396 related articles for article (PubMed ID: 17033625)
1. DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis.
Lorenz-Depiereux B; Bastepe M; Benet-Pagès A; Amyere M; Wagenstaller J; Müller-Barth U; Badenhoop K; Kaiser SM; Rittmaster RS; Shlossberg AH; Olivares JL; Loris C; Ramos FJ; Glorieux F; Vikkula M; Jüppner H; Strom TM
Nat Genet; 2006 Nov; 38(11):1248-50. PubMed ID: 17033625
[TBL] [Abstract][Full Text] [Related]
2. Hereditary hypophosphatemias: new genes in the bone-kidney axis.
Negri AL
Nephrology (Carlton); 2007 Aug; 12(4):317-20. PubMed ID: 17635744
[TBL] [Abstract][Full Text] [Related]
3. Regulation of bone-renal mineral and energy metabolism: the PHEX, FGF23, DMP1, MEPE ASARM pathway.
Rowe PS
Crit Rev Eukaryot Gene Expr; 2012; 22(1):61-86. PubMed ID: 22339660
[TBL] [Abstract][Full Text] [Related]
4. Bone proteins PHEX and DMP1 regulate fibroblastic growth factor Fgf23 expression in osteocytes through a common pathway involving FGF receptor (FGFR) signaling.
Martin A; Liu S; David V; Li H; Karydis A; Feng JQ; Quarles LD
FASEB J; 2011 Aug; 25(8):2551-62. PubMed ID: 21507898
[TBL] [Abstract][Full Text] [Related]
5. Long-term clinical outcome and carrier phenotype in autosomal recessive hypophosphatemia caused by a novel DMP1 mutation.
Mäkitie O; Pereira RC; Kaitila I; Turan S; Bastepe M; Laine T; Kröger H; Cole WG; Jüppner H
J Bone Miner Res; 2010 Oct; 25(10):2165-74. PubMed ID: 20499351
[TBL] [Abstract][Full Text] [Related]
6. PHEX, FGF23, DMP1 and beyond.
Strom TM; Jüppner H
Curr Opin Nephrol Hypertens; 2008 Jul; 17(4):357-62. PubMed ID: 18660670
[TBL] [Abstract][Full Text] [Related]
7. FGF23, PHEX, and MEPE regulation of phosphate homeostasis and skeletal mineralization.
Quarles LD
Am J Physiol Endocrinol Metab; 2003 Jul; 285(1):E1-9. PubMed ID: 12791601
[TBL] [Abstract][Full Text] [Related]
8. Emerging role of fibroblast growth factor 23 in a bone-kidney axis regulating systemic phosphate homeostasis and extracellular matrix mineralization.
Liu S; Gupta A; Quarles LD
Curr Opin Nephrol Hypertens; 2007 Jul; 16(4):329-35. PubMed ID: 17565275
[TBL] [Abstract][Full Text] [Related]
9. A Mutation in the Dmp1 Gene Alters Phosphate Responsiveness in Mice.
Ichikawa S; Gerard-O'Riley RL; Acton D; McQueen AK; Strobel IE; Witcher PC; Feng JQ; Econs MJ
Endocrinology; 2017 Mar; 158(3):470-476. PubMed ID: 28005411
[TBL] [Abstract][Full Text] [Related]
10. Phosphorylated acidic serine-aspartate-rich MEPE-associated motif peptide from matrix extracellular phosphoglycoprotein inhibits phosphate regulating gene with homologies to endopeptidases on the X-chromosome enzyme activity.
Liu S; Rowe PS; Vierthaler L; Zhou J; Quarles LD
J Endocrinol; 2007 Jan; 192(1):261-7. PubMed ID: 17210763
[TBL] [Abstract][Full Text] [Related]
11. The wrickkened pathways of FGF23, MEPE and PHEX.
Rowe PS
Crit Rev Oral Biol Med; 2004 Sep; 15(5):264-81. PubMed ID: 15470265
[TBL] [Abstract][Full Text] [Related]
12. Identification of a novel dentin matrix protein-1 (DMP-1) mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia.
Turan S; Aydin C; Bereket A; Akcay T; Güran T; Yaralioglu BA; Bastepe M; Jüppner H
Bone; 2010 Feb; 46(2):402-9. PubMed ID: 19796717
[TBL] [Abstract][Full Text] [Related]
13. Regulation of fibroblastic growth factor 23 expression but not degradation by PHEX.
Liu S; Guo R; Simpson LG; Xiao ZS; Burnham CE; Quarles LD
J Biol Chem; 2003 Sep; 278(39):37419-26. PubMed ID: 12874285
[TBL] [Abstract][Full Text] [Related]
14. [Epidemiology of FGF23-related hypophosophatemic diseases].
Endo I
Clin Calcium; 2016 Feb; 26(2):223-31. PubMed ID: 26813502
[TBL] [Abstract][Full Text] [Related]
15. Dentin matrix protein 1 (DMP1): new and important roles for biomineralization and phosphate homeostasis.
Qin C; D'Souza R; Feng JQ
J Dent Res; 2007 Dec; 86(12):1134-41. PubMed ID: 18037646
[TBL] [Abstract][Full Text] [Related]
16. ASARM peptides: PHEX-dependent and -independent regulation of serum phosphate.
David V; Martin A; Hedge AM; Drezner MK; Rowe PS
Am J Physiol Renal Physiol; 2011 Mar; 300(3):F783-91. PubMed ID: 21177780
[TBL] [Abstract][Full Text] [Related]
17. Overexpression of the DMP1 C-terminal fragment stimulates FGF23 and exacerbates the hypophosphatemic rickets phenotype in Hyp mice.
Martin A; David V; Li H; Dai B; Feng JQ; Quarles LD
Mol Endocrinol; 2012 Nov; 26(11):1883-95. PubMed ID: 22930691
[TBL] [Abstract][Full Text] [Related]
18. Mutational analysis of PHEX, FGF23, DMP1, SLC34A3 and CLCN5 in patients with hypophosphatemic rickets.
Beck-Nielsen SS; Brixen K; Gram J; Brusgaard K
J Hum Genet; 2012 Jul; 57(7):453-8. PubMed ID: 22695891
[TBL] [Abstract][Full Text] [Related]
19. Osteocyte-specific deletion of Fgfr1 suppresses FGF23.
Xiao Z; Huang J; Cao L; Liang Y; Han X; Quarles LD
PLoS One; 2014; 9(8):e104154. PubMed ID: 25089825
[TBL] [Abstract][Full Text] [Related]
20. Functional analysis of mutant FAM20C in Raine syndrome with FGF23-related hypophosphatemia.
Kinoshita Y; Hori M; Taguchi M; Fukumoto S
Bone; 2014 Oct; 67():145-51. PubMed ID: 25026495
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
