Detalhe da pesquisa
1.
Aberrant protein expression and frequent allelic loss of MSH3 in colorectal cancer with low-level microsatellite instability.
Int J Colorectal Dis
; 27(7): 911-9, 2012 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-22249440
2.
TCF-3, 4 protein expression correlates with beta-catenin expression in MSS and MSI-H colorectal cancer from HNPCC patients but not in sporadic colorectal cancers.
Int J Colorectal Dis
; 25(8): 931-9, 2010 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-20532534
3.
Genomic rearrangements in MSH2, MLH1 or MSH6 are rare in HNPCC patients carrying point mutations.
Cancer Lett
; 248(1): 89-95, 2007 Apr 08.
Artigo
Inglês
| MEDLINE | ID: mdl-16837128
4.
Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without hematological malignancy and brain tumor.
Eur J Hum Genet
; 14(5): 561-6, 2006 May.
Artigo
Inglês
| MEDLINE | ID: mdl-16418736
5.
Absence of association between cyclin D1 (CCND1) G870A polymorphism and age of onset in hereditary nonpolyposis colorectal cancer.
Cancer Lett
; 236(2): 191-7, 2006 May 18.
Artigo
Inglês
| MEDLINE | ID: mdl-16832876
6.
Loss of MSH3 protein expression is frequent in MLH1-deficient colorectal cancer and is associated with disease progression.
Cancer Res
; 64(3): 864-70, 2004 Feb 01.
Artigo
Inglês
| MEDLINE | ID: mdl-14871813
7.
Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium.
J Clin Oncol
; 22(22): 4486-94, 2004 Nov 15.
Artigo
Inglês
| MEDLINE | ID: mdl-15483016
8.
Ten novel MSH2 and MLH1 germline mutations in families with HNPCC.
Hum Mutat
; 24(4): 351-2, 2004 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-15365996
9.
Identification of six novel MSH2 and MLH1 germline mutations in HNPCC.
Hum Mutat
; 21(4): 445-6, 2003 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-12655562
10.
Eight novel MSH6 germline mutations in patients with familial and nonfamilial colorectal cancer selected by loss of protein expression in tumor tissue.
Hum Mutat
; 23(3): 285, 2004 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-14974087
11.
Seven novel MLH1 and MSH2 germline mutations in hereditary nonpolyposis colorectal cancer.
Hum Mutat
; 19(1): 82, 2002 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-11754112
12.
Methylenetetrahydrofolate reductase polymorphisms and risk of sporadic and hereditary colorectal cancer with or without microsatellite instability.
Cancer Lett
; 191(2): 179-85, 2003 Mar 10.
Artigo
Inglês
| MEDLINE | ID: mdl-12618331
13.
A novel strumpellin mutation and potential pitfalls in the molecular diagnosis of hereditary spastic paraplegia type SPG8.
J Neurol Sci
; 347(1-2): 372-4, 2014 Dec 15.
Artigo
Inglês
| MEDLINE | ID: mdl-25454649
14.
A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression.
Eur J Med Genet
; 57(5): 207-11, 2014 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-24486772
15.
Microsatellite instability and loss of heterozygosity in squamous cell carcinoma of the head and neck.
Head Neck
; 30(8): 1105-13, 2008 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-18615731
16.
N-Acetyltransferase (NAT) 2 acetylator status and age of tumour onset in patients with sporadic and familial, microsatellite stable (MSS) colorectal cancer.
Int J Colorectal Dis
; 22(2): 137-43, 2007 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-16896994
17.
Occult endometrial cancer and decision making for prophylactic hysterectomy in hereditary nonpolyposis colorectal cancer patients.
Gynecol Oncol
; 102(2): 189-94, 2006 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-16476474
18.
Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer.
Int J Cancer
; 118(1): 115-22, 2006 Jan 01.
Artigo
Inglês
| MEDLINE | ID: mdl-16003745
19.
Molecular mechanisms associated with chromosomal and microsatellite instability in sporadic glioblastoma multiforme.
Oncology
; 66(5): 395-403, 2004.
Artigo
Inglês
| MEDLINE | ID: mdl-15331927
20.
Involvement of hMSH6 in the development of hereditary and sporadic colorectal cancer revealed by immunostaining is based on germline mutations, but rarely on somatic inactivation.
Int J Cancer
; 97(5): 643-8, 2002 Feb 10.
Artigo
Inglês
| MEDLINE | ID: mdl-11807791