Modeling Psychomotor Retardation using iPSCs from MCT8-Deficient Patients Indicates a Prominent Role for the Blood-Brain Barrier. (Q46205341)

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20 March 2020

title

Modeling Psychomotor Retardation using iPSCs from MCT8-Deficient Patients Indicates a Prominent Role for the Blood-Brain Barrier (English)

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Samuel Refetoff

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Gad D Vatine

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16 May 2017

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6

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831-843.e5

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Gene regulation by thyroid hormone

20 March 2020

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Transporters MCT8 and OATP1C1 maintain murine brain thyroid hormone homeostasis

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Cerebral cortex hyperthyroidism of newborn mct8-deficient mice transiently suppressed by lat2 inactivation

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Mutations of the thyroid hormone transporter MCT8 cause prenatal brain damage and persistent hypomyelination

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The Thyroid Hormone Analog DITPA Ameliorates Metabolic Parameters of Male Mice With Mct8 Deficiency

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Endotoxin-induced inflammation down-regulates L-type amino acid transporter 1 (LAT1) expression at the blood-brain barrier of male rats and mice

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In Vivo CRISPR/Cas9 Gene Editing Corrects Retinal Dystrophy in the S334ter-3 Rat Model of Autosomal Dominant Retinitis Pigmentosa

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Purification and Characterization of Progenitor and Mature Human Astrocytes Reveals Transcriptional and Functional Differences with Mouse

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ALS disrupts spinal motor neuron maturation and aging pathways within gene co-expression networks

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Huntington's Disease iPSC-Derived Brain Microvascular Endothelial Cells Reveal WNT-Mediated Angiogenic and Blood-Brain Barrier Deficits

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12 December 2020

10.1016/J.STEM.2017.04.002

Identifiers

DOI

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20 March 2020

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20 March 2020

PubMed publication ID

28526555

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