Found: 9
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NanoSatellite: accurate characterization of expanded tandem repeat length and sequence through whole genome long-read sequencing on PromethION.
- Published in:
- Genome Biology, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s13059-019-1856-3
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- Article
Adiponectin serum level is an independent and incremental predictor of all‐cause mortality after transcatheter aortic valve replacement.
- Published in:
- Clinical Cardiology, 2022, v. 45, n. 10, p. 1060, doi. 10.1002/clc.23892
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- Article
Transcript analysis using long‐read sequencing reveals the complex splicing profile of AD‐associated gene ABCA7: Genetics: Genetics and omics of AD I.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.042815
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- Article
ABCA7 PTC mutation carriers present with Alzheimer's disease pathology and cerebral amyloid angiopathy: Basic science and pathogenesis: Genetics and omics of AD.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.041513
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- Article
ABCA7 mutations are major contributors to Alzheimer's disease in Belgian patients: Genetics/genetic factors of Alzheimer's disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.040227
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- Article
Rare missense mutations in ABCA7 might increase Alzheimer's disease risk by plasma membrane exclusion.
- Published in:
- Acta Neuropathologica Communications, 2022, v. 10, n. 1, p. 1, doi. 10.1186/s40478-022-01346-3
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- Article
The role of ATP-binding cassette subfamily A in the etiology of Alzheimer's disease.
- Published in:
- Molecular Neurodegeneration, 2022, v. 17, n. 1, p. 1, doi. 10.1186/s13024-022-00536-w
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- Article
Belgian Carriers of Rare ABCA7 Mutations Present with Pronounced Cerebral Amyloid Angiopathy and Alzheimer's Disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 4, p. 1, doi. 10.1002/alz.068101
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- Article
Rare missense mutations and compound heterozygous mutations in ABCA7 contribute to Alzheimer's disease in Belgian patients.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 1, doi. 10.1002/alz.051341
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- Article