Results 91 to 100 of about 294,685 (303)

Current trends in single‐cell RNA sequencing applications in diabetes mellitus

open access: yesFEBS Open Bio, EarlyView.
Single‐cell RNA sequencing is a powerful approach to decipher the cellular and molecular landscape at a single‐cell resolution. The rapid development of this technology has led to a wide range of applications, including the detection of cellular and molecular mechanisms and the identification and introduction of novel potential diagnostic and ...
Seyed Sajjad Zadian   +6 more
wiley   +1 more source

Editorial: Role of complement activation in kidney diseases

open access: yesFrontiers in Medicine, 2023
Takashi Oda, Toshihiro Sawai
doaj   +1 more source

Hypoxic Processes Induce Complement Activation via Classical Pathway in Porcine Neuroretinas. [PDF]

open access: yesCells, 2021
Mueller-Buehl AM   +6 more
europepmc   +1 more source

Stimulation of Prostaglandin Synthesis with Resultant Bone Resorption by the Classical and Alternative C Pathways [PDF]

open access: bronze, 1976
Ann L. Sandberg   +3 more
openalex   +1 more source

Characterization of ribosome heterogeneity during endothelial to hematopoietic transition

open access: yesFEBS Open Bio, EarlyView.
The panorama of ribosome heterogeneity during embryonic hematopoiesis has not yet been portrayed. In this study, utilizing dual‐omics data, the heterogenous dynamic of ribosome during endothelial‐to‐hematopoietic transition has been systemically described. Moreover, stage‐specific upregulation and peripheral localization of RPL27 and RACK1 in hemogenic
Xitong Tian   +4 more
wiley   +1 more source

Anticomplement activity of ginsenosides from Panax ginseng

open access: yesJournal of Functional Foods, 2013
The anticomplementary activities of 12 ginseng saponins obtained from Panax ginseng were investigated. The total saponin and its major components showed strong anticomplementary activities through classic pathway.
Hong-wei Gao   +4 more
doaj  

A Novel CHMP2B Splicing Variant in Atypical Presentation of Familial Frontotemporal Lobar Degeneration

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who
Sara Rubio‐Guerra   +17 more
wiley   +1 more source

Editorial: C1q: A Molecular Bridge to Innate and Adaptive Immunity

open access: yesFrontiers in Immunology, 2020
Uday Kishore, Berhane Ghebrehiwet
doaj   +1 more source

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