Dmp1-deficient mice display severe defects in cartilage formation responsible for a chondrodysplasia-like phenotype
about
Inactivation of a novel FGF23 regulator, FAM20C, leads to hypophosphatemic rickets in miceDentin matrix protein 1 enhances invasion potential of colon cancer cells by bridging matrix metalloproteinase-9 to integrins and CD44.DMP1 depletion decreases bone mineralization in vivo: an FTIR imaging analysisFibroblast Growth Factor 23: A New Dimension to Diseases of Calcium-Phosphorus MetabolismControl of bone mass and remodeling by PTH receptor signaling in osteocytesRole of Periostin in Adhesion and Migration of Bone Remodeling CellsProtective roles of DMP1 in high phosphate homeostasisDentin matrix protein 1 regulates dentin sialophosphoprotein gene transcription during early odontoblast differentiationA chondroitin sulfate chain attached to the bone dentin matrix protein 1 NH2-terminal fragmentRecent advances in the renal-skeletal-gut axis that controls phosphate homeostasisFilamin B mutations cause chondrocyte defects in skeletal developmentImmunohistochemical analysis of dentin matrix protein 1 (Dmp1) phosphorylation by Fam20C in bone: implications for the induction of biomineralizationImmunohistochemical study of small integrin-binding ligand, N-linked glycoproteins in reactionary dentin of rat molars at different agesOverexpression of DMP1 accelerates mineralization and alters cortical bone biomechanical properties in vivo.Distribution of small integrin-binding ligand, N-linked glycoproteins (SIBLING) in the articular cartilage of the rat femoral head.Expression profiling of Dexamethasone-treated primary chondrocytes identifies targets of glucocorticoid signalling in endochondral bone development.Single nucleotide polymorphisms in bone turnover-related genes in Koreans: ethnic differences in linkage disequilibrium and haplotype.Morphological and molecular evidence for a stepwise evolutionary transition from teeth to baleen in mysticete whales.Temperature alters solute transport in growth plate cartilage measured by in vivo multiphoton microscopy.Klf5 Mediates Odontoblastic Differentiation through Regulating Dentin-Specific Extracellular Matrix Gene Expression during Mouse Tooth DevelopmentIdentification of a novel dentin matrix protein-1 (DMP-1) mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia.Induced ablation of Bmp1 and Tll1 produces osteogenesis imperfecta in mice.Distribution of small integrin-binding ligand, N-linked glycoproteins (SIBLING) in the condylar cartilage of rat mandible.Specific ablation of mouse Fam20C in cells expressing type I collagen leads to skeletal defects and hypophosphatemia.Constitutive nuclear expression of dentin matrix protein 1 fails to rescue the Dmp1-null phenotype.Expression and distribution of SIBLING proteins in the predentin/dentin and mandible of hyp mice.Circling behavior developed in Dmp1 null mice is due to bone defects in the vestibular apparatus.Failure to process dentin matrix protein 1 (DMP1) into fragments leads to its loss of function in osteogenesisCalcium-mediated stress kinase activation by DMP1 promotes osteoblast differentiation.Expression and processing of small integrin-binding ligand N-linked glycoproteins in mouse odontoblastic cells.Stress chaperone GRP-78 functions in mineralized matrix formationIdentification of secretory odontoblasts using DMP1-GFP transgenic miceE11/gp38 selective expression in osteocytes: regulation by mechanical strain and role in dendrite elongation.Long-term clinical outcome and carrier phenotype in autosomal recessive hypophosphatemia caused by a novel DMP1 mutation.Separation of newly formed bone from older compact bone reveals clear compositional differences in bone matrixPorcine dentin matrix protein 1: gene structure, cDNA sequence, and expression in teethKey pathways regulated by HoxA9,10,11/HoxD9,10,11 during limb development.Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism.mTORC1 Prevents Preosteoblast Differentiation through the Notch Signaling Pathway.Phosphatonins: new hormones involved in numerous inherited bone disorders
P2860
Q21092419-16141722-56FD-4C5A-B559-AD91AEB1F856Q24538982-9C4FEB83-5011-4655-A7C7-632F6774999DQ24545780-26ACF3BB-68EC-449C-B6A3-52F931D7BCD6Q26866263-79F6CACD-6AB4-4572-833B-2D58BFCE4655Q27300741-96B75993-A4C3-478C-B6C4-942DF2F47739Q27324603-1B855117-B1BB-448D-90A6-C38DD7ED9FB1Q27325653-33AA9B9A-4039-4343-9176-9A2DF28B3F25Q28238781-D2A524BD-9F5E-493E-9633-FFDB58622031Q28292467-24BDD850-6DF6-4862-BEA2-D9FE9ECC26D2Q28301682-9A90364E-43FF-4F1C-965C-63B1AA0439D7Q28302896-7F54D0FB-6ED9-43D7-AAB7-244C124E772CQ28577803-01F4F0A9-86C2-4E4F-87B9-4BF688E40C35Q28583778-8184A16D-2B3B-45DD-9790-27D978A5D9C9Q30459556-1CAD6386-EB3C-4490-A7F8-9F774B091F22Q33288792-24C1E4B3-0078-40BB-A847-71B4C44A8E35Q33289555-9B065015-C2AC-45DA-806A-ADAC62BD879BQ33307072-BF6A0BF0-4607-45DE-9BB8-70B68D276054Q33319245-0AE009B3-9BCF-4EE9-A478-EB4BB06D2C0CQ33431104-D537EFA8-C41D-4009-B005-8B78976E4C69Q33600966-ED18DB41-A356-4E75-89E7-6F7569A243EFQ33636748-5732C484-0F57-4757-AFF9-3467427D3A51Q33649249-4BB08BF2-7C52-48E5-88DC-12EE336A9CD3Q33712605-E2588061-7AA8-4E53-81A2-1D35116F0BA5Q33804104-71773AD9-3CD9-44FD-AC38-0878CF8CB9CAQ33985338-56114BFC-DC6E-4C8E-A484-9FC2101EFC5FQ33992512-402B65E1-19EB-466C-82E8-565841B23A7DQ34156739-D112D52C-FC80-4133-B401-98ECA47A9D29Q34181537-EED9EEE9-E5AD-4433-AE9E-98D081B642F1Q34298989-D36D744A-6BAD-462F-BF8F-A404CB69A6F8Q34402367-A3DA59B4-63BB-46E9-9356-9BFEE32ACDF6Q34685059-D3B6ACBD-BCE7-4EFE-A8E9-E4635A3C6585Q34709275-3D3E4CB2-DD15-43F0-BDE6-F9D552164926Q34718158-0F96253D-4598-42B1-8545-3BBA6BDF5E78Q35156029-5A7FFCB1-4597-4269-A64B-2EB9DD89E688Q35566336-6E88DB43-F584-4529-9AAD-6BDD22BD5155Q35651426-088FA89C-638C-4411-B2EE-55FA76BC4EB6Q35695329-1B3D7BD7-AD56-4671-B41A-3741C54FAC11Q35728669-262D57C8-1D71-42DE-91CA-96057B091F4FQ35737544-7EFF82B7-A98E-42D6-9665-7994183CF6FDQ35755676-5D7A903A-F5B7-496B-919B-49FC808D2B39
P2860
Dmp1-deficient mice display severe defects in cartilage formation responsible for a chondrodysplasia-like phenotype
description
2004 nî lūn-bûn
@nan
2004 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Dmp1-deficient mice display se ...... hondrodysplasia-like phenotype
@ast
Dmp1-deficient mice display se ...... hondrodysplasia-like phenotype
@en
type
label
Dmp1-deficient mice display se ...... hondrodysplasia-like phenotype
@ast
Dmp1-deficient mice display se ...... hondrodysplasia-like phenotype
@en
prefLabel
Dmp1-deficient mice display se ...... hondrodysplasia-like phenotype
@ast
Dmp1-deficient mice display se ...... hondrodysplasia-like phenotype
@en
P2093
P2860
P356
P1476
Dmp1-deficient mice display se ...... hondrodysplasia-like phenotype
@en
P2093
Adele Boskey
Haiyang Huang
Jian Q Feng
Lynda F Bonewald
Mark R Dallas
Pitchumani Sivakumar
Sarah L Dallas
Takeo W Tsutsui
P2860
P304
P356
10.1074/JBC.M412911200
P407
P577
2004-12-07T00:00:00Z