Results 291 to 300 of about 321,114 (362)

MUSTN1 Interaction With SMPX Regulates Muscle Development and Regeneration

Cell Proliferation, EarlyView.
Model of the role of MUSTN1 in skeletal muscle development. MUSTN1‐KO mice display delayed muscle growth and regeneration. MUSTN1 protects SMPX from instability and maintains the morphology of muscle fibres. MUSTN1 and SMPX synergistically promote myoblast proliferation and dependently facilitate differentiation.
Yu Fu, Xin Hao, Peng Shang, Jingru Nie, Yangzom Chamba, Bo Zhang, Hao Zhang   +6 more
wiley   +1 more source

Ambient floor vibration sensing advances the accessibility of functional gait assessments for children with muscular dystrophies. [PDF]

Sci Rep
Dong Y, Iammarino M, Liu J, Codling J, Fagert J, Mirshekari M, Lowes L, Zhang P, Noh HY.   +8 more
europepmc   +1 more source

Intelligent Manufacturing for Osteoarthritis Organoids

Cell Proliferation, EarlyView.
Overall schematic of intelligent manufacturing in osteoarthritis organoids. Broad overview of the article's structure, outlining the progression from fundamental joint anatomy and OA pathogenesis to organoid construction and, ultimately, to intelligent manufacturing and future prospects.
Xukun Lyu, Jian Wang, Jiacan Su
wiley   +1 more source

The Efficacy of Sulphur Amino Acids and Related Compounds for Protection Against the Development of Muscular Dystrophy in the Chick

, 1962
K.J. Jenkins, D.C. Hill, Lilian M. Hutcheson, H.D. Branion   +3 more
openalex   +1 more source

Elucidating the Role and Mechanism of Alpha‐Enolase in Senescent Amelioration via Metabolic Reprogramming

Cell Proliferation, EarlyView.
KB2764 interacted with alpha‐enolase (ENO1) and pyruvate kinase M (PKM), ultimately leading to PKM phosphorylation of ENO1. KB2764 consequently increased mitochondrial ATP production and decreased glycolysis dependence. Furthermore, the action of KB2764 extends its application to extend the lifespan of Caenorhabditis elegans.
Yun Haeng Lee, Hyunwoong Lim, Gyungmin Kim, Geonhee Jang, Myeong Uk Kuk, Ji Ho Park, Jee hee Yoon, Yoo Jin Lee, Duyeol Kim, Byeonghyeon So, Minseon Kim, Hyung Wook Kwon, Youngjoo Byun, Joon Tae Park   +13 more
wiley   +1 more source

Oxygen Consumption and Anaerobic Glycolysis of the Muscle from the Patients with Progressive Muscular Dystrophy

, 1963
Keiya Tada, Haruko Hirono, Hisashi Miyazawa   +2 more
openalex   +2 more sources

Diagnostic approach to the congenital muscular dystrophies

Neuromuscular Disorders, 2014
C. Bönnemann, Ching H. Wang, S. Quijano-roy, N. Deconinck, E. Bertini, A. Ferreiro, F. Muntoni, C. Sewry, C. Béroud, K. Mathews, S. Moore, Jonathan Bellini, A. Rutkowski, K. North   +13 more
semanticscholar   +1 more source

Exploring Splice-Site Mutations in LAMA2-Related Muscular Dystrophies: A Comprehensive Analysis of Genotypic and Phenotypic Patterns. [PDF]

Cureus
Nmer S, Ameli A, Trhanint S, Chaouki S, Bouguenouch L, Ouldim K.   +5 more
europepmc   +1 more source

A 3D adipogenesis platform to study the fate of fibro/adipogenic progenitors in muscular dystrophies.

Dis Model Mech, 2023
Reggio A, De Paolis F, Bousselmi S, Cicciarelli F, Bernardini S, Rainer A, Seliktar D, Testa S, Cirillo C, Grumati P, Cannata S, Fuoco C, Gargioli C.   +12 more
europepmc   +1 more source

Psychometric evaluation of the PROMIS parent proxy mobility item bank for use in Duchenne muscular dystrophy

Developmental Medicine &Child Neurology, EarlyView.
Abstract Aim To evaluate the psychometric properties and measurement quality of the Patient‐Reported Outcomes Measurement Information System Parent Proxy (PROMIS PP) Mobility item bank (v1.0, 23 items) for children with Duchenne muscular dystrophy (DMD), through Rasch statistical analysis. Method De‐identified PROMIS PP Mobility items were completed by
Linda Pax Lowes, Corinne M. Le Reun, Lindsay N. Alfano, Natalie F. Reash, Megan A. Iammarino, Shivangi Patel, Ivana F. Audhya   +6 more
wiley   +1 more source