TMEM106B, a risk factor for FTLD and aging, has an intrinsically disordered cytoplasmic domain

10.1371/journal.pone.0205856

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Main Authors:	Kang J., Lim L., Song J.
Other Authors:	BIOLOGICAL SCIENCES
Format:	Article
Published:	Public Library of Science 2020
Subjects:	membrane protein intrinsically disordered protein nerve protein TMEM106B protein, human aging Article bioinformatics cytoplasm frontotemporal dementia human nuclear magnetic resonance spectroscopy protein conformation protein domain protein expression protein structure risk factor autophagy biology chemistry circular dichroism endosome genetics lysosome nerve cell phenotype protein secondary structure protein transport single nucleotide polymorphism Aging Autophagy Circular Dichroism Computational Biology Cytoplasm Endosomes Frontotemporal Lobar Degeneration Humans Intrinsically Disordered Proteins Lysosomes Magnetic Resonance Spectroscopy Membrane Proteins Nerve Tissue Proteins Neurons Phenotype Polymorphism, Single Nucleotide Protein Domains Protein Structure, Secondary Protein Transport Risk Factors
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/165893
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Institution:	National University of Singapore

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spelling	sg-nus-scholar.10635-1658932024-04-03T06:05:38Z TMEM106B, a risk factor for FTLD and aging, has an intrinsically disordered cytoplasmic domain Kang J. Lim L. Song J. BIOLOGICAL SCIENCES membrane protein intrinsically disordered protein membrane protein nerve protein TMEM106B protein, human aging Article bioinformatics cytoplasm frontotemporal dementia human nuclear magnetic resonance spectroscopy protein conformation protein domain protein expression protein structure risk factor aging autophagy biology chemistry circular dichroism cytoplasm endosome frontotemporal dementia genetics lysosome nerve cell phenotype protein domain protein secondary structure protein transport single nucleotide polymorphism Aging Autophagy Circular Dichroism Computational Biology Cytoplasm Endosomes Frontotemporal Lobar Degeneration Humans Intrinsically Disordered Proteins Lysosomes Magnetic Resonance Spectroscopy Membrane Proteins Nerve Tissue Proteins Neurons Phenotype Polymorphism, Single Nucleotide Protein Domains Protein Structure, Secondary Protein Transport Risk Factors 10.1371/journal.pone.0205856 PLoS ONE 13 10 e0205856 2020-03-23T06:18:44Z 2020-03-23T06:18:44Z 2018 Article Kang J., Lim L., Song J. (2018). TMEM106B, a risk factor for FTLD and aging, has an intrinsically disordered cytoplasmic domain. PLoS ONE 13 (10) : e0205856. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0205856 19326203 https://scholarbank.nus.edu.sg/handle/10635/165893 Public Library of Science Unpaywall 20200320
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	membrane protein intrinsically disordered protein membrane protein nerve protein TMEM106B protein, human aging Article bioinformatics cytoplasm frontotemporal dementia human nuclear magnetic resonance spectroscopy protein conformation protein domain protein expression protein structure risk factor aging autophagy biology chemistry circular dichroism cytoplasm endosome frontotemporal dementia genetics lysosome nerve cell phenotype protein domain protein secondary structure protein transport single nucleotide polymorphism Aging Autophagy Circular Dichroism Computational Biology Cytoplasm Endosomes Frontotemporal Lobar Degeneration Humans Intrinsically Disordered Proteins Lysosomes Magnetic Resonance Spectroscopy Membrane Proteins Nerve Tissue Proteins Neurons Phenotype Polymorphism, Single Nucleotide Protein Domains Protein Structure, Secondary Protein Transport Risk Factors
spellingShingle	membrane protein intrinsically disordered protein membrane protein nerve protein TMEM106B protein, human aging Article bioinformatics cytoplasm frontotemporal dementia human nuclear magnetic resonance spectroscopy protein conformation protein domain protein expression protein structure risk factor aging autophagy biology chemistry circular dichroism cytoplasm endosome frontotemporal dementia genetics lysosome nerve cell phenotype protein domain protein secondary structure protein transport single nucleotide polymorphism Aging Autophagy Circular Dichroism Computational Biology Cytoplasm Endosomes Frontotemporal Lobar Degeneration Humans Intrinsically Disordered Proteins Lysosomes Magnetic Resonance Spectroscopy Membrane Proteins Nerve Tissue Proteins Neurons Phenotype Polymorphism, Single Nucleotide Protein Domains Protein Structure, Secondary Protein Transport Risk Factors Kang J. Lim L. Song J. TMEM106B, a risk factor for FTLD and aging, has an intrinsically disordered cytoplasmic domain
description	10.1371/journal.pone.0205856
author2	BIOLOGICAL SCIENCES
author_facet	BIOLOGICAL SCIENCES Kang J. Lim L. Song J.
format	Article
author	Kang J. Lim L. Song J.
author_sort	Kang J.
title	TMEM106B, a risk factor for FTLD and aging, has an intrinsically disordered cytoplasmic domain
title_short	TMEM106B, a risk factor for FTLD and aging, has an intrinsically disordered cytoplasmic domain
title_full	TMEM106B, a risk factor for FTLD and aging, has an intrinsically disordered cytoplasmic domain
title_fullStr	TMEM106B, a risk factor for FTLD and aging, has an intrinsically disordered cytoplasmic domain
title_full_unstemmed	TMEM106B, a risk factor for FTLD and aging, has an intrinsically disordered cytoplasmic domain
title_sort	tmem106b, a risk factor for ftld and aging, has an intrinsically disordered cytoplasmic domain
publisher	Public Library of Science
publishDate	2020
url	https://scholarbank.nus.edu.sg/handle/10635/165893
_version_	1795374169659015168

TMEM106B, a risk factor for FTLD and aging, has an intrinsically disordered cytoplasmic domain

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