{"title":"神经纤维蛋白及其功能","authors":"Peluso Carla","doi":"10.35248/2155-9562.21.12.534","DOIUrl":null,"url":null,"abstract":"Neurofibromin 1 (NF1) could be a quality in people that's found on chromosome 17. NF1 codes for neurofibromin, a GTPase-activating protein that adversely controls RAS/MAPK pathway activity by quickening the hydrolysis of Rasbound GTP. NF1 incorporates a tall change rate and changes in NF1 can change cellular development control, and neural advancement, coming about in neurofibromatosis sort 1 (NF1, too known as von Recklinghausen disorder). Indications of NF1 incorporate deforming cutaneous neurofibromas (CNF), café au lait shade spots, plexiform neurofibromas (PN), skeletal abandons, optic nerve gliomas, life-threatening harmful fringe nerve sheath tumors (MPNST), pheochromocytoma, consideration shortfalls, learning shortfalls and other cognitive incapacities.","PeriodicalId":16455,"journal":{"name":"Journal of Neurology and Neurophysiology","volume":"13 1","pages":"1-2"},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Neurofibromin & Its function\",\"authors\":\"Peluso Carla\",\"doi\":\"10.35248/2155-9562.21.12.534\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Neurofibromin 1 (NF1) could be a quality in people that's found on chromosome 17. NF1 codes for neurofibromin, a GTPase-activating protein that adversely controls RAS/MAPK pathway activity by quickening the hydrolysis of Rasbound GTP. NF1 incorporates a tall change rate and changes in NF1 can change cellular development control, and neural advancement, coming about in neurofibromatosis sort 1 (NF1, too known as von Recklinghausen disorder). Indications of NF1 incorporate deforming cutaneous neurofibromas (CNF), café au lait shade spots, plexiform neurofibromas (PN), skeletal abandons, optic nerve gliomas, life-threatening harmful fringe nerve sheath tumors (MPNST), pheochromocytoma, consideration shortfalls, learning shortfalls and other cognitive incapacities.\",\"PeriodicalId\":16455,\"journal\":{\"name\":\"Journal of Neurology and Neurophysiology\",\"volume\":\"13 1\",\"pages\":\"1-2\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Neurology and Neurophysiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.35248/2155-9562.21.12.534\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Neurology and Neurophysiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.35248/2155-9562.21.12.534","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
神经纤维蛋白1 (NF1)可能是人类在17号染色体上发现的一种品质。NF1编码神经纤维蛋白,神经纤维蛋白是一种gtpase激活蛋白,通过加速Rasbound GTP的水解来抑制RAS/MAPK通路的活性。NF1的变化率很高,NF1的变化可以改变细胞发育控制和神经进展,发生在1型神经纤维瘤病(NF1,也被称为von Recklinghausen疾病)中。NF1的适应症包括变形性皮肤神经纤维瘤(CNF)、caf au lait阴影斑、网状神经纤维瘤(PN)、骨骼放弃、视神经胶质瘤、危及生命的有害边缘神经鞘肿瘤(MPNST)、嗜铬细胞瘤、考虑能力不足、学习能力不足和其他认知能力丧失。
Neurofibromin 1 (NF1) could be a quality in people that's found on chromosome 17. NF1 codes for neurofibromin, a GTPase-activating protein that adversely controls RAS/MAPK pathway activity by quickening the hydrolysis of Rasbound GTP. NF1 incorporates a tall change rate and changes in NF1 can change cellular development control, and neural advancement, coming about in neurofibromatosis sort 1 (NF1, too known as von Recklinghausen disorder). Indications of NF1 incorporate deforming cutaneous neurofibromas (CNF), café au lait shade spots, plexiform neurofibromas (PN), skeletal abandons, optic nerve gliomas, life-threatening harmful fringe nerve sheath tumors (MPNST), pheochromocytoma, consideration shortfalls, learning shortfalls and other cognitive incapacities.