HuGE Literature Finder
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| Study of diagnostic value of congenital hypertrophy of retinal pigment epithelium in Chinese familial adenomatous polyposis patients. European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 2022 Feb . Cai Shanrong, Yu Yibo, Xie Xin, Huang Yanqin, Song Yongmao, Zhan Suzhan, Zheng S |
| Germline mutations of the adenomatous polyposis coli (APC) gene in Algerian familial adenomatous polyposis cohort: first report. Molecular biology reports 2022 2 49 (5): 3823-3837. Khider Feriel, Cherbal Farid, Boumehdi Asma-Lamia, Layaida Karim, Mahfouf Hassen, Zebboudj Ferhat, Maaoui Mustap |
| Necessity of multiplex ligation probe amplification in genetic tests: Germline variant analysis of the APC gene in familial adenomatous polyposis patients. Cancer genetics 2022 2 262-263 95-101. Lee Jong Kwon, Kwon Won Kyung, Hong Sung Noh, Chang Dong Kyung, Kim Hee Cheol, Jang Ja-Hyun, Kim Jong-W |
| Heterozygous APC germline mutations impart predisposition to colorectal cancer. Scientific reports 2021 Mar 11 (1): 5113. Preisler Livia, Habib Aline, Shapira Guy, Kuznitsov-Yanovsky Liron, Mayshar Yoav, Carmel-Gross Ilana, Malcov Mira, Azem Foad, Shomron Noam, Kariv Revital, Hershkovitz Dov, Ben-Yosef Dal |
| High cumulative risk of colorectal cancers and desmoid tumours and fibromatosis in South Asian APC mutation carriers. Journal of medical genetics 2021 Mar . Ashar Shivani, Lipsa Anuja, Khan Nikhat, Sarin Raj |
| Linkage analysis revealed risk loci on 6p21 and 18p11.2-q11.2 in familial colon and rectal cancer, respectively. European journal of human genetics : EJHG 2019 Apr . von Holst Susanna, Jiao Xiang, Liu Wen, Kontham Vinaykumar, Thutkawkorapin Jessada, Ringdahl Jenny, Bryant Patrick, Lindblom Anni |
| Identification of Lynch syndrome risk variants in the Romanian population. Journal of cellular and molecular medicine 2018 Dec 22 (12): 6068-6076. Iordache Paul D, Mates Dana, Gunnarsson Bjarni, Eggertsson Hannes P, Sulem Patrick, Benonisdottir Stefania, Csiki Irma Eva, Rascu Stefan, Radavoi Daniel, Ursu Radu, Staicu Catalin, Calota Violeta, Voinoiu Angelica, Jinga Mariana, Rosoga Gabriel, Danau Razvan, Sima Sorin Cristian, Badescu Daniel, Suciu Nicoleta, Radoi Viorica, Mates Ioan Nicolae, Dobra Mihai, Nicolae Camelia, Kristjansdottir Sigrun, Jonasson Jon G, Manolescu Andrei, Arnadottir Gudny, Jensson Brynjar, Jonasdottir Aslaug, Sigurdsson Asgeir, le Roux Louise, Johannsdottir Hrefna, Rafnar Thorunn, Halldorsson Bjarni V, Jinga Viorel, Stefansson Ka |
| Synonymous mutation adenomatous polyposis coli?486s affects exon splicing and may predispose patients to adenomatous polyposis coli/mutY DNA glycosylase mutation-negative familial adenomatous polyposis. Molecular medicine reports 2018 Sep . Liu Wei Qing, Dong Jian, Peng Yan Xia, Li Wen Liang, Yang J |
| The PTPN13 Y2081D (T>G) (rs989902) polymorphism is associated with an increased risk of sporadic colorectal cancer. Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland 2017 May . Laczmanska Izabela, Karpinski Pawel, Gil Justyna, Laczmanski Lukasz, Makowska Izabela, Bebenek Marek, Ramsey David, Sasiadek Maria |
| Two subtypes of colorectal tumor with distinct molecular features in familial adenomatous polyposis. Oncotarget 2016 Aug . Takane Kiyoko, Matsusaka Keisuke, Ota Satoshi, Fukuyo Masaki, Yue Yao, Nishimura Motoi, Sakai Eiji, Matsushita Kazuyuki, Miyauchi Hideaki, Aburatani Hiroyuki, Nakatani Yukio, Takayama Tadatoshi, Matsubara Hisahiro, Akagi Kiwamu, Kaneda Atsus |
| Clinicopathological features of familial adenomatous polyposis in Korean patients. World journal of gastroenterology 2016 May 22 (17): 4380-8. Jung Sung Min, Yoon Yong Sik, Lim Seok-Byeong, Yu Chang Sik, Kim Jin Che |
| Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers. Familial cancer 2016 Feb . Ghorbanoghli Z, Nieuwenhuis M H, Houwing-Duistermaat J J, Jagmohan-Changur S, Hes F J, Tops C M, Wagner A, Aalfs C M, Verhoef S, Gómez García E B, Sijmons R H, Menko F H, Letteboer T G, Hoogerbrugge N, van Wezel T, Vasen H F A, Wijnen J |
| Copy number variants associated with 18p11.32, DCC and the promoter 1B region of APC in colorectal polyposis patients. Meta gene 2016 Feb 7 95-104. Masson Amy L, Talseth-Palmer Bente A, Evans Tiffany-Jane, McElduff Patrick, Spigelman Allan D, Hannan Garry N, Scott Rodney |
| [Molecular Pathogenesis of Colorectal Cancer]. Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti 2016 29 (6): 419-427. Král J, Slyšková J, Vodi?ka P, Špi?ák |
| Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary. Familial cancer 2015 Oct . Papp Janos, Kovacs Marietta Eva, Matrai Zoltan, Orosz Enik?, Kásler Miklós, Børresen-Dale Anne-Lise, Olah Edi |
| Adenoma development in familial adenomatous polyposis and MUTYH-associated polyposis: somatic landscape and driver genes. The Journal of pathology 2015 Sep . Rashid Mamunur, Fischer Andrej, Wilson Cathy H, Tiffen Jessamy, Rust Alistair G, Stevens Philip, Idziaszczyk Shelley, Maynard Julie, Williams Geraint T, Mustonen Ville, Sampson Julian R, Adams David |
| Common colorectal cancer risk alleles contribute to the multiple colorectal adenoma phenotype, but do not influence colonic polyposis in FAP. European journal of human genetics : EJHG 2015 Feb 23 (2): 260-3. Cheng Timothy H T, Gorman Maggie, Martin Lynn, Barclay Ella, Casey Graham, , , Saunders Brian, Thomas Huw, Clark Sue, Tomlinson I |
| Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families. Familial cancer 2013 Mar 12 (1): 35-42. Schwarzová Lucie, Štekrová Jitka, Florianová Martina, Novotný Aleš, Schneiderová Michaela, Ln?ni?ka Petr, Kebrdlová V?ra, Kotlas Jaroslav, Veselá Kamila, Kohoutová Mila |
| Clinical and molecular features of attenuated adenomatous polyposis in northern Italy. Techniques in coloproctology 2013 Feb 17 (1): 79-87. de Leon M Ponz, Urso E D L, Pucciarelli S, Agostini M, Nitti D, Roncucci L, Benatti P, Pedroni M, Kaleci S, Balsamo A, Laudi C, Di Gregorio C, Viel A, Rossi G, Venesio |
| Contribution of the MLH1 -93G>a promoter polymorphism in modulating susceptibility risk in Malaysian colorectal cancer patients. Asian Pacific journal of cancer prevention : APJCP 2013 14 (2): 619-24. Nizam Zahary Mohd, Abdul Aziz Ahmad Aizat, Kaur Gurjeet, Abu Hassan Muhammad Radzi, Mohd Sidek Ahmad Shanwani, Yeh Lee Yeong, Mazuwin Maya, Ankathil Ravindr |
| Frequencies of mtDNA mutations in primary tissues of colorectal adenopolyps. Frontiers in bioscience (Elite edition) 2013 5 809-13. Adams Gregory, Mehrabi Sharifeh, Vatcharapijarn Yupha, Iyamu Osatohamwen I, Akwe Joyce A, Grizzle William E, Yao Xuebiao, Aikhionbare Felix |
| Association study of APC polymorphisms with colorectal cancer in Han Chinese. Clinical biochemistry 2012 Jul . Huang X, Wang Y, Yu T, Liu B, Li X, Li W, Chen S, Zhao Q, Li X, Yang F, Wang Q, Wang J, Xiao Y, Xu Y, Feng G, Peng Z, He L, He G |
| Genotype-phenotype correlation in colorectal polyposis. Clinical genetics 2011 Jun . Newton K, Mallinson E, Bowen J, Lalloo F, Clancy T, Hill J, Evans D |
| MUTYH-associated polyposis - variability of the clinical phenotype in patients with biallelic and monoallelic MUTYH mutations and report on novel mutations. Clinical genetics 2010 Oct 78 (4): 353-63. Morak M, Laner A, Bacher U, Keiling C, Holinski-Feder |
| Mutation analysis of the APC gene in Taiwanese FAP families: low incidence of APC germline mutation in a distinct subgroup of FAP families. Familial cancer 2010 Jun 9 (2): 117-24. Chiang J M, Chen H W, Tang R P, Chen J S, Changchien C R, Hsieh P S, Wang J |
| APC or MUTYH mutations account for the majority of clinically well-characterized families with FAP and AFAP phenotype and patients with more than 30 adenomas. Clinical genetics 2009 Sep 76 (3): 242-55. Filipe B, Baltazar C, Albuquerque C, Fragoso S, Lage P, Vitoriano I, Mão de Ferro S, Claro I, Rodrigues P, Fidalgo P, Chaves P, Cravo M, Nobre Leitão |
| Molecular analysis of the APC and MUTYH genes in Galician and Catalonian FAP families: a different spectrum of mutations? BMC medical genetics 2009 10 . Gómez-Fernández N, Castellví-Bel S, Fernández-Rozadilla C, Balaguer F, Muñoz J, Madrigal I, Milà M, Graña B, Vega A, Castells A, Carracedo A, Ruiz-Ponte C |
| Somatic mutations of the CDC4 (FBXW7) gene in hereditary colorectal tumors. Oncology 2009 76 (6): 430-4. Miyaki Michiko, Yamaguchi Tatsuro, Iijima Takeru, Takahashi Keiichi, Matsumoto Hiroshi, Mori Tak |
| CHEK2 1100delC is a susceptibility allele for HNPCC-related colorectal cancer. Clinical cancer research : an official journal of the American Association for Cancer Research 2008 Aug 14 (15): 4989-94. Wasielewski Marijke, Vasen Hans, Wijnen Juul, Hooning Maartje, Dooijes Dennis, Tops Carli, Klijn Jan G M, Meijers-Heijboer Hanne, Schutte Mie |
| Contribution of common monoallelic MUTYH gene variants in German patients with familial colorectal cancer. Cancer biomarkers : section A of Disease markers 2008 4 (2): 55-61. Grünhage Frank, Jungck Matthias, Lamberti Christof, Schulte-Witte Hildegard, Plassmann Dominik, Becker Ursula, Rahner Nils, Aretz Stefan, Friedrichs Nicolaus, Buettner Reinhard, Sauerbruch Tilman, Lammert Fra |
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- Page last updated:Jan 27, 2023
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