Results 91 to 100 of about 2,814 (184)
Integrated Immune, Epithelial and Lipid Pathways in NSAID‐Exacerbated Respiratory Disease
Clinical and Translational Allergy, Volume 16, Issue 8, August 2026.ABSTRACT NSAID‐exacerbated respiratory disease (N‐ERD) is a chronic inflammatory disorder characterized by asthma, chronic rhinosinusitis with nasal polyps and respiratory reactions to cyclooxygenase‐1 inhibiting nonsteroidal anti‐inflammatory drugs (NSAID).
Piotr Szatkowski, Lucyna Mastalerz
wiley +1 more source
Cycloheximide Facilitates the Identification of Aberrant Transcripts Resulting from a Novel Splice-Site Mutation in COL17A1 in a Patient with Generalized Atrophic Benign Epidermolysis Bullosa [PDF]
, 1998 Patients with generalized atrophic benign epidermolysis bullosa often show decreased expression of type XVII collagen, a transmembrane hemidesmosomal protein encoded by COL17A1.
Koh, Brian +7 more
core +1 more source
Genes involved in amelogenesis imperfecta. Part II
Revista Facultad de Odontología Universidad de Antioquia, 2019 Amelogenesis imperfecta (AI) is a condition of genetic origin that alters the structure of tooth enamel. AI may exist in isolation or associated with other systemic conditions as part of a syndromic AI.
Víctor Hugo Simancas-Escorcia +2 more
doaj +1 more source
iMeta, Volume 5, Issue 4, August 2026.Spatial multi‐omics of the mouse ocular globe after retinal ischemia‐reperfusion (RIR) injury identifies the ganglion cell layer (GCL) as an immunometabolic niche where Trem2+ microglia closely associate with stressed retinal ganglion cells (RGCs) through Trem2‐Apoe signaling.
Yunhong Shi +12 more
wiley +1 more source
Upregulation of α6β4 and β1 integrins in Col17a1−/− skin.
, 2014 A and B, Skin lysates from WT and Col17a1−/− mice were immunoblotted with indicated antibodies. The graphs combine the quantification for β4 protein expression of four individuals per genotype (A) and β1 protein expression of three individuals (B ...
Claus-Werner Franzke (185138) +7 more
core +1 more source
Vertical Growth of Facial Soft Tissues: A Longitudinal Three‐Dimensional Facial Growth Study
Orthodontics &Craniofacial Research, Volume 29, Issue 4, Page 649-658, August 2026.ABSTRACT Objective This longitudinal cohort study aimed to assess changes in vertical facial landmarks in individuals aged 10 to 18 years and identify sex differences in growth patterns. Materials and Methods One hundred and one individuals (males, n = 56; females, n = 45) were observed.
Signe Silinevica +3 more
wiley +1 more source
Rotating cell culture system-induced injectable self-assembled microtissues with epidermal stem cells for full-thickness skin repair [PDF]
PeerJEpidermal stem cells (EpSCs) are crucial for wound healing and tissue regeneration, and traditional culture methods often lead to their inactivation. It is urgent to increase the yield of high quality EpSCs. In this study, primary EpSCs were isolated and
Min Zhang +6 more
doaj +2 more sources
Update on Approved Therapies for Dystrophic and Junctional Epidermolysis Bullosa
Pediatric Dermatology, Volume 43, Issue S2, Page 20-28, August 2026.ABSTRACT Dystrophic epidermolysis bullosa (DEB) and junctional EB (JEB) are severe, bullous genodermatoses induced by mutations of genes encoding structural skin proteins that disrupt epidermal adhesion. Until recently, treatment was limited to symptomatic care. Since 2022, three therapies – birch triterpenes gel (Filsuvez), beremagene geperpavec‐svdt (
Alberto Pappalardo +5 more
wiley +1 more source
, 2023 L’Epidermolisi Bollosa Giunzionale (JEB) è una malattia genetica rara causata dalla ridotta o anormale espressione del collagene 17. Tale patologia coinvolge principalmente la pelle e si caratterizza per l’insufficiente ancoraggio dell'epidermide al ...
NESTERUK, IVANNA
core
Novel Mutations Associated With Various Types of Corneal Dystrophies in a Han Chinese Population
Frontiers in Genetics, 2019 Aims: To study the genetic spectra of corneal dystrophies (CDs) in Han Chinese patients using next-generation sequencing (NGS).Methods: NGS-based targeted region sequencing was performed to evaluate 71 CD patients of Han Chinese ethnicity.
Jing Zhang +20 more
doaj +1 more source