A novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family-Reference-Cited by-同舟云学术

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A novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family

Published:2013-12 Issue:12 Volume:34 Page:2890.e1-2890.e5
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Guerreiro Rita,Bilgic Basar,Guven Gamze,Brás José,Rohrer Jonathan,Lohmann Ebba,Hanagasi Hasmet,Gurvit Hakan,Emre Murat

Funder

Wellcome Trust/MRC Joint Call in Neurodegeneration

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

Reference8 articles.

1. Mutations in TREM2 lead to pure early-onset dementia without bone cysts;Chouery;Hum. Mutat.,2008

2. Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's disease;Giraldo;Neurobiol. Aging,2013

3. TREM2 variants in Alzheimer's disease;Guerreiro;N. Engl. J. Med.,2013

4. Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement;Guerreiro;JAMA Neurol.,2013

5. Variant of TREM2 associated with the risk of Alzheimer's disease;Jonsson;N. Engl. J. Med.,2013

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1. Current understanding on TREM-2 molecular biology and physiopathological functions;International Immunopharmacology;2024-06

2. Homozygous TREM2 c.549del; p.(Leu184Serfs*5) variant causing Nasu‐Hakola disease in three siblings in a consanguineous Iraqi family: Case report and review of literature;Molecular Genetics & Genomic Medicine;2024-06

3. Microglia, Trem2, and Neurodegeneration;The Neuroscientist;2024-05-20

4. Behavioral variant of frontotemporal dementia in carriers of biallelic TREM2 variants: cases study;Folia Neuropathologica;2024

5. Lipid in microglial biology — from material to mediator;Inflammation and Regeneration;2023-07-17

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