Zobrazeno 1 - 10
of 130
pro vyhledávání: '"Abnormal mitochondria"'
Challenging Sarcopenia: Exploring AdipoRon in Aging Skeletal Muscle as a Healthspan-Extending Shield
Autor:
Camille M. Selvais, Maria A. Davis-López de Carrizosa, Romain Versele, Nicolas Dubuisson, Laurence Noel, Sonia M. Brichard, Michel Abou-Samra
Publikováno v:
Antioxidants, Vol 13, Iss 9, p 1073 (2024)
Sarcopenia, characterized by loss of muscle mass, quality, and function, poses significant risks in aging. We previously demonstrated that long-term treatment with AdipoRon (AR), an adiponectin receptor agonist, alleviated myosteatosis and muscle deg
Externí odkaz:
https://doaj.org/article/33fd684899a1494f905b661ff7d1186c
Akademický článek
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Publikováno v:
Polish Journal of Pathology, Vol 69, Iss 4, Pp 422-431 (2019)
Our studies concerned skeletal muscle biopsy specimens from a patient with clinically suspected MERRF syndrome, confirmed by genetic tests showing the presence of point mutation in the m.8344A> G in the tRNALys gene. Ultrastructurally, extensive dama
Externí odkaz:
https://doaj.org/article/1184fe4e72ae4a29a47bfe3688d09772
Autor:
Paulina Felczak, Eliza Lewandowska, Iwona Stępniak, Monika Ołdak, Agnieszka Pollak, Urszula Lechowicz, Elżbieta Pasennik, Tomasz Stępień, Teresa Wierzba-Bobrowicz
Publikováno v:
Polish Journal of Pathology, Vol 68, Iss 2, Pp 173-181 (2017)
Ultrastructural changes in skeletal muscle biopsy in a 24-year-old female patient with clinically suspected mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes (MELAS) syndrome are presented. We observed proliferation and/or pleo
Externí odkaz:
https://doaj.org/article/9eeddc026cfc4e4096a4244cca42779a
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Publikováno v:
Analytical Chemistry. 91:8415-8421
Elucidating the internal relationship between diseases and mitochondrial viscosity remains a great challenge due to the lack of the studies on multidisease living animals. So far, demonstrating abnormal mitochondria viscosity in the fatty liver and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6182cd79f5bbfe08e4d559f9604eecd
https://doi.org/10.1021/acs.analchem.9b01293
https://doi.org/10.1021/acs.analchem.9b01293
Publikováno v:
Polish Journal of Pathology, Vol 69, Iss 4, Pp 422-431 (2019)
Our studies concerned skeletal muscle biopsy specimens from a patient with clinically suspected MERRF syndrome, confirmed by genetic tests showing the presence of point mutation in the m.8344A> G in the tRNALys gene. Ultrastructurally, extensive dama
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::107fdee336d0900b7a338d29091b82f7
https://www.termedia.pl/Pathology-of-skeletal-muscle-fibers-and-small-blood-vessels-in-MERRF-syndrome-an-ultrastructural-study,55,34483,1,1.html
https://www.termedia.pl/Pathology-of-skeletal-muscle-fibers-and-small-blood-vessels-in-MERRF-syndrome-an-ultrastructural-study,55,34483,1,1.html
Autor:
Shannon Kalsow, Sarah J. Parker
Publikováno v:
The FASEB Journal. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3bca012ee62df42e61e89830e1382cf
https://doi.org/10.1096/fasebj.2021.35.s1.03352
https://doi.org/10.1096/fasebj.2021.35.s1.03352
Autor:
Long Zhang, Elizabeth P. Henske
Publikováno v:
Urologic oncology. 38(8)
Chromophobe renal cell carcinoma (chRCC) represents 5% of all RCC. ChRCC appears to arise from the distal nephron, in contrast to clear cell RCC that arises from the proximal nephron. ChRCC is distinctive because the tumor cells contain abundant abno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cf050e8c69227203ba9168d9e930efa
https://pubmed.ncbi.nlm.nih.gov/32444178
https://pubmed.ncbi.nlm.nih.gov/32444178
Autor:
Ingo Kurth, Roman Rolke, Zafer Yüksel, Martin Häusler, Dorothea Rohrmann, Simone Schrading, Marion Bienert, Joachim Weis, Annegret Quade
Publikováno v:
Neuromuscular Disorders. 28:1006-1011
We report a 9-year-old girl homozygous for a loss-of-function mutation in the PIEZO-2 gene. She showed generalized muscular hypotonia with severe scoliosis, joint deformities, deficient proprioceptive function and selective atrophy and signal alterat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1fc1f46935cf1e9f5e09fe2fb1e9dbc
https://doi.org/10.1016/j.nmd.2018.08.009
https://doi.org/10.1016/j.nmd.2018.08.009