Zobrazeno 1 - 10
of 6 646
pro vyhledávání: '"dystrophic"'
Autor:
Chen Yang, Zhong-Ping Sun, Juan Jiang, Xiao-Lu Cai, Yan Wang, Hui Wang, Chong Che, Ewen Tu, Ai-hua Pan, Yan Zhang, Xiao-Ping Wang, Mei-Zhen Cui, Xue-min Xu, Xiao-Xin Yan, Qi-Lei Zhang
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-20 (2024)
Abstract Presenilin-associated protein (PSAP) is a mitochondrial proapoptotic protein as established in cell biology studies. It remains unknown whether it involves in neurodegenerative diseases. Here, we explored PASP expression in adult and aged hu
Externí odkaz:
https://doaj.org/article/fe7c5aa21bb943f0a251463613b429aa
Autor:
T.O. Andreeva, O.M. Stoyanov, E.M. Mirdjuraev, G.M. Chebotareva, V.I. Kalashnikov, R.S. Vastyanov, V.I. Dariy
Publikováno v:
Bolʹ, Sustavy, Pozvonočnik, Vol 14, Iss 3, Pp 147-154 (2024)
Background. The neck, its bone-cartilaginous and muscle apparatus, etc. high activity is well known. Cervical spine degenerative-dystrophic processes are considered to be an urgent problem. The purpose of the study was to determine the clinical and m
Externí odkaz:
https://doaj.org/article/7414121014854b868eb2144fe87ecda0
Publikováno v:
Journal of Dermatological Treatment, Vol 35, Iss 1 (2024)
Background: The ability of mesenchymal stromal cells (MSCs) to facilitate regenerative responses in inflamed and injured tissues, coupled with preclinical data suggesting potential to restore defective collagen VII at the dermo-epidermal junction, ha
Externí odkaz:
https://doaj.org/article/efb7b29873f44fc58aad2d306a78a086
Autor:
Amy S. Paller, Shireen V. Guide, Diego Ayala, Mercedes E. Gonzalez, Anne W. Lucky, Isin Sinem Bagci, M. Peter Marinkovich
Publikováno v:
Journal of Dermatological Treatment, Vol 35, Iss 1 (2024)
Background/purpose Dystrophic epidermolysis bullosa (DEB), a rare genetic skin disease caused by loss-of-function mutations in COL7A1, the gene encoding type VII collagen (COL7), is characterized by skin blistering, scarring, and extracutaneous manif
Externí odkaz:
https://doaj.org/article/4d22581de2c841f09a639f4a31802fdc
Autor:
Dimitra Kiritsi, Franziska Schauer, Stella Gewert, Katja Reineker, Antonia Reimer-Taschenbrecker, Agnes Schwieger-Briel, Hagen Ott, Claudia Schmoor, Olga Grishina, Dedee Murrell, Brigitte Stiller, Tobias Zahn, Alexander Nyström, Leena Bruckner-Tuderman
Publikováno v:
EClinicalMedicine, Vol 77, Iss , Pp 102900- (2024)
Summary: Background: Recessive dystrophic epidermolysis bullosa (RDEB) is a skin fragility disorder characterised by life-long mechanically induced skin blistering, fibrosis-driven pseudosyndactyly, and multi-organ involvement. Preclinical studies ha
Externí odkaz:
https://doaj.org/article/ceaea83a01bb41de80f3d86b05684855
Publikováno v:
JAAD Case Reports, Vol 50, Iss , Pp 79-81 (2024)
Externí odkaz:
https://doaj.org/article/0bcd000b0c3944e092b2e0e2a80773d5
Publikováno v:
Spine Surgery and Related Research, Vol 8, Iss 4, Pp 469-472 (2024)
Externí odkaz:
https://doaj.org/article/9cb963feefbb47f983cbc65fce8c6da0
Publikováno v:
Chinese Medicine, Vol 19, Iss 1, Pp 1-14 (2024)
Abstract Background Alzheimer's disease (AD) is a common type of dementia characterized by amyloid-β (Aβ) accumulation, lysosomal dysfunction, and tau hyperphosphorylation, leading to neurite dystrophy and memory loss. This study aimed to investiga
Externí odkaz:
https://doaj.org/article/a96a43ba9f414804b02bd18f03276976
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-12 (2024)
Abstract Background Invasive cutaneous squamous cell carcinomas (cSCC) are a leading cause of death in recessive dystrophic epidermolysis bullosa (RDEB), a rare blistering genodermatosis. Outcomes of RDEB-cSCC therapies have primarily been described
Externí odkaz:
https://doaj.org/article/64f39d56a71f4cad83d2160f67236646
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.