For: |
Papp J, Kovacs ME, Olah E. Germline |
---|---|
URL: | https://www.wjgnet.com/1007-9327/full/v13/i19/2727.htm |
Number | Citing Articles |
1 |
Hidetaka Yamada, Kazuya Shinmura, Hiroaki Ito, Masako Kasami, Naomi Sasaki, Hideyuki Shima, Masami Ikeda, Hong Tao, Masanori Goto, Takachika Ozawa, Toshihiro Tsuneyoshi, Fumihiko Tanioka, Haruhiko Sugimura. Germline alterations in the CDH1 gene in familial gastric cancer in the Japanese population. Cancer Science 2011; 102(10): 1782 doi: 10.1111/j.1349-7006.2011.02038.x
|
2 |
Yasushi Yamasaki, Masashi Matsushima, Hisae Tanaka, Sakurako Tajiri, Ryuki Fukuda, Hideki Ozawa, Atsushi Takagi, Ken-ichi Hirabayashi, Sohtaro Sadahiro. Patient with Eight Metachronous Gastrointestinal Cancers Thought to be Hereditary Nonpolyposis Colorectal Cancer (HNPCC). Internal Medicine 2010; 49(3): 209 doi: 10.2169/internalmedicine.49.2316
|
3 |
Demétrius Germini, Flávia Gehrke, Daniel Lira, Beatriz Alves, Lígia Azzalis, Matheus Perez, Fernando Fonseca, Jaques Waisberg. HMSH2 and HMSH6 gene expression profiles in colorectal adenocarcinoma in patients up to 50 years of age. Biomedicine & Pharmacotherapy 2016; 83: 602 doi: 10.1016/j.biopha.2016.07.015
|
4 |
Ajay Kumar Jain, Kathleen J Motil, Oluyinka O Olutoye, Sandy Cope‐Yokoyama, Rachel A Egler, Nina Tatevian. Colon Cancer in a 16‐Year‐Old Girl: Signet‐Ring Cell Carcinoma Without Microsatellite Instability—An Unusual Suspect. Journal of Pediatric Gastroenterology and Nutrition 2009; 48(1): 110 doi: 10.1097/MPG.0b013e31815dda8c
|
5 |
Jianbiao Xu, Jianlin Song, Wenchuan Zhu, Liangyu Zuo, Jinzhi Wu, Li Zhang, Tongmin Wang, Jianhui Guo. A novel germline frameshift mutation in the MLH1 gene in a patient with Lynch syndrome. Cancer Genetics 2023; : 54 doi: 10.1016/j.cancergen.2023.03.003
|
6 |
Kyoung-Jin Park, Dong Kyung Chang, Hee Cheol Kim, Jong-Won Kim. Germline Variants in MLH1, MSH2, and MSH6 in Korean Patients with Lynch Syndrome. Laboratory Medicine Online 2018; 8(4): 156 doi: 10.3343/lmo.2018.8.4.156
|
7 |
Renata Bordeira-Carriço, Ana Paula Pêgo, Manuel Santos, Carla Oliveira. Cancer syndromes and therapy by stop-codon readthrough. Trends in Molecular Medicine 2012; 18(11): 667 doi: 10.1016/j.molmed.2012.09.004
|
8 |
Ryan Thibodeau, Abtin Jafroodifar, Dmitriy Bakrukov, Leen Alkukhun, Kavya Mirchia, Anand Majmudar, Saurabh Gupta, Ravikumar Hanumaiah. Intussusception secondary to signet ring cell adenocarcinoma in adolescent. Radiology Case Reports 2021; 16(5): 1198 doi: 10.1016/j.radcr.2021.02.027
|
9 |
H. M. Heneghan, S. T. Martin, D. C. Winter. Segmental vs extended colectomy in the management of hereditary nonpolyposis colorectal cancer: a systematic review and meta‐analysis. Colorectal Disease 2015; 17(5): 382 doi: 10.1111/codi.12868
|
10 |
Sara Ashorn, Tuuli Välineva, Katri Kaukinen, Merja Ashorn, Jonathan Braun, Hanna Raukola, Immo Rantala, Pekka Collin, Markku Mäki, Tiina Luukkaala, Sari Iltanen. Serological Responses to Microbial Antigens in Celiac Disease Patients During a Gluten-Free Diet. Journal of Clinical Immunology 2009; 29(2): 190 doi: 10.1007/s10875-008-9255-7
|
11 |
M. Tanyi, J. Olasz, J.L. Tanyi, L. Tóth, P. Antal-Szalmás, Z. Ress, T. Bubán, K. Palatka, C. András, H. Urbancsek, Z. Garami, O. Csuka, L. Damjanovich. MLH1 and MSH2 mutation screening in HNPCC families of Hungary – Two new MMR gene mutations. European Journal of Surgical Oncology (EJSO) 2014; 40(11): 1445 doi: 10.1016/j.ejso.2014.07.032
|
12 |
Keiko Suzuki, Satoshi Nakao, Akihiro Suzuki, Masahiko Inamori, Hiroshi Iida, Hiroki Endo, Tomoyuki Akiyama, Kyoko Yoneda, Koji Fujita, Hirokazu Takahashi, Masato Yoneda, Yasunobu Abe, Noritoshi Kobayashi, Kensuke Kubota, Satoru Saito, Atsushi Nakajima. Ulcerative Colitis with Positivity for Proteinase 3-Antineutrophil Cytoplasmic Antibody. Digestion 2008; 77(3-4): 157 doi: 10.1159/000140976
|
13 |
Bincy P. Abraham, Selvi Thirumurthi. Clinical significance of inflammatory markers. Current Gastroenterology Reports 2009; 11(5): 360 doi: 10.1007/s11894-009-0055-x
|
14 |
Renato Mitsunori Nisihara, Wilson Beleski de Carvalho, Shirley Ramos da Rosa Utiyama, Heda Amarante, Márcia Luiza Baptista. Diagnostic Role and Clinical Association of ASCA and ANCA in Brazilian Patients with Inflammatory Bowel Disease. Digestive Diseases and Sciences 2010; 55(8): 2309 doi: 10.1007/s10620-009-0998-7
|
15 |
Dandan Li, Fulan Hu, Fan Wang, Binbin Cui, Xinshu Dong, Wencui Zhang, Chunqing Lin, Xia Li, Da Wang, Yashuang Zhao, Amanda Ewart Toland. Prevalence of Pathological Germline Mutations of hMLH1 and hMSH2 Genes in Colorectal Cancer. PLoS ONE 2013; 8(3): e51240 doi: 10.1371/journal.pone.0051240
|
16 |
Miklós Tanyi. Hereditaer Nonpolyposis Colorectalis Carcinoma előfordulásával szerzett tapasztalatainkr. Magyar Sebészet 2009; 62(2): 87 doi: 10.1556/maseb.62.2009.2.7
|
17 |
Cynthia H Seow, Joanne M Stempak, Wei Xu, Hui Lan, Anne M Griffiths, Gordon R Greenberg, A Hillary Steinhart, Nir Dotan, Mark S Silverberg. Novel Anti-Glycan Antibodies Related to Inflammatory Bowel Disease Diagnosis and Phenotype. The American Journal of Gastroenterology 2009; 104(6): 1426 doi: 10.1038/ajg.2009.79
|
18 |
Marietta E. Kovacs, Janos Papp, Zoltan Szentirmay, Szabolcs Otto, Edith Olah. Deletions removing the last exon ofTACSTD1constitute a distinct class of mutations predisposing to Lynch syndrome. Human Mutation 2009; 30(2): 197 doi: 10.1002/humu.20942
|
19 |
Miklós Tanyi, Judit Olasz, Janos L. Tanyi, László Tóth, Péter Antal-Szalmás, Tamás Bubán, Csilla András, Hilda Urbancsek, Zoltán Garami, Orsolya Csuka, László Damjanovich. Q48P mutation in the hMLH1 gene associated with Lynch syndrome in three Hungarian families. Familial Cancer 2012; 11(3): 519 doi: 10.1007/s10689-012-9515-9
|
20 |
Paolo Nanni, Fredrik Levander, Giulia Roda, Alessandra Caponi, Peter James, Aldo Roda. A label-free nano-liquid chromatography–mass spectrometry approach for quantitative serum peptidomics in Crohn's disease patients. Journal of Chromatography B 2009; 877(27): 3127 doi: 10.1016/j.jchromb.2009.08.003
|
21 |
Natasha G. Caminsky, Eliseos J. Mucaki, Peter K. Rogan. Interpretation of mRNA splicing mutations in genetic disease: review of the literature and guidelines for information-theoretical analysis. F1000Research 2014; 3: 282 doi: 10.12688/f1000research.5654.1
|
22 |
Zhaoxiu Liu, Bo Shen. Overcoming difficulty in diagnosis and differential diagnosis of Crohn’s disease: the potential role of serological and genetic tests. Expert Review of Molecular Diagnostics 2015; 15(9): 1133 doi: 10.1586/14737159.2015.1068121
|
23 |
Janos Papp, Marietta Eva Kovacs, Zoltan Matrai, Enikő Orosz, Miklós Kásler, Anne-Lise Børresen-Dale, Edith Olah. Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary. Familial Cancer 2016; 15(1): 85 doi: 10.1007/s10689-015-9845-5
|
24 |
Janos Papp, Marietta Eva Kovacs, Szilvia Solyom, Miklos Kasler, Anne-Lise Børresen-Dale, Edith Olah. High prevalence of germline STK11mutations in Hungarian Peutz-Jeghers Syndrome patients. BMC Medical Genetics 2010; 11(1) doi: 10.1186/1471-2350-11-169
|
25 |
Natasha G. Caminsky, Eliseos J. Mucaki, Peter K. Rogan. Interpretation of mRNA splicing mutations in genetic disease: review of the literature and guidelines for information-theoretical analysis. F1000Research 2015; 3: 282 doi: 10.12688/f1000research.5654.2
|
26 |
Poonam Beniwal, Laura Harrell. The Status of Diagnostic Markers for Inflammatory Bowel Disease. Current Gastroenterology Reports 2010; 12(6): 479 doi: 10.1007/s11894-010-0145-9
|
27 |
Vince Kornél Grolmusz, Petra Nagy, István Likó, Henriett Butz, Tímea Pócza, Anikó Bozsik, János Papp, Edit Oláh, Attila Patócs. A common genetic variation in GZMB may associate with cancer risk in patients with Lynch syndrome. Frontiers in Oncology 2023; 13 doi: 10.3389/fonc.2023.1005066
|
28 |
Felipe Cavalcanti Carneiro da Silva, Mev Dominguez Valentin, Fábio de Oliveira Ferreira, Dirce Maria Carraro, Benedito Mauro Rossi. Mismatch repair genes in Lynch syndrome: a review. Sao Paulo Medical Journal 2009; 127(1): 46 doi: 10.1590/S1516-31802009000100010
|
29 |
Eva Wielders, Elly Delzenne-Goette, Rob Dekker, Martin van der Valk, Hein te Riele. Truncation of the MSH2 C-terminal 60 amino acids disrupts effective DNA mismatch repair and is causative for Lynch syndrome. Familial Cancer 2017; 16(2): 221 doi: 10.1007/s10689-016-9945-x
|