Sato C - Search Results

1

Genetic and epigenetic study of ALS-discordant identical twins with double mutations in SOD1 and ARHGEF28.

Zhang M, Xi Z, Ghani M, Jia P, Pal M, Werynska K, Moreno D, Sato C, Liang Y, Robertson J, Petronis A, Zinman L, Rogaeva E. Zhang M, et al. Among authors: sato c. J Neurol Neurosurg Psychiatry. 2016 Nov;87(11):1268-1270. doi: 10.1136/jnnp-2016-313592. Epub 2016 May 6. J Neurol Neurosurg Psychiatry. 2016. PMID: 27154192 No abstract available.

2

Nicastrin modulates presenilin-mediated notch/glp-1 signal transduction and betaAPP processing.

Yu G, Nishimura M, Arawaka S, Levitan D, Zhang L, Tandon A, Song YQ, Rogaeva E, Chen F, Kawarai T, Supala A, Levesque L, Yu H, Yang DS, Holmes E, Milman P, Liang Y, Zhang DM, Xu DH, Sato C, Rogaev E, Smith M, Janus C, Zhang Y, Aebersold R, Farrer LS, Sorbi S, Bruni A, Fraser P, St George-Hyslop P. Yu G, et al. Among authors: sato c. Nature. 2000 Sep 7;407(6800):48-54. doi: 10.1038/35024009. Nature. 2000. PMID: 10993067

3

Mutation of the conserved N-terminal cysteine (Cys92) of human presenilin 1 causes increased A beta42 secretion in mammalian cells but impaired Notch/lin-12 signalling in C. elegans.

Zhang DM, Levitan D, Yu G, Nishimura M, Chen F, Tandon A, Kawarai T, Arawaka S, Supala A, Song YQ, Rogaeva E, Liang Y, Holmes E, Milman P, Sato C, Zhang L, St George-Hyslop P. Zhang DM, et al. Among authors: sato c. Neuroreport. 2000 Sep 28;11(14):3227-30. doi: 10.1097/00001756-200009280-00035. Neuroreport. 2000. PMID: 11043553

4

Screening for PS1 mutations in a referral-based series of AD cases: 21 novel mutations.

Rogaeva EA, Fafel KC, Song YQ, Medeiros H, Sato C, Liang Y, Richard E, Rogaev EI, Frommelt P, Sadovnick AD, Meschino W, Rockwood K, Boss MA, Mayeux R, St George-Hyslop P. Rogaeva EA, et al. Among authors: sato c. Neurology. 2001 Aug 28;57(4):621-5. doi: 10.1212/wnl.57.4.621. Neurology. 2001. PMID: 11524469

5

Brain levels of CDK5 activator p25 are not increased in Alzheimer's or other neurodegenerative diseases with neurofibrillary tangles.

Tandon A, Yu H, Wang L, Rogaeva E, Sato C, Chishti MA, Kawarai T, Hasegawa H, Chen F, Davies P, Fraser PE, Westaway D, St George-Hyslop PH. Tandon A, et al. Among authors: sato c. J Neurochem. 2003 Aug;86(3):572-81. doi: 10.1046/j.1471-4159.2003.01865.x. J Neurochem. 2003. PMID: 12859671 Free article.

6

Benign hereditary chorea: clinical, genetic, and pathological findings.

Kleiner-Fisman G, Rogaeva E, Halliday W, Houle S, Kawarai T, Sato C, Medeiros H, St George-Hyslop PH, Lang AE. Kleiner-Fisman G, et al. Among authors: sato c. Ann Neurol. 2003 Aug;54(2):244-7. doi: 10.1002/ana.10637. Ann Neurol. 2003. PMID: 12891678

7

PS1 Alzheimer's disease family with spastic paraplegia: the search for a gene modifier.

Rogaeva E, Bergeron C, Sato C, Moliaka I, Kawarai T, Toulina A, Song YQ, Kolesnikova T, Orlacchio A, Bernardi G, St George-Hyslop PH. Rogaeva E, et al. Among authors: sato c. Neurology. 2003 Oct 14;61(7):1005-7. doi: 10.1212/wnl.61.7.1005. Neurology. 2003. PMID: 14557582

8

Clinical findings in a large family with a parkin ex3delta40 mutation.

Munhoz RP, Sa DS, Rogaeva E, Salehi-Rad S, Sato C, Medeiros H, Farrer M, Lang AE. Munhoz RP, et al. Among authors: sato c. Arch Neurol. 2004 May;61(5):701-4. doi: 10.1001/archneur.61.5.701. Arch Neurol. 2004. PMID: 15148147

9

Analysis of the glucocerebrosidase gene in Parkinson's disease.

Sato C, Morgan A, Lang AE, Salehi-Rad S, Kawarai T, Meng Y, Ray PN, Farrer LA, St George-Hyslop P, Rogaeva E. Sato C, et al. Mov Disord. 2005 Mar;20(3):367-70. doi: 10.1002/mds.20319. Mov Disord. 2005. PMID: 15517592

10

Genetic association study of PINK1 coding polymorphisms in Parkinson's disease.

Groen JL, Kawarai T, Toulina A, Rivoiro C, Salehi-Rad S, Sato C, Morgan A, Liang Y, Postuma RB, St George-Hyslop P, Lang AE, Rogaeva E. Groen JL, et al. Among authors: sato c. Neurosci Lett. 2004 Dec 6;372(3):226-9. doi: 10.1016/j.neulet.2004.09.043. Neurosci Lett. 2004. PMID: 15542245

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