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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2014/03/16 21:07:00」(JST)

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  • Protein Analysis of Glioblastoma Primary and Posttreatment Pairs Suggests a Mesenchymal Shift at Recurrence.
  • Wood MD1, Reis GF1, Reuss DE1, Phillips JJ2.
  • Journal of neuropathology and experimental neurology.J Neuropathol Exp Neurol.2016 Oct;75(10):925-935. Epub 2016 Aug 18.
  • Glioblastomas (GBM) are aggressive brain tumors that inevitably recur despite surgical resection, chemotherapy, and radiation. The degree to which recurrent GBM retains its initial immunophenotype is incompletely understood. We generated tissue microarrays of paired initial and posttreatment GBM (3
  • PMID 27539476
  • The Genetic Landscape of Malignant Pleural Mesothelioma: Results from Massively Parallel Sequencing.
  • Hylebos M1, Van Camp G2, van Meerbeeck JP3, Op de Beeck K4.
  • Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.J Thorac Oncol.2016 Oct;11(10):1615-26. doi: 10.1016/j.jtho.2016.05.020. Epub 2016 Jun 6.
  • Malignant pleural mesothelioma (MPM) is a rare yet aggressive tumor that is causally associated with-mostly professional-asbestos exposure. Given the long latency between exposure and disease, and because asbestos is still being used, MPM will remain a global health issue for decades to come. Notwi
  • PMID 27282309
  • Neurofibromatosis type 1 (NF1) gene: Beyond café au lait spots and dermal neurofibromas.
  • Peltonen S1, Kallionpää RA2, Peltonen J2.
  • Experimental dermatology.Exp Dermatol.2016 Sep 13. doi: 10.1111/exd.13212. [Epub ahead of print]
  • Neurofibromatosis 1 (NF1) occurs in 1:2000 births. The main diagnostic signs are visible on the skin and this opens several interesting aspects for dermatological point of view. The NF1 syndrome is caused by mutations in the NF1 gene which encodes the tumor suppressor protein neurofibromin. Neurofib
  • PMID 27622733


  • 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,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
  • … The NF1 gene product neurofibromin is thought to deliver much of its function by downregulating the oncogene ras. …
  • NAID 10025527376
  • Neurofibromatosis type 1 (NF1) tumor suppressor, neurofibromin, regulates the neuronal differentiation of PC12 cells via its associating protein, CRMP-2
  • von Recklinghausen病に合併した多発性空腸gastrointestinal stromal tumorの1例
  • 米田 浩二,平松 昌子,藤田 能久,西村 東人,辰巳 嘉章,田中 覚,江頭 由太郎,谷川 允彦
  • 日本消化器外科学会雑誌 40(2), 209-214, 2007-02-01
  • … を認め摘出した.免疫組織学的には,CD34 (+), KIT (+)でGISTと診断されたが,c-kitの遺伝子異常はみられなかった.R病に合併したGIST症例には,c-kit遺伝子・PDGFRα遺伝子に突然変異のみられないものが報告されている.R病は第17染色体に遺伝子異常がみられ,NF1遺伝子の変異によるneurofibrominの機能異常から腫瘍が発生してくるとされている.R病を合併したc-kit遺伝子・PDGFRα機能獲得性突然変異を伴わない多発性空腹GIST症例を報告する. …
  • NAID 110006163723


NF1 A gene on chromosome 17q11.2 that encodes neurofibromin 1, a protein which stimulates GTPase activity of Ras and may regulate Ras activity. Molecular pathology NF1 defects cause: • Familial spinal neurofibromatosis;
neurofibromatosis type 1 - caused by mutations in the NF1 gene More than 1,000 NF1 mutations that cause neurofibromatosis type 1 have been identified. Most of these mutations are unique to a particular family. Many NF1 ...


sc-20982250px-PBB_Protein_NF1_image.jpgneurofibromin 2 antibody www pierce Neurofibromatosis type 1 |[mdash]| a model 2d4q » NeurofibrominIn the case of neurofibromin

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