mouse model (Cyagen Biosciences)
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Cyagen Biosciences
mouse model
Mouse Model, supplied by Cyagen Biosciences, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+models/Tcfl5/pm36797258-166-1-5
Average 92 stars, based on 1 article reviews
Mouse Model, supplied by Cyagen Biosciences, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+models/Tcfl5/pm36797258-166-1-5
Average 92 stars, based on 1 article reviews
mouse model - by Bioz Stars,
2026-10
92/100 stars
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other:Article Title: Nynrin preserves hematopoietic stem cell function by inhibiting the mitochondrial permeability transition pore opening. Article Snippet: The mouse models used in this research, including Nynrinfl/fl, Nynrin-EGFP, 33FlagNynrin-Tg, Knock-Out:Article Title: LncRNA evf‐2 Exacerbates Podocyte Injury in Diabetic Nephropathy by Inducing Cell Cycle Re‐entry and Inflammation Through Distinct Mechanisms Triggered by hnRNPU Article Snippet: .. ◆ Podocyte-specific knockout of lncRNA evf-2 in mice The Cell Function Assay:Article Title: The 133-kDa N-terminal region of myosin XVa is critical for normal structure and function of auditory and hair cells. Article Snippet: Background: MYO15A is a commonly implicated gene in severe to profound sensorineural hearing loss.. Numerous studies have identified mutations in MYO15A in humans, analyzed their presence and co-segregation, and predicted their pathogenicity using software tools. however, few have investigated the pathogenic mechanisms of these mutations using mouse models. in a prior study, we identified the MYO15A c.2482 c > t mutation as a potential causative gene for deafness in a Uygur family from Xinjiang. to further explore the pathogenicity and mechanisms of this mutation, we constructed a mouse model harboring the Myo15a c.2455a > t mutation. this study demonstrates that mice with the Myo15a c.2455a > t spot knock-in exhibit the abnormal hair cell morphology, dysfunction, and hearing loss phenotype observed in humans.. Objectives: to investigate the pathogenic mechanism of deafness caused by MYO15A c.2482c > t mutation. Generated:Article Title: Development and characterization of a fully humanized ACE2 mouse model. Article Snippet: .. JMM generated Table S1 and conceived the design of the Article Title: A rare germline BMP15 missense mutation causes hereditary ovarian immature teratoma in human. Article Snippet: .. Mutagenesis:Article Title: A rare germline BMP15 missense mutation causes hereditary ovarian immature teratoma in human. Article Snippet: .. |