Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Fenghe Liang"'
Autor:
Chunyan, Qu, Fenghe, Liang, Qin, Long, Min, Zhao, Haiqiong, Shang, Lynn, Fan, Li, Wang, Joseph, Foster, Denise, Yan, Xuezhong, Liu
Publikováno v:
Hearing, Balance and Communication. 15:98-106
Introduction Usher syndrome is the most common cause of hereditary deaf-blindness. Three clinical subtypes have been classified. Usher syndrome type I is the most severe subtype characterized by congenital severe-to-profound hearing loss, retinitis p
Identification of a de novo mutation of SOX10 in a Chinese patient with Waardenburg syndrome type IV
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 91:67-71
Objectives Waardenburg syndrome is a rare genetic disorder, characterized by the association of sensorineural hearing loss and pigmentation abnormalities. Four subtypes have been classified. The present study aimed to analyze the clinical feature and
Publikováno v:
Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery. 30(5)
To investigate the feasibility of the treatment of otosclerosis using laser stapedotomy with mini incision in the external auditory meatus.Thirteen patients(15 ears) with otosclerosis evidence on clinic history. They were all operated using the laser
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 76:235-239
Objective To investigate the molecular etiologic causes of sporadic nonsyndromic hearing loss in Chinese children. Methods 179 sporadic nonsyndromic hearing loss children were subjected to microarray-based mutation detection for nine hot spot mutatio
Publikováno v:
Journal of the Association for Research in Otolaryngology. 8:205-219
Voltage-gated chloride channels (ClCs) are important mediators of cellular ion homeostasis and volume regulation. In an earlier study, we used immunohistochemical, Western blot, and reverse transcriptase PCR (RT-PCR) approaches to identify ClC-K vari
Publikováno v:
Hearing Research. 213:79-87
Current models of the lateral K + recycling pathway in the mammalian cochlea include two multicellular transport networks separated from one another by three interstitial gaps. The first gap is between outer hair cells and Deiters cells, the second i
Autor:
Cungui Mao, Fenghe Liang, Zhijun Shen, Debra J. Hazen-Martin, Chunyan Qu, Bradley A. Schulte, Wei Hu
Publikováno v:
Molecular Brain Research. 125:40-46
Intracellular free Ca 2+ levels are critical to the activity of BK channels in inner ear type I spiral ligament fibrocytes. However, the mechanisms for regulating intracellular Ca 2+ levels in these cells are currently poorly understood. Using patch-
Publikováno v:
Hearing Research. 187:35-43
Recent experimental and clinical studies have provided considerable evidence to support the phenomenon of K(+) recycling in the mammalian cochlea. However, the precise cellular and molecular mechanisms underlying and regulating this process remain on
Autor:
A. Niedzielski, Zhijun Shen, Debra J. Hazen-Martin, Samuel S. Spicer, Bradley A. Schulte, Fenghe Liang
Publikováno v:
Pflugers Archiv : European journal of physiology. 445(6)
Evidence is accruing that spiral ligament fibrocytes (SLFs) play an important role in cochlear K+ homeostasis, but little direct physiological data is available to support this concept. Here we report the presence and characterization of a voltage- a