Neystat M - Search Results

1

Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy.

Wilhelmsen KC, Blake DM, Lynch T, Mabutas J, De Vera M, Neystat M, Bernstein M, Hirano M, Gilliam TC, Murphy PL, Sola MD, Bonilla E, Schotland DL, Hays AP, Rowland LP. Wilhelmsen KC, et al. Among authors: neystat m. Ann Neurol. 1996 Apr;39(4):507-20. doi: 10.1002/ana.410390413. Ann Neurol. 1996. PMID: 8619529 Review.

2

Alpha-synuclein expression in substantia nigra and cortex in Parkinson's disease.

Neystat M, Lynch T, Przedborski S, Kholodilov N, Rzhetskaya M, Burke RE. Neystat M, et al. Mov Disord. 1999 May;14(3):417-22. doi: 10.1002/1531-8257(199905)14:3<417::aid-mds1005>3.0.co;2-x. Mov Disord. 1999. PMID: 10348463

3

A high-resolution genetic linkage map of the pericentromeric region of the human X chromosome.

Weeks DE, Nygaard TG, Neystat M, Harby LD, Wilhelmsen KC. Weeks DE, et al. Among authors: neystat m. Genomics. 1995 Mar 1;26(1):39-46. doi: 10.1016/0888-7543(95)80080-6. Genomics. 1995. PMID: 7782084 Free article.

4

Molecular genetic analysis of Lubag.

Wilhelmsen KC, Moskowitz CB, Weeks DE, Neystat M, Nygaard TG, Clark L, Dancoup M, Sobrevega EE, Rosales R, Gamez GL, Pacioles O, Perez M, Fahn S. Wilhelmsen KC, et al. Among authors: neystat m. Adv Neurol. 1998;78:341-8. Adv Neurol. 1998. PMID: 9750931 No abstract available.

5

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17.

Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H, Pickering-Brown S, Chakraverty S, Isaacs A, Grover A, Hackett J, Adamson J, Lincoln S, Dickson D, Davies P, Petersen RC, Stevens M, de Graaff E, Wauters E, van Baren J, Hillebrand M, Joosse M, Kwon JM, Nowotny P, Che LK, Norton J, Morris JC, Reed LA, Trojanowski J, Basun H, Lannfelt L, Neystat M, Fahn S, Dark F, Tannenberg T, Dodd PR, Hayward N, Kwok JB, Schofield PR, Andreadis A, Snowden J, Craufurd D, Neary D, Owen F, Oostra BA, Hardy J, Goate A, van Swieten J, Mann D, Lynch T, Heutink P. Hutton M, et al. Among authors: neystat m. Nature. 1998 Jun 18;393(6686):702-5. doi: 10.1038/31508. Nature. 1998. PMID: 9641683

6

Analysis of synphilin-1 and synuclein interactions by yeast two-hybrid beta-galactosidase liquid assay.

Neystat M, Rzhetskaya M, Kholodilov N, Burke RE. Neystat M, et al. Neurosci Lett. 2002 Jun 7;325(2):119-23. doi: 10.1016/s0304-3940(02)00253-7. Neurosci Lett. 2002. PMID: 12044636

7

Increased expression of rat synuclein in the substantia nigra pars compacta identified by mRNA differential display in a model of developmental target injury.

Kholodilov NG, Neystat M, Oo TF, Lo SE, Larsen KE, Sulzer D, Burke RE. Kholodilov NG, et al. Among authors: neystat m. J Neurochem. 1999 Dec;73(6):2586-99. doi: 10.1046/j.1471-4159.1999.0732586.x. J Neurochem. 1999. PMID: 10582622 Free article.

8

Alpha-synuclein up-regulation in substantia nigra dopaminergic neurons following administration of the parkinsonian toxin MPTP.

Vila M, Vukosavic S, Jackson-Lewis V, Neystat M, Jakowec M, Przedborski S. Vila M, et al. Among authors: neystat m. J Neurochem. 2000 Feb;74(2):721-9. doi: 10.1046/j.1471-4159.2000.740721.x. J Neurochem. 2000. PMID: 10646524 Free article.

9

Upregulation of cytosolic branched chain aminotransferase in substantia nigra following developmental striatal target injury.

Kholodilov NG, Neystat M, Oo TF, Hutson SM, Burke RE. Kholodilov NG, et al. Among authors: neystat m. Brain Res Mol Brain Res. 2000 Feb 22;75(2):281-6. doi: 10.1016/s0169-328x(99)00318-6. Brain Res Mol Brain Res. 2000. PMID: 10686349 Free article.

10

Expression of cyclin-dependent kinase 5 and its activator p35 in models of induced apoptotic death in neurons of the substantia nigra in vivo.

Neystat M, Rzhetskaya M, Oo TF, Kholodilov N, Yarygina O, Wilson A, El-Khodor BF, Burke RE. Neystat M, et al. J Neurochem. 2001 Jun;77(6):1611-25. doi: 10.1046/j.1471-4159.2001.00376.x. J Neurochem. 2001. PMID: 11413244 Free article.

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