| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1026891361 |
| P356 | DOI | 10.1186/1471-213X-8-86 |
| P932 | PMC publication ID | 2561030 |
| P698 | PubMed publication ID | 18801194 |
| P50 | author | Ulrika Blank | Q122700029 |
| Leif Oxburgh | Q54280533 | ||
| P2093 | author name string | Don M Wojchowski | |
| Derek C Adams | |||
| Michele J Karolak | |||
| Marianne L Seto | |||
| P2860 | cites work | Genetic analysis of the roles of BMP2, BMP4, and BMP7 in limb patterning and skeletogenesis | Q21145242 |
| TGF-beta signal transduction | Q22003891 | ||
| Heart specific expression of mouse BMP-10 a novel member of the TGF-beta superfamily | Q22009012 | ||
| OAZ uses distinct DNA- and protein-binding zinc fingers in separate BMP-Smad and Olf signaling pathways | Q22011195 | ||
| Identification of BMP9 and BMP10 as functional activators of the orphan activin receptor-like kinase 1 (ALK1) in endothelial cells | Q24309588 | ||
| Regulation of BMP7 expression during kidney development | Q24321655 | ||
| Bmpr1a and Bmpr1b have overlapping functions and are essential for chondrogenesis in vivo | Q24555732 | ||
| Bone morphogenetic protein-9 is a circulating vascular quiescence factor | Q24657942 | ||
| Regulation of Smad signaling through a differential recruitment of coactivators and corepressors by ZEB proteins | Q24677861 | ||
| A role for smad6 in development and homeostasis of the cardiovascular system | Q28143788 | ||
| Endogenous patterns of BMP signaling during early chick development | Q28207797 | ||
| Identification and functional characterization of distinct critically important bone morphogenetic protein-specific response elements in the Id1 promoter | Q28208212 | ||
| Human Smad3 and Smad4 are sequence-specific transcription activators | Q28276193 | ||
| BMP-9 signals via ALK1 and inhibits bFGF-induced endothelial cell proliferation and VEGF-stimulated angiogenesis | Q28289169 | ||
| Early embryonic lethality in Bmp5;Bmp7 double mutant mice suggests functional redundancy within the 60A subgroup | Q28506935 | ||
| BMP4 substitutes for loss of BMP7 during kidney development | Q28507463 | ||
| Activation of bone morphogenetic protein/Smad signaling in bronchial epithelial cells during airway inflammation | Q28507809 | ||
| Overlapping expression domains of bone morphogenetic protein family members potentially account for limited tissue defects in BMP7 deficient embryos | Q28507860 | ||
| A requirement for bone morphogenetic protein-7 during development of the mammalian kidney and eye | Q28508005 | ||
| Bmp in podocytes is essential for normal glomerular capillary formation | Q28511751 | ||
| Differential requirements for Smad4 in TGFbeta-dependent patterning of the early mouse embryo | Q28513265 | ||
| Mice deficient for BMP2 are nonviable and have defects in amnion/chorion and cardiac development | Q28513337 | ||
| TGFbeta superfamily signals are required for morphogenesis of the kidney mesenchyme progenitor population | Q28513547 | ||
| Dynamic regulation of Smad expression during mesenchyme to epithelium transition in the metanephric kidney | Q28570315 | ||
| Smad expression during kidney development | Q28585087 | ||
| BMP receptor IA is required in mammalian neural crest cells for development of the cardiac outflow tract and ventricular myocardium | Q28586500 | ||
| Foxd1-dependent signals control cellularity in the renal capsule, a structure required for normal renal development | Q28586643 | ||
| Evidence that autocrine signaling through Bmpr1a regulates the proliferation, survival and morphogenetic behavior of distal lung epithelial cells | Q28587721 | ||
| Expression of bone morphogenetic protein receptors in the developing mouse metanephros | Q77149595 | ||
| Morphogenesis during mouse embryonic kidney explant culture | Q78630765 | ||
| Patterning the embryonic kidney: BMP signaling mediates the differentiation of the pronephric tubules and duct in Xenopus laevis | Q80171752 | ||
| Essential role of Smad4 in maintaining cardiomyocyte proliferation during murine embryonic heart development | Q81297429 | ||
| Control of kidney, eye and limb expression of Bmp7 by an enhancer element highly conserved between species | Q28754463 | ||
| BMP induction of Id proteins suppresses differentiation and sustains embryonic stem cell self-renewal in collaboration with STAT3 | Q29614624 | ||
| A highly efficient recombineering-based method for generating conditional knockout mutations | Q29615157 | ||
| In vivo enhancer analysis of human conserved non-coding sequences | Q29616554 | ||
| Immunohistochemical expression of Smads 1-6 in the 15-day gestation mouse embryo: signaling by BMPs and TGF-betas | Q31911425 | ||
| Functional redundancy of TGF-beta family type I receptors and receptor-Smads in mediating anti-Mullerian hormone-induced Mullerian duct regression in the mouse | Q33621021 | ||
| Developmental expression of mouse Follistatin-like 1 (Fstl1): Dynamic regulation during organogenesis of the kidney and lung | Q33705583 | ||
| Endocardial cushion and myocardial defects after cardiac myocyte-specific conditional deletion of the bone morphogenetic protein receptor ALK3 | Q34014910 | ||
| Suv39h histone methyltransferases interact with Smads and cooperate in BMP-induced repression | Q34316282 | ||
| Requirement for BMP signaling in interdigital apoptosis and scale formation. | Q34377113 | ||
| Interaction between FGF and BMP signaling pathways regulates development of metanephric mesenchyme | Q35199256 | ||
| Conditional deletion of Smad1 and Smad5 in somatic cells of male and female gonads leads to metastatic tumor development in mice | Q36421055 | ||
| BMP signaling in dermal papilla cells is required for their hair follicle-inductive properties | Q36453561 | ||
| BMP receptor ALK3 controls collecting system development | Q36667155 | ||
| Colocalization of BMP 7 and BMP 2 RNAs suggests that these factors cooperatively mediate tissue interactions during murine development | Q36686718 | ||
| Bone morphogenetic protein 4 regulates the budding site and elongation of the mouse ureter | Q37176177 | ||
| The pro-osteogenic action of beta-catenin requires interaction with BMP signaling, but not Tcf/Lef transcriptional activity | Q37265057 | ||
| Essential pro-Bmp roles of crossveinless 2 in mouse organogenesis | Q38308645 | ||
| Enhancer analysis of the mouse HNF-3 beta gene: regulatory elements for node/notochord and floor plate are independent and consist of multiple sub-elements | Q38363013 | ||
| Spatio-temporal activation of Smad1 and Smad5 in vivo: monitoring transcriptional activity of Smad proteins | Q40521999 | ||
| p38MAPK acts in the BMP7-dependent stimulatory pathway during epithelial cell morphogenesis and is regulated by Smad1. | Q40600202 | ||
| Transcriptional regulation of BMP4 synexpression in transgenic Xenopus | Q40734215 | ||
| BMP-2 and OP-1 exert direct and opposite effects on renal branching morphogenesis | Q41070912 | ||
| Inducible expression of an hsp68-lacZ hybrid gene in transgenic mice | Q44484787 | ||
| TGF-beta superfamily members modulate growth, branching, shaping, and patterning of the ureteric bud. | Q44738676 | ||
| BMP signaling inhibits intestinal stem cell self-renewal through suppression of Wnt-beta-catenin signaling | Q45065876 | ||
| Phylogenetic footprinting and genome scanning identify vertebrate BMP response elements and new target genes. | Q45965916 | ||
| Expression of a retinoic acid response element-hsplacZ transgene defines specific domains of transcriptional activity during mouse embryogenesis | Q46255940 | ||
| De novo crypt formation and juvenile polyposis on BMP inhibition in mouse intestine | Q47961996 | ||
| Real time monitoring of BMP Smads transcriptional activity during mouse development. | Q50628619 | ||
| Localization of TGF-beta signaling intermediates Smad2, 3, 4, and 7 in developing and mature human and mouse kidney. | Q52000197 | ||
| BMP receptor type IA in limb bud mesenchyme regulates distal outgrowth and patterning. | Q52019997 | ||
| In vivo evidence that BMP signaling is necessary for apoptosis in the mouse limb. | Q52115127 | ||
| Endogenous patterns of TGFbeta superfamily signaling during early Xenopus development. | Q52167679 | ||
| Bmp signaling regulates proximal-distal differentiation of endoderm in mouse lung development. | Q52174962 | ||
| Smad5 knockout mice die at mid-gestation due to multiple embryonic and extraembryonic defects. | Q52178711 | ||
| Bone morphogenetic protein receptor 1A signaling is dispensable for hematopoietic development but essential for vessel and atrioventricular endocardial cushion formation. | Q54588887 | ||
| Expression of BMP-7 and USAG-1 (a BMP antagonist) in kidney development and injury | Q57936785 | ||
| Physical and functional interaction of SMADs and p300/CBP | Q64381971 | ||
| BMP-7 is an inducer of nephrogenesis, and is also required for eye development and skeletal patterning | Q71817916 | ||
| Mechanism of the pleiotropic effects of the short-ear mutant gene in the mouse | Q72137415 | ||
| P304 | page(s) | 86 | |
| P577 | publication date | 2008-09-18 | |
| P1433 | published in | BMC Developmental Biology | Q15761839 |
| P1476 | title | An in vivo reporter of BMP signaling in organogenesis reveals targets in the developing kidney | |
| P478 | volume | 8 |
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| Q35035999 | Adult-specific systemic over-expression reveals novel in vivo effects of the soluble forms of ActRIIA, ActRIIB and BMPRII. |
| Q37330620 | An interdigit signalling centre instructs coordinate phalanx-joint formation governed by 5'Hoxd-Gli3 antagonism. |
| Q51933152 | Analysis of early nephron patterning reveals a role for distal RV proliferation in fusion to the ureteric tip via a cap mesenchyme-derived connecting segment. |
| Q34343116 | Anti-inflammatory activity of bone morphogenetic protein signaling pathways in stomachs of mice |
| Q50678241 | BMP antagonism by Noggin is required in presumptive notochord cells for mammalian foregut morphogenesis. |
| Q38161819 | BMP signaling and its modifiers in kidney development |
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| Q37385501 | BMP7 promotes proliferation of nephron progenitor cells via a JNK-dependent mechanism |
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| Q30431055 | Cadherin 6B induces BMP signaling and de-epithelialization during the epithelial mesenchymal transition of the neural crest |
| Q38275152 | Cell signaling pathways involved in hematopoietic stem cell specification |
| Q35096652 | Chondrocyte-specific microRNA-140 regulates endochondral bone development and targets Dnpep to modulate bone morphogenetic protein signaling. |
| Q50525535 | Direct visualization of Smad1/5/8-mediated transcriptional activity identifies podocytes and collecting ducts as major targets of BMP signalling in healthy and diseased kidneys. |
| Q33792073 | Disruption of mitotic arrest precedes precocious differentiation and transdifferentiation of pregranulosa cells in the perinatal Wnt4 mutant ovary |
| Q35498717 | Distinct bone morphogenetic proteins activate indistinguishable transcriptional responses in nephron epithelia including Notch target genes. |
| Q34870630 | Dynamic analysis of BMP-responsive smad activity in live zebrafish embryos |
| Q64951976 | Expression of BMP-4 and Smad1 in patients with Hirschsprung disease and its clinical significance. |
| Q36309205 | Inactivation of the dual Bmp/Wnt inhibitor Sostdc1 enhances pancreatic islet function |
| Q35111241 | Integrated β-catenin, BMP, PTEN, and Notch signalling patterns the nephron |
| Q33573554 | Lrp4 regulates initiation of ureteric budding and is crucial for kidney formation--a mouse model for Cenani-Lenz syndrome |
| Q38649803 | On signaling pathways: hematopoietic stem cell specification from hemogenic endothelium. |
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| Q35626101 | SMAD1 and SMAD5 Expression Is Coordinately Regulated by FLI1 and GATA2 during Endothelial Development |
| Q52669131 | Stromal β-catenin overexpression contributes to the pathogenesis of renal dysplasia. |
| Q52703607 | TGF-β Family Signaling in Ductal Differentiation and Branching Morphogenesis. |
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