scholarly article | Q13442814 |
P50 | author | Ernesto Canalis | Q56269284 |
Stefano Zanotti | Q56269901 | ||
Kristen Parker | Q117248443 | ||
P2093 | author name string | Ernesto Canalis | |
P2860 | cites work | Guidelines for assessment of bone microstructure in rodents using micro-computed tomography | Q37763651 |
Effect of primary and secondary structure of oligodeoxyribonucleotides on the fluorescent properties of conjugated dyes | Q39600740 | ||
Multiplex quantitative PCR using self-quenched primers labeled with a single fluorophore | Q39600850 | ||
Notch 1 overexpression inhibits osteoblastogenesis by suppressing Wnt/beta-catenin but not bone morphogenetic protein signaling | Q40331060 | ||
Expression of the BMP 2 gene during bone cell differentiation. | Q40607137 | ||
Recombinant human bone morphogenetic protein-2 induces osteoblastic differentiation in W-20-17 stromal cells | Q41638851 | ||
The mode of bone morphogenetic protein (BMP) receptor oligomerization determines different BMP-2 signaling pathways. | Q42823613 | ||
Protein related to DAN and cerberus is a bone morphogenetic protein antagonist that participates in ovarian paracrine regulation | Q44811143 | ||
Targeted deletion of the sclerostin gene in mice results in increased bone formation and bone strength | Q46186977 | ||
Age-related changes in trabecular architecture differ in female and male C57BL/6J mice. | Q51009028 | ||
C/EBP homologous protein is necessary for normal osteoblastic function. | Q53566901 | ||
Skeletal Overexpression of Noggin Results in Osteopenia and Reduced Bone Formation | Q57936901 | ||
Bone morphogenetic proteins in bone stimulate osteoclasts and osteoblasts during bone development | Q79822578 | ||
Activation of the ERK pathway in osteoblastic cells, role of gremlin and BMP-2 | Q80735928 | ||
Deletion of a single allele of the Dkk1 gene leads to an increase in bone formation and bone mass | Q83924358 | ||
Skeletal overexpression of gremlin impairs bone formation and causes osteopenia | Q24314447 | ||
The Xenopus dorsalizing factor Gremlin identifies a novel family of secreted proteins that antagonize BMP activities | Q24314690 | ||
Two doses of sclerostin antibody in cynomolgus monkeys increases bone formation, bone mineral density, and bone strength | Q28274891 | ||
Sclerostin inhibition of Wnt-3a-induced C3H10T1/2 cell differentiation is indirect and mediated by bone morphogenetic proteins | Q28293474 | ||
Sclerostin antibody treatment increases bone formation, bone mass, and bone strength in a rat model of postmenopausal osteoporosis | Q28302443 | ||
Gremlin-mediated BMP antagonism induces the epithelial-mesenchymal feedback signaling controlling metanephric kidney and limb organogenesis | Q28506504 | ||
Gremlin is the BMP antagonist required for maintenance of Shh and Fgf signals during limb patterning | Q28507504 | ||
Identification of drm, a novel gene whose expression is suppressed in transformed cells and which can inhibit growth of normal but not transformed cells in culture | Q28576024 | ||
Biosynthesis, post-translation modification, and functional characterization of Drm/Gremlin | Q28578839 | ||
Bone histomorphometry: standardization of nomenclature, symbols, and units. Report of the ASBMR Histomorphometry Nomenclature Committee | Q29616160 | ||
Generation and Selection of Novel Fully Human Monoclonal Antibodies That Neutralize Dickkopf-1 (DKK1) Inhibitory Function in Vitro and Increase Bone Mass in Vivo | Q30497635 | ||
Validation of peripheral dual-energy X-ray absorptiometry for the measurement of bone mineral in intact and excised long bones of rats | Q31970416 | ||
Signal transduction by bone morphogenetic protein receptors: functional roles of Smad proteins | Q33697455 | ||
Bone morphogenetic proteins induce gremlin, a protein that limits their activity in osteoblasts | Q33927389 | ||
Connective tissue growth factor is required for skeletal development and postnatal skeletal homeostasis in male mice | Q34132427 | ||
Bone morphogenetic protein antagonist gremlin 1 is widely expressed by cancer-associated stromal cells and can promote tumor cell proliferation | Q34569128 | ||
Bone morphogenetic proteins and their antagonists | Q34572394 | ||
Conditional deletion of gremlin causes a transient increase in bone formation and bone mass | Q34676851 | ||
Bone morphogenetic proteins, their antagonists, and the skeleton | Q35109618 | ||
Wnt inhibitors Dkk1 and Sost are downstream targets of BMP signaling through the type IA receptor (BMPRIA) in osteoblasts. | Q35156225 | ||
The CCN family: a new stimulus package | Q35194555 | ||
Wnt signaling in osteoblasts and bone diseases | Q35913119 | ||
Connective-tissue growth factor (CTGF) modulates cell signalling by BMP and TGF-beta | Q36663630 | ||
Skeletal overexpression of connective tissue growth factor impairs bone formation and causes osteopenia | Q36908891 | ||
BMP signaling negatively regulates bone mass through sclerostin by inhibiting the canonical Wnt pathway. | Q37222697 | ||
Bone morphogenetic proteins induce the expression of noggin, which limits their activity in cultured rat osteoblasts | Q37388231 | ||
Enhanced osteoclastogenesis causes osteopenia in twisted gastrulation-deficient mice through increased BMP signaling | Q37396641 | ||
Phosphatidylinositol 3 kinase/Akt signal relay cooperates with smad in bone morphogenetic protein-2-induced colony stimulating factor-1 (CSF-1) expression and osteoclast differentiation | Q37418214 | ||
P433 | issue | 1 | |
P304 | page(s) | 269-277 | |
P577 | publication date | 2012-01-01 | |
P1433 | published in | Journal of Cellular Physiology | Q1524270 |
P1476 | title | Gremlin1 is required for skeletal development and postnatal skeletal homeostasis | |
P478 | volume | 227 |
Q36132931 | A soluble bone morphogenetic protein type IA receptor increases bone mass and bone strength |
Q36219733 | Adipose Tissue Residing Progenitors (Adipocyte Lineage Progenitors and Adipose Derived Stem Cells (ADSC). |
Q38896053 | Agonists and Antagonists of TGF-β Family Ligands |
Q36889250 | Bone mineral properties in growing Col1a2(+/G610C) mice, an animal model of osteogenesis imperfecta |
Q35872773 | Conditional inactivation of noggin in the postnatal skeleton causes osteopenia |
Q46012172 | Expression of Noggin and Gremlin1 and its implications in fine-tuning BMP activities in mouse cartilage tissues. |
Q27323315 | Gremlin 1 identifies a skeletal stem cell with bone, cartilage, and reticular stromal potential. |
Q33867359 | Gremlin1 plays a key role in kidney development and renal fibrosis |
Q38942069 | Gremlin1 preferentially binds to bone morphogenetic protein-2 (BMP-2) and BMP-4 over BMP-7. |
Q35755147 | High-throughput screening of mouse gene knockouts identifies established and novel skeletal phenotypes |
Q91688877 | New Insights on Properties and Spatial Distributions of Skeletal Stem Cells |
Q44824506 | Use of locally weighted scatterplot smoothing (LOWESS) regression to study selection signatures in Piedmontese and Italian Brown cattle breeds. |
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