Results 201 to 210 of about 516,267 (425)

Squamate ventricular cardiomyocytes: Ploidy, proliferation, and heart muscle cell size in the leopard gecko (Eublepharis macularius)

open access: yesDevelopmental Dynamics, EarlyView.
Abstract Background While heart function is broadly conserved across vertebrates, the cellular phenotype of muscle cells (cardiomyocytes) varies across taxa and throughout ontogeny. Emerging evidence suggests that some attributes may correlate with the capacity for spontaneous cardiomyocyte replacement following injury.
Kathy Jacyniak   +4 more
wiley   +1 more source

Clinical value of right subclavian artery atheromatosis presented as the marker of early carotid artery arteriosclerosis

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2013
Background There are many reports regarding the harmful effect of arteriosclerosis at the bifurcation of common carotid artery, but few researches involving the application of color Doppler sonography scanning for the diagnosis of arteriosclerosis at the
Pan CHENG, De-lin YU, Ren-guang MA
doaj  

Bilateral Common Carotid Artery Occlusion in the Rat as a Model of Retinal Ischaemia

open access: yesNeuro-ophthalmology (Aeolus Press. 1980), 2014
Yingxiang Huang   +3 more
semanticscholar   +1 more source

Pre‐oviposition development of the brown anole (Anolis sagrei)

open access: yesDevelopmental Dynamics, EarlyView.
Abstract Background The brown anole, Anolis sagrei, has emerged as a representative squamate species for developmental studies during the past decades. Novel functional tools have been established to manipulate embryogenesis through genome editing or the introduction of small molecule inhibitors, and their effective use requires a thorough ...
Antonia Weberling   +9 more
wiley   +1 more source

Prediction of stroke before and after unilateral occlusion of the common carotid artery in gerbils. [PDF]

open access: bronze, 1988
Masayasu Matsumoto   +4 more
openalex   +1 more source

Transthyretin amyloid cardiomyopathy: Literature review and red‐flag symptom clusters for each cardiology specialty

open access: yesESC Heart Failure, Volume 12, Issue 2, Page 955-967, April 2025.
Abstract Wild‐type transthyretin amyloid cardiomyopathy (ATTRwt‐CM) is a progressive and infiltrative cardiac disorder that may cause fatal consequences if left untreated. The estimated survival time from diagnosis is approximately 3–6 years. Because of the non‐specificity of initial symptom manifestation and insufficient awareness among treating ...
Yasuhiro Izumiya   +9 more
wiley   +1 more source

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