Results 101 to 110 of about 110,072 (307)

A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal and mdx mice Immunological evidence [PDF]

, 1991
F. Pons, N Augier, Jocelyne Léger, Aude Robert, F.M.S. Tomé, Michel Fardeau, Thomas Voit, L. V. B. Nicholson, Dominique Mornet, J. Léger   +9 more
openalex   +1 more source

In Vivo Cytoskeletal AMPA Receptor Transport Imaging in C. elegans

Cytoskeleton, EarlyView.
ABSTRACT Long‐distance intracellular transport of ionotropic glutamate receptors (iGluRs) is essential for proper excitatory synaptic function underlying learning and memory. Many neuropsychiatric and neurodegenerative conditions have abnormal iGluR transport and trafficking, leading to an intense interest in the mechanisms and factors regulating these
Michaelis A. K., Hoerndli F. J.
wiley   +1 more source

Where You Place, How You Load: A Scoping Review of the Determinants of Orthodontic Mini-Implant Success

Applied Sciences
Objective: This scoping review identifies and analyzes factors influencing the effectiveness of orthodontic mini-implants and temporary anchorage devices in orthodontic treatments, including clinical applications, success rates, and associated ...
Jacob Daniel Gardner, Ambrose Ha, Samantha Lee, Amir Mohajeri, Connor Schwartz, Man Hung   +5 more
doaj   +1 more source

Identification of a new DMD gene deletion by ectopic transcript analysis. [PDF]

, 1992
Frauke Rininsland, Andreas Hahn, Susanne C. Niemann‐Seyde, Ryszard Słomski, F. Hanefeld, Jochen Reiss   +5 more
openalex   +1 more source

Reviewer #1 (Public Review): Development and validation of a high throughput screening platform to enable target identification in skeletal muscle cells from Duchenne Muscular Dystrophy (DMD) patients

, 2023
Santosh Hariharan, Oana Lorintiu, Chia-Chin Lee, Eve Duchemin-Pelletier, Xianfeng Li, Aileen M. Healy, Régis Doyonnas, Luc Selig, Pauline Poydenot, Erwann Ventre, Andrea D. Weston, Jane Owens, Nicolas Christoforou   +12 more
openalex   +1 more source

Fhod3 in zebrafish supports myofibril stability during growth of embryonic skeletal muscle

Developmental Dynamics, EarlyView.
Abstract Background Actin filament organization in cardiomyocytes critically depends on the formin Fhod3, but a role for Fhod3 in skeletal muscle development has not yet been described. Results We demonstrate here that in zebrafish mutated for one of two fhod3 paralog genes, fhod3a, skeletal muscle of the trunk appears normal through 2 days post ...
Aubrie Russell, Tracy Eng, Jeffrey D. Amack, David Pruyne   +3 more
wiley   +1 more source

A clinical case of severe Duchenne muscular dystrophy caused by a nonsense mutation in the DMD gene in a girl

, 2021
Tatyana V. Podkletnova, Olga B. Kondakova, Eugeniya V. Uvakina, Dariya A. Fisenko, Anastasiya A. Lyalina, Sophiya G. Popovich, Л. М. Кузенкова, Aleksey L. Kurenkov, Л. А. Пак, Б. И. Бурсагова   +9 more
openalex   +1 more source

Developing a Suitable Anion Exchange Layer Structure for Pure–Water Fed Bipolar Membrane CO2 Electrolysis

ENERGY &ENVIRONMENTAL MATERIALS, EarlyView.
A porous anion exchange layer (AEL) is implemented in a forward‐biased bipolar membrane CO2 electrolyzer to suppress carbonate crossover, support CO2 regeneration and maintain cathode alkalinity. Two fabrication strategies are compared—deposition on a silver gas diffusion electrode (GDE) or on the CEM—showing that a porous AEL‐coated GDE provides the ...
Henning Lorenz, Nico Roubicek, Simon Thiele, Chuyen van Pham   +3 more
wiley   +1 more source

Dystrophinopathy with a <i>DMD</i> exon 49-50 deletion in a female patient who developed schizophrenia: An autopsy case. [PDF]

PCN Rep
Abstract Background Mutations in DMD affect not only muscles but also the brain. Cases of schizophrenia with DMD mutations have been described previously. Although female dystrophinopathy often has a milder phenotype, some affected females also have intellectual disabilities and psychiatric disorders.
Arafuka S, Torii Y, Miwa A, Kushima I, Sekiguchi H, Fujishiro H, Habuchi C, Miyahara H, Kawai Y, Wei R, Tokunaga K, Ozaki N, Yoshida M, Iritani S, Iwasaki Y, Ikeda M.   +15 more
europepmc   +2 more sources

Prevention of early-onset cardiomyopathy in Dmd exon 52–54 deletion mice by CRISPR-Cas9-mediated exon skipping [PDF]

, 2023
M. Rok, Tatianna Wai Ying Wong, Eleonora Maino, Abdalla Ahmed, Grace Meijuan Yang, Elzbieta Hyatt, Kyle Lindsay, Sina Fatehi, Ryan M. Marks, Paul Delgado-Olguı́n, Evgueni A. Ivakine, Ronald D. Cohn   +11 more
openalex   +1 more source