Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Melanoma and MLH1[original query] |
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| Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes. Familial cancer 2008 7 (4): 331-7. Magnusson Susanne, Borg Ake, Kristoffersson Ulf, Nilbert Mef, Wiebe Thomas, Olsson Håk |
| Effect of DNA repair host factors on temozolomide or dacarbazine melanoma treatment in Caucasians. Pharmacogenetics and genomics 2009 Oct 19 (10): 760-9. Boeckmann Lars, Schirmer Markus, Rosenberger Albert, Struever Diana, Thoms Kai-Martin, Gutzmer Ralf, Has Cristina, Kunz Manfred, Kuschal Christiane, Laspe Petra, Schoen Michael P, Brockmoeller Juergen, Emmert Steff |
| Multiplex ligation-dependent probe amplification of conjunctival melanoma reveals common BRAF V600E gene mutation and gene copy number changes. Investigative ophthalmology & visual science 2011 Jun . Lake SL, Jmor F, Dopierala J, Taktak AF, Coupland SE, Damato BE |
| Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations. Human genetics 2016 Jul . Yang Xiaohong R, Rotunno Melissa, Xiao Yanzi, Ingvar Christian, Helgadottir Hildur, Pastorino Lorenza, van Doorn Remco, Bennett Hunter, Graham Cole, Sampson Joshua N, Malasky Michael, Vogt Aurelie, Zhu Bin, Bianchi-Scarra Giovanna, Bruno William, Queirolo Paola, Fornarini Giuseppe, Hansson Johan, Tuominen Rainer, Burdett Laurie, Hicks Belynda, Hutchinson Amy, Jones Kristine, Yeager Meredith, Chanock Stephen J, Landi Maria Teresa, Höiom Veronica, Olsson Håkan, Gruis Nelleke, Ghiorzo Paola, Tucker Margaret A, Goldstein Alisa |
| A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome families. Hereditary cancer in clinical practice 2018 11 16 16. Karimi Masoud, von Salomé Jenny, Aravidis Christos, Silander Gustav, Askmalm Marie Stenmark, Henriksson Isabelle, Gebre-Medhin Samuel, Frödin Jan-Erik, Björck Erik, Lagerstedt-Robinson Kristina, Lindblom Annika, Tham Em |
| Microsatellite Instability Is Associated With the Presence of Lynch Syndrome Pan-Cancer. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2018 10 37 (4): 286-295. Latham Alicia, Srinivasan Preethi, Kemel Yelena, Shia Jinru, Bandlamudi Chaitanya, Mandelker Diana, Middha Sumit, Hechtman Jaclyn, Zehir Ahmet, Dubard-Gault Marianne, Tran Christina, Stewart Carolyn, Sheehan Margaret, Penson Alexander, DeLair Deborah, Yaeger Rona, Vijai Joseph, Mukherjee Semanti, Galle Jesse, Dickson Mark A, Janjigian Yelena, O'Reilly Eileen M, Segal Neil, Saltz Leonard B, Reidy-Lagunes Diane, Varghese Anna M, Bajorin Dean, Carlo Maria I, Cadoo Karen, Walsh Michael F, Weiser Martin, Aguilar Julio Garcia, Klimstra David S, Diaz Luis A, Baselga Jose, Zhang Liying, Ladanyi Marc, Hyman David M, Solit David B, Robson Mark E, Taylor Barry S, Offit Kenneth, Berger Michael F, Stadler Zsofia |
| Genetic analysis of subsequent second primary malignant neoplasms in long-term pancreatic cancer survivors suggests new potential hereditary genetic alterations. Cancer management and research 2019 11 599-609. Lovecek Martin, Janatova Marketa, Skalicky Pavel, Zemanek Tomas, Havlik Roman, Ehrmann Jiri, Strouhal Ondrej, Zemankova Petra, Lhotova Klara, Borecka Marianna, Soukupova Jana, Svebisova Hana, Soucek Pavel, Hlavac Viktor, Kleibl Zdenek, Neoral Cestmir, Melichar Bohuslav, Mohelnikova-Duchonova Beatri |
| PREVALENCE OF MISMATCH REPAIR GENE MUTATIONS IN UVEAL MELANOMA. Retina (Philadelphia, Pa.) 2020 2 40 (11): 2216-2220. Toomey Christopher B, Protopsaltis Nicholas J, Phou Samantha, Bakhoum Mathieu F, Thorson John A, Ediriwickrema Lilangi S, Korn Bobby S, Kikkawa Don O, Goldbaum Michael H, Lin Jonathan |
| Whole Exome Sequencing Identifies Candidate Genes Associated with Hereditary Predisposition to Uveal Melanoma. Ophthalmology 2019 Nov . Abdel-Rahman Mohamed H, Sample Klarke M, Pilarski Robert, Walsh Tomas, Grosel Timothy, Kinnamon Daniel, Boru Getachew, Massengill James B, Schoenfield Lynn, Kelly Ben, Gordon David, Johansson Peter, DeBenedictis Meghan J, Singh Arun, Casadei Silvia, Davidorf Frederick H, White Peter, Stacey Andrew W, Scarth James, Fewings Ellie, Tischkowitz Marc, King Mary-Claire, Hayward Nicholas K, Cebulla Colleen |
| DACH1 mutation frequency in endometrial cancer is associated with high tumor mutation burden. PloS one 2020 12 15 (12): e0244558. Riggs McKayla J, Lin Nan, Wang Chi, Piecoro Dava W, Miller Rachel W, Hampton Oliver A, Rao Mahadev, Ueland Frederick R, Kolesar Jill |
| MC1R Is a Prognostic Marker and Its Expression Is Correlated with MSI in Colorectal Cancer. Current issues in molecular biology 2021 10 43 (3): 1529-1547. Peng Lixiong, Chang Jiang, Liu Xilin, Lu Shiying, Ren Honglin, Zhou Xiaoshi, Liu Zengshan, Hu P |
| Differential Expression of the TLR4 Gene in Pan-Cancer and Its Related Mechanism. Frontiers in cell and developmental biology 2021 10 9 700661. Hu Jialing, Xu Jiasheng, Feng Xiaojin, Li Yiran, Hua Fuzhou, Xu Guoh |
| Pancreatic Cancer with Mutation in BRCA1/2, MLH1, and APC Genes: Phenotype Correlation and Detection of a Novel Germline BRCA2 Mutation. Genes 2022 2 13 (2): . Vietri Maria Teresa, D'Elia Giovanna, Caliendo Gemma, Albanese Luisa, Signoriello Giuseppe, Napoli Claudio, Molinari Anna Mar |
| Risk of Syndrome-Associated Cancers Among First-Degree Relatives of Patients With Pancreatic Ductal Adenocarcinoma With Pathogenic or Likely Pathogenic Germline Variants. JAMA oncology 2023 5 . Xuan Chen, Margaret A Meyer, Jennifer L Kemppainen, Masayasu Horibe, Shruti Chandra, Shounak Majumder, Gloria M Petersen, Kari G Ra |
| Molecular profiling of primary uveal melanoma: results of a Polish cohort. Melanoma research 2023 1 33 (2): 104-115. Kowalik Artur, Karpinski Pawel, Markiewicz Anna, Orlowska-Heitzman Jolanta, Romanowska-Dixon Bozena, Donizy Piotr, Hoang Mai |
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