Defective pulmonary vascular remodeling in Smad8 mutant mice
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Transforming growth factor β signaling in uterine development and functionThe molecular genetics and cellular mechanisms underlying pulmonary arterial hypertensionTenascin-C in development and disease of blood vesselsHepatic deletion of Smad7 in mouse leads to spontaneous liver dysfunction and aggravates alcoholic liver injury.Expression of bone morphogenetic protein 2, 4, and related components of the BMP signaling pathway in the mouse uterus during the estrous cycleBone Morphogenetic Protein (BMP) signaling in development and human diseasesTenascins and the importance of adhesion modulation.Anti-Müllerian hormone recruits BMPR-IA in immature granulosa cells.Inhibitory SMADs: potential regulators of ovarian functionAdvances in tenascin-C biology.The genetics of pulmonary arterial hypertension in the post-BMPR2 era.Altered MicroRNA processing in heritable pulmonary arterial hypertension: an important role for Smad-8High Frequency of Pulmonary Hypertension-Causing Gene Mutation in Chinese Patients with Chronic Thromboembolic Pulmonary HypertensionSmad1/5/8 are myogenic regulators of murine and human mesoangioblastsPulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects.BMP signaling is essential in neonatal surfactant production during respiratory adaptationTranscription factors, transcriptional coregulators, and epigenetic modulation in the control of pulmonary vascular cell phenotype: therapeutic implications for pulmonary hypertension (2015 Grover Conference series).BMP signaling in vascular development and disease.BMP signaling in congenital heart disease: new developments and future directions.TGFβ signaling and cardiovascular diseases.Spatial regulation of BMP activity.Transforming Growth Factor β Superfamily Signaling in Development of Colorectal Cancer.Smad1 and its target gene Wif1 coordinate BMP and Wnt signaling activities to regulate fetal lung development.Endothelial chromosome 13 deletion in congenital heart disease-associated pulmonary arterial hypertension dysregulates SMAD9 signaling.Minimal fertility defects in mice deficient in oocyte-expressed Smad4.Identification of a rare BMP pathway mutation in a non-syndromic human brain arteriovenous malformation via exome sequencing.
P2860
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P2860
Defective pulmonary vascular remodeling in Smad8 mutant mice
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 05 May 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Defective pulmonary vascular remodeling in Smad8 mutant mice
@en
Defective pulmonary vascular remodeling in Smad8 mutant mice.
@nl
type
label
Defective pulmonary vascular remodeling in Smad8 mutant mice
@en
Defective pulmonary vascular remodeling in Smad8 mutant mice.
@nl
prefLabel
Defective pulmonary vascular remodeling in Smad8 mutant mice
@en
Defective pulmonary vascular remodeling in Smad8 mutant mice.
@nl
P2093
P2860
P356
P1476
Defective pulmonary vascular remodeling in Smad8 mutant mice
@en
P2093
Degang Wang
James F Martin
Kaori Ihida-Stansbury
Peter Lloyd Jones
Zheng Huang
P2860
P304
P356
10.1093/HMG/DDP214
P577
2009-05-05T00:00:00Z