Evidence that autocrine signaling through Bmpr1a regulates the proliferation, survival and morphogenetic behavior of distal lung epithelial cells
about
Cathespin H is an Fgf10 target involved in Bmp4 degradation during lung branching morphogenesisTip cells: master regulators of tubulogenesis?Activation of the canonical bone morphogenetic protein (BMP) pathway during lung morphogenesis and adult lung tissue repairStructure analysis of bone morphogenetic protein-2 type I receptor complexes reveals a mechanism of receptor inactivation in juvenile polyposis syndromeUnderstanding the development of the respiratory glandsBranch mode selection during early lung developmentTbx2 controls lung growth by direct repression of the cell cycle inhibitor genes Cdkn1a and Cdkn1bWnt7b stimulates embryonic lung growth by coordinately increasing the replication of epithelium and mesenchymeWnt2/2b and beta-catenin signaling are necessary and sufficient to specify lung progenitors in the foregutBmp4 is required for tracheal formation: a novel mouse model for tracheal agenesisComparative molecular developmental aspects of the mammalian- and the avian lungs, and the insectan tracheal system by branching morphogenesis: recent advances and future directionsSuppression of Bmp4 signaling by the zinc-finger repressors Osr1 and Osr2 is required for Wnt/β-catenin-mediated lung specification in Xenopus.Human bronchial epithelial cells differentiate to 3D glandular acini on basement membrane matrixThe origin of bmp16, a novel Bmp2/4 relative, retained in teleost fish genomesTranscriptional program induced by Wnt protein in human fibroblasts suggests mechanisms for cell cooperativity in defining tissue microenvironments.FGF10 maintains distal lung bud epithelium and excessive signaling leads to progenitor state arrest, distalization, and goblet cell metaplasia.An in vivo reporter of BMP signaling in organogenesis reveals targets in the developing kidney.Early mortality and cardiorespiratory failure in patients with fibrodysplasia ossificans progressiva.Bmp2 and Bmp4 genetically interact to support multiple aspects of mouse development including functional heart development.Chronic respiratory aeroallergen exposure in mice induces epithelial-mesenchymal transition in the large airwaysSignaling through BMP receptors promotes respiratory identity in the foregut via repression of Sox2.Analysis of gene expression in PTHrP-/- mammary buds supports a role for BMP signaling and MMP2 in the initiation of ductal morphogenesis.Genetic interaction between Bmp2 and Bmp4 reveals shared functions during multiple aspects of mouse organogenesis.Two nested developmental waves demarcate a compartment boundary in the mouse lungMesothelial- and epithelial-derived FGF9 have distinct functions in the regulation of lung development.Progesterone receptor activates Msx2 expression by downregulating TNAP/Akp2 and activating the Bmp pathway in EpH4 mouse mammary epithelial cells.Bone Morphogenetic Protein (BMP) signaling in development and human diseasesThe three R's of lung health and disease: repair, remodeling, and regeneration.Wnt and FGF mediated epithelial-mesenchymal crosstalk during lung development.Lung development and repair: contribution of the ciliated lineage.Lung organogenesisTargeted deletion of Jun/AP-1 in alveolar epithelial cells causes progressive emphysema and worsens cigarette smoke-induced lung inflammationSignaling in cell differentiation and morphogenesisGATA-6 promotes cell survival by up-regulating BMP-2 expression during embryonic stem cell differentiationBranching morphogenesis: from cells to organs and back.Reduced bone morphogenetic protein receptor type 1A signaling in neural-crest-derived cells causes facial dysmorphism.Prenatal lung epithelial cell-specific abrogation of Alk3-bone morphogenetic protein signaling causes neonatal respiratory distress by disrupting distal airway formationGenome-scale study of transcription factor expression in the branching mouse lung.Comparative mechanisms of branching morphogenesis in diverse systems.Key mechanisms of early lung development.
P2860
Q24305496-1347B0EF-1374-4C50-A73F-B9BB70E31FCBQ26991847-410467F9-CC7A-4C0B-B4C2-8C68DF8ED60BQ27331890-EA3914F9-7832-49F8-9646-FC43A6136B0AQ27649432-5D251C03-F5BA-42E4-8EFD-A0B8FE664CA6Q28081046-04588DA0-9978-4026-AB21-969C4D666538Q28480872-2DC816E6-CC79-449E-B910-FFD61E4F79D7Q28485157-AE9FE1DE-D05E-4122-A035-AA6623F84C95Q28506294-E6A7BAF9-1B95-4387-976A-92D9495C7C63Q28509406-597FE814-8191-44C4-B235-BD15F1C3400FQ28510349-05BE49E9-E7BE-45C0-87FB-6461C6603E7BQ28710584-2A9204DD-3B0F-4B2A-9D60-991C8508DE95Q30417661-9194F34B-4591-45D7-909C-22AB7FA17A19Q30502453-95BAC1CF-58B5-4E7B-993D-DC34F16DA6B3Q30936691-431841DD-F3C5-4410-BAC5-33368A9D290FQ33300355-795BFAA2-18CD-45F8-B488-E8FC3279801CQ33314149-E806FA91-C055-4B81-8BBE-5EAA819A6A85Q33370427-E2E25902-0C46-4E6A-8277-2BC44C3861F0Q33685088-90FB70F8-06A7-4BC5-B4C0-7BAB46C2229BQ33761311-5E688754-EB18-4E32-A61A-5119391DCD35Q33809320-B948BC9F-304B-4CB1-9764-3A8861F5A8F2Q33818155-38C1EE89-2460-49E9-8060-0B6EBCF5F08EQ33822636-E49E4509-58FD-486F-9C9A-AC37EB2F638BQ33938401-E86F69D2-1270-4E99-97F4-AFA7C1280C21Q33969488-30B2F752-A179-4288-A6B7-90E730BBC0E2Q34199875-7DEE58E2-A2ED-4E96-BB97-05BD574852E1Q34212149-B5957B01-8006-46F6-98AE-F212DA02AF8FQ34512444-7E60D7EC-5EA9-4691-9967-DDEDD563A60AQ35015756-C895E663-BD6B-4990-BD27-886676D5A483Q35132288-7EBC8A63-5981-4AB3-8579-67B6942C9B5DQ35546713-FEBE147B-2DCD-4710-BA86-B2CDAFA53C42Q35922155-F6DB16FC-63D0-4EF7-9924-F731A405D84CQ35951960-19463D40-DC8C-4A60-8F4A-DB2D2D7EBE76Q36009264-F54CE516-AA2D-45DD-BFF3-A7AEBDEEC948Q36234535-26CD70B1-9F45-4EBE-9CFD-BACA7A6B737DQ36329454-A1646FAB-9D42-44D3-88AB-BCD5972A305FQ36359280-F569AAAC-BD68-41FB-BB39-4A5980D639CEQ36482223-E59B0C4A-2960-4D60-BBE5-797062395314Q36485563-C698BF5F-3B03-4A5A-BC26-EE037FAABDC0Q36660547-DEC363A7-37B1-4CAB-B4C4-5891BA5C55CCQ36968027-5D31A178-D18A-47A4-9E90-46FBF8EA858B
P2860
Evidence that autocrine signaling through Bmpr1a regulates the proliferation, survival and morphogenetic behavior of distal lung epithelial cells
description
2006 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մարտին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2006
@ast
im März 2006 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2006/03/01)
@sk
vědecký článek publikovaný v roce 2006
@cs
wetenschappelijk artikel (gepubliceerd op 2006/03/01)
@nl
наукова стаття, опублікована в березні 2006
@uk
مقالة علمية (نشرت في مارس 2006)
@ar
name
Evidence that autocrine signal ...... f distal lung epithelial cells
@ast
Evidence that autocrine signal ...... f distal lung epithelial cells
@en
Evidence that autocrine signal ...... f distal lung epithelial cells
@nl
type
label
Evidence that autocrine signal ...... f distal lung epithelial cells
@ast
Evidence that autocrine signal ...... f distal lung epithelial cells
@en
Evidence that autocrine signal ...... f distal lung epithelial cells
@nl
prefLabel
Evidence that autocrine signal ...... f distal lung epithelial cells
@ast
Evidence that autocrine signal ...... f distal lung epithelial cells
@en
Evidence that autocrine signal ...... f distal lung epithelial cells
@nl
P2093
P921
P1476
Evidence that autocrine signal ...... f distal lung epithelial cells
@en
P2093
Brigid L. M. Hogan
Mary Reedy
Maxwell C. Eblaghie
Tim Oliver
Yuji Mishina
P356
10.1016/J.YDBIO.2005.12.006
P407
P577
2006-03-01T00:00:00Z