Davis RL - Search Results

1

Neuroserpin binds Abeta and is a neuroprotective component of amyloid plaques in Alzheimer disease.

Kinghorn KJ, Crowther DC, Sharp LK, Nerelius C, Davis RL, Chang HT, Green C, Gubb DC, Johansson J, Lomas DA. Kinghorn KJ, et al. Among authors: davis rl. J Biol Chem. 2006 Sep 29;281(39):29268-77. doi: 10.1074/jbc.M600690200. Epub 2006 Jul 17. J Biol Chem. 2006. PMID: 16849336 Free article.

2

Association between conformational mutations in neuroserpin and onset and severity of dementia.

Davis RL, Shrimpton AE, Carrell RW, Lomas DA, Gerhard L, Baumann B, Lawrence DA, Yepes M, Kim TS, Ghetti B, Piccardo P, Takao M, Lacbawan F, Muenke M, Sifers RN, Bradshaw CB, Kent PF, Collins GH, Larocca D, Holohan PD. Davis RL, et al. Lancet. 2002 Jun 29;359(9325):2242-7. doi: 10.1016/S0140-6736(02)09293-0. Lancet. 2002. PMID: 12103288

3

Familial dementia caused by polymerization of mutant neuroserpin.

Davis RL, Shrimpton AE, Holohan PD, Bradshaw C, Feiglin D, Collins GH, Sonderegger P, Kinter J, Becker LM, Lacbawan F, Krasnewich D, Muenke M, Lawrence DA, Yerby MS, Shaw CM, Gooptu B, Elliott PR, Finch JT, Carrell RW, Lomas DA. Davis RL, et al. Nature. 1999 Sep 23;401(6751):376-9. doi: 10.1038/43894. Nature. 1999. PMID: 10517635

4

A presenilin 1 mutation (L420R) in a family with early onset Alzheimer disease, seizures and cotton wool plaques, but not spastic paraparesis.

Shrimpton AE, Schelper RL, Linke RP, Hardy J, Crook R, Dickson DW, Ishizawa T, Davis RL. Shrimpton AE, et al. Among authors: davis rl. Neuropathology. 2007 Jun;27(3):228-32. doi: 10.1111/j.1440-1789.2007.00766.x. Neuropathology. 2007. PMID: 17645236

5

Familial encephalopathy with neuroserpin inclusion bodies.

Davis RL, Holohan PD, Shrimpton AE, Tatum AH, Daucher J, Collins GH, Todd R, Bradshaw C, Kent P, Feiglin D, Rosenbaum A, Yerby MS, Shaw CM, Lacbawan F, Lawrence DA. Davis RL, et al. Am J Pathol. 1999 Dec;155(6):1901-13. doi: 10.1016/S0002-9440(10)65510-1. Am J Pathol. 1999. PMID: 10595921 Free PMC article.

6

Cognitive deficits associated with a recently reported familial neurodegenerative disease: familial encephalopathy with neuroserpin inclusion bodies.

Bradshaw CB, Davis RL, Shrimpton AE, Holohan PD, Rea CB, Fieglin D, Kent P, Collins GH. Bradshaw CB, et al. Among authors: davis rl. Arch Neurol. 2001 Sep;58(9):1429-34. doi: 10.1001/archneur.58.9.1429. Arch Neurol. 2001. PMID: 11559315

7

Neuroserpin mutation S52R causes neuroserpin accumulation in neurons and is associated with progressive myoclonus epilepsy.

Takao M, Benson MD, Murrell JR, Yazaki M, Piccardo P, Unverzagt FW, Davis RL, Holohan PD, Lawrence DA, Richardson R, Farlow MR, Ghetti B. Takao M, et al. Among authors: davis rl. J Neuropathol Exp Neurol. 2000 Dec;59(12):1070-86. doi: 10.1093/jnen/59.12.1070. J Neuropathol Exp Neurol. 2000. PMID: 11138927

8

Genome sequencing reanalysis increases the diagnostic yield in dystonia.

Fellner A, Wali GM, Mahant N, Grosz BR, Ellis M, Narayanan RK, Ng K, Davis RL, Tchan MC, Kotschet K, Yeow D, Rudaks LI, Siow SF, Wali G, Yiannikas C, Hobbs M, Copty J, Geaghan M, Darveniza P, Liang C, Williams LJ, Chang FCF, Morales-Briceño H, Tisch S, Hayes M, Whyte S, Kummerfeld S, Kennerson ML, Cowley MJ, Fung VSC, Sue CM, Kumar KR. Fellner A, et al. Among authors: davis rl. Parkinsonism Relat Disord. 2024 May 14;124:107010. doi: 10.1016/j.parkreldis.2024.107010. Online ahead of print. Parkinsonism Relat Disord. 2024. PMID: 38772265 Free article.

9

The Next, Next-Generation of Sequencing, Promising to Boost Research and Clinical Practice.

Kumar KR, Cowley MJ, Davis RL. Kumar KR, et al. Among authors: davis rl. Semin Thromb Hemost. 2024 May 11. doi: 10.1055/s-0044-1786756. Online ahead of print. Semin Thromb Hemost. 2024. PMID: 38733978 No abstract available.

10

Next-Generation Sequencing and Emerging Technologies.

Kumar KR, Cowley MJ, Davis RL. Kumar KR, et al. Among authors: davis rl. Semin Thromb Hemost. 2024 May 1. doi: 10.1055/s-0044-1786397. Online ahead of print. Semin Thromb Hemost. 2024. PMID: 38692283

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