Results 81 to 90 of about 15,101 (190)

Improvement of neuropsychological performances and reduction of immune-activation markers after probiotic supplementation and change of life-style in an HIV positive male: targeting the microbiota to act on gut-brain axis [PDF]

, 2017
The gut-brain axis is widely in uenced by the intestinal microbiota and dysbiosis is consequently associated with a large dysregulation of its functions. Probiotic supplementation, reducing the harmful effects of dysbiosis, has shown positive effects not
Bianchi, Luigi, Cavallari, EUGENIO NELSON, Ceccarelli, Giancarlo, Corano Scheri, Giuseppe, D'Ettorre, Gabriella, Gabriella Di Girolamo,, Martiangela, Fratino, Vassalini, Paolo, Vullo, Vincenzo   +8 more
core  

Soluble two-species diffusion-limited Models in arbitrary dimensions

, 2001
A class of two-species ({\it three-states}) bimolecular diffusion-limited models of classical particles with hard-core reacting and diffusing in a hypercubic lattice of arbitrary dimension is investigated.
A. A. Lushnikov, B. Chopard, B. P. Lee, D. C. Mattis, D. Toussaint, E. Ben-Naim, E. Clément, G. M. Schütz, G. M. Schütz, G. M. Schütz, J. L. Cardy, J. Marro, K. Fichthorn, M. Bramson, M. Bramson, M. D. Grynberg, M. D. Grynberg, M. Droz, M. Henkel, M. Mobilia, P.-A. Bares, P.-A. Bares, R. B. Stinchcombe, R. J. Glauber, R. Kopelman, R. Kroon, V. Belitsky, Y. Fujii, Z. Racz   +28 more
core   +1 more source

DASH: a versatile and high‐capacity gene stacking system for plant synthetic biology

Plant Biotechnology Journal, Volume 23, Issue 9, Page 3697-3712, September 2025.
Summary DNA assembly systems based on the Golden Gate method are popular in synthetic biology but have several limitations: small insert size, incompatibility with other cloning platforms, DNA domestication requirement, generation of fusion scars, and lack of post‐assembly modification.
Chengsong Zhao, Anna N. Stepanova, Jose M. Alonso   +2 more
wiley   +1 more source

The sum rule for the structure functions of the deuteron from the current algebra on the null-plane

, 2009
The fixed-mass sum rules for the deuteron target have been derived by using the connected matrix element of the current anti-commutation relation on the null-plane.
Koretune, Susumu
core   +1 more source

Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome [PDF]

, 2015
SPOAN syndrome is a neurodegenerative disorder mainly characterized by spastic paraplegia, optic atrophy and neuropathy (SPOAN). Affected patients are wheelchair bound after 15 years old, with progressive joint contractures and spine deformities.
Amorim, Simone, Armas, Pablo, Calcaterra, Nora Beatriz, Coatti, Giuliana C., Coux, Gabriela, Figueiredo, Thalita, Gleeson, Joseph G., Griesi Oliveira, Karina, Kitajima, João P., Kok, Fernando, Macedo Souza, Lucia I., Martins Pinheiro, Marinalva, Melo, Uira S., Menck, Carlos F.M., Muotri, Alysson R, Olávio, Thiago R., Rocha, Clarissa R.R, Santos, Silvana, Zaki, Maha S., Zatz, Mayana   +19 more
core   +1 more source

Pathway Analyses of Inherited Neuropathies Identify Putative Common Mechanisms of Axon Degeneration

Annals of Clinical and Translational Neurology, Volume 12, Issue 7, Page 1454-1464, July 2025.
ABSTRACT Objective Inherited neuropathies (IN) are associated with over 100 different genetic mutations presenting with a variety of phenotypes. This complexity suggests multiple pathways may converge onto a limited number of downstream pathways to effect axonal injury.
Christopher R. Cashman, Craig Blackstone, Reza Sadjadi   +2 more
wiley   +1 more source

Functional and genetic characterization of the non-lysosomal glucosylceramidase 2 as a modifier for Gaucher disease [PDF]

, 2013
Background: Gaucher disease (GD) is the most common inherited lysosomal storage disorder in humans, caused by mutations in the gene encoding the lysosomal enzyme glucocerebrosidase (GBA1).
Beck, Michael, Breiden, Bernadette, Elstein, Deborah, Filocamo, Mirella, Gonzalez, Maria C., Hoffmann, Per, Horwitz, Mia, Karlsson, Stefan,, Lund University., Lund University., Mattheisen, Manuel, Mengel, Eugen, Niederau, Claus, Noethen, Markus M., Sandhoff, Konrad, Sandhoff, Roger, Sidransky, Ellen, vom Dahl, Stefan, Yildiz, Yildiz, Zimran, Ari   +19 more
core   +2 more sources

Neurodevelopmental Implications Underpinning Hereditary Spastic Paraplegia

CNS Neuroscience &Therapeutics, Volume 31, Issue 2, February 2025.
Hereditary spastic paraplegia (HSP) is a group of rare genetic neurodegenerative disorders. This review comprehensively outlines the clinical manifestations, gene expression trajectories, and protein function of HSP subtypes from the perspective of neurodevelopment.
Yiqiang Zhi, Yan Shi, Danping Lu, Dan Xu
wiley   +1 more source

Candidate genes for plasma triglyceride, FFA, and glucose revealed from an intercross between inbred mouse strains NZB/B1NJ and NZW/LacJ*s⃞

Journal of Lipid Research, 2008
To identify the genes controlling plasma concentrations of triglycerides (TGs), FFAs, and glucose, we carried out a quantitative trait loci (QTL) analysis of the closely related mouse strains New Zealand Black (NZB/B1NJ) and New Zealand White (NZW/LacJ),
Zhiguang Su, Shirng-wern Tsaih, Jin Szatkiewicz, Yuan Shen, Beverly Paigen   +4 more
doaj   +1 more source

Human genetic defects of sphingolipid synthesis

Journal of Inherited Metabolic Disease, Volume 48, Issue 1, January 2025.
Abstract Sphingolipids are ubiquitous lipids, present in the membranes of all cell types, the stratum corneum and the circulating lipoproteins. Autosomal recessive as well as dominant diseases due to disturbed sphingolipid biosynthesis have been identified, including defects in the synthesis of ceramides, sphingomyelins and glycosphingolipids.
Patricia Dubot, Frédérique Sabourdy, Thierry Levade   +2 more
wiley   +1 more source