Works matching DE "PRESENILIN genetics"
Results: 12
A case of atypical early-onset Alzheimer's disease carrying the missense mutation Thr354Ile in exon 10 of the PSEN1 gene.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Linkage analysis for plasma amyloid beta levels in persons with hypertension implicates Aβ-40 levels to presenilin 2.
- Published in:
- Human Genetics, 2012, v. 131, n. 12, p. 1869, doi. 10.1007/s00439-012-1210-2
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- Publication type:
- Article
Wybrane mysie modele oparte na mutacji genów APP, MAPT oraz presenilin wykorzystywane w badaniach nad patogenez ą choroby Alzheimera.
- Published in:
- Advances in Hygiene & Experimental Medicine / Postepy Higieny i Medycyny Doswiadczalnej, 2012, v. 66, p. 415, doi. 10.5604/17322693.1001098
- By:
- Publication type:
- Article
Common variants of the PINK1 and PARL genes do not confer genetic susceptibility to schizophrenia in Han Chinese.
- Published in:
- Molecular Genetics & Genomics, 2015, v. 290, n. 2, p. 585, doi. 10.1007/s00438-014-0942-1
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- Publication type:
- Article
Gene mutations in a Han Chinese Alzheimer's disease cohort.
- Published in:
- Brain & Behavior, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1002/brb3.1180
- By:
- Publication type:
- Article
Análisis in silico a nivel proteico de la estructura de presenilina-1 en homínidos.
- Published in:
- Revista Lasallista de Investigación, 2022, v. 19, n. 2, p. 149, doi. 10.22507/rli.v19n2a10
- By:
- Publication type:
- Article
Intraneuronal APP and extracellular Aβ independently cause dendritic spine pathology in transgenic mouse models of Alzheimer's disease.
- Published in:
- Acta Neuropathologica, 2015, v. 129, n. 6, p. 909, doi. 10.1007/s00401-015-1421-4
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- Publication type:
- Article
Neuroprotective Effect of Arctigenin via Upregulation of P-CREB in Mouse Primary Neurons and Human SH-SY5Y Neuroblastoma Cells.
- Published in:
- International Journal of Molecular Sciences, 2013, v. 14, n. 9, p. 18657, doi. 10.3390/ijms140918657
- By:
- Publication type:
- Article
GENETIC AND NON-GENETIC FACTORS RESPONSIBLE FOR MITOCHONDRIAL FAILURE AND ALZHEIMER'S DISEASE.
- Published in:
- Genetika (0534-0012), 2014, v. 46, n. 2, p. 631, doi. 10.2298/GENSR1402631G
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- Publication type:
- Article
Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene.
- Published in:
- Acta Neuropathologica Communications, 2017, v. 5, p. 1, doi. 10.1186/s40478-017-0441-9
- By:
- Publication type:
- Article
Molecular cloning and characterization of presenilin gene in Bombyx mori.
- Published in:
- Molecular Medicine Reports, 2015, v. 12, n. 4, p. 5508, doi. 10.3892/mmr.2015.4019
- By:
- Publication type:
- Article
The E280A Presenilin Mutation Reduces Voltage-Gated Sodium Channel Levels in Neuronal Cells.
- Published in:
- Neurodegenerative Diseases, 2014, v. 13, n. 2/3, p. 64, doi. 10.1159/000354669
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- Publication type:
- Article