| scholarly article | Q13442814 |
| review article | Q7318358 |
| P2093 | author name string | Michael B O'Connor | |
| Seth S Blair | |||
| David Umulis | |||
| P2860 | cites work | Glypicans | Q21183908 |
| DRAGON, a bone morphogenetic protein co-receptor | Q24292739 | ||
| Glypican LON-2 is a conserved negative regulator of BMP-like signaling in Caenorhabditis elegans | Q24293743 | ||
| Bone morphogenetic proteins signal through the transforming growth factor-beta type III receptor | Q24306137 | ||
| BMPER is an endothelial cell regulator and controls bone morphogenetic protein-4-dependent angiogenesis | Q24312066 | ||
| Biglycan is a new extracellular component of the Chordin-BMP4 signaling pathway | Q24529120 | ||
| GDF11 forms a bone morphogenetic protein 1-activated latent complex that can modulate nerve growth factor-induced differentiation of PC12 cells | Q24531973 | ||
| BMP-2 antagonists emerge from alterations in the low-affinity binding epitope for receptor BMPR-II | Q24631766 | ||
| A new model for growth factor activation: type II receptors compete with the prodomain for BMP-7 | Q24653867 | ||
| The evolutionarily conserved BMP-binding protein Twisted gastrulation promotes BMP signalling | Q24656491 | ||
| BMPER, a novel endothelial cell precursor-derived protein, antagonizes bone morphogenetic protein signaling and endothelial cell differentiation | Q24679290 | ||
| Regulation of limb patterning by extracellular microfibrils | Q24685602 | ||
| Type I receptor binding of bone morphogenetic protein 6 is dependent on N-glycosylation of the ligand | Q27649251 | ||
| Crystal structure analysis reveals how the Chordin family member crossveinless 2 blocks BMP-2 receptor binding | Q27650592 | ||
| Targeting of bone morphogenetic protein growth factor complexes to fibrillin | Q28118178 | ||
| Identification of the ligand-binding site of the BMP type IA receptor for BMP-4 | Q28203953 | ||
| Heparan sulfate proteoglycans retain Noggin at the cell surface: a potential mechanism for shaping bone morphogenetic protein gradients | Q28204970 | ||
| Homologues of Twisted gastrulation are extracellular cofactors in antagonism of BMP signalling | Q28205891 | ||
| Lipoprotein particles are required for Hedgehog and Wingless signalling | Q28248673 | ||
| BMP antagonists: their roles in development and involvement in pathophysiology | Q28255986 | ||
| TGFbeta family signaling: novel insights in development and disease | Q28262452 | ||
| Cellular trafficking of the glypican Dally-like is required for full-strength Hedgehog signaling and wingless transcytosis | Q28279926 | ||
| The Twisted gastrulation family of proteins, together with the IGFBP and CCN families, comprise the TIC superfamily of cysteine rich secreted factors | Q28360508 | ||
| glypican-3 controls cellular responses to Bmp4 in limb patterning and skeletal development | Q28507693 | ||
| Kielin/chordin-like protein, a novel enhancer of BMP signaling, attenuates renal fibrotic disease | Q28508295 | ||
| Repulsive guidance molecule (RGMa), a DRAGON homologue, is a bone morphogenetic protein co-receptor | Q28510682 | ||
| Cell-surface heparan sulfate proteoglycans potentiate chordin antagonism of bone morphogenetic protein signaling and are necessary for cellular uptake of chordin | Q28512603 | ||
| HSPG modification by the secreted enzyme Notum shapes the Wingless morphogen gradient | Q28609767 | ||
| Evo-devo: variations on ancestral themes | Q28755209 | ||
| Positional information and the spatial pattern of cellular differentiation | Q29616635 | ||
| Analysis of dynamic morphogen scale invariance | Q41832321 | ||
| Proteolytic cleavage of Chordin as a switch for the dual activities of Twisted gastrulation in BMP signaling | Q41835575 | ||
| Mouse Crossveinless-2 is the vertebrate homolog of a Drosophila extracellular regulator of BMP signaling | Q41850839 | ||
| Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos | Q41858943 | ||
| The endocytic pathway and formation of the Wingless morphogen gradient | Q42487988 | ||
| Elucidation of subfamily segregation and intramolecular coevolution of the olfactomedin-like proteins by comprehensive phylogenetic analysis and gene expression pattern assessment. | Q42670137 | ||
| Dally regulates Dpp morphogen gradient formation by stabilizing Dpp on the cell surface. | Q43029966 | ||
| Regulation of ADMP and BMP2/4/7 at opposite embryonic poles generates a self-regulating morphogenetic field | Q43073793 | ||
| The BMP signaling gradient patterns dorsoventral tissues in a temporally progressive manner along the anteroposterior axis | Q43074864 | ||
| dlx3b/4b are required for the formation of the preplacodal region and otic placode through local modulation of BMP activity | Q43138530 | ||
| Crossveinless-2 Is a BMP feedback inhibitor that binds Chordin/BMP to regulate Xenopus embryonic patterning | Q43244356 | ||
| Type IV collagens and Dpp: positive and negative regulators of signaling | Q44257725 | ||
| Vertebrate crossveinless 2 is secreted and acts as an extracellular modulator of the BMP signaling cascade | Q44930072 | ||
| Silencing of TGF-beta signalling by the pseudoreceptor BAMBI. | Q45345819 | ||
| Combinatorial signaling by Twisted Gastrulation and Decapentaplegic. | Q46019495 | ||
| On the role of glypicans in the process of morphogen gradient formation | Q46050552 | ||
| Creation of a Sog morphogen gradient in the Drosophila embryo | Q46099920 | ||
| The Drosophila decapentaplegic and short gastrulation genes function antagonistically during adult wing vein development. | Q46182535 | ||
| Abrogation of heparan sulfate synthesis in Drosophila disrupts the Wingless, Hedgehog and Decapentaplegic signaling pathways | Q46222991 | ||
| Regulation of BMP-induced ectopic bone formation by Ahsg | Q46483432 | ||
| Do morphogen gradients arise by diffusion? | Q46502677 | ||
| Dorsal-ventral patterning of the Drosophila embryo depends on a putative negative growth factor encoded by the short gastrulation gene | Q46783591 | ||
| Knockdown of zebrafish crim1 results in a bent tail phenotype with defects in somite and vascular development | Q46981063 | ||
| Type IV collagens regulate BMP signalling in Drosophila | Q47070333 | ||
| Three Drosophila EXT genes shape morphogen gradients through synthesis of heparan sulfate proteoglycans | Q47070505 | ||
| Regulation of dally, an integral membrane proteoglycan, and its function during adult sensory organ formation of Drosophila | Q47070527 | ||
| Opposing activities of Dally-like glypican at high and low levels of Wingless morphogen activity | Q47070543 | ||
| Matching catalytic activity to developmental function: tolloid-related processes Sog in order to help specify the posterior crossvein in the Drosophila wing | Q47071229 | ||
| Long-range Dpp signaling is regulated to restrict BMP signaling to a crossvein competent zone. | Q47071235 | ||
| Facilitated transport of a Dpp/Scw heterodimer by Sog/Tsg leads to robust patterning of the Drosophila blastoderm embryo | Q47071657 | ||
| Crossveinless 2 contains cysteine-rich domains and is required for high levels of BMP-like activity during the formation of the cross veins in Drosophila | Q47071708 | ||
| Gradient formation of the TGF-beta homolog Dpp. | Q47071783 | ||
| Dpp gradient formation in the Drosophila wing imaginal disc | Q47072140 | ||
| Expression of a secreted form of Dally, a Drosophila glypican, induces overgrowth phenotype by affecting action range of Hedgehog | Q47072245 | ||
| Crossveinless 2 is an essential positive feedback regulator of Bmp signaling during zebrafish gastrulation | Q47074038 | ||
| crm-1 facilitates BMP signaling to control body size in Caenorhabditis elegans | Q47270276 | ||
| Physical properties of Tld, Sog, Tsg and Dpp protein interactions are predicted to help create a sharp boundary in Bmp signals during dorsoventral patterning of the Drosophila embryo | Q47681453 | ||
| DRAGON, a GPI-anchored membrane protein, inhibits BMP signaling in C2C12 myoblasts | Q47862467 | ||
| Anti-dorsalizing morphogenetic protein is a novel TGF-beta homolog expressed in the Spemann organizer | Q48068846 | ||
| Lipoprotein-heparan sulfate interactions in the Hh pathway | Q50336941 | ||
| Mammalian Notum induces the release of glypicans and other GPI-anchored proteins from the cell surface | Q50336949 | ||
| Syndecan-1 regulates BMP signaling and dorso-ventral patterning of the ectoderm during early Xenopus development. | Q51756884 | ||
| Kinetics of morphogen gradient formation. | Q51924455 | ||
| The mechanism of sudden stripe formation during dorso-ventral patterning in Drosophila. | Q51928749 | ||
| Twisted gastrulation mutation suppresses skeletal defect phenotypes in Crossveinless 2 mutant mice. | Q51952135 | ||
| Heparan sulfate proteoglycans at a glance. | Q51985397 | ||
| Crim1KST264/KST264 mice implicate Crim1 in the regulation of vascular endothelial growth factor-A activity during glomerular vascular development. | Q51987898 | ||
| Tolloid gets Sizzled competing with Chordin. | Q52026716 | ||
| Drosophila Dpp morphogen movement is independent of dynamin-mediated endocytosis but regulated by the glypican members of heparan sulfate proteoglycans. | Q52086756 | ||
| A vertebrate crossveinless 2 homologue modulates BMP activity and neural crest cell migration. | Q52087210 | ||
| Robustness of the BMP morphogen gradient in Drosophila embryonic patterning. | Q52114692 | ||
| Follistatin regulates bone morphogenetic protein-7 (BMP-7) activity to stimulate embryonic muscle growth. | Q52123833 | ||
| Dpp receptor levels contribute to shaping the Dpp morphogen gradient in the Drosophila wing imaginal disc. | Q52182365 | ||
| Dpp gradient formation by dynamin-dependent endocytosis: receptor trafficking and the diffusion model. | Q52650937 | ||
| The crossveinless gene encodes a new member of the Twisted gastrulation family of BMP-binding proteins which, with Short gastrulation, promotes BMP signaling in the crossveins of the Drosophila wing. | Q52657937 | ||
| α2-HS Glycoprotein/Fetuin, a Transforming Growth Factor-β/Bone Morphogenetic Protein Antagonist, Regulates Postnatal Bone Growth and Remodeling | Q56999751 | ||
| Scaling of the BMP activation gradient in Xenopus embryos | Q59064240 | ||
| Modulation of the binding of matrix Gla protein (MGP) to bone morphogenetic protein-2 (BMP-2) | Q73387646 | ||
| Site-specific interaction of bone morphogenetic protein 2 with procollagen II | Q74484057 | ||
| Mechanisms for positional signalling by morphogen transport: a theoretical study | Q74567323 | ||
| von Willebrand factor type C domain-containing proteins regulate bone morphogenetic protein signaling through different recognition mechanisms | Q80273766 | ||
| Heparan sulfate proteoglycans including syndecan-3 modulate BMP activity during limb cartilage differentiation | Q81354471 | ||
| Bmp signaling: turning a half into a whole | Q81636894 | ||
| Order out of chaos: assembly of ligand binding sites in heparan sulfate | Q29620085 | ||
| The interpretation of position in a morphogen gradient as revealed by occupancy of activin receptors | Q30052356 | ||
| crossveinless defines a new family of Twisted-gastrulation-like modulators of bone morphogenetic protein signalling | Q30982795 | ||
| Tsukushi functions as an organizer inducer by inhibition of BMP activity in cooperation with chordin. | Q33206751 | ||
| BMP stimulation of alkaline phosphatase activity in pluripotent mouse C2C12 cells is inhibited by dermatopontin, one of the most abundant low molecular weight proteins in demineralized bone matrix | Q33264254 | ||
| Synergistic effects of Nell-1 and BMP-2 on the osteogenic differentiation of myoblasts | Q33835530 | ||
| Why cytoplasmic signalling proteins should be recruited to cell membranes. | Q33885449 | ||
| Spemann's organizer and self-regulation in amphibian embryos | Q33993579 | ||
| Action range of BMP is defined by its N-terminal basic amino acid core | Q34113614 | ||
| CRIM1 regulates the rate of processing and delivery of bone morphogenetic proteins to the cell surface. | Q34205739 | ||
| Domain-specific modification of heparan sulfate by Qsulf1 modulates the binding of the bone morphogenetic protein antagonist Noggin | Q34279840 | ||
| Human Crossveinless-2 is a novel inhibitor of bone morphogenetic proteins | Q34295177 | ||
| Patched controls the Hedgehog gradient by endocytosis in a dynamin-dependent manner, but this internalization does not play a major role in signal transduction | Q34315554 | ||
| A common plan for dorsoventral patterning in Bilateria | Q34374917 | ||
| Cleavage of Chordin by Xolloid metalloprotease suggests a role for proteolytic processing in the regulation of Spemann organizer activity | Q34445698 | ||
| A translational block to HSPG synthesis permits BMP signaling in the early Drosophila embryo | Q34454099 | ||
| Embryonic dorsal-ventral signaling: secreted frizzled-related proteins as inhibitors of tolloid proteinases | Q34484724 | ||
| Robust, bistable patterning of the dorsal surface of the Drosophila embryo | Q34550702 | ||
| Bone morphogenetic proteins and their antagonists | Q34572394 | ||
| Crim1KST264/KST264 mice display a disruption of the Crim1 gene resulting in perinatal lethality with defects in multiple organ systems | Q34581812 | ||
| Chordin-like CR domains and the regulation of evolutionarily conserved extracellular signaling systems. | Q34626087 | ||
| The cysteine-rich domain protein KCP is a suppressor of transforming growth factor beta/activin signaling in renal epithelia | Q34718144 | ||
| Activation of latent myostatin by the BMP-1/tolloid family of metalloproteinases | Q34792315 | ||
| Extracellular regulation of BMP signaling in vertebrates: a cocktail of modulators | Q34958533 | ||
| Comparative Genomic Analysis of the Eight-Membered Ring Cystine Knot-Containing Bone Morphogenetic Protein Antagonists | Q35549994 | ||
| Crossveinless-2 controls bone morphogenetic protein signaling during early cardiomyocyte differentiation in P19 cells | Q35674506 | ||
| Formation of the BMP activity gradient in the Drosophila embryo | Q35690799 | ||
| Wingful, an extracellular feedback inhibitor of Wingless | Q35776013 | ||
| Molecular recognition in bone morphogenetic protein (BMP)/receptor interaction | Q35902283 | ||
| Interpreting clone-mediated perturbations of morphogen profiles. | Q36008793 | ||
| Direct binding of follistatin to a complex of bone-morphogenetic protein and its receptor inhibits ventral and epidermal cell fates in early Xenopus embryo | Q36257576 | ||
| Type IIA procollagen containing the cysteine-rich amino propeptide is deposited in the extracellular matrix of prechondrogenic tissue and binds to TGF-beta1 and BMP-2. | Q36288339 | ||
| Shaping BMP morphogen gradients in the Drosophila embryo and pupal wing. | Q36348381 | ||
| The interpretation of morphogen gradients | Q36367278 | ||
| Quantitative models of developmental pattern formation | Q36584506 | ||
| Extracellular modulation of BMP activity in patterning the dorsoventral axis. | Q36633269 | ||
| Mathematical modeling identifies Smad nucleocytoplasmic shuttling as a dynamic signal-interpreting system | Q36638792 | ||
| Morpheus unbound: reimagining the morphogen gradient | Q36718804 | ||
| Tinkering with heparan sulfate sulfation to steer development | Q36744373 | ||
| Xenopus kielin: A dorsalizing factor containing multiple chordin-type repeats secreted from the embryonic midline. | Q36970265 | ||
| Robustness of embryonic spatial patterning in Drosophila melanogaster. | Q37006654 | ||
| Theoretical and experimental approaches to understand morphogen gradients | Q37118479 | ||
| A concentration-dependent endocytic trap and sink mechanism converts Bmper from an activator to an inhibitor of Bmp signaling | Q37124350 | ||
| BMPER is a conserved regulator of hematopoietic and vascular development in zebrafish | Q37258951 | ||
| Interaction between proteins localized in membranes | Q37396417 | ||
| Informatics approaches to understanding TGFbeta pathway regulation. | Q37397518 | ||
| Bone morphogenetic protein-2 activity is regulated by secreted phosphoprotein-24 kd, an extracellular pseudoreceptor, the gene for which maps to a region of the human genome important for bone quality | Q37449764 | ||
| The regulation of TGFbeta signal transduction | Q37621155 | ||
| Twisted gastrulation is a conserved extracellular BMP antagonist | Q38303086 | ||
| Essential pro-Bmp roles of crossveinless 2 in mouse organogenesis | Q38308645 | ||
| Sizzled controls dorso-ventral polarity by repressing cleavage of the Chordin protein | Q38315245 | ||
| Cerberus functions as a BMP agonist to synergistically induce nodal expression during left-right axis determination in the chick embryo. | Q39921132 | ||
| Robust stability of the embryonic axial pattern requires a secreted scaffold for chordin degradation | Q39942706 | ||
| Amelogenin binds to both heparan sulfate and bone morphogenetic protein 2 and pharmacologically suppresses the effect of noggin. | Q39976665 | ||
| Proline and gamma-carboxylated glutamate residues in matrix Gla protein are critical for binding of bone morphogenetic protein-4. | Q39998162 | ||
| Development of the vertebral morphogenetic field in the mouse: interactions between Crossveinless-2 and Twisted Gastrulation | Q40047807 | ||
| HSPG modulation of BMP signaling in fibrodysplasia ossificans progressiva cells | Q40129950 | ||
| The function of a Drosophila glypican does not depend entirely on heparan sulfate modification | Q40217255 | ||
| The prodomain of BMP-7 targets the BMP-7 complex to the extracellular matrix | Q40414698 | ||
| Spatial bistability of Dpp-receptor interactions during Drosophila dorsal-ventral patterning. | Q40439096 | ||
| The BMP-binding protein Crossveinless 2 is a short-range, concentration-dependent, biphasic modulator of BMP signaling in Drosophila. | Q41063878 | ||
| Production of a DPP activity gradient in the early Drosophila embryo through the opposing actions of the SOG and TLD proteins | Q41080207 | ||
| Human bone morphogenetic protein 2 contains a heparin-binding site which modifies its biological activity | Q41211589 | ||
| Fish are like flies are like frogs: conservation of dorsal-ventral patterning mechanisms. | Q41459424 | ||
| P433 | issue | 22 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | morphogenesis | Q815547 |
| sequestering of BMP from receptor via BMP binding | Q21115972 | ||
| sequestering of TGFbeta from receptor via TGFbeta binding | Q22303643 | ||
| P1104 | number of pages | 14 | |
| P304 | page(s) | 3715-3728 | |
| P577 | publication date | 2009-11-01 | |
| P1433 | published in | Development | Q3025404 |
| P1476 | title | The extracellular regulation of bone morphogenetic protein signaling | |
| P478 | volume | 136 |
| Q40710612 | Accelerating protein release from microparticles for regenerative medicine applications |
| Q35676399 | Anterior segment alterations and comparative aqueous humor proteomics in the buphthalmic rabbit (an American Ophthalmological Society thesis). |
| Q27347557 | Anterograde Activin signaling regulates postsynaptic membrane potential and GluRIIA/B abundance at the Drosophila neuromuscular junction |
| Q48148998 | Anti-Müllerian hormone signaling is influenced by Follistatin 288, but not 14 other transforming growth factor beta superfamily regulators. |
| Q93153182 | Apcdd1 is a dual BMP/Wnt inhibitor in the developing nervous system and skin |
| Q37127457 | BMP Antagonist Gremlin 2 Limits Inflammation After Myocardial Infarction. |
| Q22065324 | BMP signaling components in embryonic transcriptomes of the hover fly Episyrphus balteatus (Syrphidae) |
| Q41591432 | BMP signaling in the development of the mouse esophagus and forestomach |
| Q37776859 | BMP signaling in vascular development and disease |
| Q38019707 | BMP signaling in wing development: A critical perspective on quantitative image analysis |
| Q51701151 | BMP2 Transfer to Neighboring Cells and Activation of Signaling. |
| Q33707750 | Binding between Crossveinless-2 and Chordin von Willebrand factor type C domains promotes BMP signaling by blocking Chordin activity |
| Q36268982 | Bmp2 conditional knockout in osteoblasts and endothelial cells does not impair bone formation after injury or mechanical loading in adult mice |
| Q38872877 | Bone Morphogenetic Proteins in Vascular Homeostasis and Disease |
| Q36035290 | Bone morphogenetic protein modulator BMPER is highly expressed in malignant tumors and controls invasive cell behavior |
| Q33804968 | CD44 and hyaluronan promote the bone morphogenetic protein 7 signaling response in murine chondrocytes |
| Q38812866 | CRIM1, a newfound cancer-related player, regulates the adhesion and migration of lung cancer cells |
| Q27347461 | Caenorhabditis elegans SMA-10/LRIG is a conserved transmembrane protein that enhances bone morphogenetic protein signaling |
| Q37409544 | Chordin forms a self-organizing morphogen gradient in the extracellular space between ectoderm and mesoderm in the Xenopus embryo |
| Q47071676 | Control of Dpp morphogen signalling by a secreted feedback regulator |
| Q35098166 | Crimpy inhibits the BMP homolog Gbb in motoneurons to enable proper growth control at the Drosophila neuromuscular junction |
| Q36010310 | Crossveinless 2 regulates bone morphogenetic protein 9 in human and mouse vascular endothelium |
| Q35978899 | Crossveinless d is a vitellogenin-like lipoprotein that binds BMPs and HSPGs, and is required for normal BMP signaling in the Drosophila wing |
| Q92488443 | Crossveinless is a direct transcriptional target of Trachealess and Tango in Drosophila tracheal precursor cells |
| Q42377350 | Crossveinless-2 is required for the relocalization of Chordin protein within the vertebral field in mouse embryos |
| Q39774510 | Cv2, functioning as a pro-BMP factor via twisted gastrulation, is required for early development of nephron precursors |
| Q34626056 | Development of Physiologically Based Pharmacokinetic Model (PBPK) of BMP2 in Mice |
| Q36476190 | Differential diffusivity of Nodal and Lefty underlies a reaction-diffusion patterning system. |
| Q90304779 | Disordered linkers in multidomain allosteric proteins: Entropic effect to favor the open state or enhanced local concentration to favor the closed state? |
| Q42131909 | Dorsal-ventral patterning: Crescent is a dorsally secreted Frizzled-related protein that competitively inhibits Tolloid proteases |
| Q42622861 | Dynamics of BMP signaling and distribution during zebrafish dorsal-ventral patterning |
| Q38538339 | EMBRYO DEVELOPMENT. BMP gradients: A paradigm for morphogen-mediated developmental patterning |
| Q34470346 | Efficient calculation of steady state probability distribution for stochastic biochemical reaction network |
| Q34341320 | Efficient reverse-engineering of a developmental gene regulatory network |
| Q34661949 | Expression and functional study of extracellular BMP antagonists during the morphogenesis of the digits and their associated connective tissues. |
| Q37066518 | Extracellular Regulation of Bone Morphogenetic Protein Activity by the Microfibril Component Fibrillin-1. |
| Q37932245 | Extracellular matrix in development: insights from mechanisms conserved between invertebrates and vertebrates |
| Q35561452 | Extracellular movement of signaling molecules. |
| Q37689990 | Extracellular regulation of BMP signaling |
| Q27026644 | Fine-tuned shuttles for bone morphogenetic proteins |
| Q41830263 | Free extracellular diffusion creates the Dpp morphogen gradient of the Drosophila wing disc |
| Q27005904 | Heparan sulfate in skeletal development, growth, and pathology: the case of hereditary multiple exostoses |
| Q89729149 | Homeobox D3, A Novel Link Between Bone Morphogenetic Protein 9 and Transforming Growth Factor Beta 1 Signaling |
| Q34429113 | ID family protein expression and regulation in hypoxic pulmonary hypertension |
| Q41636712 | Identification of a p53 target, CD137L, that mediates growth suppression and immune response of osteosarcoma cells. |
| Q28547838 | In silico Mechano-Chemical Model of Bone Healing for the Regeneration of Critical Defects: The Effect of BMP-2 |
| Q37397518 | Informatics approaches to understanding TGFbeta pathway regulation. |
| Q34365597 | Inhibition of bone morphogenetic proteins protects against atherosclerosis and vascular calcification |
| Q51412572 | Interplay between binding affinity and kinetics in protein-protein interactions. |
| Q39317513 | LRP1-dependent endocytic mechanism governs the signaling output of the bmp system in endothelial cells and in angiogenesis |
| Q26864974 | Making models match measurements: model optimization for morphogen patterning networks |
| Q37801803 | Mechanisms driving neural crest induction and migration in the zebrafish and Xenopus laevis |
| Q37358716 | Mechanisms of scaling in pattern formation |
| Q36752931 | Morphogen transport |
| Q36094301 | Multistep molecular mechanism for bone morphogenetic protein extracellular transport in the Drosophila embryo |
| Q88352257 | Nodal and BMP dispersal during early zebrafish development |
| Q34826199 | Notch and PKC are involved in formation of the lateral region of the dorso-ventral axis in Drosophila embryos |
| Q37047239 | Pentagone internalises glypicans to fine-tune multiple signalling pathways |
| Q37069124 | Perichondrium phenotype and border function are regulated by Ext1 and heparan sulfate in developing long bones: a mechanism likely deranged in Hereditary Multiple Exostoses |
| Q37889211 | Position matters: variability in the spatial pattern of BMP modulators generates functional diversity |
| Q22065789 | Primordial germ cells in mice |
| Q27311143 | Promotion of bone morphogenetic protein signaling by tetraspanins and glycosphingolipids |
| Q35873728 | Regulation of BMP activity and range in Drosophila wing development |
| Q42770522 | Regulation of TGFβ superfamily signaling by two separable domains of glypican LON-2 in C. elegans |
| Q47621324 | Regulation of glycosaminoglycan biogenesis is critical for sensitive-period-dependent vocal ontogeny. |
| Q38465654 | Regulators and effectors of bone morphogenetic protein signalling in the cardiovascular system. |
| Q38112402 | Repulsive guidance molecules (RGMs) and neogenin in bone morphogenetic protein (BMP) signaling |
| Q50229613 | Role of interleukin-10 in endochondral bone formation in mice: anabolic effect via the bone morphogenetic protein/Smad pathway |
| Q38890487 | SMOC can act as both an antagonist and an expander of BMP signaling. |
| Q42257664 | Secreted, receptor-associated bone morphogenetic protein regulators reduce stochastic noise intrinsic to many extracellular morphogen distributions |
| Q33755839 | Signaling pathways in cartilage repair |
| Q38019713 | Spatial regulation of BMP activity |
| Q35126888 | Spatiotemporal delivery of bone morphogenetic protein enhances functional repair of segmental bone defects. |
| Q27013995 | Systems control of BMP morphogen flow in vertebrate embryos |
| Q39107096 | TGF-β Family Signaling in Drosophila |
| Q21135289 | The BMP antagonist follistatin-like 1 is required for skeletal and lung organogenesis |
| Q36126757 | The Gyc76C Receptor Guanylyl Cyclase and the Foraging cGMP-Dependent Kinase Regulate Extracellular Matrix Organization and BMP Signaling in the Developing Wing of Drosophila melanogaster |
| Q41268124 | The RGM protein DRAG-1 positively regulates a BMP-like signaling pathway in Caenorhabditis elegans |
| Q38116934 | The TGFbeta superfamily signaling pathway |
| Q91767495 | The calcium channel subunit α2δ-3 organizes synapses via an activity-dependent and autocrine BMP signaling pathway |
| Q40733179 | The cell-surface proteins Dally-like and Ihog differentially regulate Hedgehog signaling strength and range during development |
| Q57180801 | The extracellular protease AdamTS-B inhibits vein formation in the Drosophila wing |
| Q38056252 | The importance of geometry in mathematical models of developing systems |
| Q38071469 | The myotomal basement membrane: insight into laminin-111 function and its control by Sonic hedgehog signaling |
| Q37178004 | The neogenin/DCC homolog UNC-40 promotes BMP signaling via the RGM protein DRAG-1 in C. elegans |
| Q37919693 | The regulation of valvular and vascular sclerosis by osteogenic morphogens |
| Q33614316 | The role of inflammatory and anti-inflammatory cytokines in the pathogenesis of osteoarthritis. |
| Q36760208 | The role of mathematical models in understanding pattern formation in developmental biology |
| Q37962474 | Transforming growth factor-β in normal nociceptive processing and pathological pain models |
| Q47102060 | Two functional domains in C. elegans glypican LON-2 can independently inhibit BMP-like signaling |
| Q38853714 | Where do we stand on vascular calcification? |
| Q52736010 | You're going to need a bigger (glass bottom) boat. |
Search more.