Results 261 to 270 of about 2,435,950 (372)

Exosome Proteomics of SOD1D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Amyotrophic lateral sclerosis (ALS) is a neuromuscular disease. Super oxide dismutase 1 (SOD1) gene mutations cause ALS, and the D90A mutation is associated with primarily upper motor neuron (UMN) loss. Objective Our goal is to reveal the early cellular events in ALS pathology and identify potential pharmacokinetic biomarkers, using well ...
Mukesh Gautam, Ali Laith, Aslihan Gunel, Melda Yilmaz, Nazli Basak, Halil Idrisoglu, P. Hande Ozdinler   +6 more
wiley   +1 more source

Optimizing implant hygiene: the added value of interproximal cleaning devices around implant-supported restorations-a systematic review and meta-analysis. [PDF]

Int J Implant Dent
Bishti S, Wolfart S, Tuna T.
europepmc   +1 more source

Frequency-resolved Raman for transient thermal probing and thermal diffusivity measurement

, 2015
Tianyu Wang, Shen Xu, David H. Hurley, Yanan Yue, Xinwei Wang   +4 more
openalex   +2 more sources

Growth Differentiation Factor 15 Elevation in the Central Nervous System Is Associated With Failure to Thrive in Alexander Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Alexander disease (AxD) is a severe neurodegenerative disorder caused by gain‐of‐function mutations in the gene for GFAP, which lead to protein aggregation and a primary astrocytopathy. Symptoms vary, but failure to thrive (FTT) and frequent emesis are common and cause significant morbidity. Here we investigate GDF15, a member of the
Tracy L. Hagemann, Michelle M. Sonsalla, Cora Luzinski, Fernando Zacahua, David A. Harris, Dudley W. Lamming, Albee Messing   +6 more
wiley   +1 more source

Salivary glucose, salivary interleukin-18, glycemic control, and periodontal status in patients with type 2 diabetes mellitus. [PDF]

Sci Rep
Techatanawat S, Puangmaliwan P, Thanathornwong B, Chairatvit K, Bhattarai BP, Khovidhunkit W, Khovidhunkit SP.   +6 more
europepmc   +1 more source

Probing questions [PDF]

Nature Chemical Biology, 2015
openaire   +2 more sources

Nationwide Characterization of MFN2‐Related CMT in 176 Japanese Patients: Clinical and Genetic Insights

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Mitofusin 2 (MFN2) is a major causative gene for axonal Charcot – Marie – Tooth disease type 2A (CMT2A), with a wide phenotypic spectrum. Comprehensive large ‐ scale genotype – phenotype association studies are essential for understanding disease pathogenesis and improved clinical management.
Masahiro Ando, Yujiro Higuchi, Jun‐Hui Yuan, Akiko Yoshimura, Chikashi Yano, Takahiro Hobara, Fumikazu Kojima, Yu Hiramatsu, Satoshi Nozuma, Tomonori Nakamura, Yusuke Sakiyama, Jun Mitsui, Shoji Tsuji, Hiroshi Takashima   +13 more
wiley   +1 more source

Regular home use of dual-light photodynamic therapy as an adjunct to non-surgical periodontal treatment in smokers: a single-center randomized controlled clinical trial. [PDF]

Clin Oral Investig
Vakaki C, Fragkioudakis I, Pätilä T, Sakellari D.   +3 more
europepmc   +1 more source

Probing Interactions in Fixed and Multilevel Regression: Inferential and Graphical Techniques

Multivariate Behavioral Research, 2005
Daniel J. Bauer, P. Curran
semanticscholar   +1 more source