202 related articles for article (PubMed ID: 23188710)
1. Gpr177, a novel locus for bone mineral density and osteoporosis, regulates osteogenesis and chondrogenesis in skeletal development.
Maruyama T; Jiang M; Hsu W
J Bone Miner Res; 2013 May; 28(5):1150-9. PubMed ID: 23188710
[TBL] [Abstract][Full Text] [Related]
2. Gpr177/mouse Wntless is essential for Wnt-mediated craniofacial and brain development.
Fu J; Ivy Yu HM; Maruyama T; Mirando AJ; Hsu W
Dev Dyn; 2011 Feb; 240(2):365-71. PubMed ID: 21246653
[TBL] [Abstract][Full Text] [Related]
3. Expression of Gpr177, a Wnt trafficking regulator, in mouse embryogenesis.
Yu HM; Jin Y; Fu J; Hsu W
Dev Dyn; 2010 Jul; 239(7):2102-9. PubMed ID: 20549736
[TBL] [Abstract][Full Text] [Related]
4. Reciprocal regulation of Wnt and Gpr177/mouse Wntless is required for embryonic axis formation.
Fu J; Jiang M; Mirando AJ; Yu HM; Hsu W
Proc Natl Acad Sci U S A; 2009 Nov; 106(44):18598-603. PubMed ID: 19841259
[TBL] [Abstract][Full Text] [Related]
5. Wntless spatially regulates bone development through β-catenin-dependent and independent mechanisms.
Zhong ZA; Zahatnansky J; Snider J; Van Wieren E; Diegel CR; Williams BO
Dev Dyn; 2015 Oct; 244(10):1347-55. PubMed ID: 26249818
[TBL] [Abstract][Full Text] [Related]
6. Gpr177-mediated Wnt Signaling Is Required for Secondary Palate Development.
Liu Y; Wang M; Zhao W; Yuan X; Yang X; Li Y; Qiu M; Zhu XJ; Zhang Z
J Dent Res; 2015 Jul; 94(7):961-7. PubMed ID: 25922332
[TBL] [Abstract][Full Text] [Related]
7. Intra-epithelial requirement of canonical Wnt signaling for tooth morphogenesis.
Zhu X; Zhao P; Liu Y; Zhang X; Fu J; Ivy Yu HM; Qiu M; Chen Y; Hsu W; Zhang Z
J Biol Chem; 2013 Apr; 288(17):12080-9. PubMed ID: 23525146
[TBL] [Abstract][Full Text] [Related]
8. Wnt/beta-catenin signaling in mesenchymal progenitors controls osteoblast and chondrocyte differentiation during vertebrate skeletogenesis.
Day TF; Guo X; Garrett-Beal L; Yang Y
Dev Cell; 2005 May; 8(5):739-50. PubMed ID: 15866164
[TBL] [Abstract][Full Text] [Related]
9. Gpr177 deficiency impairs mammary development and prohibits Wnt-induced tumorigenesis.
Maruyama EO; Yu HM; Jiang M; Fu J; Hsu W
PLoS One; 2013; 8(2):e56644. PubMed ID: 23457599
[TBL] [Abstract][Full Text] [Related]
10. Interaction of the mu-opioid receptor with GPR177 (Wntless) inhibits Wnt secretion: potential implications for opioid dependence.
Jin J; Kittanakom S; Wong V; Reyes BA; Van Bockstaele EJ; Stagljar I; Berrettini W; Levenson R
BMC Neurosci; 2010 Mar; 11():33. PubMed ID: 20214800
[TBL] [Abstract][Full Text] [Related]
11. Rap1b Is an Effector of Axin2 Regulating Crosstalk of Signaling Pathways During Skeletal Development.
Maruyama T; Jiang M; Abbott A; Yu HI; Huang Q; Chrzanowska-Wodnicka M; Chen EI; Hsu W
J Bone Miner Res; 2017 Sep; 32(9):1816-1828. PubMed ID: 28520221
[TBL] [Abstract][Full Text] [Related]
12. Expression of GPR177 (Wntless/Evi/Sprinter), a highly conserved Wnt-transport protein, in rat tissues, zebrafish embryos, and cultured human cells.
Jin J; Morse M; Frey C; Petko J; Levenson R
Dev Dyn; 2010 Sep; 239(9):2426-34. PubMed ID: 20652957
[TBL] [Abstract][Full Text] [Related]
13. The Wnt secretion protein Evi/Gpr177 promotes glioma tumourigenesis.
Augustin I; Goidts V; Bongers A; Kerr G; Vollert G; Radlwimmer B; Hartmann C; Herold-Mende C; Reifenberger G; von Deimling A; Boutros M
EMBO Mol Med; 2012 Jan; 4(1):38-51. PubMed ID: 22147553
[TBL] [Abstract][Full Text] [Related]
14. Does murine spermatogenesis require WNT signalling? A lesson from Gpr177 conditional knockout mouse models.
Chen SR; Tang JX; Cheng JM; Hao XX; Wang YQ; Wang XX; Liu YX
Cell Death Dis; 2016 Jun; 7(6):e2281. PubMed ID: 27362799
[TBL] [Abstract][Full Text] [Related]
15. Wnt-mediated reciprocal regulation between cartilage and bone development during endochondral ossification.
Lu C; Wan Y; Cao J; Zhu X; Yu J; Zhou R; Yao Y; Zhang L; Zhao H; Li H; Zhao J; He L; Ma G; Yang X; Yao Z; Guo X
Bone; 2013 Apr; 53(2):566-74. PubMed ID: 23274346
[TBL] [Abstract][Full Text] [Related]
16. Wntless functions in mature osteoblasts to regulate bone mass.
Zhong Z; Zylstra-Diegel CR; Schumacher CA; Baker JJ; Carpenter AC; Rao S; Yao W; Guan M; Helms JA; Lane NE; Lang RA; Williams BO
Proc Natl Acad Sci U S A; 2012 Aug; 109(33):E2197-204. PubMed ID: 22745162
[TBL] [Abstract][Full Text] [Related]
17. Gpr177-mediated Wnt Signaling is Required for Fungiform Placode Initiation.
Zhu X; Liu Y; Zhao P; Dai Z; Yang X; Li Y; Qiu M; Zhang Z
J Dent Res; 2014 Jun; 93(6):582-8. PubMed ID: 24736288
[TBL] [Abstract][Full Text] [Related]
18. Epidermal Wnt controls hair follicle induction by orchestrating dynamic signaling crosstalk between the epidermis and dermis.
Fu J; Hsu W
J Invest Dermatol; 2013 Apr; 133(4):890-8. PubMed ID: 23190887
[TBL] [Abstract][Full Text] [Related]
19. Polymorphisms in genes involved in the NF-κB signalling pathway are associated with bone mineral density, geometry and turnover in men.
Roshandel D; Thomson W; Pye SR; Boonen S; Borghs H; Vanderschueren D; Huhtaniemi IT; Adams JE; Ward KA; Bartfai G; Casanueva FF; Finn JD; Forti G; Giwercman A; Han TS; Kula K; Lean ME; Pendleton N; Punab M; Wu FC; Holliday KL; O'Neill TW;
PLoS One; 2011; 6(11):e28031. PubMed ID: 22132199
[TBL] [Abstract][Full Text] [Related]
20. Osteoblast-derived NOTUM reduces cortical bone mass in mice and the
Movérare-Skrtic S; Nilsson KH; Henning P; Funck-Brentano T; Nethander M; Rivadeneira F; Coletto Nunes G; Koskela A; Tuukkanen J; Tuckermann J; Perret C; Souza PPC; Lerner UH; Ohlsson C
FASEB J; 2019 Oct; 33(10):11163-11179. PubMed ID: 31307226
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
