Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
about
Inactivation of a novel FGF23 regulator, FAM20C, leads to hypophosphatemic rickets in miceSLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasisTissue-specific expression of betaKlotho and fibroblast growth factor (FGF) receptor isoforms determines metabolic activity of FGF19 and FGF21Secreted frizzled-related protein 4 is a potent tumor-derived phosphaturic agentHereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3.Fibroblast growth factorsFibroblast growth factor 23 inhibits extrarenal synthesis of 1,25-dihydroxyvitamin D in human monocytesA mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected]Cloning and characterization of FGF23 as a causative factor of tumor-induced osteomalaciaThe FGF23-Klotho axis: endocrine regulation of phosphate homeostasisEndocrine fibroblast growth factors 15/19 and 21: from feast to famineChronic kidney disease mineral and bone disorder in childrenFGF23-mediated regulation of systemic phosphate homeostasis: is Klotho an essential player?Klotho and agingBetaKlotho is required for metabolic activity of fibroblast growth factor 21Molecular insights into the klotho-dependent, endocrine mode of action of fibroblast growth factor 19 subfamily membersEndocrine FGFs: Evolution, Physiology, Pathophysiology, and PharmacotherapySignificant roles of anti-aging protein klotho and fibroblast growth factor23 in cardiovascular diseaseAlpha Klotho and phosphate homeostasisMiscellaneous non-inflammatory musculoskeletal conditions. Hyperphosphatemic familial tumoral calcinosis (FGF23, GALNT3 and αKlotho)FGF23 and Phosphate Wasting DisordersRegulation of serum phosphateRegulation and function of the FGF23/klotho endocrine pathwaysFibroblast Growth Factor 23: A New Dimension to Diseases of Calcium-Phosphorus MetabolismExtracellular matrix mineralization in periodontal tissues: Noncollagenous matrix proteins, enzymes, and relationship to hypophosphatasia and X-linked hypophosphatemiaEndocrine crosstalk between muscle and boneFibrous dysplasia and fibroblast growth factor-23 regulationFamilial tumoral calcinosis: a valuable vehicle for discoveryExploring mechanisms of FGF signalling through the lens of structural biologyGenetic disorders of phosphate regulationCardiovascular Risk Factors and Chronic Kidney Disease-FGF23: A Key Molecule in the Cardiovascular DiseaseDysregulated gene expression in the primary osteoblasts and osteocytes isolated from hypophosphatemic Hyp miceLeads for development of new naphthalenesulfonate derivatives with enhanced antiangiogenic activity: crystal structure of acidic fibroblast growth factor in complex with 5-amino-2-naphthalene sulfonateA potential link between phosphate and aging--lessons from Klotho-deficient miceTumour-induced osteomalacia: a literature review and a case reportVascular calcification: When should we interfere in chronic kidney disease patients and how?Enzymes, dentinogenesis and dental caries: a literature reviewThe secretory pathway kinasesDysregulation of phosphate metabolism and conditions associated with phosphate toxicityFunctional diversity of fibroblast growth factors in bone formation
P2860
Q21092419-6012631C-18B7-4DB8-9105-B63CC2AE0235Q24299058-D921EB32-2406-443F-95FB-3EF501546730Q24318639-65E3181C-E9C7-4D5C-843C-777655359BB9Q24319643-D5765907-F4E7-444B-927E-DAF8CA21FBDCQ24540520-6F88AA7E-FB0E-47AD-A968-3902371788C9Q24542507-D53C905D-B9E3-4B69-B5BC-E3F5E476D2C3Q24604832-B9C440CE-E6AE-4744-9E9B-534B4BE46A0EQ24615444-F309BA98-C818-4612-A40E-943E842C883AQ24623628-6948D75C-5AF2-47CA-99FA-C48771B396EEQ24625902-3724283A-C49A-4902-8AE0-48A57923BDB4Q24629260-419946C6-63D7-4827-89C9-914A4BE31152Q24642788-86427C2C-E160-4C8F-8882-28CCFC802E29Q24653541-2ADC6B45-F50C-434F-9B96-6094E76202C6Q24654902-25B78E5B-DBEA-4AF0-9C30-FB21F67F043AQ24681531-FF0DA684-BAD9-458B-AAED-02989A32666DQ24683254-B3273F74-B663-42A5-B507-E07B5F533689Q26781556-3F752D6E-D14D-4665-BCB4-6EB137C5B72EQ26782946-F840D8EB-DA10-4E12-9E93-D9598511D5E7Q26825471-ACC7AC19-4BF7-40BB-8E6C-0A3C68B98EFEQ26827280-2455CC4C-A789-4B07-81DE-5F01ED73CA27Q26851904-555F9502-A517-449D-B718-DEB637CFB711Q26852177-A4585787-37C3-47DA-AE42-6FE1C4FED512Q26860470-49A6EBEA-6D83-4FE2-B92B-3809F9A746EEQ26866263-C0B41546-6C64-4F88-8B81-7AF01F188A7AQ27002346-5CEC7A89-AAB3-45C5-B77E-8641452966F0Q27008987-D1301312-FEFB-4482-84C6-D6E6739989DDQ27010789-BF3EC176-2E42-416B-82E5-BDD638CCF771Q27013868-9C2DF377-64F5-4989-B96F-5E18A045564FQ27015054-FD57EFA2-C9B4-4E70-ACD9-44A7CA0E01C6Q27022049-970DA7D3-7E57-4309-A6B3-B2AD5044D48DQ27024043-6BAD1843-C647-4F0F-B9DB-20A32B3D43CCQ27345068-F9CBC528-0963-478E-ADC5-D60AA31E7E5CQ27640887-103B7648-A2B8-421E-B429-25E1AF96B672Q27687316-A44F59AC-F535-41D6-A259-F294E4147767Q28069314-C3C0FA37-A9EA-4FC8-A517-9858ADA63047Q28071582-B17FCC2F-AE1C-4B58-8E5F-8E021DB21553Q28081854-DB77DD74-92BB-4D5E-8E00-A8F517E8BAEEQ28085305-D3CF00C8-D19C-4ABB-A46B-11167F5CC47AQ28085476-03E54D14-FCCD-4459-8B61-664B6D9CC6EAQ28086929-6DBA49AC-B2F6-41E2-BD62-3DC323A2B2AA
P2860
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
description
2000 nî lūn-bûn
@nan
2000 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
@ast
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
@en
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
@nl
type
label
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
@ast
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
@en
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
@nl
prefLabel
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
@ast
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
@en
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
@nl
P3181
P356
P1433
P1476
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
@en
P2888
P3181
P356
10.1038/81664
P407
P577
2000-11-01T00:00:00Z
P5875
P6179
1050621705