144 related articles for article (PubMed ID: 21805247)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. A novel mutation in the mouse Pcsk1 gene showing obesity and diabetes.
Muhsin NIA; Bentley L; Bai Y; Goldsworthy M; Cox RD
Mamm Genome; 2020 Feb; 31(1-2):17-29. PubMed ID: 31974728
[TBL] [Abstract][Full Text] [Related]
9. Effects of rs6234/rs6235 and rs6232/rs6234/rs6235 PCSK1 single-nucleotide polymorphism clusters on proprotein convertase 1/3 biosynthesis and activity.
Mbikay M; Sirois F; Nkongolo KK; Basak A; Chrétien M
Mol Genet Metab; 2011 Dec; 104(4):682-7. PubMed ID: 22000902
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Congenital proprotein convertase 1/3 deficiency causes malabsorptive diarrhea and other endocrinopathies in a pediatric cohort.
Martín MG; Lindberg I; Solorzano-Vargas RS; Wang J; Avitzur Y; Bandsma R; Sokollik C; Lawrence S; Pickett LA; Chen Z; Egritas O; Dalgic B; Albornoz V; de Ridder L; Hulst J; Gok F; Aydoğan A; Al-Hussaini A; Gok DE; Yourshaw M; Wu SV; Cortina G; Stanford S; Georgia S
Gastroenterology; 2013 Jul; 145(1):138-148. PubMed ID: 23562752
[TBL] [Abstract][Full Text] [Related]
13. PCSK1 Mutations and Human Endocrinopathies: From Obesity to Gastrointestinal Disorders.
Stijnen P; Ramos-Molina B; O'Rahilly S; Creemers JW
Endocr Rev; 2016 Aug; 37(4):347-71. PubMed ID: 27187081
[TBL] [Abstract][Full Text] [Related]
14. Defective transport of the obesity mutant PC1/3 N222D contributes to loss of function.
Prabhu Y; Blanco EH; Liu M; Peinado JR; Wheeler MC; Gekakis N; Arvan P; Lindberg I
Endocrinology; 2014 Jul; 155(7):2391-401. PubMed ID: 24828610
[TBL] [Abstract][Full Text] [Related]
15. A novel familial mutation in the PCSK1 gene that alters the oxyanion hole residue of proprotein convertase 1/3 and impairs its enzymatic activity.
Wilschanski M; Abbasi M; Blanco E; Lindberg I; Yourshaw M; Zangen D; Berger I; Shteyer E; Pappo O; Bar-Oz B; Martín MG; Elpeleg O
PLoS One; 2014; 9(10):e108878. PubMed ID: 25272002
[TBL] [Abstract][Full Text] [Related]
16. Novel Homozygous Inactivating Mutation in the
Aerts L; Terry NA; Sainath NN; Torres C; Martín MG; Ramos-Molina B; Creemers JW
Genes (Basel); 2021 May; 12(5):. PubMed ID: 34068683
[TBL] [Abstract][Full Text] [Related]
17. Revisiting PC1/3 Mutants: Dominant-Negative Effect of Endoplasmic Reticulum-Retained Mutants.
Blanco EH; Ramos-Molina B; Lindberg I
Endocrinology; 2015 Oct; 156(10):3625-37. PubMed ID: 26207343
[TBL] [Abstract][Full Text] [Related]
18. Modulation of prohormone convertase 1/3 properties using site-directed mutagenesis.
Ozawa A; Peinado JR; Lindberg I
Endocrinology; 2010 Sep; 151(9):4437-45. PubMed ID: 20610561
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Polymorphisms in an obesity-related gene (PCSK1) are associated with fat deposition and production traits in Italian heavy pigs.
Fontanesi L; Bertolini F; Scotti E; Trevisi P; Buttazzoni L; Dall'olio S; Davoli R; Bosi P; Russo V
Animal; 2012 Dec; 6(12):1913-24. PubMed ID: 23032090
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]