213 related articles for article (PubMed ID: 24890885)
1. A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity.
Philippe J; Stijnen P; Meyre D; De Graeve F; Thuillier D; Delplanque J; Gyapay G; Sand O; Creemers JW; Froguel P; Bonnefond A
Int J Obes (Lond); 2015 Feb; 39(2):295-302. PubMed ID: 24890885
[TBL] [Abstract][Full Text] [Related]
2. Contribution of heterozygous PCSK1 variants to obesity and implications for precision medicine: a case-control study.
Folon L; Baron M; Toussaint B; Vaillant E; Boissel M; Scherrer V; Loiselle H; Leloire A; Badreddine A; Balkau B; Charpentier G; Franc S; Marre M; Aboulouard S; Salzet M; Canouil M; Derhourhi M; Froguel P; Bonnefond A
Lancet Diabetes Endocrinol; 2023 Mar; 11(3):182-190. PubMed ID: 36822744
[TBL] [Abstract][Full Text] [Related]
3. Heterozygous mutations causing partial prohormone convertase 1 deficiency contribute to human obesity.
Creemers JW; Choquet H; Stijnen P; Vatin V; Pigeyre M; Beckers S; Meulemans S; Than ME; Yengo L; Tauber M; Balkau B; Elliott P; Jarvelin MR; Van Hul W; Van Gaal L; Horber F; Pattou F; Froguel P; Meyre D
Diabetes; 2012 Feb; 61(2):383-90. PubMed ID: 22210313
[TBL] [Abstract][Full Text] [Related]
4. Association between rs155971 in the PCSK1 gene and the lipid profile of obese Thai children: a family-based study.
Kulanuwat S; Santiprabhob J; Phonrat B; Limwongse C; Tungtrongchitr A; Chongviriyaphan N; Tungtrongchitr R
Genet Mol Res; 2015 Aug; 14(3):9136-44. PubMed ID: 26345846
[TBL] [Abstract][Full Text] [Related]
5. Next-generation sequencing of the monogenic obesity genes LEP, LEPR, MC4R, PCSK1 and POMC in a Norwegian cohort of patients with morbid obesity and normal weight controls.
Nordang GBN; Busk ØL; Tveten K; Hanevik HI; Fell AKM; Hjelmesæth J; Holla ØL; Hertel JK
Mol Genet Metab; 2017 May; 121(1):51-56. PubMed ID: 28377240
[TBL] [Abstract][Full Text] [Related]
6. Genetic and functional characterization of PCSK1.
Choquet H; Stijnen P; Creemers JW
Methods Mol Biol; 2011; 768():247-53. PubMed ID: 21805247
[TBL] [Abstract][Full Text] [Related]
7. Common nonsynonymous variants in PCSK1 confer risk of obesity.
Benzinou M; Creemers JW; Choquet H; Lobbens S; Dina C; Durand E; Guerardel A; Boutin P; Jouret B; Heude B; Balkau B; Tichet J; Marre M; Potoczna N; Horber F; Le Stunff C; Czernichow S; Sandbaek A; Lauritzen T; Borch-Johnsen K; Andersen G; Kiess W; Körner A; Kovacs P; Jacobson P; Carlsson LM; Walley AJ; Jørgensen T; Hansen T; Pedersen O; Meyre D; Froguel P
Nat Genet; 2008 Aug; 40(8):943-5. PubMed ID: 18604207
[TBL] [Abstract][Full Text] [Related]
8. Functional and clinical relevance of novel and known
Löffler D; Behrendt S; Creemers JWM; Klammt J; Aust G; Stanik J; Kiess W; Kovacs P; Körner A
Mol Metab; 2017 Mar; 6(3):295-305. PubMed ID: 28271036
[TBL] [Abstract][Full Text] [Related]
9. Rare Heterozygous
Van Dijck E; Beckers S; Diels S; Huybrechts T; Verrijken A; Van Hoorenbeeck K; Verhulst S; Massa G; Van Gaal L; Van Hul W
Genes (Basel); 2022 Sep; 13(10):. PubMed ID: 36292633
[TBL] [Abstract][Full Text] [Related]
10. Melanocortin 4 Receptor Pathway Dysfunction in Obesity: Patient Stratification Aimed at MC4R Agonist Treatment.
Ayers KL; Glicksberg BS; Garfield AS; Longerich S; White JA; Yang P; Du L; Chittenden TW; Gulcher JR; Roy S; Fiedorek F; Gottesdiener K; Cohen S; North KE; Schadt EE; Li SD; Chen R; Van der Ploeg LHT
J Clin Endocrinol Metab; 2018 Jul; 103(7):2601-2612. PubMed ID: 29726959
[TBL] [Abstract][Full Text] [Related]
11. Endoplasmic reticulum-associated degradation of the mouse PC1/3-N222D hypomorph and human PCSK1 mutations contributes to obesity.
Stijnen P; Brouwers B; Dirkx E; Ramos-Molina B; Van Lommel L; Schuit F; Thorrez L; Declercq J; Creemers JW
Int J Obes (Lond); 2016 Jun; 40(6):973-81. PubMed ID: 26786350
[TBL] [Abstract][Full Text] [Related]
12. Common variants in PCSK1 influence blood pressure and body mass index.
Gu Q; Yazdanpanah M; van Hoek M; Hofman A; Gao X; de Rooij FW; Sijbrands EJ
J Hum Hypertens; 2015 Feb; 29(2):82-6. PubMed ID: 25031086
[TBL] [Abstract][Full Text] [Related]
13. PCSK1 Variants and Human Obesity.
Ramos-Molina B; Martin MG; Lindberg I
Prog Mol Biol Transl Sci; 2016; 140():47-74. PubMed ID: 27288825
[TBL] [Abstract][Full Text] [Related]
14. Effects of PCSK1 genetic variants on obesity among Thai children and their family members: in relation to health risk, and biochemical and anthropometric parameters.
Kulanuwat S; Phonrat B; Tungtrongchitr A; Limwongse C; Chongviriyaphan N; Tungtrongchitr R; Santiprabhob J
Southeast Asian J Trop Med Public Health; 2014 Jan; 45(1):214-25. PubMed ID: 24964673
[TBL] [Abstract][Full Text] [Related]
15. Contribution of common PCSK1 genetic variants to obesity in 8,359 subjects from multi-ethnic American population.
Choquet H; Kasberger J; Hamidovic A; Jorgenson E
PLoS One; 2013; 8(2):e57857. PubMed ID: 23451278
[TBL] [Abstract][Full Text] [Related]
16. A New Case of PCSK1 Pathogenic Variant With Congenital Proprotein Convertase 1/3 Deficiency and Literature Review.
Pépin L; Colin E; Tessarech M; Rouleau S; Bouhours-Nouet N; Bonneau D; Coutant R
J Clin Endocrinol Metab; 2019 Apr; 104(4):985-993. PubMed ID: 30383237
[TBL] [Abstract][Full Text] [Related]
17. Differential sex-association between PCSK1 polymorphisms and obesity risk in Portuguese children.
Manco L; Albuquerque D; Aranda B; Rodrigues D; Machado-Rodrigues AM; Padez C
Am J Hum Biol; 2024 May; 36(5):e24023. PubMed ID: 38009939
[TBL] [Abstract][Full Text] [Related]
18. Functional characterization of all missense variants in
Shah BP; Sleiman PM; Mc Donald J; Moeller IH; Kleyn P
Expert Rev Endocrinol Metab; 2023 Mar; 18(2):209-219. PubMed ID: 36864747
[TBL] [Abstract][Full Text] [Related]
19. Early Clinical Diagnosis of PC1/3 Deficiency in a Patient With a Novel Homozygous PCSK1 Splice-Site Mutation.
Härter B; Fuchs I; Müller T; Akbulut UE; Cakir M; Janecke AR
J Pediatr Gastroenterol Nutr; 2016 Apr; 62(4):577-80. PubMed ID: 26488123
[TBL] [Abstract][Full Text] [Related]
20. Severe obesity and diabetes insipidus in a patient with PCSK1 deficiency.
Frank GR; Fox J; Candela N; Jovanovic Z; Bochukova E; Levine J; Papenhausen PR; O'Rahilly S; Farooqi IS
Mol Genet Metab; 2013; 110(1-2):191-4. PubMed ID: 23800642
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]