Detalhe da pesquisa
1.
A complementary study approach unravels novel players in the pathoetiology of Hirschsprung disease.
PLoS Genet
; 16(11): e1009106, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33151932
2.
Allele-specific expression at the RET locus in blood and gut tissue of individuals carrying risk alleles for Hirschsprung disease.
Hum Mutat
; 34(5): 754-62, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23441071
3.
Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability.
Am J Hum Genet
; 87(1): 60-74, 2010 Jul 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-20598273
4.
Reduced RET expression in gut tissue of individuals carrying risk alleles of Hirschsprung's disease.
Hum Mol Genet
; 19(8): 1461-7, 2010 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20089534
5.
Genetic basis of Hirschsprung's disease.
Pediatr Surg Int
; 25(7): 543-58, 2009 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19521704
6.
Prophylactic thyroidectomy in ethnic Chinese patients with multiple endocrine neoplasia type 2A syndrome after the introduction of genetic testing.
Hong Kong Med J
; 15(5): 326-31, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19801688
7.
Implications of endocrine gland-derived vascular endothelial growth factor/prokineticin-1 signaling in human neuroblastoma progression.
Clin Cancer Res
; 13(3): 868-75, 2007 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17289879
8.
Epidemiological characteristics of Hirschsprung's disease (HSCR): Results of a case series of fifty patients from Bangladesh.
J Pediatr Surg
; 53(10): 1955-1959, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29429767
9.
Liver intestine-cadherin (CDH17) haplotype is associated with increased risk of hepatocellular carcinoma.
Clin Cancer Res
; 12(17): 5248-52, 2006 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-16951245
10.
Are psychiatric comorbidities and associated cognitive functions related to treatment response to methylphenidate in boys with attention-deficit/hyperactivity disorder?
Neuropsychiatr Dis Treat
; 13: 1071-1080, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28442911
11.
Male and female differential reproductive rate could explain parental transmission asymmetry of mutation origin in Hirschsprung disease.
Eur J Hum Genet
; 20(9): 917-20, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22395866
12.
Hirschsprung's disease.
Semin Pediatr Surg
; 19(3): 194-200, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20610192
13.
Molecular genetics of Hirschsprung's disease.
Semin Pediatr Surg
; 13(4): 236-48, 2004 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-15660317
14.
Application of HapMap data to the evaluation of 8 candidate genes for pediatric slow transit constipation.
J Pediatr Surg
; 42(4): 666-71, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17448763
15.
Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndrome.
Clin Chem
; 52(1): 46-52, 2006 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-16254195
16.
TTF-1 and RET promoter SNPs: regulation of RET transcription in Hirschsprung's disease.
Hum Mol Genet
; 14(2): 191-204, 2005 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-15548547
17.
Mapping of nasopharyngeal carcinoma tumor-suppressive activity to a 1.8-megabase region of chromosome band 11q13.
Genes Chromosomes Cancer
; 34(1): 97-103, 2002 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-11921287
18.
Highly recurrent RET mutations and novel mutations in genes of the receptor tyrosine kinase and endothelin receptor B pathways in Chinese patients with sporadic Hirschsprung disease.
Clin Chem
; 50(1): 93-100, 2004 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-14633923