| 1 |
32782434 |
10.1186/s12935-020-01457-8 |
2022 |
Evaluation of the upregulation and surface expression of hypoxanthine guanine phosphoribosyltransferase in acute lymphoblastic leukemia and Burkitt's B cell lymphoma. |
MSH6 |
| 2 |
33811277 |
10.1007/s10689-021-00244-2 |
2022 |
Constitutional 2p16.3 deletion including MSH6 and FBXO11 in a boy with developmental delay and diffuse large B-cell lymphoma. |
MSH6 |
| 3 |
33928678 |
10.1111/den.14004 |
2022 |
Clinicopathological features and risk factors for developing colorectal neoplasia in Hodgkin's lymphoma survivors. |
MSH6 |
| 4 |
34538134 |
10.1177/03009858211022704 |
2022 |
Mismatch repair deficiency in canine neoplasms. |
MSH6 |
| 5 |
34787334 |
10.1111/pde.14861 |
2022 |
Eruptive nevi in a patient with constitutional mismatch repair deficiency (CMMRD). |
MSH6 |
| 6 |
35227120 |
10.1177/10935266221075605 |
2022 |
Diffuse Large B-Cell Lymphoma, Epstein-Barr Virus -Positive Kappa Monotypic Plasma Cell Proliferation and Invasive Carcinoma, Developing in a Child With Defective Mismatch Repair. |
MSH6 |
| 7 |
35359413 |
10.3389/fonc.2022.817635 |
2022 |
Analysis of Genetic Alterations in Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma With Whole-Exome Sequencing. |
MSH6 |
| 8 |
35812033 |
10.1136/flgastro-2022-102123 |
2022 |
Diagnosis and management of Lynch syndrome. |
MSH6 |
| 9 |
36097110 |
10.1007/s11033-022-07761-y |
2022 |
Looking beyond the cytogenetics in haematological malignancies: decoding the role of tandem repeats in DNA repair genes. |
MSH6 |
| 10 |
32022486 |
10.1002/cam4.2870 |
2021 |
Microsatellite instability and its associations with the clinicopathologic characteristics of diffuse large B-cell lymphoma. |
MSH6 |
| 11 |
32866816 |
10.1016/j.jns.2020.117102 |
2021 |
Preconditioning with INC280 and LDK378 drugs sensitizes MGMT-unmethylated glioblastoma to temozolomide: Pre-clinical assessment. |
MSH6 |
| 12 |
34086170 |
10.1007/s10549-021-06258-9 |
2021 |
Double heterozygotes of BRCA1/BRCA2 and mismatch repair gene pathogenic variants: case series and clinical implications. |
MSH6 |
| 13 |
34425783 |
10.1186/s12876-021-01902-6 |
2021 |
Intensive surveillance endoscopy for multiple gastrointestinal tumors in a patient with constitutional mismatch repair deficiency: case report. |
MSH6 |
| 14 |
30147880 |
10.1002/ccr3.1564 |
2020 |
Rare compound heterozygous mutations in gene <i>MSH6</i> cause constitutive mismatch repair deficiency syndrome. |
MSH6 |
| 15 |
30456894 |
10.1002/jcp.27620 |
2020 |
Inhibitory effect of MSH6 gene silencing in combination with cisplatin on cell proliferation of human osteosarcoma cell line MG63. |
MSH6 |
| 16 |
31697823 |
10.1182/blood.2019002220 |
2020 |
Therapy-induced mutations drive the genomic landscape of relapsed acute lymphoblastic leukemia. |
MSH6 |
| 17 |
33143351 |
10.3390/pathogens9110909 |
2020 |
Bovine Leukemia Virus Infection Affects Host Gene Expression Associated with DNA Mismatch Repair. |
MSH6 |
| 18 |
29449434 |
10.3324/haematol.2017.176362 |
2019 |
MSH6 haploinsufficiency at relapse contributes to the development of thiopurine resistance in pediatric B-lymphoblastic leukemia. |
MSH6 |
| 19 |
29904176 |
10.1038/s41431-018-0197-0 |
2019 |
Cancer prevention by aspirin in children with Constitutional Mismatch Repair Deficiency (CMMRD). |
MSH6 |
| 20 |
30551794 |
10.1016/j.bulcan.2018.10.008 |
2019 |
[Constitutional MMR deficiency: Genetic bases and clinical implications]. |
MSH6 |
| 21 |
30734108 |
10.1007/s00428-019-02528-6 |
2019 |
Comprehensive analysis of PD-L1 expression, HER2 amplification, ALK/EML4 fusion, and mismatch repair deficiency as putative predictive and prognostic factors in ovarian carcinoma. |
MSH6 |
| 22 |
28142295 |
10.1080/10428194.2017.1283029 |
2018 |
Identification of a tumor suppressor network in T-cell leukemia. |
MSH6 |
| 23 |
28465297 |
10.1158/1541-7786.MCR-16-0305 |
2018 |
Comprehensive Transcriptome and Mutational Profiling of Endemic Burkitt Lymphoma Reveals EBV Type-Specific Differences. |
MSH6 |
| 24 |
28728506 |
10.1080/10245332.2017.1354428 |
2018 |
Microsatellite Instability and Promoter Hypermethylation of DNA repair genes in Hematologic Malignancies: a forthcoming direction toward diagnostics. |
MSH6 |
| 25 |
28923119 |
10.1186/s13000-017-0645-0 |
2018 |
ALK-positive gastric inflammatory myofibroblastic tumor in an adult with familial adenomatous polyposis and diffuse fundic polyposis. |
MSH6 |
| 26 |
29439113 |
10.1136/gutjnl-2016-312608 |
2018 |
Double somatic mutations in mismatch repair genes are frequent in colorectal cancer after Hodgkin's lymphoma treatment. |
MSH6 |
| 27 |
27017609 |
10.1007/s10689-016-9894-4 |
2017 |
MSI detection and its pitfalls in CMMRD syndrome in a family with a bi-allelic MLH1 mutation. |
MSH6 |
| 28 |
28157215 |
10.1038/bcj.2017.3 |
2017 |
Identification of a genetically defined ultra-high-risk group in relapsed pediatric T-lymphoblastic leukemia. |
MSH6 |
| 29 |
28562508 |
10.1097/MPH.0000000000000863 |
2017 |
Biallelic PMS2 Mutation and Heterozygous DICER1 Mutation Presenting as Constitutional Mismatch Repair Deficiency With Corpus Callosum Agenesis: Case Report and Review of Literature. |
MSH6 |
| 30 |
28981733 |
10.1093/jjco/hyx098 |
2017 |
Prognostic factors for primary central nervous system lymphomas treated with high-dose methotrexate-based chemo-radiotherapy. |
MSH6 |
| 31 |
25978431 |
10.1038/bcj.2015.35 |
2016 |
NPM-ALK mediates phosphorylation of MSH2 at tyrosine 238, creating a functional deficiency in MSH2 and the loss of mismatch repair. |
MSH6 |
| 32 |
26004186 |
10.1016/j.celrep.2015.04.052 |
2016 |
The CREB Coactivator CRTC2 Is a Lymphoma Tumor Suppressor that Preserves Genome Integrity through Transcription of DNA Mismatch Repair Genes. |
MSH6 |
| 33 |
26318770 |
10.1136/jmedgenet-2015-103299 |
2016 |
Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort. |
MSH6 |
| 34 |
26498208 |
10.1016/j.mrfmmm.2015.10.001 |
2016 |
Microsatellite instability detected in tumor-related genes in C57BL/6J mice with thymic lymphoma induced by N-methyl-N-nitrosourea. |
MSH6 |
| 35 |
26544533 |
10.1002/pbc.25818 |
2016 |
Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity. |
MSH6 |
| 36 |
26558945 |
10.1615/critreveukaryotgeneexpr.2015013893 |
2016 |
Genes Associated with Human Cancers: Their Expressions, Features, Functions, and Significance. |
MSH6 |
| 37 |
26599546 |
10.1371/journal.pone.0139663 |
2016 |
Genomic Landscape of Primary Mediastinal B-Cell Lymphoma Cell Lines. |
MSH6 |
| 38 |
26743104 |
10.1016/j.ejmg.2015.12.014 |
2016 |
Acute lymphoblastic leukemia and lymphoma in the context of constitutional mismatch repair deficiency syndrome. |
MSH6 |
| 39 |
24068316 |
10.1007/s10689-013-9676-1 |
2015 |
Diversity of the clinical presentation of the MMR gene biallelic mutations. |
MSH6 |
| 40 |
24662245 |
10.1038/ncomms4469 |
2015 |
Mutations in epigenetic regulators including SETD2 are gained during relapse in paediatric acute lymphoblastic leukaemia. |
MSH6 |
| 41 |
25431869 |
10.1055/s-0034-1389905 |
2015 |
Constitutional mismatch repair-deficiency and whole-exome sequencing as the means of the rapid detection of the causative MSH6 defect. |
MSH6 |
| 42 |
22916837 |
10.3109/10428194.2012.723211 |
2013 |
Analysis of microsatellite instability in gastric mucosa-associated lymphoid tissue lymphoma. |
MSH6 |
| 43 |
23066952 |
10.3109/10428194.2012.739687 |
2013 |
Mutation mismatch repair gene deletions in diffuse large B-cell lymphoma. |
MSH6 |
| 44 |
23960188 |
10.1084/jem.20122842 |
2013 |
DNA repair genes are selectively mutated in diffuse large B cell lymphomas. |
MSH6 |
| 45 |
21674763 |
10.1002/pbc.23217 |
2012 |
High-grade brain tumors in siblings with biallelic MSH6 mutations. |
MSH6 |
| 46 |
22000951 |
10.1016/j.jcpa.2011.08.009 |
2012 |
Widespread mismatch repair expression in feline small intestinal lymphomas. |
MSH6 |
| 47 |
22083360 |
10.3791/3573 |
2012 |
Assessing somatic hypermutation in Ramos B cells after overexpression or knockdown of specific genes. |
MSH6 |
| 48 |
22493294 |
10.1182/blood-2011-10-386862 |
2012 |
Phenotype diversity in type 1 Gaucher disease: discovering the genetic basis of Gaucher disease/hematologic malignancy phenotype by individual genome analysis. |
MSH6 |
| 49 |
22920205 |
|
2012 |
[Constitutional mismatch repair-deficiency syndrome (CMMR-D) - a case report of a family with biallelic MSH6 mutation]. |
MSH6 |
| 50 |
20015892 |
10.3324/haematol.2009.015503 |
2011 |
Constitutional mismatch repair deficiency and childhood leukemia/lymphoma--report on a novel biallelic MSH6 mutation. |
MSH6 |
| 51 |
20846793 |
10.1016/j.prp.2010.07.007 |
2011 |
Concomitant adenocarcinoma and colonic non-Hodgkin's lymphoma in a patient with ulcerative colitis: a case report and molecular analysis. |
MSH6 |
| 52 |
20934970 |
10.2353/ajpath.2010.100234 |
2011 |
Msh6 protects mature B cells from lymphoma by preserving genomic stability. |
MSH6 |
| 53 |
21703420 |
10.1016/j.ajpath.2011.03.045 |
2011 |
Fusion tyrosine kinase NPM-ALK Deregulates MSH2 and suppresses DNA mismatch repair function novel insights into a potent oncoprotein. |
MSH6 |
| 54 |
22164924 |
|
2011 |
[Management of hereditary non-polyposis syndrome (Lynch syndrome)]. |
MSH6 |
| 55 |
20305618 |
10.1038/modpathol.2010.41 |
2010 |
Endometrial and ovarian carcinomas with undifferentiated components: clinically aggressive and frequently underrecognized neoplasms. |
MSH6 |
| 56 |
20567595 |
10.1371/journal.pone.0011182 |
2010 |
MSH2/MSH6 complex promotes error-free repair of AID-induced dU:G mispairs as well as error-prone hypermutation of A:T sites. |
MSH6 |
| 57 |
19194194 |
10.1097/MPH.0b013e31818b3774 |
2009 |
Compound heterozygosity for MSH6 mutations in a pediatric lymphoma patient. |
MSH6 |
| 58 |
19551857 |
10.1002/ijc.24681 |
2009 |
The mechanisms underlying MMR deficiency in immunodeficiency-related non-Hodgkin lymphomas are different from those in other sporadic microsatellite instable neoplasms. |
MSH6 |
| 59 |
17601929 |
10.1136/jmg.2007.048942 |
2008 |
Familial T-cell non-Hodgkin lymphoma caused by biallelic MSH2 mutations. |
MSH6 |
| 60 |
17851451 |
10.1038/sj.ejhg.5201923 |
2008 |
Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1. |
MSH6 |
| 61 |
18593904 |
10.1158/0008-5472.CAN-08-0019 |
2008 |
Zebrafish with mutations in mismatch repair genes develop neurofibromas and other tumors. |
MSH6 |
| 62 |
18768390 |
10.1182/blood-2008-06-165027 |
2008 |
Genome-wide copy number profiling reveals molecular evolution from diagnosis to relapse in childhood acute lymphoblastic leukemia. |
MSH6 |
| 63 |
17240451 |
10.1016/j.molimm.2006.12.006 |
2007 |
Known components of the immunoglobulin A:T mutational machinery are intact in Burkitt lymphoma cell lines with G:C bias. |
MSH6 |
| 64 |
17440981 |
10.1002/cncr.22697 |
2007 |
Biallelic germline mutations of mismatch-repair genes: a possible cause for multiple pediatric malignancies. |
MSH6 |
| 65 |
16283678 |
10.1002/ajmg.a.30998 |
2006 |
Neurofibromatosis von Recklinghausen type I phenotype and early onset of cancers in siblings compound heterozygous for mutations in MSH6. |
MSH6 |
| 66 |
15805259 |
10.1158/0008-5472.CAN-04-3158 |
2005 |
A lack of DNA mismatch repair on an athymic murine background predisposes to hematologic malignancy. |
MSH6 |
| 67 |
16000562 |
10.1158/1078-0432.CCR-04-2025 |
2005 |
A homozygous mutation in MSH6 causes Turcot syndrome. |
MSH6 |
| 68 |
14762794 |
10.1053/j.gastro.2003.11.008 |
2004 |
Gastrointestinal cancers and neurofibromatosis type 1 features in children with a germline homozygous MLH1 mutation. |
MSH6 |
| 69 |
12400605 |
10.1080/1042819021000002956 |
2003 |
Analysis of mismatch repair defects in the familial occurrence of lymphoma and colorectal cancer. |
MSH6 |
| 70 |
12538346 |
10.1093/carcin/24.1.31 |
2003 |
Assessment of mismatch repair function in leukaemic cell lines and blasts from children with acute lymphoblastic leukaemia. |
MSH6 |
| 71 |
10498615 |
|
1999 |
Mutator phenotype in human hematopoietic neoplasms and its association with deletions disabling DNA repair genes and bcl-2 rearrangements. |
MSH6 |
| 72 |
10500837 |
10.1007/978-1-4615-4811-9_64 |
1999 |
Expression of DNA mismatch repair proteins in acute lymphoblastic leukaemia and normal bone marrow. |
MSH6 |
| 73 |
10545954 |
10.1038/15544 |
1999 |
HNPCC-like cancer predisposition in mice through simultaneous loss of Msh3 and Msh6 mismatch-repair protein functions. |
MSH6 |
| 74 |
9510473 |
10.1111/j.1349-7006.1998.tb00476.x |
1998 |
Frameshift mutations of the hMSH6 gene in human leukemia cell lines. |
MSH6 |
| 75 |
9390556 |
10.1016/s0092-8674(00)80433-x |
1997 |
Mutation in the mismatch repair gene Msh6 causes cancer susceptibility. |
MSH6 |
Datasets
Models
