Detalhe da pesquisa
1.
Clinical and Pathological Characterization of Lynch-Like Syndrome.
Clin Gastroenterol Hepatol
; 18(2): 368-374.e1, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31220642
2.
Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (FamCan-NGS).
Hered Cancer Clin Pract
; 17: 3, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30675318
3.
The heritability and patterns of DNA methylation in normal human colorectum.
Hum Mol Genet
; 25(12): 2600-2611, 2016 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26936820
4.
Primary constitutional MLH1 epimutations: a focal epigenetic event.
Br J Cancer
; 119(8): 978-987, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30283143
5.
Increased Risk of Colorectal Cancer in Patients With Multiple Serrated Polyps and Their First-Degree Relatives.
Gastroenterology
; 153(1): 106-112.e2, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28400194
6.
Characterization of a novel POLD1 missense founder mutation in a Spanish population.
J Gene Med
; 19(4)2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28306219
7.
New insights into POLE and POLD1 germline mutations in familial colorectal cancer and polyposis.
Hum Mol Genet
; 23(13): 3506-12, 2014 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24501277
8.
Prevalence of MLH1 constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancer.
J Med Genet
; 52(7): 498-502, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25908759
9.
HGUE-C-1 is an atypical and novel colon carcinoma cell line.
BMC Cancer
; 15: 240, 2015 Apr 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-25885658
10.
Risk of cancer in cases of suspected lynch syndrome without germline mutation.
Gastroenterology
; 144(5): 926-932.e1; quiz e13-4, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23354017
11.
Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndrome.
Orphanet J Rare Dis
; 19(1): 26, 2024 Jan 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38279137
12.
Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer.
Gut
; 61(6): 865-72, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21868491
13.
Lynch-like Syndrome: Potential Mechanisms and Management.
Cancers (Basel)
; 14(5)2022 Feb 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35267422
14.
Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome.
BMC Med Genet
; 12: 12, 2011 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-21247423
15.
Metagenomic analysis of formalin-fixed paraffin-embedded tumor and normal mucosa reveals differences in the microbiome of colorectal cancer patients.
Sci Rep
; 11(1): 391, 2021 01 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33432015
16.
Co-occurrence of germline pathogenic variants for different hereditary cancer syndromes in patients with Lynch syndrome.
Cancer Commun (Lond)
; 41(3): 218-228, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33630411
17.
Utility of p16 immunohistochemistry for the identification of Lynch syndrome.
Clin Cancer Res
; 15(9): 3156-62, 2009 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19383812
18.
Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome in Spain: Clinical and Genetic Characterization.
Cancers (Basel)
; 12(11)2020 Nov 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33167498
19.
Risk of Cancer in Family Members of Patients with Lynch-Like Syndrome.
Cancers (Basel)
; 12(8)2020 Aug 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32784934
20.
TGFB1 and TGFBR1 polymorphic variants in relationship to bladder cancer risk and prognosis.
Int J Cancer
; 124(3): 608-13, 2009 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19004027