HuGE Literature Finder
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| Clinical and genetic profiling of nevoid basal cell carcinoma syndrome in Korean patients by whole-exome sequencing. Scientific reports 2021 Jan 11 (1): 1163. Kim Boram, Kim Man Jin, Hur Keunyoung, Jo Seong Jin, Ko Jung Min, Park Sung Sup, Seong Moon-Woo, Mun Je- |
| Prevalence and spectrum of pathogenic germline variants in intestinal and pancreatobiliary type of ampullary cancer. Pathology, research and practice 2020 Dec 217 153309. Kumari Niraj, Singh Rajneesh K, Mishra Shravan K, L Raghvendra, Mohindra Samir, Krishnani Narend |
| Prevalence of Germline Mutations Associated With Cancer Risk in Patients With Intraductal Papillary Mucinous Neoplasms. Gastroenterology 2019 Feb . Skaro Michael, Nanda Neha, Gauthier Christian, Felsenstein Matthäus, Jiang Zhengdong, Qiu Miaozhen, Shindo Koji, Yu Jun, Hutchings Danielle, Javed Ammar A, Beckman Ross, He Jin, Wolfgang Christopher L, Thompson Elizabeth, Hruban Ralph H, Klein Alison P, Goggins Michael, Wood Laura D, Roberts Nicholas |
| Absence of BRAFV600E mutation in odontogenic keratocysts. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology 2018 Feb 47 (2): 186-191. França Josiane Alves, de Sousa Sílvia Ferreira, Diniz Marina Gonçalves, Pereira Thaís Dos Santos Fontes, de Resende Taynara Asevedo Campos, Santos Jean Nunes Dos, Gomez Ricardo Santiago, Gomes Carolina Cavalie |
| A mutational signature associated with alcohol consumption and prognostically significantly mutated driver genes in esophageal squamous cell carcinoma. Annals of oncology : official journal of the European Society for Medical Oncology 2018 Jan . Li X C, Wang M Y, Yang M, Dai H J, Zhang B F, Wang W, Chu X L, Wang X, Zheng H, Niu R F, Zhang W, Chen K |
| Whole-exome sequencing to identify novel mutations of nevoid basal cell carcinoma syndrome in a Chinese population. Cancer biomarkers : section A of Disease markers 2017 Oct . Lu Nanhang, Wang Jinzeng, Zhu Bijun, Zhang Miaomiao, Qi Fazhi, Wang Xiangdong, Gu Jianyi |
| Genomic analyses reveal mutational signatures and frequently altered genes in esophageal squamous cell carcinoma. American journal of human genetics 2015 Apr 96 (4): 597-611. Zhang Ling, Zhou Yong, Cheng Caixia, Cui Heyang, Cheng Le, Kong Pengzhou, Wang Jiaqian, Li Yin, Chen Wenliang, Song Bin, Wang Fang, Jia Zhiwu, Li Lin, Li Yaoping, Yang Bin, Liu Jing, Shi Ruyi, Bi Yanghui, Zhang Yanyan, Wang Juan, Zhao Zhenxiang, Hu Xiaoling, Yang Jie, Li Hongyi, Gao Zhibo, Chen Gang, Huang Xuanlin, Yang Xukui, Wan Shengqing, Chen Chao, Li Bin, Tan Yongkai, Chen Longyun, He Minghui, Xie Sha, Li Xiangchun, Zhuang Xuehan, Wang Mengyao, Xia Zhi, Luo Longhai, Ma Jie, Dong Bing, Zhao Jiuzhou, Song Yongmei, Ou Yunwei, Li Enming, Xu Liyan, Wang Jinfen, Xi Yanfeng, Li Guodong, Xu Enwei, Liang Jianfang, Yang Xiaofeng, Guo Jiansheng, Chen Xing, Zhang Yanbo, Li Qingshan, Liu Lixin, Li Yingrui, Zhang Xiuqing, Yang Huanming, Lin Dongxin, Cheng Xiaolong, Guo Yongjun, Wang Jun, Zhan Qimin, Cui Yongpi |
| PTCH1 mutation is a frequent event in oesophageal basaloid squamous cell carcinoma. Mutagenesis 2015 Mar 30 (2): 297-301. Saito Tsuyoshi, Mitomi Hiroyuki, Imamhasan Abdukadir, Hayashi Takuo, Kurisaki-Arakawa Aiko, Mitani Keiko, Takahashi Michiko, Kajiyama Yoshiaki, Yao Takas |
| Underestimated PTCH1 mutation rate in sporadic keratocystic odontogenic tumors. Oral oncology 2015 Jan 51 (1): 40-5. Qu Jiafei, Yu Feiyan, Hong Yingying, Guo Yanyan, Sun Lisha, Li Xuefen, Zhang Jianyun, Zhang Heyu, Shi Ruirui, Chen Feng, Li Tiej |
| Frequency and features of TP53 mutation in 30 Chinese patients with sporadic basal cell carcinoma. Clinical and experimental dermatology 2014 Oct 39 (7): 829-34. Wang Y M, Huang Y S, Ma Z H, Bu D F, Wang Y, Tu P, Li |
| PTCH1 gene polymorphisms in ovarian tumors: potential protective role of c.3944T allele. Gene 2013 Jan . Musani V, Sabol M, Car D, Ozreti? P, Kalafati? D, Maurac I, Oreškovi? S, Levanat S |
| PTCH1 gene mutations in Keratocystic odontogenic tumors: a study of 43 Chinese patients and a systematic review. PloS one 2013 8 (10): e77305. Guo Yan-Yan, Zhang Jian-Yun, Li Xue-Fen, Luo Hai-Yan, Chen Feng, Li Tie-J |
| Association of FANCC and PTCH1 with the development of early dysplastic lesions of the head and neck. Annals of surgical oncology 2012 Jul 19 Suppl 3 S528-38. Ghosh Amlan, Ghosh Susmita, Maiti Guru Prasad, Mukherjee Sudeshna, Mukherjee Nupur, Chakraborty Jayanta, Roy Anup, Roychoudhury Susanta, Panda C |
| Unique features of PTCH1 mutation spectrum in Chinese sporadic basal cell carcinoma. Journal of the European Academy of Dermatology and Venereology : JEADV 2012 Feb . Huang YS, Bu DF, Li XY, Ma ZH, Yang Y, Lin ZM, Lu FM, Tu P, Li H |
| Association of copy number loss of CDKN2B and PTCH1 with poor overall survival in patients with pulmonary squamous cell carcinoma. Clinical lung cancer 2011 Sep 12 (5): 328-34. Zhao Yushi, Li Ye, Lu Hongguang, Chen Jianxin, Zhang Zhijie, Zhu Zhong-Zhe |
| PTCH1 gene haplotype association with basal cell carcinoma after transplantation. The British journal of dermatology 2010 Aug 163 (2): 364-70. Begnini A, Tessari G, Turco A, Malerba G, Naldi L, Gotti E, Boschiero L, Forni A, Rugiu C, Piaserico S, Fortina A B, Brunello A, Cascone C, Girolomoni G, Gomez Lira |
| Expression patterns and polymorphisms of PTCH in Chinese hepatocellular carcinoma patients. Experimental and molecular pathology 2008 Jun 84 (3): 195-9. Fu Xinhui, Wang Qian, Chen Xilin, Huang Xiaohui, Cao Liangqi, Tan Haoxiang, Li Wen, Zhang Longjuan, Bi Jiong, Su Qiao, Chen Lianzh |
| The patched polymorphism Pro1315Leu (C3944T) may modulate the association between use of oral contraceptives and breast cancer risk. International journal of cancer. Journal international du cancer 2003 Mar 103 (6): 779-83. Chang-Claude Jenny, Dunning Alison, Schnitzbauer Udo, Galmbacher Petra, Tee Louise, Wjst Matthias, Chalmers Jennifer, Zemzoum Iris, Harbeck Nadia, Pharoah Paul D P, Hahn Hei |
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- Page last updated:Jun 22, 2022
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