Detalhe da pesquisa
1.
The orphan nuclear receptor NR0B2 could be a novel susceptibility locus associated with microsatellite-stable, APC mutation-negative early-onset colorectal carcinomas with metabolic manifestation.
Genes Chromosomes Cancer
; 60(2): 61-72, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33094510
2.
A Theory-Based, Multidisciplinary Approach to Cocreate a Patient-Centric Digital Solution to Enhance Perioperative Health Outcomes Among Colorectal Cancer Patients and Their Family Caregivers: Development and Evaluation Study.
J Med Internet Res
; 23(12): e31917, 2021 12 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34878991
3.
Living With Cancer Alone? The Experiences of Singles Diagnosed With Colorectal Cancer.
J Psychosoc Oncol
; 33(4): 354-76, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25996668
4.
Germline bone morphogenesis protein receptor 1A mutation causes colorectal tumorigenesis in hereditary mixed polyposis syndrome.
Am J Gastroenterol
; 104(12): 3027-33, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19773747
5.
Chromosome 19q13 disruption alters expressions of CYP2A7, MIA and MIA-RAB4B lncRNA and contributes to FAP-like phenotype in APC mutation-negative familial colorectal cancer patients.
PLoS One
; 12(3): e0173772, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28306719
6.
Critical appraisal of laparoscopic vs open rectal cancer surgery.
World J Gastrointest Surg
; 8(6): 452-60, 2016 Jun 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-27358678
7.
Genomics of Hereditary Colorectal Cancer: Lessons Learnt from 25 Years of the Singapore Polyposis Registry.
Ann Acad Med Singap
; 44(8): 290-6, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26477961
8.
A novel indel in exon 9 of APC upregulates a 'skip exon 9' isoform and causes very severe familial adenomatous polyposis.
Eur J Hum Genet
; 22(6): 833-6, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24169521
9.
Systematic study on genetic and epimutational profile of a cohort of Amsterdam criteria-defined Lynch Syndrome in Singapore.
PLoS One
; 9(4): e94170, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24710284
10.
Peutz-Jeghers syndrome: data from the Singapore Polyposis Registry and a shifting paradigm in management.
Ann Acad Med Singap
; 39(1): 17-21, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20126809
11.
Mesenteric desmoid tumors in Singapore familial adenomatous polyposis patients: clinical course and genetic profile in a predominantly Chinese population.
Dis Colon Rectum
; 50(1): 75-82, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17082890
12.
Singapore familial adenomatous polyposis (FAP) patients with classical adenomatous polyposis but undetectable APC mutations have accelerated cancer progression.
Am J Gastroenterol
; 101(12): 2810-7, 2006 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17026565