Detalhe da pesquisa
1.
MC4R-dependent suppression of appetite by bone-derived lipocalin 2.
Nature
; 543(7645): 385-390, 2017 03 16.
Artigo
Inglês
| MEDLINE | ID: mdl-28273060
2.
Corrigendum: MC4R-dependent suppression of appetite by bone-derived lipocalin 2.
Nature
; 546(7658): 440, 2017 06 14.
Artigo
Inglês
| MEDLINE | ID: mdl-28617454
3.
Bitter taste phenotype and body weight predict children's selection of sweet and savory foods at a palatable test-meal.
Appetite
; 77: 113-21, 2014 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-24607656
4.
Mutations in ZIC3 and ACVR2B are a common cause of heterotaxy and associated cardiovascular anomalies.
Cardiol Young
; 22(2): 194-201, 2012 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-21864452
5.
Frequency and characterization of mutations in genes in a large cohort of patients referred to MODY registry.
J Pediatr Endocrinol Metab
; 34(5): 633-638, 2021 May 26.
Artigo
Inglês
| MEDLINE | ID: mdl-33852230
6.
Whole-exome sequencing identifies novel LEPR mutations in individuals with severe early onset obesity.
Obesity (Silver Spring)
; 22(2): 576-84, 2014 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-23616257
7.
Hypomorphism for RPGRIP1L, a ciliary gene vicinal to the FTO locus, causes increased adiposity in mice.
Cell Metab
; 19(5): 767-79, 2014 May 06.
Artigo
Inglês
| MEDLINE | ID: mdl-24807221
8.
Common variants in the CD36 gene are associated with oral fat perception, fat preferences, and obesity in African Americans.
Obesity (Silver Spring)
; 20(5): 1066-73, 2012 May.
Artigo
Inglês
| MEDLINE | ID: mdl-22240721
9.
Association of candidate genes with nonsyndromic clefts in Honduran and Colombian populations.
Laryngoscope
; 122(9): 2082-7, 2012 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-22753311
10.
Sex differences in the effects of inherited bitter thiourea sensitivity on body weight in 4-6-year-old children.
Obesity (Silver Spring)
; 18(6): 1194-200, 2010 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-19779476
11.
Association of plastin 3 expression with disease severity in spinal muscular atrophy only in postpubertal females.
Arch Neurol
; 67(10): 1252-6, 2010 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-20937953
12.
Glucokinase mutations in young children with hyperglycemia.
Diabetes Metab Res Rev
; 22(5): 348-55, 2006.
Artigo
Inglês
| MEDLINE | ID: mdl-16444761
13.
Prenatal diagnosis of factor X deficiency using a combination of direct mutation detection and linkage analysis with an intragenic single nucleotide polymorphism.
Prenat Diagn
; 23(6): 457-60, 2003 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-12813758
14.
Rapid prenatal diagnosis of sickle cell diseases using oligonucleotide ligation assay coupled with laser-induced capillary fluorescence detection.
Prenat Diagn
; 22(8): 686-91, 2002 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-12210577