Pesquisa
Educação
Soluções
Entrar
PT
EN - English
CN - 中文
DE - Deutsch
ES - Español
KR - 한국어
IT - Italiano
FR - Français
PT - Português
TR - Turkish
JA - Japanese
Oregon Hearing Research Center,
Department of Otolaryngology/Head & Neck Surgery,
Oregon Hearing Research Center, Department of Otolaryngology/Head & Neck Surgery
Lingling Neng has not added Biography.
If you are Lingling Neng and would like to personalize this page please email our Author Liaison for assistance.
Perivascular-resident macrophage-like melanocytes in the inner ear are essential for the integrity of the intrastrial fluid-blood barrier.
Proceedings of the National Academy of Sciences of the United States of America Jun, 2012 | Pubmed ID: 22689949
Endothelial cell, pericyte, and perivascular resident macrophage-type melanocyte interactions regulate cochlear intrastrial fluid-blood barrier permeability.
Journal of the Association for Research in Otolaryngology : JARO Apr, 2013 | Pubmed ID: 23247886
Isolation and culture of endothelial cells, pericytes and perivascular resident macrophage-like melanocytes from the young mouse ear.
Nature protocols Apr, 2013 | Pubmed ID: 23493068
Perivascular macrophage-like melanocyte responsiveness to acoustic trauma--a salient feature of strial barrier associated hearing loss.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology Sep, 2013 | Pubmed ID: 23729595
Characterization and inflammatory response of perivascular-resident macrophage-like melanocytes in the vestibular system.
Journal of the Association for Research in Otolaryngology : JARO Oct, 2013 | Pubmed ID: 23821347
Thin and open vessel windows for intra-vital fluorescence imaging of murine cochlear blood flow.
Hearing research Jul, 2014 | Pubmed ID: 24780131
Structural changes in thestrial blood-labyrinth barrier of aged C57BL/6 mice.
Cell and tissue research Sep, 2015 | Pubmed ID: 25740201
A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60.
Human genetics May, 2016 | Pubmed ID: 27023905
Acoustic Trauma Causes Cochlear Pericyte-to-Myofibroblast-Like Cell Transformation and Vascular Degeneration, and Transplantation of New Pericytes Prevents Vascular Atrophy.
The American journal of pathology 09, 2020 | Pubmed ID: 32562655
Suppression of Connexin 43 Leads to Strial Vascular Hyper-Permeability, Decrease in Endocochlear Potential, and Mild Hearing Loss.
Frontiers in physiology , 2020 | Pubmed ID: 32922309
VEGFA165 gene therapy ameliorates blood-labyrinth barrier breakdown and hearing loss.
JCI insight Apr, 2021 | Pubmed ID: 33690221
Oregon Health & Science University
Zhiqiang Hou1,
Yunpei Zhang1,
Lingling Neng1,
Jinhui Zhangundefined,
Xiaorui Shi1
1Oregon Hearing Research Center, Department of Otolaryngology/Head & Neck Surgery, Oregon Health & Science University
Privacidade
Termos de uso
Políticas
Entre em contato
recomende à biblioteca
Newsletter
JoVE Journal
Coleções de métodos
JoVE Encyclopedia of Experiments
Arquivo
JoVE Core
JoVE Business
JoVE Science Education
JoVE Lab Manual
Centro de Recursos para Docentes
Autores
Bibliotecários
Acesso
SOBRE A JoVE
Copyright © 2024 MyJoVE Corporation. Todos os direitos reservados