448 related articles for article (PubMed ID: 17332414)
1. LRP6 mutation in a family with early coronary disease and metabolic risk factors.
Mani A; Radhakrishnan J; Wang H; Mani A; Mani MA; Nelson-Williams C; Carew KS; Mane S; Najmabadi H; Wu D; Lifton RP
Science; 2007 Mar; 315(5816):1278-82. PubMed ID: 17332414
[TBL] [Abstract][Full Text] [Related]
2. Rare nonconservative LRP6 mutations are associated with metabolic syndrome.
Singh R; Smith E; Fathzadeh M; Liu W; Go GW; Subrahmanyan L; Faramarzi S; McKenna W; Mani A
Hum Mutat; 2013 Sep; 34(9):1221-5. PubMed ID: 23703864
[TBL] [Abstract][Full Text] [Related]
3. [Cytokines in bone diseases. Wnt signaling and osteoporosis-pseudoglioma syndrome].
Ozono K
Clin Calcium; 2010 Oct; 20(10):1520-5. PubMed ID: 20890034
[TBL] [Abstract][Full Text] [Related]
4. LRP5 in premature adrenarche and in metabolic characteristics of prepubertal children.
Lappalainen S; Saarinen A; Utriainen P; Voutilainen R; Jääskeläinen J; Mäkitie O
Clin Endocrinol (Oxf); 2009 May; 70(5):725-31. PubMed ID: 18721193
[TBL] [Abstract][Full Text] [Related]
5. Combined effects of apoE-CI-CII cluster and LDL-R gene polymorphisms on chromosome 19 and coronary artery disease risk.
Wang C; Zhou X; Ye S; Han D; Tan X; Zheng F; Shi Q
Int J Hyg Environ Health; 2006 May; 209(3):265-73. PubMed ID: 16459141
[TBL] [Abstract][Full Text] [Related]
6. Mutant LRP6 Impairs Endothelial Cell Functions Associated with Familial Normolipidemic Coronary Artery Disease.
Guo J; Li Y; Ren YH; Sun Z; Dong J; Yan H; Xu Y; Wang DW; Zheng GY; Du J; Tian XL
Int J Mol Sci; 2016 Jul; 17(7):. PubMed ID: 27455246
[TBL] [Abstract][Full Text] [Related]
7. Mutation in EGFP domain of LDL receptor-related protein 6 impairs cellular LDL clearance.
Liu W; Mani S; Davis NR; Sarrafzadegan N; Kavathas PB; Mani A
Circ Res; 2008 Nov; 103(11):1280-8. PubMed ID: 18948618
[TBL] [Abstract][Full Text] [Related]
8. Carotid artery atherosclerosis in hypertensive patients with a functional LDL receptor-related protein 6 gene variant.
Sarzani R; Salvi F; Bordicchia M; Guerra F; Battistoni I; Pagliariccio G; Carbonari L; Dessì-Fulgheri P; Rappelli A
Nutr Metab Cardiovasc Dis; 2011 Feb; 21(2):150-6. PubMed ID: 19833493
[TBL] [Abstract][Full Text] [Related]
9. Functional analysis LRP6 novel mutations in patients with coronary artery disease.
Xu Y; Gong W; Peng J; Wang H; Huang J; Ding H; Wang DW
PLoS One; 2014; 9(1):e84345. PubMed ID: 24427284
[TBL] [Abstract][Full Text] [Related]
10. Genetic flaw linked to early heart disease: association with osteoporosis also found.
Hampton T
JAMA; 2007 Apr; 297(15):1643-4. PubMed ID: 17440136
[No Abstract] [Full Text] [Related]
11. [Regulation of bone metabolism by pathogenic mutations and polymorphism in the LRP5-Wnt signaling genes].
Urano T
Nihon Rinsho; 2007 Nov; 65 Suppl 9():95-100. PubMed ID: 18161089
[No Abstract] [Full Text] [Related]
12. Wnt signaling, de novo lipogenesis, adipogenesis and ectopic fat.
Song K; Wang S; Mani M; Mani A
Oncotarget; 2014 Nov; 5(22):11000-3. PubMed ID: 25526027
[TBL] [Abstract][Full Text] [Related]
13. Nonalcoholic fatty liver disease induced by noncanonical Wnt and its rescue by Wnt3a.
Wang S; Song K; Srivastava R; Dong C; Go GW; Li N; Iwakiri Y; Mani A
FASEB J; 2015 Aug; 29(8):3436-45. PubMed ID: 25917329
[TBL] [Abstract][Full Text] [Related]
14. A family with osteoporosis pseudoglioma syndrome due to compound heterozygosity of two novel mutations in the LRP5 gene.
Cheung WM; Jin LY; Smith DK; Cheung PT; Kwan EY; Low L; Kung AW
Bone; 2006 Sep; 39(3):470-6. PubMed ID: 16679074
[TBL] [Abstract][Full Text] [Related]
15. Ocular coloboma and dorsoventral neuroretinal patterning defects in Lrp6 mutant eyes.
Zhou CJ; Molotkov A; Song L; Li Y; Pleasure DE; Pleasure SJ; Wang YZ
Dev Dyn; 2008 Dec; 237(12):3681-9. PubMed ID: 18985738
[TBL] [Abstract][Full Text] [Related]
16. [The LDL receptor related protein type 6 (LRP6) deficiency: implications for the pathogenesis of type 2 diabetes, arterial hypertension and atherosclerosis].
Aguilar-Salinas CA
Rev Invest Clin; 2007; 59(2):98-102. PubMed ID: 17633795
[No Abstract] [Full Text] [Related]
17. A mutation in the signal sequence of LRP5 in a family with an osteoporosis-pseudoglioma syndrome (OPPG)-like phenotype indicates a novel disease mechanism for trinucleotide repeats.
Chung BD; Kayserili H; Ai M; Freudenberg J; Uzümcü A; Uyguner O; Bartels CF; Höning S; Ramirez A; Hanisch FG; Nürnberg G; Nürnberg P; Warman ML; Wollnik B; Kubisch C; Netzer C
Hum Mutat; 2009 Apr; 30(4):641-8. PubMed ID: 19177549
[TBL] [Abstract][Full Text] [Related]
18. Missense mutations in LRP5 are not a common cause of idiopathic osteoporosis in adult men.
Crabbe P; Balemans W; Willaert A; van Pottelbergh I; Cleiren E; Coucke PJ; Ai M; Goemaere S; van Hul W; de Paepe A; Kaufman JM
J Bone Miner Res; 2005 Nov; 20(11):1951-9. PubMed ID: 16234968
[TBL] [Abstract][Full Text] [Related]
19. Cenani-Lenz syndrome restricted to limb and kidney anomalies associated with a novel LRP4 missense mutation.
Khan TN; Klar J; Ali Z; Khan F; Baig SM; Dahl N
Eur J Med Genet; 2013 Jul; 56(7):371-4. PubMed ID: 23664847
[TBL] [Abstract][Full Text] [Related]
20. Lrp6-mediated canonical Wnt signaling is required for lip formation and fusion.
Song L; Li Y; Wang K; Wang YZ; Molotkov A; Gao L; Zhao T; Yamagami T; Wang Y; Gan Q; Pleasure DE; Zhou CJ
Development; 2009 Sep; 136(18):3161-71. PubMed ID: 19700620
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
