Detalles de la búsqueda
1.
Randomized, double-blind, placebo-controlled dose-finding study of the dipeptidyl peptidase-4 inhibitor linagliptin in pediatric patients with type 2 diabetes.
Pediatr Diabetes
; 19(4): 640-648, 2018 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-29171139
2.
Relationship between salivary/pancreatic amylase and body mass index: a systems biology approach.
BMC Med
; 15(1): 37, 2017 02 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-28228143
3.
Rfx6 directs islet formation and insulin production in mice and humans.
Nature
; 463(7282): 775-80, 2010 Feb 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-20148032
4.
Contribution of the low-frequency, loss-of-function p.R270H mutation in FFAR4 (GPR120) to increased fasting plasma glucose levels.
J Med Genet
; 52(9): 595-8, 2015 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-26025001
5.
Variation in FTO contributes to childhood obesity and severe adult obesity.
Nat Genet
; 39(6): 724-6, 2007 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-17496892
6.
Monocytes of Patients with Type 1 Diabetes Harbour Enterovirus RNA.
Eur J Clin Invest
; 45(9): 918-24, 2015 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-26108863
7.
Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes.
Nat Genet
; 37(8): 863-7, 2005 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-16025115
8.
Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups.
PLoS Genet
; 6(4): e1000916, 2010 Apr 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-20421936
9.
The p.Pro2232Leu variant in the ChEL domain of thyroglobulin gene causes intracellular transport disorder and congenital hypothyroidism.
Endocrine
; 80(1): 47-53, 2023 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-36547798
10.
Barriers to Physical Activity in Children and Adults Living With Type 1 Diabetes: A Complex Link With Real-life Glycemic Excursions.
Can J Diabetes
; 47(2): 124-132, 2023 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-36411182
11.
New insights into the pathogenesis of Beckwith-Wiedemann and Silver-Russell syndromes: contribution of small copy number variations to 11p15 imprinting defects.
Hum Mutat
; 32(10): 1171-82, 2011 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-21780245
12.
Identification by array-Comparative Genomic Hybridization (array-CGH) of a large deletion of luteinizing hormone receptor gene combined with a missense mutation in a patient diagnosed with a 46,XY disorder of sex development and application to prenatal diagnosis.
Endocr J
; 58(9): 769-76, 2011.
Artículo
en Inglés
| MEDLINE | ID: mdl-21720050
13.
SHP2 drives inflammation-triggered insulin resistance by reshaping tissue macrophage populations.
Sci Transl Med
; 13(591)2021 04 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-33910978
14.
R125W coding variant in TBC1D1 confers risk for familial obesity and contributes to linkage on chromosome 4p14 in the French population.
Hum Mol Genet
; 17(12): 1798-802, 2008 Jun 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-18325908
15.
Craniopharyngioma and hypothalamic obesity in children.
Childs Nerv Syst
; 25(3): 347-52, 2009 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-19057910
16.
Loss-of-function mutations in MRAP2 are pathogenic in hyperphagic obesity with hyperglycemia and hypertension.
Nat Med
; 25(11): 1733-1738, 2019 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-31700171
17.
Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism.
Mol Cell Endocrinol
; 473: 1-16, 2018 09 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-29275168
18.
CoDE-seq, an augmented whole-exome sequencing, enables the accurate detection of CNVs and mutations in Mendelian obesity and intellectual disability.
Mol Metab
; 13: 1-9, 2018 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-29784605
19.
Genetic study of the melanin-concentrating hormone receptor 2 in childhood and adulthood severe obesity.
J Clin Endocrinol Metab
; 92(11): 4403-9, 2007 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-17698913
20.
No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseases.
Eur J Hum Genet
; 15(3): 320-7, 2007 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-17164796