Detalhe da pesquisa
1.
Individual-specific levels of CTGâ¢CAG somatic instability are shared across multiple tissues in myotonic dystrophy type 1.
Hum Mol Genet
; 32(4): 621-631, 2023 01 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-36099027
2.
Myotonic dystrophy type 1 (DM1) clinical subtypes and CTCF site methylation status flanking the CTG expansion are mutant allele length-dependent.
Hum Mol Genet
; 31(2): 262-274, 2021 12 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-34432028
3.
Longitudinal increases in somatic mosaicism of the expanded CTG repeat in myotonic dystrophy type 1 are associated with variation in age-at-onset.
Hum Mol Genet
; 29(15): 2496-2507, 2020 08 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-32601694
4.
Reliable Route Selection for Wireless Sensor Networks with Connection Failure Uncertainties.
Sensors (Basel)
; 21(21)2021 Oct 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-34770561
5.
Multi-omics Analysis Reveals Immune Features Associated with Immunotherapy Benefit in Patients with Squamous Cell Lung Cancer from Phase III Lung-MAP S1400I Trial.
Clin Cancer Res
; 30(8): 1655-1668, 2024 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38277235
6.
Sex-specific effect of the TP53 PIN3 polymorphism on cancer risk in a cohort study of TP53 germline mutation carriers.
Hum Genet
; 130(6): 789-94, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21688173
7.
Joint effects of germ-line TP53 mutation, MDM2 SNP309, and gender on cancer risk in family studies of Li-Fraumeni syndrome.
Hum Genet
; 129(6): 663-73, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21305319
8.
Development and Validation of a Gene Signature Classifier for Consensus Molecular Subtyping of Colorectal Carcinoma in a CLIA-Certified Setting.
Clin Cancer Res
; 27(1): 120-130, 2021 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33109741
9.
Immune evolution from preneoplasia to invasive lung adenocarcinomas and underlying molecular features.
Nat Commun
; 12(1): 2722, 2021 05 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33976164
10.
DEAR1 is a dominant regulator of acinar morphogenesis and an independent predictor of local recurrence-free survival in early-onset breast cancer.
PLoS Med
; 6(5): e1000068, 2009 May 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-19536326
11.
Analysis of mutational dynamics at the DMPK (CTG)n locus identifies saliva as a suitable DNA sample source for genetic analysis in myotonic dystrophy type 1.
PLoS One
; 14(5): e0216407, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31048891
12.
Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism.
Nat Genet
; 45(11): 1405-8, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24076603
13.
Methylation of the candidate biomarker TCF21 is very frequent across a spectrum of early-stage nonsmall cell lung cancers.
Cancer
; 117(3): 606-17, 2011 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20945327
14.
Effects of MDM2, MDM4 and TP53 codon 72 polymorphisms on cancer risk in a cohort study of carriers of TP53 germline mutations.
PLoS One
; 5(5): e10813, 2010 May 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-20520810
15.
Genome-wide hypomethylation in head and neck cancer is more pronounced in HPV-negative tumors and is associated with genomic instability.
PLoS One
; 4(3): e4941, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19293934