about
Recombinant human extracellular matrix protein 1 inhibits alkaline phosphatase activity and mineralization of mouse embryonic metatarsals in vitroExtracellular matrix protein 1 (ECM1) has angiogenic properties and is expressed by breast tumor cellsSmad-interacting protein 1 is a repressor of liver/bone/kidney alkaline phosphatase transcription in bone morphogenetic protein-induced osteogenic differentiation of C2C12 cellsMolecular cloning, characterization, and genetic mapping of the cDNA coding for a novel secretory protein of mouse. Demonstration of alternative splicing in skin and cartilageMeta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22Cystinosis (ctns) zebrafish mutant shows pronephric glomerular and tubular dysfunction.delta-EF1 is a negative regulator of Ihh in the developing growth plate.Differentiation-dependent alternative splicing and expression of the extracellular matrix protein 1 gene in human keratinocytes.Isolation and characterization of chondrolectin (Chodl), a novel C-type lectin predominantly expressed in muscle cells.Orphan G-protein coupled receptor 22 (Gpr22) regulates cilia length and structure in the zebrafish Kupffer's vesicleWnt signaling and osteoarthritis.Limb skeletal malformations - what the HOX is going on?Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation.Noggin haploinsufficiency differentially affects tissue responses in destructive and remodeling arthritis.Wnt-ligand-dependent interaction of TAK1 (TGF-beta-activated kinase-1) with the receptor tyrosine kinase Ror2 modulates canonical Wnt-signalling.Characterization of Frzb-Cre transgenic mouse.The bone morphogenetic protein 2 signaling mediator Smad1 participates predominantly in osteogenic and not in chondrogenic differentiation in mesenchymal progenitors C3H10T1/2.Noggin inactivation affects the number and differentiation potential of muscle progenitor cells in vivo.Relationships between translation of pro alpha1(I) and pro alpha2(I) mRNAs during synthesis of the type I procollagen heterotrimer.Smoc2 modulates embryonic myelopoiesis during zebrafish development.Novel Mutation of the RUNX2 Gene in Patients with Cleidocranial Dysplasia.The C-terminal domain of Mad-like signal transducers is sufficient for biological activity in the Xenopus embryo and transcriptional activation.Expression profile and thyroid hormone responsiveness of transporters and deiodinases in early embryonic chicken brain development.Zfhx1a and Zfhx1b mRNAs have non-overlapping expression domains during chick and mouse midgestation limb development.Cooperation of BMP and IHH signaling in interdigital cell fate determination.SMOC2 inhibits calcification of osteoprogenitor and endothelial cells.A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to aCol2a1mutationJoining the fingers: a HOXD13 StoryAn N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterningStrategies for Modulating Oxidative Stress under Diverse Physiological and Pathological ConditionsMultipotent mesenchymal stem cells from adult human synovial membraneArticular cartilage and biomechanical properties of the long bones in Frzb-knockout miceThe Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defectsNoggin haploinsufficiency influences severity of arthritis in different mouse models
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Przemko Tylzanowski
@ast
Przemko Tylzanowski
@en
Przemko Tylzanowski
@es
Przemko Tylzanowski
@nl
Przemko Tylzanowski
@sl
type
label
Przemko Tylzanowski
@ast
Przemko Tylzanowski
@en
Przemko Tylzanowski
@es
Przemko Tylzanowski
@nl
Przemko Tylzanowski
@sl
prefLabel
Przemko Tylzanowski
@ast
Przemko Tylzanowski
@en
Przemko Tylzanowski
@es
Przemko Tylzanowski
@nl
Przemko Tylzanowski
@sl
P106
P21
P31
P496
0000-0003-0769-559X