Neuronal 3′,3,5-triiodothyronine (T3) uptake and behavioral phenotype of mice deficient in Mct8, the neuronal T3 transporter mutated in Allan-Herndon-Dudley syndrome

Journal of Neuroscience

Volumn 29, Issue 30, 2009, Pages 9439-9449

  Wirth, Eva K ^a   Roth, Stephan ^a   Blechschmidt, Cristiane ^a   Hölter, Sabine M ^b   Becker, Lore ^b,c   Racz, Ildiko ^b,d   Zimmer, Andreas ^d   Klopstock, Thomas ^c   Gailus Durner, Valerie ^b   Fuchs, Helmut ^b   Wurst, Wolfgang ^b   Naumann, Thomas ^a   Bräuer, Anja ^a   De Angelis, Martin Hrabé ^b   Köhrle, Josef ^a   Grüters, Annette ^a   Schweizer, Ulrich ^a  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^b INSTITUTE OF EPIDEMIOLOGY   (Germany)

^c LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

^d UNIVERSITY OF BONN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID TRANSPORTER; LAT PROTEIN; LAT2 PROTEIN; LIOTHYRONINE; MESSENGER RNA; MONOCARBOXYLATE TRANSPORTER 8; UNCLASSIFIED DRUG; CARRIER PROTEIN; CD98 ANTIGEN; SLC16A2 PROTEIN, MOUSE; SLC7A8 PROTEIN, MOUSE;

ALLAN HERNDON DUDLEY SYNDROME; ANIMAL BEHAVIOR; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BEHAVIOR CHANGE; BEHAVIOR DISORDER; BRAIN CELL; BRAIN DEVELOPMENT; CELL ISOLATION; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE MODEL; FEMALE; GENE EXPRESSION; GENE MUTATION; HORMONE TRANSPORT; HYPERTHYROIDISM; HYPOTHYROIDISM; MALE; MICROGLIA; MOUSE; MOUSE MUTANT; NERVE CELL CULTURE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; THYROID HORMONE BLOOD LEVEL; X LINKED MENTAL RETARDATION; ANIMAL; BRAIN; CELL CULTURE; GENETICS; GROWTH, DEVELOPMENT AND AGING; HUMAN; METABOLISM; NERVE CELL; NEUROPSYCHOLOGICAL TEST; PATHOPHYSIOLOGY; PHYSIOLOGY; PRENATAL DEVELOPMENT; SYNDROME;

AMINO ACID TRANSPORT SYSTEM Y+; ANIMALS; ANTIGENS, CD98 LIGHT CHAINS; BEHAVIOR, ANIMAL; BRAIN; CELLS, CULTURED; HUMANS; HYPERTHYROIDISM; HYPOTHYROIDISM; MEMBRANE TRANSPORT PROTEINS; MENTAL RETARDATION, X-LINKED; MICE; MICE, KNOCKOUT; MICROGLIA; NEURONS; NEUROPSYCHOLOGICAL TESTS; PHENOTYPE; RNA, MESSENGER; SYNDROME; TRIIODOTHYRONINE;

EID: 68049138998     PISSN: 02706474     EISSN: 15292401     Source Type: Journal    
DOI: 10.1523/JNEUROSCI.6055-08.2009     Document Type: Article

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