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Somatic mutations of the MEN1 tumor suppressor gene detected in sporadic angiofibromas.

作者信息

Böni R, Vortmeyer A O, Pack S, Park W S, Burg G, Hofbauer G, Darling T, Liotta L, Zhuang Z

出版信息

J Invest Dermatol. 1998 Sep;111(3):539-40. doi: 10.1046/j.1523-1747.1998.00317.x.

DOI:10.1046/j.1523-1747.1998.00317.x
PMID:9740255
Abstract
摘要

相似文献

1
Somatic mutations of the MEN1 tumor suppressor gene detected in sporadic angiofibromas.
J Invest Dermatol. 1998 Sep;111(3):539-40. doi: 10.1046/j.1523-1747.1998.00317.x.
2
Cutaneous tumors in patients with multiple endocrine neoplasia type 1 show allelic deletion of the MEN1 gene.1型多发性内分泌肿瘤患者的皮肤肿瘤显示MEN1基因的等位基因缺失。
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Molecular characterization of the men1 tumor suppressor gene in sporadic pituitary tumors.散发性垂体瘤中men1肿瘤抑制基因的分子特征
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Multiple facial angiofibromas and collagenomas in patients with multiple endocrine neoplasia type 1.1型多发性内分泌肿瘤患者的多发性面部血管纤维瘤和胶原瘤。
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Somatic mutations of the MEN1 tumor suppressor gene in sporadic gastrinomas and insulinomas.散发性胃泌素瘤和胰岛素瘤中MEN1肿瘤抑制基因的体细胞突变。
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Perivascular cells harboring multiple endocrine neoplasia type 1 alterations are neoplastic cells in angiofibromas.携带1型多发性内分泌肿瘤改变的血管周围细胞是血管纤维瘤中的肿瘤细胞。
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Frequency of facial angiofibromas in Japanese patients with multiple endocrine neoplasia type 1.日本1型多发性内分泌肿瘤患者面部血管纤维瘤的发生率
Endocr J. 2000 Oct;47(5):569-73. doi: 10.1507/endocrj.47.569.
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Angiofibromas in multiple endocrine neoplasia type 1.1型多发性内分泌肿瘤中的血管纤维瘤
Dermatol Online J. 2012 Dec 15;18(12):20.
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Mutations of the MEN1 tumor suppressor gene in pituitary tumors.垂体瘤中MEN1肿瘤抑制基因的突变
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Multiple endocrine neoplasia type 1: clinical and genetic features of the hereditary endocrine neoplasias.1型多发性内分泌腺瘤病：遗传性内分泌肿瘤的临床和遗传特征
Recent Prog Horm Res. 1999;54:397-438; discussion 438-9.

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Approach of Multiple Endocrine Neoplasia Type 1 (MEN1) Syndrome-Related Skin Tumors.1型多发性内分泌腺瘤病（MEN1）综合征相关皮肤肿瘤的治疗方法。
Diagnostics (Basel). 2022 Nov 12;12(11):2768. doi: 10.3390/diagnostics12112768.
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Beyond the "3 Ps": A critical appraisal of the non-endocrine manifestations of multiple endocrine neoplasia type 1.超越“3P”：对 1 型多发性内分泌肿瘤非内分泌表现的批判性评估。
Front Endocrinol (Lausanne). 2022 Oct 17;13:1029041. doi: 10.3389/fendo.2022.1029041. eCollection 2022.
3
Multi-omics analyses of MEN1 missense mutations identify disruption of menin-MLL and menin-JunD interactions as critical requirements for molecular pathogenicity.
MEN1 错义突变的多组学分析确定了 menin-MLL 和 menin-JunD 相互作用的破坏是分子发病机制的关键要求。
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Causes of death and prognostic factors in multiple endocrine neoplasia type 1: a prospective study: comparison of 106 MEN1/Zollinger-Ellison syndrome patients with 1613 literature MEN1 patients with or without pancreatic endocrine tumors.1型多发性内分泌腺瘤病的死亡原因及预后因素：一项前瞻性研究：106例MEN1/卓艾综合征患者与1613例有或无胰腺内分泌肿瘤的文献报道的MEN1患者的比较
Medicine (Baltimore). 2013 May;92(3):135-181. doi: 10.1097/MD.0b013e3182954af1.
5
Characterisation of prostate cancer lesions in heterozygous Men1 mutant mice.杂合 Men1 突变小鼠前列腺癌病变的特征。
BMC Cancer. 2010 Jul 27;10:395. doi: 10.1186/1471-2407-10-395.
6
Multiple angiofibromas and collagenomas in a 45-year-old man with recurrent nephrolithiasis, fatigue, and vision loss.一名45岁男性患有多发性血管纤维瘤和胶原瘤，伴有复发性肾结石、疲劳和视力丧失。
J Am Acad Dermatol. 2009 Aug;61(2):319-22. doi: 10.1016/j.jaad.2009.01.026.
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Multiple leiomyomas of the esophagus, lung, and uterus in multiple endocrine neoplasia type 1.1型多发性内分泌肿瘤中的食管、肺和子宫多发性平滑肌瘤
Am J Pathol. 2001 Sep;159(3):1121-7. doi: 10.1016/S0002-9440(10)61788-9.
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Identification of somatic mutations of the MEN1 gene in sporadic endocrine tumours.散发性内分泌肿瘤中MEN1基因体细胞突变的鉴定
Br J Cancer. 2000 Oct;83(8):1003-8. doi: 10.1054/bjoc.2000.1385.