Results 161 to 170 of about 2,602,328 (411)
A new model for non-typeable Haemophilus influenzae middle ear infection in the Junbo mutant mouse [PDF]
Acute otitis media, inflammation of the middle ear, is the most common bacterial infection in children and, as a consequence, is the most common reason for antimicrobial prescription to this age group.
Azar, Ali+10 more
core +2 more sources
Pinoresinol diglucoside, a bioactive component extracted from traditional Chinese medicine, attenuates cisplatin‐induced ototoxicity in vivo and in vitro. The protective effect is achieved by downregulation of Socs1. The present study is the first to investigate the expression and function of Socs1 in inner ear, which is known to promote ferroptosis ...
Yin Chen+12 more
wiley +1 more source
Abstract GTF2IRD1, a gene on chromosome 7 which encodes a transcription factor, is of significant clinical interest due to its heterozygous loss as part of the classical deletion associated with Williams–Beuren syndrome (WBS). However, biallelic variants in GTF2IRD1 alone as part of an autosomal recessive disease have not been previously reported. Here,
Christopher Thomas Cummings+1 more
wiley +1 more source
EXTENSIVE VENOUS INFECTION COMPLICATING MIDDLE - EAR DISEASE: THORACIC EMPYEMA: RECOVERY [PDF]
Noelle B. Patterson
openalex +1 more source
The role of KRT5+ progenitors in chronic otitis media [PDF]
Background: Chronic inflammation of the middle ear, known as chronic otitis media, is a debilitating condition of unknown aetiology that causes hearing loss in children and adults.
Chandrasekharan, Deepak P.
core
The fusion peptide LR27‐modified thermosensitive nanodelivery system exhibits both hair cell targeting and inner ear penetrating properties. This system sustainably and effectively delivers PTH1‐34 to the inner ear of a hearing loss mouse model via the synergistic effects of multiple peptides, achieving satisfactory hearing protection through ...
Jiawen Li+12 more
wiley +1 more source
Abstract Chromosome 1p36 deletion syndrome (1p36DS) is one of the most common terminal deletion syndromes (incidence between 1/5000 and 1/10,000 live births in the American population), due to a heterozygous deletion of part of the short arm of chromosome 1.
Clémence Jacquin+47 more
wiley +1 more source
Application of laser autodyne for vibration assessment of tympanic membrane [PDF]
Research is devoted to assessing the state of the middle ear structures by usage of modern nanotechnology methods. The history of the problem, various ancient and modern methods for studying the mobility of the middle ear structures have been described ...
Skripal A.V.+4 more
doaj
Realistic 3D computer model of the gerbil middle ear, featuring accurate morphology of bone and soft tissue structures [PDF]
In order to improve realism in middle ear (ME) finite element modeling (FEM), comprehensive and precise morphological data are needed. To date, micro-scale X-ray computed tomography (\mu CT) recordings have been used as geometric input data for FEM models of the ME ossicles.
arxiv