Detalhe da pesquisa
1.
GDF15 linked to maternal risk of nausea and vomiting during pregnancy.
Nature
; 625(7996): 760-767, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38092039
2.
MC3R links nutritional state to childhood growth and the timing of puberty.
Nature
; 599(7885): 436-441, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34732894
3.
Ethnic differences in complement system biomarkers and their association with metabolic health in men of Black African and White European ethnicity.
Clin Exp Immunol
; 212(1): 52-60, 2023 04 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36722378
4.
Circulating levels of GDF15 in patients with myalgic encephalomyelitis/chronic fatigue syndrome.
J Transl Med
; 17(1): 409, 2019 12 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31801546
5.
GWAS for BMI: a treasure trove of fundamental insights into the genetic basis of obesity.
Int J Obes (Lond)
; 42(8): 1524-1531, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29980761
6.
Effects of the mu-opioid receptor antagonist GSK1521498 on hedonic and consummatory eating behaviour: a proof of mechanism study in binge-eating obese subjects.
Mol Psychiatry
; 18(12): 1287-93, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23147384
7.
FTO expression is regulated by availability of essential amino acids.
Int J Obes (Lond)
; 37(5): 744-7, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22614055
8.
Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene.
Nat Genet
; 16(3): 303-6, 1997 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-9207799
9.
LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.
Nat Genet
; 24(2): 153-6, 2000 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-10655060
10.
Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.
Nat Genet
; 28(4): 365-70, 2001 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-11479539
11.
Fetally-encoded GDF15 and maternal GDF15 sensitivity are major determinants of nausea and vomiting in human pregnancy.
bioRxiv
; 2023 Jun 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37398065
12.
Investigating the involvement of the ATF6α pathway of the unfolded protein response in adipogenesis.
Int J Obes (Lond)
; 36(9): 1248-51, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22124452
13.
Founder effect in the Horn of Africa for an insulin receptor mutation that may impair receptor recycling.
Diabetologia
; 54(5): 1057-65, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21318406
14.
Mechanistic insights into insulin resistance in the genetic era.
Diabet Med
; 28(12): 1476-86, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21992440
15.
A multicomponent screen for feeding behaviour and nutritional status in Drosophila to interrogate mammalian appetite-related genes.
Mol Metab
; 43: 101127, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33242659
16.
Morbid obesity exposes the association between PNPLA3 I148M (rs738409) and indices of hepatic injury in individuals of European descent.
Int J Obes (Lond)
; 34(1): 190-4, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19844213
17.
Loss of NPC1 function in a patient with a co-inherited novel insulin receptor mutation does not grossly modify the severity of the associated insulin resistance.
J Inherit Metab Dis
; 33 Suppl 3: S227-32, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20521171
18.
Correlation of the leptin:adiponectin ratio with measures of insulin resistance in non-diabetic individuals.
Diabetologia
; 52(11): 2345-2349, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19756488
19.
Severe insulin resistance due to anti-insulin antibodies: response to plasma exchange and immunosuppressive therapy.
Diabet Med
; 26(1): 79-82, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19125765
20.
Human obesity as a heritable disorder of the central control of energy balance.
Int J Obes (Lond)
; 32 Suppl 7: S55-61, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19136992