Lynch Syndrome || Public Health Genomics Knowledge Base (v1.2)

Public Health Genomics Knowledge Base (v1.2)

From HuGE Literature Finder Database

This database contains published literature on genetic associations and other human genome epidemiology

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• Rare germline alterations in cancer-related genes associated with the risk of multiple primary tumor development.
  Journal of molecular medicine (Berlin, Germany) 2017 Jan .
  Villacis Rolando A R, Basso Tatiane R, Canto Luisa M, Pinheiro Maísa, Santiago Karina M, Giacomazzi Juliana, de Paula Cláudia A A, Carraro Dirce M, Ashton-Prolla Patrícia, Achatz Maria I, Rogatto Silvia
• [Lynch syndrome, Muir Torre variant: 2 cases].
  Rev Gastroenterol Peru 2016 Jan-Mar (36): 81-5.
  Castro-Mujica María Del Carmen, Barletta-Carrillo Claudia, Acosta-Aliaga Marisa, Montenegro-Garreaud Xime
• [Evaluation of BRAF V600E Mutations in High-Level Microsatellite Instability(MSI-H)Colon Cancer - Comparison Between Genetic Testing and Immunohistochemical Staining].
  Gan to kagaku ryoho. Cancer & chemotherapy 2016 Nov 43 (12): 1693-1695.
  Sakimoto Takehiko, Chika Noriyasu, Suzuki Okihide, Ishibashi Keiichiro, Tachikawa Tetsuhiko, Akagi Kiwamu, Eguchi Hidetaka, Okazaki Yasushi, Ishida Hideyu
• Pathogenic germline MCM9 variants are rare in Australian Lynch-like syndrome patients.
  Cancer genetics 2016 Nov 209 (11): 497-500.
  Liu Qing, Hesson Luke B, Nunez Andrea C, Packham Deborah, Hawkins Nicholas J, Ward Robyn L, Sloane Mathew
• Prevalence of Lynch syndrome in unselected patients with endometrial or ovarian cancer.
  Archives of gynecology and obstetrics 2016 Nov 294 (6): 1299-1303.
  Kast Karin, Dobberschütz Catharina, Sadowski Carolin Eva, Pistorius Steffen, Wimberger Pauli

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Public Health Genomics Knowledge Base (v1.2)