Wragg M - Search Results

1

A mutation in Alzheimer's disease destroying a splice acceptor site in the presenilin-1 gene.

Perez-Tur J, Froelich S, Prihar G, Crook R, Baker M, Duff K, Wragg M, Busfield F, Lendon C, Clark RF, et al. Perez-Tur J, et al. Among authors: wragg m. Neuroreport. 1995 Dec 29;7(1):297-301. Neuroreport. 1995. PMID: 8742474

2

Complete analysis of the presenilin 1 gene in early onset Alzheimer's disease.

Hutton M, Busfield F, Wragg M, Crook R, Perez-Tur J, Clark RF, Prihar G, Talbot C, Phillips H, Wright K, Baker M, Lendon C, Duff K, Martinez A, Houlden H, Nichols A, Karran E, Roberts G, Roques P, Rossor M, Venter JC, Adams MD, Cline RT, Phillips CA, Goate A, et al. Hutton M, et al. Among authors: wragg m. Neuroreport. 1996 Feb 29;7(3):801-5. doi: 10.1097/00001756-199602290-00029. Neuroreport. 1996. PMID: 8733749

3

The role of presenilin 1 in the genetics of Alzheimer's disease.

Clark RF, Hutton M, Talbot C, Wragg M, Lendon C, Busfield F, Han SW, Perez-Tur J, Adams M, Fuldner R, Roberts G, Karran E, Hardy J, Goate A. Clark RF, et al. Among authors: wragg m. Cold Spring Harb Symp Quant Biol. 1996;61:551-8. Cold Spring Harb Symp Quant Biol. 1996. PMID: 9246481

4

No association found between Alzheimer's disease and a mitochondrial tRNA glutamine gene variant.

Wragg MA, Talbot CJ, Morris JC, Lendon CL, Goate AM. Wragg MA, et al. Neurosci Lett. 1995 Dec 8;201(2):107-10. doi: 10.1016/0304-3940(95)12146-3. Neurosci Lett. 1995. PMID: 8848229

5

E280A PS-1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles.

Lendon CL, Martinez A, Behrens IM, Kosik KS, Madrigal L, Norton J, Neuman R, Myers A, Busfield F, Wragg M, Arcos M, Arango Viana JC, Ossa J, Ruiz A, Goate AM, Lopera F. Lendon CL, et al. Among authors: wragg m. Hum Mutat. 1997;10(3):186-95. doi: 10.1002/(SICI)1098-1004(1997)10:3<186::AID-HUMU2>3.0.CO;2-H. Hum Mutat. 1997. PMID: 9298817

6

Genetic association studies between dementia of the Alzheimer's type and three receptors for apolipoprotein E in a Caucasian population.

Lendon CL, Talbot CJ, Craddock NJ, Han SW, Wragg M, Morris JC, Goate AM. Lendon CL, et al. Among authors: wragg m. Neurosci Lett. 1997 Feb 7;222(3):187-90. doi: 10.1016/s0304-3940(97)13381-x. Neurosci Lett. 1997. PMID: 9148246

7

Genetic association between intronic polymorphism in presenilin-1 gene and late-onset Alzheimer's disease. Alzheimer's Disease Collaborative Group.

Wragg M, Hutton M, Talbot C. Wragg M, et al. Lancet. 1996 Feb 24;347(9000):509-12. doi: 10.1016/s0140-6736(96)91140-x. Lancet. 1996. PMID: 8596269

8

Autosomal dominant dementia with widespread neurofibrillary tangles.

Reed LA, Grabowski TJ, Schmidt ML, Morris JC, Goate A, Solodkin A, Van Hoesen GW, Schelper RL, Talbot CJ, Wragg MA, Trojanowski JQ. Reed LA, et al. Among authors: wragg ma. Ann Neurol. 1997 Oct;42(4):564-72. doi: 10.1002/ana.410420406. Ann Neurol. 1997. PMID: 9382467

9

Acute rehabilitation following traumatic anterior shoulder dislocation (ARTISAN): pragmatic, multicentre, randomised controlled trial.

Kearney RS, Ellard DR, Parsons H, Haque A, Mason J, Nwankwo H, Bradley H, Drew S, Modi C, Bush H, Torgerson D, Underwood M; The ARTISAN collaborators; ARTISAN collaborators. Kearney RS, et al. BMJ. 2024 Jan 17;384:e076925. doi: 10.1136/bmj-2023-076925. BMJ. 2024. PMID: 38233068 Free PMC article. Clinical Trial.

10

The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families.

Alzheimer's Disease Collaborative Group. Alzheimer's Disease Collaborative Group. Nat Genet. 1995 Oct;11(2):219-22. doi: 10.1038/ng1095-219. Nat Genet. 1995. PMID: 7550356

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