Found: 38
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Mucin gene expression in intraductal papillary-mucinous pancreatic tumours and related lesions.
- Published in:
- Journal of Pathology, 2002, v. 197, n. 5, p. 632, doi. 10.1002/path.1146
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- Publication type:
- Article
Mucin gene transcripts in benign and borderline mucinous tumours of the ovary: an in situ hybridization study.
- Published in:
- Journal of Pathology, 2001, v. 193, n. 3, p. 339, doi. 10.1002/1096-9896(2000)9999:9999<::AID-PATH798>3.0.CO;2-9
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- Publication type:
- Article
The MUC6 secretory mucin gene is expressed in a wide variety of epithelial tissues.
- Published in:
- Journal of Pathology, 1998, v. 186, n. 4, p. 398, doi. 10.1002/(SICI)1096-9896(199812)186:4<398::AID-PATH192>3.0.CO;2-X
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- Publication type:
- Article
Diagnostic value of MUC4 immunostaining in distinguishing epithelial mesothelioma and lung adenocarcinoma.
- Published in:
- Modern Pathology, 2004, v. 17, n. 2, p. 150, doi. 10.1038/modpathol.3800027
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- Publication type:
- Article
MSH2 c.1022T>C, p.Leu341Pro is a founder pathogenic variation and a major cause of Lynch syndrome in the North of France.
- Published in:
- Genes, Chromosomes & Cancer, 2020, v. 59, n. 2, p. 111, doi. 10.1002/gcc.22804
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- Publication type:
- Article
Diagnosis of Lynch Syndrome and Strategies to Distinguish Lynch-Related Tumors from Sporadic MSI/dMMR Tumors.
- Published in:
- Cancers, 2021, v. 13, n. 3, p. 467, doi. 10.3390/cancers13030467
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- Publication type:
- Article
UMD-MLH1/MSH2/MSH6 databases: description and analysis of genetic variations in French Lynch syndrome families.
- Published in:
- Database: The Journal of Biological Databases & Curation, 2013, v. 2013, p. 1, doi. 10.1093/database/bat036
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- Publication type:
- Article
Reply to Talseth-Palmer et al.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 5, p. 488, doi. 10.1038/ejhg.2011.235
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- Publication type:
- Article
Contribution of bioinformatics predictions and functional splicing assays to the interpretation of unclassified variants of the BRCA genes.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 10, p. 1052, doi. 10.1038/ejhg.2011.100
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- Publication type:
- Article
Evaluation of Lynch syndrome modifier genes in 748 MMR mutation carriers.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 887, doi. 10.1038/ejhg.2011.44
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- Publication type:
- Article
Partial duplications of the MSH2 and MLH1 genes in hereditary nonpolyposis colorectal cancer.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 383, doi. 10.1038/sj.ejhg.5201765
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- Publication type:
- Article
Trefoil Factor Family 3 Peptide Promotes Human Airway Epithelial Ciliated Cell Differentiation.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2007, v. 36, n. 3, p. 296, doi. 10.1165/rcmb.2006-0270OC
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- Publication type:
- Article
TP53 mutations in colorectal cancer from Tunisia: relationships with site of tumor origin, microsatellite instability and KRAS mutations.
- Published in:
- Molecular Biology Reports, 2014, v. 41, n. 3, p. 1807, doi. 10.1007/s11033-014-3030-z
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- Publication type:
- Article
KRAS mutations in colorectal cancer from Tunisia: relationships with clinicopathologic variables and data on TP53 mutations and microsatellite instability.
- Published in:
- Molecular Biology Reports, 2013, v. 40, n. 11, p. 6107, doi. 10.1007/s11033-013-2722-0
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- Publication type:
- Article
Lynch syndrome in Tunisia: first description of clinical features and germline mutations.
- Published in:
- International Journal of Colorectal Disease, 2011, v. 26, n. 4, p. 455, doi. 10.1007/s00384-010-1129-9
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- Publication type:
- Article
Mucin gene expression and cell differentiation in human normal, premalignant and malignant esophagus.
- Published in:
- International Journal of Cancer, 2000, v. 88, n. 6, p. 856, doi. 10.1002/1097-0215(20001215)88:6<856::AID-IJC3>3.0.CO;2-D
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- Publication type:
- Article
From normal respiratory mucosa to epidermoid carcinoma: Expression of human mucin genes.
- Published in:
- International Journal of Cancer, 2000, v. 86, n. 2, p. 162, doi. 10.1002/(SICI)1097-0215(20000415)86:2<162::AID-IJC3>3.0.CO;2-R
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- Publication type:
- Article
Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic Consortium.
- Published in:
- Clinical Genetics, 2021, v. 99, n. 5, p. 662, doi. 10.1111/cge.13925
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- Publication type:
- Article
The Complex Intratumoral Heterogeneity of Colon Cancer Highlighted by Laser Microdissection.
- Published in:
- Digestive Diseases & Sciences, 2012, v. 57, n. 5, p. 1271, doi. 10.1007/s10620-011-2023-1
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- Publication type:
- Article
Mucin gene expression in the human endocervix.
- Published in:
- 1995
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- Publication type:
- journal article
The serrated neoplasia pathway of colorectal tumors: Identification of MUC5AC hypomethylation as an early marker of polyps with malignant potential.
- Published in:
- International Journal of Cancer, 2016, v. 138, n. 6, p. 1472, doi. 10.1002/ijc.29891
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- Publication type:
- Article
MUC5 AC hypomethylation is a predictor of microsatellite instability independently of clinical factors associated with colorectal cancer.
- Published in:
- International Journal of Cancer, 2015, v. 136, n. 12, p. 2811, doi. 10.1002/ijc.29342
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- Publication type:
- Article
Identification and management of Lynch syndrome in the Middle East and North African countries: outcome of a survey in 12 countries.
- Published in:
- Familial Cancer, 2021, v. 20, n. 3, p. 215, doi. 10.1007/s10689-020-00211-3
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- Publication type:
- Article
Is the controversy on breast cancer as part of the Lynch-related tumor spectrum still open?
- Published in:
- 2012
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- Publication type:
- Letter
French experts report on MUTYH-associated polyposis (MAP).
- Published in:
- Familial Cancer, 2012, v. 11, n. 3, p. 321, doi. 10.1007/s10689-012-9511-0
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- Publication type:
- Article
Identification and characterization of a novel MLH1 genomic rearrangement as the cause of HNPCC in a Tunisian family: evidence for a homologous Alu-mediated recombination.
- Published in:
- Familial Cancer, 2009, v. 8, n. 2, p. 119, doi. 10.1007/s10689-008-9215-7
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- Publication type:
- Article
Familial adenomatous polyposis associated craniopharyngioma secondary to both germline and somatic mutations in the APC gene.
- Published in:
- Acta Neuropathologica, 2020, v. 140, n. 6, p. 967, doi. 10.1007/s00401-020-02232-9
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- Publication type:
- Article
Age-Dependent Cancer Risk Is Not Different in between MSH2 and MLH1 Mutation Carriers.
- Published in:
- Journal of Cancer Epidemiology, 2009, p. 1, doi. 10.1155/2009/791754
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- Publication type:
- Article
La polypose associée à MUTYH : synthèse des données disponibles en 2020 et actualisation des recommandations françaises établies en 2012 sous l'égide de l'Institut National du Cancer (INCa).
- Published in:
- Hépato-Gastro & Oncologie Digestive, 2020, v. 27, n. 4, p. 396, doi. 10.1684/hpg.2020.1944
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- Publication type:
- Article
DiNAMO: highly sensitive DNA motif discovery in high-throughput sequencing data.
- Published in:
- BMC Bioinformatics, 2018, v. 19, n. 1, p. 1, doi. 10.1186/s12859-018-2215-1
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- Publication type:
- Article
Identification of mobile retrocopies during genetic testing: Consequences for routine diagnosis.
- Published in:
- Human Mutation, 2019, v. 40, n. 11, p. 1993, doi. 10.1002/humu.23845
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- Publication type:
- Article
The UMD- APC Database, a Model of Nation-Wide Knowledge Base: Update with Data from 3,581 Variations.
- Published in:
- Human Mutation, 2014, v. 35, n. 5, p. 532, doi. 10.1002/humu.22539
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- Publication type:
- Article
Evidence of constitutional MLH1 epimutation associated to transgenerational inheritance of cancer susceptibility.
- Published in:
- Human Mutation, 2012, v. 33, n. 1, p. 180, doi. 10.1002/humu.21617
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- Publication type:
- Article
Leiden open variation database of the MUTYH gene.
- Published in:
- 2010
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- Publication type:
- Other
A large fraction of unclassified variants of the mismatch repair genes MLH1 and MSH2 is associated with splicing defects.
- Published in:
- Human Mutation, 2008, v. 29, n. 12, p. 1412, doi. 10.1002/humu.20796
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- Publication type:
- Article
Low frequency of AXIN2 mutations and high frequency of MUTYH mutations in patients with multiple polyposis.
- Published in:
- Human Mutation, 2006, v. 27, n. 10, p. 1064, doi. 10.1002/humu.9460
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- Publication type:
- Article
The 5′ region of the MSH2 gene involved in hereditary non-polyposis colorectal cancer contains a high density of recombinogenic sequences.
- Published in:
- Human Mutation, 2005, v. 26, n. 3, p. 255, doi. 10.1002/humu.20216
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- Publication type:
- Article
Analysis of the allele-specific expression of the mismatch repair gene MLH1 using a simple DHPLC-Based Method.
- Published in:
- Human Mutation, 2004, v. 23, n. 4, p. 379, doi. 10.1002/humu.20008
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- Publication type:
- Article