Works matching DE "LYNCH syndrome II"
Results: 189
Mechanism of mismatch recognition revealed by human MutS? bound to unpaired DNA loops.
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- Nature Structural & Molecular Biology, 2012, v. 19, n. 1, p. 72, doi. 10.1038/nsmb.2175
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- Publication type:
- Article
Current Hypotheses on How Microsatellite Instability Leads to Enhanced Survival of Lynch Syndrome Patients.
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- Clinical & Developmental Immunology, 2010, p. 1, doi. 10.1155/2010/170432
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- Publication type:
- Article
Colorectal Adenocarcinoma: A Pediatric Case Review with a Focus on Mismatch Repair Gene Mutations and E-Cadherin Expression.
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- Pediatric & Developmental Pathology, 2012, v. 15, n. 3, p. 192, doi. 10.2350/11-04-1015-OA.1
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- Publication type:
- Article
Urothelkarzinom des oberen und unteren Harntrakts – welche Risikofaktoren machen Früherkennungsmaßnahmen sinnvoll?
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- Die Urologie, 2025, v. 64, n. 1, p. 4, doi. 10.1007/s00120-024-02479-0
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- Article
Metastatic Prostate Cancer: Effects of genetic testing on care.
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- Clinical Journal of Oncology Nursing, 2019, v. 23, n. 1, p. 32, doi. 10.1188/19.CJON.32-35
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- Article
Lynch syndrome: following the leads to save lives.
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- Journal of Community Nursing, 2023, v. 37, n. 2, p. 14
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- Article
A rare case of Crohn's ileitis in a patient with constitutional mismatch repair deficiency.
- Published in:
- 2017
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- Publication type:
- Case Study
Patient and tumor characteristics may raise clinicians' awareness of familial colorectal cancer: A Norwegian population-based study.
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- Scandinavian Journal of Gastroenterology, 2011, v. 46, n. 10, p. 1236, doi. 10.3109/00365521.2011.594086
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- Article
Who Should Have Genetic Testing for the Lynch Syndrome?
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- 2011
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- Publication type:
- Editorial
Strategies to Identify the Lynch Syndrome Among Patients With Colorectal Cancer.
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- Annals of Internal Medicine, 2011, v. 155, n. 2, p. 69, doi. 10.7326/0003-4819-155-2-201107190-00002
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- Publication type:
- Article
CoDP: predicting the impact of unclassified genetic variants in MSH6 by the combination of different properties of the protein.
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- Journal of Biomedical Science, 2013, v. 20, n. 1, p. 1, doi. 10.1186/1423-0127-20-25
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- Article
Distinct gene expression signatures in Lynch syndrome and familial colorectal cancer type X.
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- BMC Proceedings, 2013, v. 7, n. Suppl 2, p. 1, doi. 10.1186/1753-6561-7-S2-P52
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- Publication type:
- Article
Evaluation of a new panel of six mononucleotide repeat markers for the detection of DNA mismatch repair-deficient tumours.
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- British Journal of Cancer, 2013, v. 108, n. 10, p. 2079, doi. 10.1038/bjc.2013.213
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- Publication type:
- Article
Performance of clinical guidelines compared with molecular tumour screening methods in identifying possible Lynch syndrome among colorectal cancer patients: a Norwegian population-based study.
- Published in:
- 2010
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- Publication type:
- journal article
Systematic review of the impact of registration and screening on colorectal cancer incidence and mortality in familial adenomatous polyposis and Lynch syndrome.
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- British Journal of Surgery, 2013, v. 100, n. 13, p. 1719, doi. 10.1002/bjs.9316
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- Publication type:
- Article
Transanal endoscopic microsurgery approach for rectal stump resection as an alternative to transperitoneal stump resection.
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- British Journal of Surgery, 2013, v. 100, n. 4, p. 568, doi. 10.1002/bjs.9005
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- Publication type:
- Article
Select Biomarkers for Tumors of the Gastrointestinal Tract.
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- Archives of Pathology & Laboratory Medicine, 2015, v. 139, n. 4, p. 457, doi. 10.5858/arpa.2014-0189-RA
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- Article
BRAF Mutation Testing in Colorectal Cancer.
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- Archives of Pathology & Laboratory Medicine, 2010, v. 134, n. 8, p. 1225, doi. 10.5858/2009-0232-rs.1
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- Article
Cáncer sincrónico: neoplasias ginecológicas concurrentes de cuello, ovario y trompa. Caso clínico.
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- Revista Chilena de Obstetricia y Ginecología, 2011, v. 76, n. 6, p. 417, doi. 10.4067/S0717-75262011000600008
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- Article
Making a Difference in the Lives of Lynch Syndrome Patients.
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- Journal of Gynecologic Oncology Nursing, 2015, v. 24, n. 2, p. 21
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- Publication type:
- Article
Clinical significance of microsatellite instability in colorectal cancer.
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- Langenbeck's Archives of Surgery, 2014, v. 399, n. 1, p. 23, doi. 10.1007/s00423-013-1112-3
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- Publication type:
- Article
Lynch syndrome: clinical, pathological, and genetic insights.
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- Langenbeck's Archives of Surgery, 2012, v. 397, n. 4, p. 513, doi. 10.1007/s00423-012-0918-8
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- Publication type:
- Article
Annual outpatient hysteroscopy and endometrial sampling (OHES) in HNPCC/Lynch syndrome (LS).
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- Archives of Gynecology & Obstetrics, 2012, v. 286, n. 6, p. 1555, doi. 10.1007/s00404-012-2492-2
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- Publication type:
- Article
Lesions of the Lower Uterine Segment.
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- Journal of Gynecologic Surgery, 2016, v. 32, n. 1, p. 1, doi. 10.1089/gyn.2015.0071
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- Publication type:
- Article
Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.
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- BMC Medical Genomics, 2013, v. 6, n. 1, p. 1, doi. 10.1186/1755-8794-6-10
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- Publication type:
- Article
Mismatch Repair Deficiency Screening via Immunohistochemical Staining in Young Asians with Colorectal Cancers.
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- World Journal of Surgery, 2013, v. 37, n. 10, p. 2468, doi. 10.1007/s00268-013-2134-2
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- Publication type:
- Article
Clinical, dermoscopic and reflectance confocal microscopy features of sebaceous neoplasms in Muir-Torre syndrome.
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- Journal of the European Academy of Dermatology & Venereology, 2013, v. 27, n. 6, p. 699, doi. 10.1111/j.1468-3083.2012.04539.x
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- Publication type:
- Article
Risk of gynecologic cancers in Danish hereditary non-polyposis colorectal cancer families.
- Published in:
- 2008
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- Publication type:
- journal article
Risks of Colorectal and Other Cancers After Endometrial Cancer for Women With Lynch Syndrome.
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- JNCI: Journal of the National Cancer Institute, 2013, v. 105, n. 4, p. 274, doi. 10.1093/jnci/djs525
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- Publication type:
- Article
Cancer Risks After Endometrial Cancer in Mismatch Repair Mutation Carriers.
- Published in:
- 2013
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- Publication type:
- Editorial
PDQ (Physician Data Query).
- Published in:
- JNCI: Journal of the National Cancer Institute, 2013, v. 105, n. 3, p. 156, doi. 10.1093/jnci/djt012
- Publication type:
- Article
PDQ (Physician Data Query).
- Published in:
- JNCI: Journal of the National Cancer Institute, 2012, v. 104, n. 23, p. 1777, doi. 10.1093/jnci/djs497
- Publication type:
- Article
Risks of Primary Extracolonic Cancers Following Colorectal Cancer in Lynch Syndrome.
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- JNCI: Journal of the National Cancer Institute, 2012, v. 104, n. 18, p. 1363, doi. 10.1093/jnci/djs351
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- Publication type:
- Article
Lynch Syndrome in Patients With Colorectal Cancer.
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- 2012
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- Publication type:
- Editorial
Identification of Lynch Syndrome Among Patients With Colorectal Cancer.
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- JAMA: Journal of the American Medical Association, 2012, v. 308, n. 15, p. 1555, doi. 10.1001/jama.2012.13088
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- Publication type:
- Article
Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch Syndrome.
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- JAMA: Journal of the American Medical Association, 2011, v. 305, n. 22, p. 2304, doi. 10.1001/jama.2011.743
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- Publication type:
- Article
Epigenetic mechanisms in the pathogenesis of Lynch syndrome.
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- Clinical Genetics, 2014, v. 85, n. 5, p. 403, doi. 10.1111/cge.12349
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- Publication type:
- Article
Dawning of the epigenetic era in hereditary cancer.
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- Clinical Genetics, 2014, v. 85, n. 5, p. 413, doi. 10.1111/cge.12369
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- Publication type:
- Article
A population-based study of hereditary non-polyposis colorectal cancer: evidence of pathologic and genetic heterogeneity.
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- Clinical Genetics, 2013, v. 84, n. 6, p. 522, doi. 10.1111/cge.12080
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- Publication type:
- Article
The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families.
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- Clinical Genetics, 2013, v. 84, n. 3, p. 244, doi. 10.1111/cge.12062
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- Publication type:
- Article
First successful double-factor PGD for Lynch syndrome: monogenic analysis and comprehensive aneuploidy screening.
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- Clinical Genetics, 2013, v. 84, n. 1, p. 70, doi. 10.1111/cge.12025
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- Publication type:
- Article
Absence of PMS2 mutations in colon- CFR participants whose colorectal cancers demonstrate unexplained loss of MLH1 expression.
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- Clinical Genetics, 2013, v. 83, n. 6, p. 591, doi. 10.1111/cge.12011
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- Publication type:
- Article
Impact of gynecological screening in Lynch syndrome carriers with an MSH2 mutation.
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- Clinical Genetics, 2013, v. 83, n. 4, p. 359, doi. 10.1111/j.1399-0004.2012.01929.x
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- Publication type:
- Article
Changes in screening behaviors and attitudes toward screening from pre-test genetic counseling to post-disclosure in Lynch syndrome families.
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- Clinical Genetics, 2013, v. 83, n. 3, p. 215, doi. 10.1111/cge.12091
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- Publication type:
- Article
Recurrent and founder mutations in the PMS2 gene.
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- Clinical Genetics, 2013, v. 83, n. 3, p. 238, doi. 10.1111/j.1399-0004.2012.01898.x
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- Publication type:
- Article
Impact of colonoscopic screening in male and female Lynch syndrome carriers with an MSH2 mutation.
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- Clinical Genetics, 2012, v. 82, n. 5, p. 439, doi. 10.1111/j.1399-0004.2011.01802.x
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- Publication type:
- Article
Colon-specific phenotype in Lynch syndrome associated with EPCAM deletion.
- Published in:
- Clinical Genetics, 2012, v. 82, n. 1, p. 97, doi. 10.1111/j.1399-0004.2011.01826.x
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- Publication type:
- Article
The MLH1 c.-27C>A and c.85G>T variants are linked to dominantly inherited MLH1 epimutation and are borne on a European ancestral haplotype.
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- European Journal of Human Genetics, 2014, v. 22, n. 5, p. 617, doi. 10.1038/ejhg.2013.200
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- Publication type:
- Article
Genetic variant in the telomerase gene modifies cancer risk in Lynch syndrome.
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- European Journal of Human Genetics, 2013, v. 21, n. 5, p. 511, doi. 10.1038/ejhg.2012.204
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- Publication type:
- Article
A unique MSH2 exon 8 deletion accounts for a major portion of all mismatch repair gene mutations in Lynch syndrome families of Sardinian origin.
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- European Journal of Human Genetics, 2013, v. 21, n. 2, p. 154, doi. 10.1038/ejhg.2012.150
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- Publication type:
- Article