Results 201 to 210 of about 1,044,161 (293)

Revitalizing equine metabolism: how SHBG improves mitochondrial function and reduces inflammation. [PDF]

BMC Vet Res
Bourebaba N, Domagała J, Bourebaba L.
europepmc   +1 more source

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

Harnessing Mitochondrial Function for Post-Stroke Rehabilitation: Unlocking Antioxidant Power. [PDF]

Antioxidants (Basel)
Olaru G, Buga AM, Sandu RE, Padureanu V, Popa DG, Calina D.   +5 more
europepmc   +1 more source

The study of the moize mitochondrial linear plasmids function in intact plants [PDF]

, 1992
S. A. Martynov, I. G. Bukh, A. Yu. Miruta, T. S. Danilenko, Т. П. Перерва, S. S. Malyuta   +5 more
openalex   +1 more source

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

TRAP1 Improves Diabetic Retinopathy by Preserving Mitochondrial Function. [PDF]

Clin Ophthalmol
Li Y, Xu W, Zhao G, Guo Y, Wang L, Du Q, Fei Y, Hu X, Hu H, Chen L, Xu Y.   +10 more
europepmc   +1 more source

Mitochondrial function in oncogene-transfected rat fibroblasts isolated from multicellular spheroids [PDF]

, 1997
Leoni A. Kunz‐Schughart, R C Habbersett, James P. Freyer   +2 more
openalex   +1 more source

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas, Pablo Iruzubieta, Alberto Damborenea, Laura Pérez‐Fernández, Inmaculada Azorín, Juan Carlos Jiménez García, Ana Töpf, Pilar Martí, Lorena Fores‐Toribio, María Manterola, Rosana Blanco‐Mañez, Oihane Pikatza‐Menoio, Sonia Alonso‐Martín, Volker Straub, Aitziber L. Cortajarena, Adolfo López de Munain, David De Sancho, Lorea Blázquez, Juan J. Vilchez   +18 more
wiley   +1 more source

MCEE Promotes Intramuscular Fat Deposition in Pigs Through Regulating Mitochondrial Function. [PDF]

Animals (Basel)
Li Y, Chen X, Chen D, Wu J, Chen T, Qiao M, Peng X, Mei S, Feng Y.   +8 more
europepmc   +1 more source

Germination conditions that require mitochondrial function in Saccharomyces cerevisiae: utilization of acetate and galactose

, 1986
Claudia Donnini, N Artoni, Nelson Marmiroli   +2 more
openalex   +1 more source