Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("Spinocerebellar heredodegeneration")

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Language

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 355

  • Page / 15
Export

Selection :

  • and

The characteristics of a visual-guided tracking movement in responce [response] to variable elastic loads in patients with spinocerebellar degenerationTAKEMURA, T; ITO, M; TAHARA, N et al.Journal of the Faculty of Engineering. Shinshu University. 1995, Num 75, pp 1-7, issn 0037-3818Article

Method to introduce stable, expanded, polyglutamine-encoding CAG/CAA trinucleotide repeats into CAG repeat-containing genesMICHALIK, Andrej; KAZANTSEV, Aleksey; VAN BROECKHOVEN, Christine et al.BioTechniques. 2001, Vol 31, Num 2, pp 250-254, issn 0736-6205, 3 p.Article

Ataxin-3 binds VCP/p97 and regulates retrotranslocation of ERAD substratesXIAOYAN ZHONG; PITTMAN, Randall N.Human molecular genetics (Print). 2006, Vol 15, Num 16, pp 2409-2420, issn 0964-6906, 12 p.Article

Elucidation of ataxin-3 and ataxin-7 function by integrative bioinformaticsSCHEEL, Hartmut; TOMIUK, Stefan; HOFMANN, Kay et al.Human molecular genetics (Print). 2003, Vol 12, Num 21, pp 2845-2852, issn 0964-6906, 8 p.Article

Un nouveau regard sur les hérédodégénérescences spino-cérébelleuses = New insight of spino-cerebellar heredodegeneration syndromeDURR, A; BRICE, A; AGID, Y et al.La Revue du praticien (Paris). 1995, Vol 45, Num 5, pp 536-540, issn 0035-2640Article

Ataxin-2 and huntingtin interact with endophilin-A complexes to function in plastin-associated pathwaysRALSER, Markus; NONHOFF, Ute; ALBRECHT, Mario et al.Human molecular genetics (Print). 2005, Vol 14, Num 19, pp 2893-2909, issn 0964-6906, 17 p.Article

Ataxin-2 repeat-length variation and neurodegenerationROSS, Owen A; RUTHERFORD, Nicola J; SEELEY, William W et al.Human molecular genetics (Print). 2011, Vol 20, Num 16, pp 3207-3212, issn 0964-6906, 6 p.Article

Gp78, an ER associated E3, promotes SOD1 and ataxin-3 degradationZHENG YING; HONGFENG WANG; HUADONGFAN et al.Human molecular genetics (Print). 2009, Vol 18, Num 22, pp 4268-4281, issn 0964-6906, 14 p.Article

Mapping of the Sca1 and pcd genes on mouse chromosome 13 provides evidence that they are different genesSERVADIO, A; MCCALL, A; ZOGHBI, H et al.Genomics (San Diego, Calif.). 1995, Vol 29, Num 3, pp 812-813, issn 0888-7543Article

Neuron-specific proteotoxicity of mutant ataxin-3 in C. elegans: rescue by the DAF-16 and HSF-1 pathwaysTEIXEIRA-CASTRO, Andreia; AILION, Michael; MACIEL, Patrícia et al.Human molecular genetics (Print). 2011, Vol 20, Num 15, pp 2996-3009, issn 0964-6906, 14 p.Article

Proteolytic cleavage of polyglutamine-expanded ataxin-3 is critical for aggregation and sequestration of non-expanded ataxin-3HAACKE, Annette; BROADLEY, Sarah A; BOTEVA, Raina et al.Human molecular genetics (Print). 2006, Vol 15, Num 4, pp 555-568, issn 0964-6906, 14 p.Article

A cell-based screen for modulators of ataxin-1 phosphorylationKAYTOR, Michael D; BYAM, Courtney E; TOUSEY, Susan K et al.Human molecular genetics (Print). 2005, Vol 14, Num 8, pp 1095-1105, issn 0964-6906, 11 p.Article

Proteotoxic stress increases nuclear localization of ataxin-3REINA, Christopher P; XIAOYAN ZHONG; PITTMAN, Randall N et al.Human molecular genetics (Print). 2010, Vol 19, Num 2, pp 235-249, issn 0964-6906, 15 p.Article

Duplication of Atxn1l suppresses SCA1 neuropathology by decreasing incorporation of polyglutamine-expanded ataxin-1 into native complexesBOWMAN, Aaron B; LAM, Yung C; JAFAR-NEJAD, Paymaan et al.Nature genetics. 2007, Vol 39, Num 3, pp 373-379, issn 1061-4036, 7 p.Article

Ataxin-2 intermediate-length polyglutamine expansions in European ALS patientsLEE, Teresa; LI, Yun R; GISPERT, Suzana et al.Human molecular genetics (Print). 2011, Vol 20, Num 9, pp 1697-1700, issn 0964-6906, 4 p.Article

SUMOylation attenuates the aggregation propensity and cellular toxicity of the polyglutamine expanded ataxin-7JANER, Alexandre; WERNER, Andreas; TAKAHASHI-FUJIGASAKI, Junko et al.Human molecular genetics (Print). 2010, Vol 19, Num 1, pp 181-195, issn 0964-6906, 15 p.Article

Defective DNA single-strand break repair in spinocerebellar ataxia with axonal neuropathy-1EL-KHAMISY, Sherif F; SAIFI, Gulam M; WEINFELD, Michael et al.Nature (London). 2005, Vol 434, Num 7029, pp 108-113, issn 0028-0836, 6 p.Article

Ambulatory blood pressure monitoring in patients with spinocerebellar degenerationAZUMA, T; UEMICHI, T; FUNAUCHI, M et al.Acta neurologica scandinavica. 2002, Vol 106, Num 4, pp 213-217, issn 0001-6314Article

A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1VUILLAUME, Isabelle; DEVOS, David; DESTEE, Alain et al.Annals of neurology. 2002, Vol 52, Num 5, pp 666-670, issn 0364-5134, 5 p.Article

Dissociation of smooth pursuit and vestibulo-ocular reflex cancellation in SCA-6TAKEICHI, N; FUKUSHIMA, K; SASAKI, H et al.Neurology. 2000, Vol 54, Num 4, pp 860-866, issn 0028-3878Article

Branched-chain amino acid therapy for spinocerebellar degeneration : A pilot clinical crossover trialMORI, N; ADACHI, Y; TAKESHIMA, T et al.Internal medicine (Tokyo. 1992). 1999, Vol 38, Num 5, pp 401-406, issn 0918-2918Article

Clinical, neuropathological, and molecular study in two families with spinocerebellar ataxia type 6 (SCA6)ISHIKAWA, K; WATANABE, M; DOI, M et al.Journal of neurology, neurosurgery and psychiatry. 1999, Vol 67, Num 1, pp 86-89, issn 0022-3050Article

Contribution clinique à l'étude génétique des ataxies cérébelleuses héréditaires = Clinical contribution to the genetic study of inherited cerebellar ataxiasDurr, Alexandra; Feingold, Josue.1998, 170 p.Thesis

A simple and rapid nonisotopic method for sizing CAG repeats in the SCA1 geneANNESI, G; MUGLIA, M; CONFORTI, F. L et al.Human heredity. 1997, Vol 47, Num 1, pp 47-51, issn 0001-5652Article

CNS sequelae in langerhans cell histiocytosis : Progressive spinocerebellar degeneration as a late manifestation of the diseaseCERVERA, A; MADERO, L; GARCIA PENAS, J. J et al.Pediatric hematology and oncology. 1997, Vol 14, Num 6, pp 577-584, issn 0888-0018Article

  • Page / 15