Failure of postnatal ductus arteriosus closure in prostaglandin transporter-deficient mice.
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The Prostaglandin Transporter: Eicosanoid Reuptake, Control of Signaling, and Development of High-Affinity Inhibitors as Drug CandidatesMutations in the prostaglandin transporter encoding gene SLCO2A1 cause primary hypertrophic osteoarthropathy and isolated digital clubbingAdditional sex combs-like family genes are required for normal cardiovascular developmentExome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathyPatent ductus arteriosus in mice with smooth muscle-specific Jag1 deletion.A link between smooth muscle cell death and extracellular matrix degradation during vascular atrophyDevelopment of a high-affinity inhibitor of the prostaglandin transporterProstaglandin Transporter (PGT/SLCO2A1) Protects the Lung from Bleomycin-Induced Fibrosis.Inhibition of the Prostaglandin Transporter PGT Lowers Blood Pressure in Hypertensive Rats and MiceInhibition of Prostaglandin Transporter (PGT) Promotes Perfusion and Vascularization and Accelerates Wound Healing in Non-Diabetic and Diabetic RatsAging-shifted prostaglandin profile in endothelium as a factor in cardiovascular disordersEffects of Advancing Gestation and Non-Caucasian Race on Ductus Arteriosus Gene Expression.Current Perspectives on Pathobiology of the Ductus Arteriosus.Identification of the Mutations in the Prostaglandin Transporter Gene, SLCO2A1 and Clinical Characterization in Korean Patients with Pachydermoperiostosis.Diabetes-induced birth defects: what do we know? What can we do?Primary hypertrophic osteoarthropathy: an update.PGE2 through the EP4 receptor controls smooth muscle gene expression patterns in the ductus arteriosus critical for remodeling at birth.Regulation of prostaglandin EP1 and EP4 receptor signaling by carrier-mediated ligand reuptake.Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis.A novel role for OATP2A1/SLCO2A1 in a murine model of colon cancer.The organic anion transporter SLCO2A1 constitutes the core component of the Maxi-Cl channel.Genetics of the patent ductus arteriosus (PDA) and pharmacogenetics of PDA treatment.Homozygous SLCO2A1 translation initiation codon mutation in a Pakistani family with recessive isolated congenital nail clubbing.The prostaglandin transporter (PGT) as a potential mediator of ovulation.
P2860
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P2860
Failure of postnatal ductus arteriosus closure in prostaglandin transporter-deficient mice.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Failure of postnatal ductus ar ...... in transporter-deficient mice.
@ast
Failure of postnatal ductus ar ...... in transporter-deficient mice.
@en
type
label
Failure of postnatal ductus ar ...... in transporter-deficient mice.
@ast
Failure of postnatal ductus ar ...... in transporter-deficient mice.
@en
prefLabel
Failure of postnatal ductus ar ...... in transporter-deficient mice.
@ast
Failure of postnatal ductus ar ...... in transporter-deficient mice.
@en
P2093
P2860
P1433
P1476
Failure of postnatal ductus ar ...... in transporter-deficient mice.
@en
P2093
Hee-Yoon Chang
Joseph Locker
Victor L Schuster
P2860
P304
P356
10.1161/CIRCULATIONAHA.109.862946
P407
P577
2010-01-18T00:00:00Z