Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Arthur G. Kristiansen"'
Autor:
Dongjun Han, Michael J. McKenna, Sasa Vasilijic, Lukas D. Landegger, Sachiyo Katsumi, Konstantina M. Stankovic, Shyan-Yuan Kao, Argyro J. Bizaki-Vallaskangas, Arthur G. Kristiansen
Publikováno v:
Bone. 145:115837
The bone encasing the inner ear, known as the otic capsule, is unique because it remodels little postnatally compared to other bones in the body. Previous studies established that osteoprotegerin (OPG) in the inner ear inhibits otic capsule remodelin
Autor:
Vítor Yamashiro Rocha Soares, Konstantina M. Stankovic, Shyan-Yuan Kao, Arthur G. Kristiansen
Publikováno v:
Aging Cell
Summary Tumor necrosis factor (TNF) family cytokines are important mediators of inflammation. Elevated levels of serum TNF‐α are associated with human sensorineural hearing loss via poorly understood mechanisms. We demonstrate, for the first time,
Autor:
Arthur G. Kristiansen, Joe C. Adams, Michael J. McKenna, Andreas F. Zehnder, Saumil N. Merchant
Publikováno v:
The Laryngoscope. 115:172-177
Objectives: To elucidate factors that may be responsible for the inhibition of remodeling of bone within the otic capsule. Methods: Expression of osteoprotegerin (OPG), receptor activator of nuclear factor kappa B (RANK), and RANK ligand (RANKL) were
Autor:
Arthur G. Kristiansen, Saumil N. Merchant, Lisbeth Tranebjærg, Anke Tropitzsch, Michael J. McKenna
Publikováno v:
Otology & Neurotology. 23:789-792
Hypothesis: Contamination of archival human temporal bones with extraneous deoxyribonucleic acid may represent a potentially significant problem in the analysis of nucleic acids isolated from archival specimens. Background: During the past decade, th
Publikováno v:
Oto-Rhino-Laryngologia Nova. 11:267-270
Because of the clinical and histopathologic similarities between otosclerosis and type I osteogenesis imperfecta and prior evidence that some cases of clinical otosclerosis have reduced expression of one COL1A1 allele, we analyzed the COL1A1 and COL1
Publikováno v:
Oto-Rhino-Laryngologia Nova. 10:232-236
Mutations in the connexin 26 gene have been found to be associated with approximately half of all cases of congenital nonsyndromic sensorineural hearing loss, and represent the single most common cause of genetic sensorineural hearing loss. Seven set
Publikováno v:
The Journal of Neuroscience. 19:10116-10124
The inner ear can be permanently damaged by overexposure to high-level noise; however, damage can be decreased by previous exposure to moderate level, nontraumatic noise (Canlon et al., 1988). The mechanism of this “protective” effect is unclear,
Autor:
Arthur G. Kristiansen, Osamu Adachi, Vicki Rosen, Kunikazu Tsuji, Konstantina M. Stankovic, Joe C. Adams, Michael J. McKenna
Publikováno v:
Hearing research. 265(1-2)
Our long term goal is to understand the molecular pathology of otosclerosis and to develop better forms of therapy. Toward this goal, the current study focused on characterizing the molecular factors responsible for the unique biological features of
Publikováno v:
Advances in oto-rhino-laryngology. 65
Otosclerosis is a bone disease of the human otic capsule, which is among the most common causes of acquired hearing loss. The pathologic process is characterized by a wave of abnormal bone remodeling in specific sites of predilection within the endoc
Otosclerosis is a bone disease of the human otic capsule, which is among the most common causes of acquired hearing loss. The pathologic process is characterized by a wave of abnormal bone remodeling in specific sites of predilection within the endoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de45ba7f5334e348d74e04853e303d35
https://doi.org/10.1159/000098674
https://doi.org/10.1159/000098674