Tsugio Seki

Sequencing analysis of a putative human O-sialoglycoprotein endopeptidase gene (OSGEP) and analysis of a bidirectional promoter between the OSGEP and APEX genes.

Arterial endothelium-specific activin receptor-like kinase 1 expression suggests its role in arterialization and vascular remodeling.

Isolation of a regulatory region of activin receptor-like kinase 1 gene sufficient for arterial endothelium-specific expression.

B-cell translocation gene 2 (Btg2) regulates vertebral patterning by modulating bone morphogenetic protein/smad signaling.

Nonoverlapping expression patterns of ALK1 and ALK5 reveal distinct roles of each receptor in vascular development.

P2 receptor regulation of [Ca2+]i in cultured mouse mesangial cells.

Activin receptor-like kinase 1 is essential for placental vascular development in mice.

Evolutionarily conserved mammalian adenine nucleotide translocase 4 is essential for spermatogenesis.

ALK5- and TGFBR2-independent role of ALK1 in the pathogenesis of hereditary hemorrhagic telangiectasia type 2.

Perinatal loss of Nkx2-5 results in rapid conduction and contraction defects.

Glomerular 20-HETE, EETs, and TGF-beta1 in diabetic nephropathy.

Differential role of Nkx2-5 in activation of the atrial natriuretic factor gene in the developing versus failing heart.

Age-dependent lethality in novel transgenic mouse models of central nervous system arteriovenous malformations.

Transcriptome analysis reveals differentially expressed transcripts in rat adrenal zona glomerulosa and zona fasciculata.

Lessons from the gene expression pattern of the rat zona glomerulosa.

Sodium deficiency regulates rat adrenal zona glomerulosa gene expression.

Combined therapy with COX-2 inhibitor and 20-HETE inhibitor reduces colon tumor growth and the adverse effects of ischemic stroke associated with COX-2 inhibition.

Flow regulation of endothelin-1 production in the inner medullary collecting duct.

Case Report: Nodule Development From Subcapsular Aldosterone-Producing Cell Clusters Causes Hyperaldosteronism.

Disorganized Steroidogenesis in Adrenocortical Carcinoma, a Case Study.

Somatic KCNJ5 mutation occurring early in adrenal development may cause a novel form of juvenile primary aldosteronism.

Human Adrenocortical Remodeling Leading to Aldosterone-Producing Cell Cluster Generation.

Immunohistochemistry of aldosterone synthase leads the way to the pathogenesis of primary aldosteronism.