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Aging of skeletal muscle fibers.

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TLDR
Muscle size and architecture are both altered with advanced adult age and changes in myofibers include impairments in several physiological domains including muscle fiber activation, excitation-contraction coupling, actin-myosin cross-bridge interaction, energy production, and repair and regeneration.
Abstract
Aging has become an important topic for scientific research because life expectancy and the number of men and women in older age groups have increased dramatically in the last century. This is true in most countries of the world including the Republic of Korea and the United States. From a rehabilitation perspective, the most important associated issue is a progressive decline in functional capacity and independence. Sarcopenia is partly responsible for this decline. Many changes underlying the loss of muscle mass and force-generating capacity of skeletal muscle can be understood at the cellular and molecular levels. Muscle size and architecture are both altered with advanced adult age. Further, changes in myofibers include impairments in several physiological domains including muscle fiber activation, excitation-contraction coupling, actin-myosin cross-bridge interaction, energy production, and repair and regeneration. A thorough understanding of these alterations can lead to the design of improved preventative and rehabilitative interventions, such as personalized exercise training programs.

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Gerry Purdy
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Japan Society of Hepatology guidelines for sarcopenia in liver disease (1st edition): Recommendation from the working group for creation of sarcopenia assessment criteria.

TL;DR: The assessment criteria for sarcopenia in liver disease proposed by the Japan Society of Hepatology (JSH) are summarized in this article, where the authors present the assessment criteria to the best of their knowledge.
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The bystander effect contributes to the accumulation of senescent cells in vivo.

TL;DR: A significant impact of the bystander effect for accumulation of senescent hepatocytes in liver is suggested and senostatic interventions like dietary restriction may act as senolytics in immunocompetent animals.
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Frailty and sarcopenia as the basis for the phenotypic manifestation of chronic diseases in older adults.

TL;DR: Cell response to stress pathways such as Nrf2, sirtuins and klotho could be considered as future therapeutic interventions for the management of frailty phenotype and aging-related chronic diseases.
References
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A longitudinal study

TL;DR: A longitudinal study of service delivery within MRI services at Auckland University for patients, researchers and referring practitioners has been carried out since 2006 as mentioned in this paper, with a focus on the effects of service provision on patient satisfaction.
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Skeletal muscle mass and distribution in 468 men and women aged 18–88 yr

TL;DR: It is indicated that men have more SM than women and that these gender differences are greater in the upper body.
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Sarcopenia: Origins and Clinical Relevance

TL;DR: Sarcopenia as mentioned in this paper is a Greek word that describes important changes in body composition and related functions, which can be used to classify patients and examine underlying pathogenic mechanisms and will allow funding agencies to appropriately target research funds to a taxonomically distinct syndrome.
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Satellite Cells and the Muscle Stem Cell Niche

TL;DR: For the last half century, the advance of molecular biology, cell biology, and genetics has greatly improved the understanding of skeletal muscle biology, with focuses on functions of satellite cells and their niche during the process ofletal muscle regeneration.
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