Feed Preview

Fast Growing

Misfolding & Aggregation Diseases

Misfolding & Aggregation Diseases diagram by

Misfolding and aggregation of proteins can lead to several diseases. For instance, misfolding of prion or tau proteins are associated with several neurodegenerative diseases. Here is the latest research on diseases caused by protein misfolding and aggregation.

Top 20 most recent papers
Methods in Molecular Biology

Immobilization of Enzymes on Supports Activated with Glutaraldehyde: A Very Simple Immobilization Protocol

Methods in Molecular BiologyJanuary 16, 2020
Fernando López-GallegoLorena Betancor
Molecules : a Journal of Synthetic Chemistry and Natural Product Chemistry

Exploring the Multi-Target Performance of Mitochondriotropic Antioxidants against the Pivotal Alzheimer's Disease Pathophysiological Hallmarks

Molecules : a Journal of Synthetic Chemistry and Natural Product ChemistryJanuary 16, 2020
Sofia BenfeitoFernanda Borges
International Journal of Molecular Sciences

Increased Cardiovascular Risk Associated with Chemical Sensitivity to Perfluoro-Octanoic Acid: Role of Impaired Platelet Aggregation

International Journal of Molecular SciencesJanuary 16, 2020
Luca De ToniCarlo Foresta
1
bioRxiv

Disentangling the effects of sampling scale and size on the shape of species abundance distributions

bioRxivJanuary 16, 2020
Renato A.F. LimaPaulo Inacio Prado
Arteriosclerosis, Thrombosis, and Vascular Biology

Short-Term Exposure to Waterpipe/Hookah Smoke Triggers a Hyperactive Platelet Activation State and Increases the Risk of Thrombogenesis

Arteriosclerosis, Thrombosis, and Vascular BiologyJanuary 17, 2020
Ahmed B AlarabiFadi T Khasawneh
Dalton Transactions : an International Journal of Inorganic Chemistry

Enhanced pseudocapacitive energy storage properties of budding-branch like MoO2 @C/CNT nanorods

Dalton Transactions : an International Journal of Inorganic ChemistryJanuary 17, 2020
Haochen SiYihe Zhang
ENeuro

Hsc70 Ameliorates the Vesicle Recycling Defects Caused by Excess α-Synuclein at Synapses

ENeuroJanuary 17, 2020
Susan M L BanksJennifer R Morgan
Analytical Chemistry

Real-Time Monitoring of Self-Aggregation of β-Amyloid by a Fluorescent Probe based on Ruthenium Complex

Analytical ChemistryJanuary 17, 2020
Hui-Juan YuLin Yu
Sub-cellular Biochemistry

Structure and Function of the AAA+ ATPase p97, a Key Player in Protein Homeostasis

Sub-cellular BiochemistryJanuary 16, 2020
Petra HänzelmannHermann Schindelin
Cells

pH-Dependent Aggregation in Intrinsically Disordered Proteins Is Determined by Charge and Lipophilicity

CellsJanuary 16, 2020
Jaime SantosSalvador Ventura
10
The Biochemical Journal

The molecular chaperone β-casein prevents amorphous and fibrillar aggregation of α-lactalbumin by stabilisation of dynamic disorder

The Biochemical JournalJanuary 16, 2020
Henry M SandersTara Louise Pukala
2
Journal of Endodontics

Contribution of Bone Marrow-derived Cells to Reparative Dentinogenesis Using Bone Marrow Transplantation Model

Journal of EndodonticsJanuary 16, 2020
Marcos FrozoniAlexandre Augusto Zaia
Journal of Environmental Management

Bentonite-supported nano zero-valent iron composite as a green catalyst for bisphenol A degradation: Preparation, performance, and mechanism of action

Journal of Environmental ManagementJanuary 17, 2020
Teng BaoBing-Jie Ni
Cells

VAPB ER-Aggregates, A Possible New Biomarker in ALS Pathology

CellsJanuary 16, 2020
Maria Piera L CadoniGrazia Galleri
ACS Chemical Neuroscience

The role of oxidized Gly25, Gly29 and Gly33 residues on the interactions of Aβ1-42 with lipid membranes

ACS Chemical NeuroscienceJanuary 16, 2020
Hebah FataftaMichael C Owen
1
Sub-cellular Biochemistry

Crystallins and Their Complexes

Sub-cellular BiochemistryJanuary 16, 2020
Kalyan Sundar Ghosh, Priyanka Chauhan
Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery

The fabrication and related properties study of chitosan-poly (lactide-co-glycolide) double-walled microspheres loaded with nerve growth factor

Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgeryJanuary 16, 2020
Mengyao RongQi Liu
Sub-cellular Biochemistry

Amyloid Oligomers, Protofibrils and Fibrils

Sub-cellular BiochemistryJanuary 16, 2020
Mohammad Khursheed SiddiqiRizwan Hasan Khan
Nanomaterials

Silica-Coated Magnetic Iron Oxide Nanoparticles Grafted onto Graphene Oxide for Protein Isolation

NanomaterialsJanuary 16, 2020
Xuan-Hung PhamBong-Hyun Jun
The Biochemical Journal

Scutellarin Inhibits the Uninduced and Metal-Induced Aggregation of ɑ-Synuclein and Disaggregates Preformed Fibrils: Implications for Parkinson's disease

The Biochemical JournalJanuary 16, 2020
Fatima Kamal Zaidi, Shashank Deep
1

See more papers from this feed

Related Feeds

ALS

Amyotrophic Lateral Sclerosis (ALS), also known as motor neuron disease, is associated with the death of neurons that control voluntary muscles. Discover the latest research on ALS here.

ALS & FTD: TDP-43

ALS shares with a considerable proportion of FTD cases the same neuropathological substrate, namely, inclusions of abnormally phosphorylated protein tdp-43 (ptdp-43). Here are the latest discoveries pertaining to ptdp-43 and these diseases.

ALS - Pathogenic Mechanisms

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder characterized by muscle weakness. Here is the latest research investigating pathogenic mechanisms that underlie this genetically heterogeneous disorder.

ALS - Phenotypes

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder characterized by muscle weakness. Here is the latest research investigating phenotypes associated with this genetically heterogeneous disorder.

ALS: Genetics

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder characterized by muscle weakness. ALS is a genetically heterogeneous disorder with several causative genes. Here are the latest discoveries pertaining to the genetics of this disease.

ALS: Prions

Prions are misfolded proteins which characterize several fatal neurodegenerative diseases. Prion-like mechanisms are associated with the pathogenesis of Amyotrophic Lateral Sclerosis (ALS). Here are the latest discoveries pertaining to this disease.

ALS: Stress Granules

Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disease characterized by cytoplasmic protein aggregates within motor neurons. TDP-43 is an ALS-linked protein that is known to regulate splicing and storage of specific mRNAs into stress granules, which have been implicated in formation of ALS protein aggregates. Here is the latest research.

ALS: Therapies

Amyotrophic Lateral Sclerosis (ALS), also known as motor neuron disease, is associated with the death of neurons that control voluntary muscles. Discover the latest research on ALS therapies here.

ALS: Transposon de-silencing

Transposon silencing is a form of transcriptional gene silencing. These gene silencing mechanisms are impaired in Amyotrophic lateral sclerosis (ALS). Here are the latest discoveries pertaining to transposon silencing and this disease.

Age-related Dementia

Age-related dementia (Alzheimer's disease) results from the destructive impact of the pulse on cerebral vasculature. Evidence is reviewed that the neuropathology of the dementia is caused by the breakdown of small cerebral vessels (silent microbleeds), that the microbleeds result from pulse-induced damage to the cerebral vessels, and that pulse becomes increasingly destructive with age, because of the age-related stiffening of the aorta and great arteries, which causes an increase in the intensity of the pressure pulse. Discover the latest research on age-related dementia here.

© 2020 Meta ULC. All rights reserved
/feed-previews/misfolding-aggregation-diseases/c1d6d464-2924-4167-a6ab-6fc6d69c1321