- Merlin; NF2 Tumor Suppressor and Regulator of Receptor Distribution/Signaling
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Lee JH
- KMID: 2277240
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2011 Jun;54(6):379-385.
- doi: 10.3342/kjorl-hns.2011.54.6.379
Acoustic tumor is the most common tumor originating from cerebellopontine angle. Acoustic tumor is benign and main origin of this tumor is vestibular nerve. This tumor arises in Schwann cell... -
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- Expression of NF2 Modulates the Progression of BRAFV600E Mutated Thyroid Cancer Cells
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You MH, Jeon MJ, Kim TY, Kim WB, Shong YK, Kim WG
- KMID: 2450521
- Endocrinol Metab.
- 2019 Jun;34(2):203-212.
- doi: 10.3803/EnM.2019.34.2.203
BACKGROUND: We previously reported the frequent neurofibromatosis 2 (NF2) gene mutations in anaplastic thyroid cancers in association with the BRAF V600E mutation. We aimed to investigate the role of NF2 in... -
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- Genetic and clinical characteristics of Korean patients with neurofibromatosis type 2
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Kim HJ, Seo GH, Kim YM, Kim GH, Seo EJ, Ra YS, Choi JH, Yoo HW, Lee BH
- KMID: 2401806
- J Genet Med.
- 2017 Dec;14(2):56-61.
- doi: 10.5734/JGM.2017.14.2.56
PURPOSE: Neurofibromatosis type 2 (NF2) is characterized by multiple tumors, including vestibular schwannoma (VS) and others affecting cranial and peripheral nerves. NF2 is caused by mutation of the NF2 gene.... -
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- Intraneural Perineurioma in the Tongue: A Case Report
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Kang J, Khang SK, Choi J, Kim JW, Seo EJ, Lee BK, Yu E
- KMID: 1521696
- Korean J Pathol.
- 2007 Feb;41(1):51-54.
We report a case of an intraneural perineurioma that developed in an unusual location, the tongue. A 16-year-old male presented with a 1 cm sized protruding submucosal mass in his... -
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- Molecular Characterization of the NF2 Gene in Korean Patients with Neurofibromatosis Type 2: A Report of Four Novel Mutations
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Seong MW, Yeo IK, Cho SI, Park CK, Kim SK, Paek SH, Kim DG, Jung HW, Park H, Kim SY, Kim JY, Park SS
- KMID: 1096807
- Korean J Lab Med.
- 2010 Apr;30(2):190-194.
- doi: 10.3343/kjlm.2010.30.2.190
BACKGROUND: Neurofibromatosis type 2 (NF2) is an autosomal dominant syndrome caused by the NF2 tumor suppressor gene. However, the NF2 mutation characteristics in Korean patients are not sufficiently understood. In... -
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