Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: Nevus and NRAS[original query] |
---|
Number of nevi and early-life ambient UV exposure are associated with BRAF-mutant melanoma. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2007 May 16 (5): 991-7. Thomas Nancy E, Edmiston Sharon N, Alexander Audrey, Millikan Robert C, Groben Pamela A, Hao Honglin, Tolbert Dawn, Berwick Marianne, Busam Klaus, Begg Colin B, Mattingly Dianne, Ollila David W, Tse Chiu Kit, Hummer Amanda, Lee-Taylor Julia, Conway Kathle |
The association between MC1R genotype and BRAF mutation status in cutaneous melanoma: findings from an Australian population. The Journal of investigative dermatology 2010 Jan 130 (1): 241-8. Hacker Elke, Hayward Nicholas K, Dumenil Troy, James Michael R, Whiteman David |
NRAS and BRAF mutations in melanoma-associated nevi and uninvolved nevi. PloS one 2013 8 (7): e69639. Tschandl Philipp, Berghoff Anna Sophie, Preusser Matthias, Burgstaller-Muehlbacher Sebastian, Pehamberger Hubert, Okamoto Ichiro, Kittler Hara |
NRAS mutation is the sole recurrent somatic mutation in large congenital melanocytic nevi. The Journal of investigative dermatology 2014 Apr 134 (4): 1067-74. Charbel Christelle, Fontaine Romain H, Malouf Gabriel G, Picard Arnaud, Kadlub Natacha, El-Murr Nizar, How-Kit Alexandre, Su Xiaoping, Coulomb-L'Hermine Aurore, Tost Jorg, Mourah Samia, Aractingi Selim, Guégan Sar |
Increased levels of ß-catenin, LEF-1, and HPA-1 correlate with poor prognosis for acral melanoma with negative BRAF and NRAS mutation in BRAF exons 11 and 15 and NRAS exons 1 and 2. DNA and cell biology 2015 Jan 34 (1): 69-77. Xu Sanxiong, Yang Zuozhang, Zhang Jinyu, Jiang Yongxin, Chen Yongbin, Li Hongjun, Liu Xuefeng, Xu Da, Chen Yanjin, Yang Yihao, Zhang Ya, Li Dongxu, Xia Junfe |
BRAF, KIT, NRAS, GNAQ and GNA11 mutation analysis in cutaneous melanomas in Turkish population. Indian journal of pathology & microbiology 0 58 (3): 279-84. Yilmaz Ismail, Gamsizkan Mehmet, Kucukodaci Zafer, Berber Ufuk, Demirel Dilaver, Haholu Aptullah, Narli Giz |
Immunohistochemical Detection of NRASQ61R Mutation in Diverse Tumor Types. American journal of clinical pathology 2016 Jan 145 (1): 29-34. Dias-Santagata Dora, Su Yuhua, Hoang Mai |
Histologic and Phenotypic Factors and MC1R Status Associated with BRAF(V600E), BRAF(V600K), and NRAS Mutations in a Community-Based Sample of 414 Cutaneous Melanomas. The Journal of investigative dermatology 2016 Apr 136 (4): 829-837. Hacker Elke, Olsen Catherine M, Kvaskoff Marina, Pandeya Nirmala, Yeo Abrey, Green Adèle C, Williamson Richard M, Triscott Joe, Wood Dominic, Mortimore Rohan, Hayward Nicholas K, Whiteman David |
Genetic Alterations in Primary Acral Melanoma and Acral Melanocytic Nevus in Korea: Common Mutated Genes Show Distinct Cytomorphological Features. The Journal of investigative dermatology 2017 Nov . Moon Ki Rang, Choi Yoo Duk, Kim Jung Min, Jin Suna, Shin Min-Ho, Shim Hyun-Jeong, Lee Jee-Bum, Yun Sook Ju |
Association of the POT1 Germline Missense Variant p.I78T With Familial Melanoma. JAMA dermatology 2018 12 155 (5): 604-609. Wong Kim, Robles-Espinoza Carla Daniela, Rodriguez David, Rudat Saskia S, Puig Susana, Potrony Miriam, Wong Chi C, Hewinson James, Aguilera Paula, Puig-Butille Joan Anton, Bressac-de Paillerets Brigitte, Zattara Hélène, van der Weyden Louise, Fletcher Christopher D M, Brenn Thomas, Arends Mark J, Quesada Víctor, Newton-Bishop Julia A, Lopez-Otin Carlos, Bishop D Timothy, Harms Paul W, Johnson Timothy M, Durham Alison B, Lombard David B, Adams David |
Neurocutaneous Melanosis in Association With Large Congenital Melanocytic Nevi in Children: A Report of 2 Cases With Clinical, Radiological, and Pathogenetic Evaluation. Frontiers in neurology 2019 2 10 79. Chen Lei, Zhai Liqin, Al-Kzayer Lika'a Fasih Y, Sarsam Shamil Naji, Liu Tingting, Alzakar Riyadh H, Nakazawa Yo |
Novel genetic alteration in congenital melanocytic nevus: MAP2K1 germline mutation with BRAF somatic mutation. Hereditas 2020 8 157 (1): 35. Zou Yun, Sun Yi, Zeng Xiaojing, Liu Yun, Cen Qingqing, Gu Hao, Lin Xiaoxi, Cai Ren, Chen H |
Definition of Biologically Distinct Groups of Conjunctival Melanomas According to Etiological Factors and Implications for Precision Medicine. Cancers 2021 8 13 (15): . Gardrat Sophie, Houy Alexandre, Brooks Kelly, Cassoux Nathalie, Barnhill Raymond, Dayot Stéphane, Bièche Ivan, Raynal Virginie, Baulande Sylvain, Marais Richard, Roman-Roman Sergio, Stern Marc-Henri, Rodrigues Manu |
Genetic and Methylation Analysis of CTNNB1 in Benign and Malignant Melanocytic Lesions. Cancers 2022 9 14 (17): . Zaremba Anne, Jansen Philipp, Murali Rajmohan, Mayakonda Anand, Riedel Anna, Krahl Dieter, Burkhardt Hans, John Stefan, Géraud Cyrill, Philip Manuel, Kretz Julia, Möller Inga, Stadtler Nadine, Sucker Antje, Paschen Annette, Ugurel Selma, Zimmer Lisa, Livingstone Elisabeth, Horn Susanne, Plass Christoph, Schadendorf Dirk, Hadaschik Eva, Lutsik Pavlo, Griewank Kla |
Association of novel MUC16, MAP3K15 and ABCA1 mutation with giant congenital melanocytic nevus. Hereditas 2022 9 159 (1): 33. Zhou Renpeng, Wang Qirui, Hou Jialin, Wang Danru, Liang Yim |
Missense mutation of NRAS is associated with malignant progression in neurocutaneous melanosis. Acta neuropathologica communications 2024 1 12 (1): 14. Haruhiko Takahashi, Manabu Natsumeda, Norikazu Hara, Akihide Koyama, Hiroshi Shimizu, Akinori Miyashita, Daiken Satake, Yoshihiro Mouri, Jun Tsukano, Keita Kawabe, Yoshihiro Tsukamoto, Masayasu Okada, Ryosuke Ogura, Akihiko Yuki, Hajime Umezu, Akiyoshi Kakita, Takeshi Ikeuchi, Makoto Ois |
- Page last reviewed:Feb 1, 2024
- Content source: