Results 41 to 50 of about 483,797 (293)

Membrane Repair Deficit in Facioscapulohumeral Muscular Dystrophy. [PDF]

open access: yes, 2020
Deficits in plasma membrane repair have been identified in dysferlinopathy and Duchenne Muscular Dystrophy, and contribute to progressive myopathy. Although Facioscapulohumeral Muscular Dystrophy (FSHD) shares clinicopathological features with these ...
Yokota, Toshifumi   +27 more
core   +1 more source

Welding, control and repair of membrane welds

open access: yesZavarivanje i zavarene konstrukcije, 2021
The paper describes design, production and inspection of membrane welds according to EN 12952-5 [1]. Stated procedures and technologies are based on water tube boiler manufacturing in the company ĐĐ Termoenergetska postrojenja d.o.o. Paper gives the overview of the standard manufacturing process: welding technology, marking and identification of welds,
Samardžić, Mijat   +4 more
openaire   +2 more sources

Multiple Parameters Beyond Lipid Binding Affinity Drive Cytotoxicity of Cholesterol-Dependent Cytolysins

open access: yesToxins, 2018
The largest superfamily of bacterial virulence factors is pore-forming toxins (PFTs). PFTs are secreted by both pathogenic and non-pathogenic bacteria. PFTs sometimes kill or induce pro-pathogen signaling in mammalian cells, all primarily through plasma ...
Sucharit Ray   +2 more
doaj   +1 more source

Is the Bacterial Cellulose Membrane Feasible for Osteopromotive Property? [PDF]

open access: yes, 2020
Guided bone regeneration was studied to establish protocols and develop new biomaterials that revealed satisfactory results. The present study aimed to comparatively evaluate the efficiency of the bacterial cellulose membrane (Nanoskin®) and collagen
Leonardo P. Faverani   +15 more
core   +1 more source

Reduced Sarcolemmal Membrane Repair Exacerbates Striated Muscle Pathology in a Mouse Model of Duchenne Muscular Dystrophy

open access: yesCells, 2022
Duchenne muscular dystrophy (DMD) is a common X-linked degenerative muscle disorder that involves mutations in the DMD gene that frequently reduce the expression of the dystrophin protein, compromising the structural integrity of the sarcolemmal membrane
Brian J. Paleo   +9 more
doaj   +1 more source

Attaching and effacing Escherichia coli downregulate DNA mismatch repair protein in vitro and are associated with colorectal adenocarcinomas in humans [PDF]

open access: yes, 2009
Background: Mucosa-associated Escherichia coli are frequently found in the colonic mucosa of patients with colorectal adenocarcinoma, but rarely in healthy controls. Chronic mucosal E. coli infection has therefore been linked to colonic tumourigenesis. E.
Short, Abigail J.   +14 more
core   +1 more source

Membrane repair and immunological danger [PDF]

open access: yesThe EMBO Reports, 2005
Antigens are able to elicit productive immune responses only when second signals are provided by adjuvant molecules. It is well established that exogenously acquired, pathogen-associated molecular patterns fulfil this adjuvant role when recognized by specific receptors on antigen-presenting cells.
openaire   +2 more sources

ER-Golgi in membrane repair in cardiomyocytes [PDF]

open access: yes, 2022
Impaired membrane repair leads to muscular dystrophies like Miyoshi Myopathy and LGMD2B1. The mechanism behind membrane repair is not well understood, and there are few studies on membrane repair in cardiomyocytes.
Michele, Daniel   +2 more
core   +1 more source

Fer1L5, a Dysferlin Homologue Present in Vesicles and Involved in C2C12 Myoblast Fusion and Membrane Repair

open access: yesBiology, 2020
Fer1L5 is a dysferlin and myoferlin related protein, which has been predicted to have a role in vesicle trafficking and muscle membrane fusion events. Mutations in dysferlin and otoferlin genes cause heredity diseases: muscular dystrophy and deafness in ...
R. Usha Kalyani   +8 more
doaj   +1 more source

Dystrophin deficiency exacerbates skeletal muscle pathology in dysferlin-null mice

open access: yesSkeletal Muscle, 2011
Background Mutations in the genes coding for either dystrophin or dysferlin cause distinct forms of muscular dystrophy. Dystrophin links the cytoskeleton to the sarcolemma through direct interaction with β-dystroglycan.
Han Renzhi   +4 more
doaj   +1 more source

Home - About - Disclaimer - Privacy