Works matching DE "HEREDITARY nonpolyposis colorectal cancer"

Results: 2170

Colorectal Cancers and Microsatellite Instability.

Published in:

Turkish Journal of Oncology / Türk Onkoloji Dergisi, 2025, v. 40, n. 1, p. 83, doi. 10.5505/tjo.2024.4477

By:

ESMKHANI, Sahra;
EMREM, Mustafa;
ŞAHIN, Ali;
BABAYEV, Hüseyn;
ZEYNELOĞLU, Can;
ARDIÇLI, Sena;
YAZICI, Hilal;
YAZICI, Hülya

Publication type:

Article

Predisposing conditions in patients with small intestinal adenocarcinomas in the Netherlands: A 20‐year nationwide cohort study.

Published in:

International Journal of Cancer, 2025, v. 157, n. 2, p. 218, doi. 10.1002/ijc.35354

By:

Linssen, Jasmijn D. G.;
Schafrat, Pascale J. M.;
de Back, Tim R.;
van Erning, Felice N.;
van Leerdam, Monique E.;
Dekker, Evelien;
Vermeulen, Louis;
de Hingh, Ignace H. J. T.;
Sommeijer, Dirkje W.

Publication type:

Article

MSH2 -Mutated Lynch Syndrome With 9 Synchronous Colon and Rectum Adenocarcinomas: An Extremely Rare Case Report.

Published in:

International Journal of Surgical Pathology, 2025, v. 33, n. 4, p. 1062, doi. 10.1177/10668969241295691

By:

Kavus, Haluk;
Dorion, Robert Patrick

Publication type:

Article

Hereditary Gastrointestinal Cancer Syndromes and Early‐Onset Gastrointestinal Cancers.

Published in:

Journal of Gastroenterology & Hepatology, 2025, v. 40, n. 5, p. 1037, doi. 10.1111/jgh.16965

By:

Lui, Rashid N.;
Chiu, Han‐Mo

Publication type:

Article

Pathological complete response after monotherapy with immune checkpoint inhibitors for bifocal colon cancer in a patient with lynch syndrome and situs inversus totalis: a case report.

Published in:

Frontiers in Immunology, 2025, p. 1, doi. 10.3389/fimmu.2025.1571607

By:

Feng, Jun;
Niu, Wenbo;
Zhang, Juan;
Ding, Yuanyi;
Li, Zheng;
Zhang, Jianfeng;
Li, Baokun;
Li, Chenhui;
Wang, Feifei;
Wang, Guiying;
Yu, Bin

Publication type:

Article

Risk of colorectal cancer in patients with diabetes mellitus: A Swedish nationwide cohort study.

Published in:

2020

By:

Ali Khan, Uzair;
Fallah, Mahdi;
Sundquist, Kristina;
Sundquist, Jan;
Brenner, Hermann;
Kharazmi, Elham

Publication type:

journal article

The proportion of endometrial tumours associated with Lynch syndrome (PETALS): A prospective cross-sectional study.

Published in:

2020

By:

Ryan, Neil A. J.;
McMahon, Raymond;
Tobi, Simon;
Snowsill, Tristan;
Esquibel, Shona;
Wallace, Andrew J.;
Bunstone, Sancha;
Bowers, Naomi;
Mosneag, Ioana E.;
Kitson, Sarah J.;
O'Flynn, Helena;
Ramchander, Neal C.;
Sivalingam, Vanitha N.;
Frayling, Ian M.;
Bolton, James;
McVey, Rhona J.;
Evans, D. Gareth;
Crosbie, Emma J.

Publication type:

journal article

Universal screening for Lynch syndrome in endometrial cancer diagnoses in Auckland, New Zealand: The initial experience.

Published in:

Australian & New Zealand Journal of Obstetrics & Gynaecology, 2025, v. 65, n. 1, p. 47, doi. 10.1111/ajo.13857

By:

Naiqiso, Silipa Lock Sam;
Moses, Jo;
Tan, Ai Ling;
Eva, Lois

Publication type:

Article

RACIAL DIFFERENCES IN MLH1 AND MSH2 MUTATION:: AN ANALYSIS OF YELLOW RACE AND WHITE RACE BASED ON THE INSIGHT DATABASE.

Published in:

Journal of Bioinformatics & Computational Biology, 2010, v. 8, p. 111, doi. 10.1142/S0219720010005154

By:

WEI, WENQIAN;
LIU, LEI;
CHEN, JIAN;
JIN, KE;
JIANG, FAN;
LIU, FANGQI;
FAN, RONG;
CHENG, ZHE;
SHEN, MENG;
XUE, CHENYI;
CAI, SANJUN;
XU, YE;
NAN, PENG

Publication type:

Article

Glioma arising in the setting of mismatch repair deficiency—rare or are we missing it?

Published in:

2024

By:

Goyal, Aditi;
Rao, Shilpa;
Rishi, Karthik S;
Ramaswamy, Veena;
Sadashiva, Nishanth;
Santosh, Vani

Publication type:

Case Study

Immunohistochemical screening for mismatch repair protein deficiency in paediatric high-grade gliomas — institutional experience and review of literature.

Published in:

Child's Nervous System, 2021, v. 37, n. 8, p. 2521, doi. 10.1007/s00381-021-05229-1

By:

Alphones, Sheena;
Chatterjee, Uttara;
Singh, Angad;
Das, Anirban;
Zameer, Lateef;
Achari, Rimpa;
Bhattacharya, Arpita;
Roy, Paromita

Publication type:

Article

Constitutional mismatch repair deficiency (CMMRD) presenting with high-grade glioma, multiple developmental venous anomalies and malformations of cortical development—a multidisciplinary/multicentre approach and neuroimaging clues to clinching the diagnosis

Published in:

Child's Nervous System, 2021, v. 37, n. 7, p. 2375, doi. 10.1007/s00381-020-04986-9

By:

Chhabda, Sahil;
Sudhakar, Sniya;
Mankad, Kshitij;
Jorgensen, Mette;
Carceller, Fernando;
Jacques, Thomas S.;
Merve, Ashirwad;
Aizpurua, Miren;
Chalker, Jane;
Garimberti, Elisa;
D'Arco, Felice

Publication type:

Article

Increased Number of Colorectal Interval Cancers in Lynch Syndrome after the SARS-CoV-2 Pandemic: A Survey-Based Study.

Published in:

Digestive Diseases, 2023, v. 41, n. 2, p. 227, doi. 10.1159/000524393

By:

Russo, Michele;
Barchi, Alberto;
Mannucci, Alessandro;
Puzzono, Marta;
Zuppardo, Raffaella Alessia;
Biamonte, Paolo;
Bencardino, Sarah;
Leandro, Gioacchino;
Cannizzaro, Renato;
Monica, Fabio;
Zagari, Rocco Maurizio;
Pasquale, Luigi;
Goni, Elisabetta;
Di Leo, Milena;
Ricciardiello, Luigi;
Cavestro, Giulia Martina

Publication type:

Article

Chromoendoscopy Is Not Superior to White Light Endoscopy in Improving Adenoma Detection in Lynch Syndrome Cohort Undergoing Surveillance with High-Resolution Colonoscopy: A Real-World Evidence Study.

Published in:

Digestive Diseases, 2022, v. 40, n. 4, p. 517, doi. 10.1159/000518840

By:

Montale, Amedeo;
Buttitta, Francesco;
Pierantoni, Chiara;
Ferrari, Clarissa;
Cameletti, Michela;
Colussi, Dora;
Miccoli, Sara;
Bazzoli, Franco;
Turchetti, Daniela;
Ricciardiello, Luigi

Publication type:

Article

Towards precision oncology discovery: four less known genes and their unknown interactions as highest-performed biomarkers for colorectal cancer.

Published in:

NPJ Precision Oncology, 2024, p. 1, doi. 10.1038/s41698-024-00512-1

By:

Liu, Yongjun;
Xu, Yuqing;
Li, Xiaoxing;
Chen, Mengke;
Wang, Xueqin;
Zhang, Ning;
Zhang, Heping;
Zhang, Zhengjun

Publication type:

Article

Compound heterozygous MSH3 germline variants and associated tumor somatic DNA mismatch repair dysfunction.

Published in:

NPJ Precision Oncology, 2024, v. 8, n. 1, p. 1, doi. 10.1038/s41698-024-00511-2

By:

Koi, Minoru;
Leach, Brandie H.;
McGee, Sarah;
Tseng-Rogenski, Stephanie S.;
Burke, Carol A.;
Carethers, John M.

Publication type:

Article

Colorectal cancer risk stratification on histological slides based on survival curves predicted by deep learning.

Published in:

NPJ Precision Oncology, 2023, v. 7, n. 1, p. 1, doi. 10.1038/s41698-023-00451-3

By:

Höhn, Julia;
Krieghoff-Henning, Eva;
Wies, Christoph;
Kiehl, Lennard;
Hetz, Martin J.;
Bucher, Tabea-Clara;
Jonnagaddala, Jitendra;
Zatloukal, Kurt;
Müller, Heimo;
Plass, Markus;
Jungwirth, Emilian;
Gaiser, Timo;
Steeg, Matthias;
Holland-Letz, Tim;
Brenner, Hermann;
Hoffmeister, Michael;
Brinker, Titus J.

Publication type:

Article

Molecular disparities in colorectal cancers of White Americans, Alabama African Americans, and Oklahoma American Indians.

Published in:

NPJ Precision Oncology, 2023, v. 7, n. 1, p. 1, doi. 10.1038/s41698-023-00433-5

By:

Yamada, Hiroshi Y.;
Xu, Chao;
Jones, Kenneth L.;
O'Neill, Philip H.;
Venkateshwar, Madka;
Chiliveru, Srikanth;
Kim, Hyung-Gyoon;
Doescher, Mark;
Morris, Katherine T.;
Manne, Upender;
Rao, Chinthalapally V.

Publication type:

Article

Molecular characteristics of microsatellite stable early-onset colorectal cancer as predictors of prognosis and immunotherapeutic response.

Published in:

NPJ Precision Oncology, 2023, v. 7, n. 1, p. 1, doi. 10.1038/s41698-023-00414-8

By:

Lu, Can;
Zhang, Xiaopeng;
Schardey, Josefine;
Wirth, Ulrich;
Heinrich, Kathrin;
Massiminio, Luca;
Cavestro, Giulia Martina;
Neumann, Jens;
Bazhin, Alexandr V.;
Werner, Jens;
Kühn, Florian

Publication type:

Article

High-throughput proteomics profiling-derived signature associated with chemotherapy response and survival for stage II/III colorectal cancer.

Published in:

NPJ Precision Oncology, 2023, v. 7, n. 1, p. 1, doi. 10.1038/s41698-023-00400-0

By:

Ye, Shu-Biao;
Cheng, Yi-Kan;
Li, Pei-Si;
Zhang, Lin;
Zhang, Lian-Hai;
Huang, Yan;
Chen, Ping;
Wang, Yi;
Wang, Chao;
Peng, Jian-Hong;
Shi, Li-Shuo;
Ling, Li;
Wu, Xiao-Jian;
Qin, Jun;
Yang, Zi-Huan;
Lan, Ping

Publication type:

Article

Comprehensive pan-cancer genomic landscape of KRAS altered cancers and real-world outcomes in solid tumors.

Published in:

NPJ Precision Oncology, 2022, v. 6, n. 1, p. 1, doi. 10.1038/s41698-022-00334-z

By:

Lee, Jessica K.;
Sivakumar, Smruthy;
Schrock, Alexa B.;
Madison, Russell;
Fabrizio, David;
Gjoerup, Ole;
Ross, Jeffrey S.;
Frampton, Garrett M.;
Napalkov, Pavel;
Montesion, Meagan;
Schutzman, Jennifer L.;
Ye, Xin;
Hegde, Priti S.;
Nagasaka, Misako;
Oxnard, Geoffrey R.;
Sokol, Ethan S.;
Ou, Sai-Hong Ignatius;
Shi, Zhen

Publication type:

Article

Clinical prospects of WRN inhibition as a treatment for MSI tumours.

Published in:

NPJ Precision Oncology, 2022, v. 6, n. 1, p. 1, doi. 10.1038/s41698-022-00319-y

By:

Morales-Juarez, David A.;
Jackson, Stephen P.

Publication type:

Article

Collision of germline POLE and PMS2 variants in a young patient treated with immune checkpoint inhibitors.

Published in:

NPJ Precision Oncology, 2022, v. 6, n. 1, p. 1, doi. 10.1038/s41698-022-00258-8

By:

Berrino, Enrico;
Filippi, Roberto;
Visintin, Clara;
Peirone, Serena;
Fenocchio, Elisabetta;
Farinea, Giovanni;
Veglio, Franco;
Aglietta, Massimo;
Sapino, Anna;
Cereda, Matteo;
Visintin, Rosella;
Pasini, Barbara;
Marchiò, Caterina

Publication type:

Article

Analysis of the Genetic Characteristics and Metastatic Pathways of G1 and G2 Colorectal Neuroendocrine Neoplasms.

Published in:

Journal of the Endocrine Society, 2024, v. 8, n. 2, p. 1, doi. 10.1210/jendso/bvad168

By:

Wang, Zhijie;
Chen, Qichen;
Zhao, Fuqiang;
Sun, Li;
Qiu, Yixian;
Cheng, Huanqing;
Qin, Jiayue;
Wang, Huina;
Shi, Susheng;
Cao, Shanbo;
Liu, Qian

Publication type:

Article

Adrenal Cortical Carcinoma Associated With Lynch Syndrome: A Case Report and Review of Literature.

Published in:

Journal of the Endocrine Society, 2019, v. 3, n. 4, p. 784, doi. 10.1210/js.2019-00050

By:

Kaur, Ravinder Jeet;
Pichurin, Pavel N;
Hines, Jolaine M;
Singh, Ravinder J;
Grebe, Stefan K;
Bancos, Irina

Publication type:

Article

Refining Risk Estimates in Hereditary Nonpolyposis Colorectal Cancer: Are We There Yet?

Published in:

JNCI Cancer Spectrum, 2020, v. 4, n. 5, p. 1, doi. 10.1093/jncics/pkaa030

By:

Lynch, Patrick M;
Pande, Mala

Publication type:

Article

Penetrance of Colorectal Cancer Among Mismatch Repair Gene Mutation Carriers: A Meta-Analysis.

Published in:

JNCI Cancer Spectrum, 2020, v. 4, n. 5, p. 1, doi. 10.1093/jncics/pkaa027

By:

Wang, Cathy;
Wang, Yan;
Hughes, Kevin S;
Parmigiani, Giovanni;
Braun, Danielle

Publication type:

Article

Choosing not to undergo predictive genetic testing for hereditary colorectal cancer syndromes: expanding our understanding of decliners and declining.

Published in:

Journal of Behavioral Medicine, 2017, v. 40, n. 4, p. 583, doi. 10.1007/s10865-016-9820-0

By:

Keogh, Louise;
Niven, Heather;
Rutstein, Alison;
Flander, Louisa;
Gaff, Clara;
Jenkins, Mark

Publication type:

Article

Physician trust moderates the relationship between intolerance of uncertainty and cancer worry interference among women with Lynch syndrome.

Published in:

Journal of Behavioral Medicine, 2016, v. 39, n. 3, p. 420, doi. 10.1007/s10865-016-9711-4

By:

Torbit, Lindsey;
Albiani, Jenna;
Aronson, Melyssa;
Holter, Spring;
Semotiuk, Kara;
Cohen, Zane;
Hart, Tae

Publication type:

Article

How calm should I keep? Café-au-lait macules as potential manifestations of cancer susceptibility syndromes.

Published in:

Oncolog-Hematolog, 2023, n. 64, p. 33

By:

Cismaru, Andrei;
Berindan-Neagoe, Ioana

Publication type:

Article

Colorectal cancer in patient younger than 50-year-old in Kelantan: Two case reports.

Published in:

Malaysian Journal of Pathology, 2022, v. 44, n. 2, p. 285

By:

CHE JALIL, Nur Asyilla;
OTHMAN, Nor Hayati;
WAN ABDUL RAHMAN, Wan Faiziah;
ZAKARIA, Andee Dzulkarnaen;
SAMSUDIN, Ahmad Hadif Zaidin;
MOHD NAFI, Siti Norasikin;
MAZUKI, Nur Ain Nabila

Publication type:

Article

Hereditary colorectal cancer syndromes and the COVID-19 pandemic: results from a survey conducted in patients enrolled in a dedicated registry.

Published in:

Quality of Life Research, 2022, v. 31, n. 4, p. 1105, doi. 10.1007/s11136-021-02973-4

By:

Signoroni, Stefano;
Ciniselli, Chiara Maura;
Piozzi, Guglielmo Niccolò;
Ricci, Maria Teresa;
Pastori, Marta;
Merola, Paolo;
Bellazzi, Marco;
Smaldone, Tatiana;
Rosito, Giuseppe;
Borreani, Claudia;
Verderio, Paolo;
Apolone, Giovanni;
Vitellaro, Marco

Publication type:

Article

Clinicopathological features of Lynch syndrome pedigrees with MSH2 c.351G>A gene variant.

Published in:

Molecular Genetics & Genomic Medicine, 2025, v. 13, n. 1, p. 1, doi. 10.1002/mgg3.2506

By:

Zhang, Shuai;
Fu, Guanyu;
Sun, Gongping;
Tang, Yuanxin;
Meng, Jin;
Wang, Zhigang;
Su, Rongjun;
Liu, Wei;
Li, Xiaoxia

Publication type:

Article

Reclassification of Two MLH1 Variants of Uncertain Significance Utilizing Clinical and Functional Data.

Published in:

Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 11, p. 1, doi. 10.1002/mgg3.70026

By:

Frederiksen, Jane Hübertz;
Birkedal, Ulf;
Bachmann, Sarah;
Eliesen, Elisabeth Victoria;
Rasmussen, Lene Juel;
Pedersen, Katja Venborg;
Al‐Zehhawi, Lana;
Boonen, Susanne E.;
Krogh, Lotte;
Rønlund, Karina;
Graversen, Lise;
Assenholt, Jannie;
Schmiegelow, Kjeld;
Wadt, Karin;
Gerdes, Anne‐Marie;
Hansen, Thomas v. O.

Publication type:

Article

Genotype–phenotype correlations in carriers of the PMS2 founder variant c.1831dup.

Published in:

Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 1, p. 1, doi. 10.1002/mgg3.2360

By:

Gass, Melanie;
Seebauer, Britta;
Thommen, Aline;
Fischler, Alexandra;
Heinimann, Karl

Publication type:

Article

From variant of unknown significance to likely pathogenic: Characterization and pathogenicity determination of a large genomic deletion in the MLH1 gene.

Published in:

Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 9, p. 1, doi. 10.1002/mgg3.2231

By:

Bouras, Ahmed;
Legrand, Clementine;
Kourda, Jihen;
Ruano, Eric;
Grand‐Masson, Chloé;
Lefol, Cedrick;
Wang, Qing

Publication type:

Article

Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndrome.

Published in:

Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 6, p. 1, doi. 10.1002/mgg3.2151

By:

Witt, Dennis;
Faust, Ulrike;
Strobl‐Wildemann, Gertrud;
Sturm, Marc;
Buchert, Rebecca;
Zuleger, Theresia;
Admard, Jakob;
Casadei, Nicolas;
Ossowski, Stephan;
Haack, Tobias B.;
Rieß, Olaf;
Schroeder, Christopher

Publication type:

Article

Characterization of a germline variant MSH6 c.4001G > C in a Lynch syndrome family.

Published in:

Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 2, p. 1, doi. 10.1002/mgg3.2104

By:

Yang, Ciyu;
Misyura, Maksym;
Kane, Sarah;
Rai, Vikas;
Latham, Alicia;
Zhang, Liying

Publication type:

Article

PMS2 variant results in loss of ATPase activity without compromising mismatch repair.

Published in:

Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 5, p. 1, doi. 10.1002/mgg3.1908

By:

D'Arcy, Brandon M.;
Arrington, Jennifer;
Weisman, Justin;
McClellan, Steven B.;
Vandana;
Yang, Zhengrong;
Deivanayagam, Champion;
Blount, Jessa;
Prakash, Aishwarya

Publication type:

Article

Insertion of an Alu‐like element in MLH1 intron 7 as a novel cause of Lynch syndrome.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 12, p. 1, doi. 10.1002/mgg3.1523

By:

Li, Yirong;
Salo‐Mullen, Erin;
Varghese, Anna;
Trottier, Magan;
Stadler, Zsofia K.;
Zhang, Liying

Publication type:

Article

Comparison of suspected Lynch syndrome patients carrying BRCA and BRCA‐like variants with Lynch syndrome probands: Phenotypic characteristics and pedigree analyses.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 8, p. 1, doi. 10.1002/mgg3.1359

By:

Xu, Yun;
Li, Cong;
Wang, Zhimin;
Liu, Fangqi;
Xu, Ye

Publication type:

Article

Identification of a novel pathogenic MLH1 mutation and recommended genetic screening strategy: An investigation of three Chinese Lynch syndrome pedigrees.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 8, p. 1, doi. 10.1002/mgg3.1295

By:

Li, Fan;
Xia, Yunwei;
Wang, Guoguang;
Tang, Chaoyang;
Zhan, Tian;
Shen, Jian;
Zhang, Jianping

Publication type:

Article

Family still matters: Counseling patients with complex family histories of colon and endometrial cancers.

Published in:

Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 9, p. N.PAG, doi. 10.1002/mgg3.886

By:

Gemmell, Amber P.;
Mauer, Caitlin B.;
Reys, Brian D.;
Pirzadeh‐Miller, Sara;
Ross, Theodora S.

Publication type:

Article

Tumor mutational signatures in sebaceous skin lesions from individuals with Lynch syndrome.

Published in:

Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 7, p. N.PAG, doi. 10.1002/mgg3.781

By:

Georgeson, Peter;
Walsh, Michael D.;
Clendenning, Mark;
Daneshvar, Simin;
Pope, Bernard J.;
Mahmood, Khalid;
Joo, Jihoon E.;
Jayasekara, Harindra;
Jenkins, Mark A.;
Winship, Ingrid M.;
Buchanan, Daniel D.

Publication type:

Article

Somatic mosaicism by a de novo MLH1 mutation as a cause of Lynch syndrome.

Published in:

Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 7, p. N.PAG, doi. 10.1002/mgg3.699

By:

Geurts‐Giele, Willemina R.;
Rosenberg, Efraim H.;
Rens, Anja van;
Leerdam, Monique E. van;
Dinjens, Winand N.;
Bleeker, Fonnet E.

Publication type:

Article

PMS2 germline mutation c.943C>T (p.Arg315*)‐induced Lynch syndrome‐associated ovarian cancer.

Published in:

Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 6, p. N.PAG, doi. 10.1002/mgg3.721

By:

Guo, Xiaoqing;
Wu, Weimin;
Gao, Hao;
Li, Xiaofeng;
He, Qizhi;
Zhu, Yong;
Liu, Na

Publication type:

Article

Toward a better definition of EPCAM deletions in Lynch Syndrome: Report of new variants in Italy and the associated molecular phenotype.

Published in:

Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 5, p. N.PAG, doi. 10.1002/mgg3.587

By:

Cini, Giulia;
Quaia, Michele;
Canzonieri, Vincenzo;
Fornasarig, Mara;
Maestro, Roberta;
Morabito, Alberto;
D'Elia, Angela Valentina;
Urso, Emanuele Damiano;
Mammi, Isabella;
Viel, Alessandra

Publication type:

Article

Impact of colonoscopic screening in Familial Colorectal Cancer Type X.

Published in:

Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 6, p. 1021, doi. 10.1002/mgg3.478

By:

Hatfield, Elizabeth;
Green, Jane S.;
Woods, Michael O.;
Warden, Geoff;
Parfrey, Patrick S.

Publication type:

Article

HLA‐DQβ1 amino acid position 87 and DQB1*0301 are associated with Chinese Han SLE.

Published in:

Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 4, p. 541, doi. 10.1002/mgg3.403

By:

Sun, Jingying;
Yang, Chao;
Fei, Wenmin;
Zhang, Xuelei;
Sheng, Yujun;
Zheng, Xiaodong;
Tang, Huayang;
Yang, Wanling;
Yang, Sen;
Fan, Xing;
Zhang, Xuejun

Publication type:

Article

Polymorphisms of DNA repair genes are associated with colorectal cancer in patients with Lynch syndrome.

Published in:

Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 4, p. 533, doi. 10.1002/mgg3.402

By:

Kamiza, Abram B.;
Hsieh, Ling‐Ling;
Tang, Reiping;
Chien, Huei‐Tzu;
Lai, Chih‐Hsiung;
Chiu, Li‐Ling;
Lo, Tsai‐Ping;
Hung, Kuan‐Yi;
You, Jeng‐Fu;
Wang, Wen‐Chang;
Hsiung, Chao A.;
Yeh, Chih‐Ching

Publication type:

Article