「Congenital goitrous hypothyroidism is caused by dysfunction of the iodide transporter SLC26A7<Abstract of dissertation>」の関連論文
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Prophylactic treatment of rapamycin ameliorates naturally developing and episode -induced heterotopic ossification in mice expressing human mutant ACVR1
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Elucidation of the Mechanism for Intestinal Phosphate Absorption
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Analysis of Anti-metabolic Syndrome Effect of Kaempferol in TSOD Mice
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Study of Mitochonic Acid 5 to improve neuromuscular dysfunction associated with aging and diseases using C. elegans
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Embryonal erythropoiesis and aging exploit ferroptosis
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Phosphorylation of the anaphase promoting complex activator FZR1/CDH1 is required for meiosis II entry in mouse male germ cell (本文)
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Dilated cardiomyopathy-linked heat shock protein family D member 1 mutations cause up-regulation of reactive oxygen species and autophagy through mitochondrial dysfunction (本文)
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A RUNX-targeted gene switch-off approach modulates the BIRC5/PIF1-p21 pathway and reduces glioblastoma growth in mice
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The crosstalk between aldosterone production and extracellular calcium metabolism in primary aldosteronism
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Histological analysis of the skin of Abca1-deleted mice : A potential model for dry skin
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Long-Surviving Adult Siblings With Joubert Syndrome Harboring a Novel Compound Heterozygous CPLANE1 Variant
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A Single RET Mutation in Hirschsprung Disease Induces Intestinal Aganglionosis Via a Dominant-Negative Mechanism
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Remote solid cancers rewire hepatic nitrogen metabolism via host nicotinamide-N-methyltransferase
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Lionheart LincRNA alleviates cardiac systolic dysfunction under pressure overload
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The role of autophagy in Arabidopsis plants exposed to ultraviolet-B or high temperature stress
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A proteome signature of umbilical cord serum associated with congenital diaphragmatic hernia
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Three-dimensional spheroid culture induces apical-basal polarity and the original characteristics of immortalized human renal proximal tubular epithelial cells
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Immunobiochemical, molecular biological, and reverse genetical studies on vitellogenin receptor candidates in medaka, Oryzias latipes [an abstract of entire text]
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The role of H3K27 demethylation in retinal development
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Studies on Thermoregulation and Growth Performance in Chicks with av-UCP mutation
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PCBP2 knockdown promotes ferroptosis in malignant mesothelioma
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Conformational change of RNA‐helicase DHX30 by ALS/FTD‐linked FUS induces mitochondrial dysfunction and cytosolic aggregates
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Gut contractile organoids: a novel model system to study the cellular synchronization in gastrointestinal motility
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A type 2C protein phosphatase activates high-affinity nitrate uptake by dephosphorylating NRT2.1
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Pitfalls in establishing mouse model of female infertility by immunization with human centromere protein
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Prickle2 and Igsf9b coordinately regulate the cytoarchitecture of the axon initial segment
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Combination of target site mutation and associated CYPs confers high-level resistance to pyridaben in Tetranychus urticae
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Development of the first clinically used radiotracer [18F]T-401 for positron emission tomography imaging of monoacylglycerol lipase in brain (Monoacylglycerol lipase (MAGL)を標的としたPETトレーサー[18F]T-401の開発)
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Forced expression of α2,3-sialyltransferase IV rescues impaired heart development in α2,6-sialyltransferase I-deficient medaka
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高純度間葉系幹細胞は機能的ミトコンドリア投入に優れている
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Inhibition of heat shock protein 90 destabilizes receptor tyrosine kinase ROR1 in lung adenocarcinoma
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Constitutively active signaling of MDA5 in Treg cells causes apoptosis of Treg cells and results in autoimmune diseases
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Cellular senescence in white matter microglia is induced during ageing in mice and exacerbates the neuroinflammatory phenotype
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Automated screening procedure for the phenotypes of congenital fibrinogen disorders using novel parameters, |min1|c and Ac/|min1|c, obtained from clot waveform analysis using the Clauss method
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miR-142 induces accumulation of reactive oxygen species (ROS) by inhibiting pexophagy in aged bone marrow mesenchymal stem cells
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Cardio- and reno-protective effects of dipeptidyl peptidase III in diabetic mice.
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Presenilin is essential for ApoE secretion, a novel role of presenilin involved in Alzheimer’s disease pathogenesis
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Pluripotent stem cell model of Shwachman-Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors
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Roles of Energy Production Pathways in Sperm Motility Regulation in Chickens
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Quantitative Prediction of P-Glycoprotein-Mediated Intestinal Absorption for Molecules Beyond the Rule of Five Using Model Animals
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成獣ライディッヒ細胞における性染色体の機能解析
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A novel cancer immunotherapy using tumor-infiltrating B cells in the APC (min/+) mouse model
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Identification and analysis of mechanisms that bypass the essentiality of Polo, a mitotic regulator
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Characterization of a bicistronic knock-in reporter mouse model for investigating the role of Cables2 in vivo
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Tenascin C Aggravates Autoimmune Myocarditis via Dendritic Cell Activation and Th17 Cell Differentiation
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Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
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Study on biological functions of Pentraxin 4 in liver
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Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings
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Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings
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Setd1a plays pivotal roles for the survival and proliferation of retinal progenitors via histone modifications of Uhrf1