An allograft mouse model for the study of hearing loss secondary to vestibular schwannoma growth-Reference-Cited by-同舟云学术

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An allograft mouse model for the study of hearing loss secondary to vestibular schwannoma growth

Published:2016-05-13 Issue:1 Volume:129 Page:47-56
ISSN:0167-594X
Container-title:Journal of Neuro-Oncology
language:en
Short-container-title:J Neurooncol

Author:

Bonne Nicolas-Xavier,Vitte Jérémie,Chareyre Fabrice,Karapetyan Gevorg,Khankaldyyan Vazgen,Tanaka Karo,Moats Rex A.,Giovannini Marco

Funder

Children's Tumor Foundation

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Clinical Neurology,Neurology,Oncology

Link

http://link.springer.com/content/pdf/10.1007/s11060-016-2150-9.pdf

Reference42 articles.

1. Kshettry VR, Hsieh JK, Ostrom QT, Kruchko C, Barnholtz-Sloan JS (2015) Incidence of vestibular schwannomas in the United States. J Neurooncol 124:223–228. doi: 10.1007/s11060-015-1827-9

2. Evans DG, Moran A, King A, Saeed S, Gurusinghe N, Ramsden R (2005) Incidence of vestibular schwannoma and neurofibromatosis 2 in the North West of England over a 10-year period: higher incidence than previously thought. Otol Neurotol 26:93–97

3. Rouleau GA, Merel P, Lutchman M, Sanson M, Zucman J, Marineau C, Hoang-Xuan K, Demczuk S, Desmaze C, Plougastel B et al (1993) Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2. Nature 363:515–521. doi: 10.1038/363515a0

4. Trofatter JA, MacCollin MM, Rutter JL, Murrell JR, Duyao MP, Parry DM, Eldridge R, Kley N, Menon AG, Pulaski K et al (1993) A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor. Cell 72:791–800

5. Bijlsma EK, Merel P, Bosch DA, Westerveld A, Delattre O, Thomas G, Hulsebos TJ (1994) Analysis of mutations in the SCH gene in schwannomas. Genes Chromosom Cancer 11:7–14

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