrophy—a multigene disorder Larkin, Ken
 2001
 56 3-4 p. 389-395
7 p.
 artikel
19 New anti-huntingtin monoclonal antibodies: implications for huntingtin conformation and its binding proteins Ko, Jan
 2001
 56 3-4 p. 319-329
11 p.
 artikel
20 Onset and pre-onset studies to define the Huntington’s disease natural history Squitieri, F.
 2001
 56 3-4 p. 233-238
6 p.
 artikel
21 Pharmacological reactivation of inactive genes: the fragile X experience Chiurazzi, Pietro
 2001
 56 3-4 p. 383-387
5 p.
 artikel
22 Phenotypic effects of expanded ataxin-1 polyglutamines with interruptions in vitro Calabresi, Valentina
 2001
 56 3-4 p. 337-342
6 p.
 artikel
23 Polyglutamine expansion neurodegenerative disease Fischbeck, Kenneth H.
 2001
 56 3-4 p. 161-163
3 p.
 artikel
24 Polyglutamine tract expansion of the androgen receptor in a motoneuronal model of spinal and bulbar muscular atrophy Piccioni, F.
 2001
 56 3-4 p. 215-220
6 p.
 artikel
25 PQBP-1 (Np/PQ): a polyglutamine tract-binding and nuclear inclusion-forming protein Okazawa, Hitoshi
 2001
 56 3-4 p. 273-280
8 p.
 artikel
26 Protective effect of chaperones on polyglutamine diseases Kobayashi, Yasushi
 2001
 56 3-4 p. 165-168
4 p.
 artikel
27 SCA12: an unusual mutation leads to an unusual spinocerebellar ataxia Holmes, Susan E.
 2001
 56 3-4 p. 397-403
7 p.
 artikel
28 Spinocerebellar ataxia type 6: channelopathy or glutamine repeat disorder? Frontali, Marina
 2001
 56 3-4 p. 227-231
5 p.
 artikel
29 The channel hypothesis of Huntington’s disease Kagan, Bruce L.
 2001
 56 3-4 p. 281-284
4 p.
 artikel
30 The Fragile X mental retardation protein Bardoni, Barbara
 2001
 56 3-4 p. 375-382
8 p.
 artikel
31 Tissue-transglutaminase in rat and human brain: light and electron immunocytochemical analysis and in situ hybridization study Maggio, Nicola
 2001
 56 3-4 p. 173-182
10 p.
 artikel
32 Transglutaminase-dependent formation of protein aggregates as possible biochemical mechanism for polyglutamine diseases Violante, V.
 2001
 56 3-4 p. 169-172
4 p.
 artikel
33 Trinucleotide repeat expansions: do they contribute to bipolar disorder? Goossens, Dirk
 2001
 56 3-4 p. 243-257
15 p.
 artikel
34 Triplet repeat diseases: from basic to clinical aspects Servadio, Antonio
 2001
 56 3-4 p. 159-
1 p.
 artikel
35 Triplet repeats, over-expanded in neuromuscular diseases, are under-represented in mammalian DNA: a survey of models Astolfi, P
 2001
 56 3-4 p. 265-271
7 p.
 artikel
36 Triplet repeats, RNA secondary structure and toxic gain-of-function models for pathogenesis Galvão, Rui
 2001
 56 3-4 p. 191-201
11 p.
 artikel
                             36 gevonden resultaten
 
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