- 関
- NF2 gene
WordNet
- (genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity; "genes were formerly called factors" (同)cistron, factor
- autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalities (同)von Recklinghausen''s disease
- informal term for information; "give me the gen on your new line of computers"
PrepTutorEJDIC
- 遺伝子
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English Journal
- Application of COLD-PCR for improved detection of NF2 mosaic mutations.
- Paganini I1, Mancini I2, Baroncelli M1, Arena G1, Gensini F1, Papi L1, Sestini R3.
- The Journal of molecular diagnostics : JMD.J Mol Diagn.2014 Jul;16(4):393-9. doi: 10.1016/j.jmoldx.2014.02.007. Epub 2014 May 9.
- Somatic mosaicism represents the coexistence of two or more cell populations with different genotypes in one person, and it is involved in >30 monogenic disorders. Somatic mosaicism characterizes approximately 25% to 33% of patients with de novo neurofibromatosis type 2 (NF2). The identification
- PMID 24815379
- The role of NF2 gene mutations and pathogenesis-related proteins in sporadic vestibular schwannomas in young individuals.
- Chen H1, Zhang X, Zhang Z, Yang T, Wang Z, Wu H.
- Molecular and cellular biochemistry.Mol Cell Biochem.2014 Jul;392(1-2):145-52. doi: 10.1007/s11010-014-2011-9. Epub 2014 Mar 12.
- Vestibular schwannomas (VSs) are benign tumors arising from eighth cranial nerve and most often occur sporadically in individuals of middle age group. Sporadic VSs are rarely reported in the young population. In this study, we evaluated clinical behaviors of 12 young sporadic VSs by the statistical
- PMID 24619252
- Cutaneous and ophthalmic signs as a clue to early diagnosis of severe neurofibromatosis type 2: report of a novel mutation that predicts this poor prognosis.
- Casado-Verrier B1, Feito-Rodriguez M, Noval S, Martínez-Glez V, Lapunzina P, De Lucas-Laguna R.
- Clinical and experimental dermatology.Clin Exp Dermatol.2014 Jun;39(4):557-9. doi: 10.1111/ced.12306. Epub 2014 Apr 8.
- PMID 24708049
Japanese Journal
- 神経線維腫症I型(von Recklinghausen 病)に合併した鼻腔平滑筋肉腫例
- 尾上 義浩,小池 修治,那須 隆 [他],野田 大介,石田 晃弘,石井 健一,青柳 優
- 耳鼻咽喉科臨床 102(11), 931-937, 2009-11-01
- … We report a case of leiomyosarcoma of the nasal cavity with neurofibromatosis type 1 (NF1). … The risk of malignancy among NF1 patients is higher than among the general population, i.e., the NF1 gene is a tumor suppressor gene of which mutation involves a fourfold increased risk for cancer. … The NF1 gene product neurofibromin is thought to deliver much of its function by downregulating the oncogene ras. …
- NAID 10025527376
- GASTRIC SCHWANNOMA WITH ADJACENT EXTERNAL PROGRESSION HARBORED ABERRANT NF2 GENE
- OGASAWARA NAOTAKA,SASAKI MAKOTO,ISHIGURO HIDEYUKI,ITOH YUKIMI,NOJIRI SYUNSUKE,KUBOTA EIJI,WADA TSUNEYA,KATAOKA HIROMI,KUWABARA YOSHIYUKI,JOH TAKASHI
- Digestive endoscopy : official journal of the Japan Gastroenterological Endoscopy Society 21(3), 192-195, 2009-07-01
- NAID 10026611357
- Inducible and Transmissible Genetic Events and Pediatric Tumors of the Nervous System
- Rice Jerry M.,NAKANE Chiyoko,TAKIMOTO Koichi
- Journal of radiation research 47(Supplement_B), B1-B11, 2006-09-00
- … Tumors of the nervous system most often occur in both children and adults as sporadic events with no family history of the disease, but they are also among the clinical manifestations of a significant number of familial cancer syndromes, including familial retinoblastoma, neurofibromatosis 1 and 2, tuberous sclerosis, and Cowden, Turcot, Li-Fraumeni and nevoid basal cell carcinoma (Gorlin) syndromes. …
- NAID 110004810212
Related Links
- The distribution of constitutional and somatic mutations in the neurofibromatosis 2 gene. Hum Mutat. 2006; 27:297–306. [PubMed: 16521120] Baser ME, Evans DG, Jackler RK, Sujansky E, Rubinstein A. Malignant peripheralBr J ...
- forum Join the Word of the Day Mailing List For webmasters TheFreeDictionary Google Bing? Word / Article Starts with Ends with Text ... neurofibromatosis type 2 gene (NF2), a mutation of the gene responsible for neurofibrosis 2 ...
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- 関
- neurofibromatosis 2 gene
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- 英
- neurofibromatosis 2 gene、NF2 gene
- 関
- NF2遺伝子
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神経線維腫症 NF