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Direct induction of chondrogenic cells from human dermal fibroblast culture by defined factorsCOL11A2 collagen gene transcription is differentially regulated by EWS/ERG sarcoma fusion protein and wild-type ERGDifferential expression of an acidic domain in the amino-terminal propeptide of mouse pro-alpha 2(XI) collagen by complex alternative splicingSIK3 is essential for chondrocyte hypertrophy during skeletal development in miceWwp2 is essential for palatogenesis mediated by the interaction between Sox9 and mediator subunit 25Identification of an enhancer sequence within the first intron required for cartilage-specific transcription of the alpha2(XI) collagen geneRole of CDMP-1 in skeletal morphogenesis: promotion of mesenchymal cell recruitment and chondrocyte differentiationIdentification of small molecular compounds and fabrication of its aqueous solution by laser-ablation, expanding primordial cartilage.Enhancer analysis of the alpha 1(II) and alpha 2(XI) collagen genes in transfected chondrocytes and transgenic mice.Generation of hyaline cartilaginous tissue from mouse adult dermal fibroblast culture by defined factorsSalt-inducible Kinase 3 Signaling Is Important for the Gluconeogenic Programs in Mouse Hepatocytes.Pterosin B prevents chondrocyte hypertrophy and osteoarthritis in mice by inhibiting Sik3.Sox9 reprogrammed dermal fibroblasts undergo hypertrophic differentiation in vitro and trigger endochondral ossification in vivo.Essential mesenchymal role of small GTPase Rac1 in interdigital programmed cell death during limb development.Generation of scaffoldless hyaline cartilaginous tissue from human iPSCs.Limited Immunogenicity of Human Induced Pluripotent Stem Cell-Derived Cartilages.Oxygen tension regulates chondrocyte differentiation and function during endochondral ossification.Differential expression of aggrecan mRNA isoforms by chondrosarcoma cells.Separable cis-regulatory elements that contribute to tissue- and site-specific alpha 2(XI) collagen gene expression in the embryonic mouse cartilage.Corrigendum: Pterosin B prevents chondrocyte hypertrophy and osteoarthritis in mice by inhibiting Sik3.Cell reprogramming for skeletal dysplasia drug repositioning.Characteristics of fracture and related factors in patients with rheumatoid arthritis.Time-lapse observation of the dedifferentiation process in mouse chondrocytes using chondrocyte-specific reporters.Identification of an enhancer sequence within the first intron required for cartilage-specific transcription of the α2(XI) collagen gene. VOLUME 275 (2000) PAGES 12712-12718.A selective inhibition of c-Fos/activator protein-1 as a potential therapeutic target for intervertebral disc degeneration and associated pain.A-674563 increases chondrocyte marker expression in cultured chondrocytes by inhibiting Sox9 degradation.Repair of articular cartilage defects in rabbits using CDMP1 gene-transfected autologous mesenchymal cells derived from bone marrow.Modular arrangement of cartilage- and neural tissue-specific cis-elements in the mouse alpha2(XI) collagen promoter.Loss of Mob1a/b in mice results in chondrodysplasia due to YAP1/TAZ-TEADs-dependent repression of SOX9.Bone morphogenetic protein signals are required for cartilage formation and differently regulate joint development during skeletogenesis.Statin treatment rescues FGFR3 skeletal dysplasia phenotypes.Modeling type II collagenopathy skeletal dysplasia by directed conversion and induced pluripotent stem cells.Integration Capacity of Human Induced Pluripotent Stem Cell-Derived CartilageConsiderations in hiPSC-derived cartilage for articular cartilage repairCervical spondylotic radiculopathy involving two adjacent nerve roots. Anterior decompression through a single level intervertebral approachProgressive degeneration of articular cartilage and intervertebral discs. An experimental study in transgenic mice bearing a type IX collagen mutation[Collagen genes and skeletal disorders]A recurrent 1992delCT mutation of the type X collagen gene in a Japanese patient with Schmid metaphyseal chondrodysplasiaA novel type X collagen gene mutation (G595R) associated with Schmid-type metaphyseal chondrodysplasiaAlternative splicing of fibronectin transcripts in osteochondrogenic tumors
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description
researcher
@en
name
N Tsumaki
@en
N Tsumaki
@nl
type
label
N Tsumaki
@en
N Tsumaki
@nl
prefLabel
N Tsumaki
@en
N Tsumaki
@nl
P106
P31
P496
0000-0002-0520-3654