Cerebellar abnormalities in mice lacking type 3 deiodinase and partial reversal of phenotype by deletion of thyroid hormone receptor α1

Endocrinology

Volumn 154, Issue 1, 2013, Pages 550-561

  Peeters, Robin P ^a,b   Hernandez, Arturo ^c   Ng, Lily ^b   Ma, Michelle ^b   Sharlin, David S ^b,d   Pandey, Mritunjay ^b   Simonds, William F ^b   St Germain, Donald L ^c   Forrest, Douglas ^b  

^a ERASMUS MEDICAL CENTER   (Netherlands)

^b NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

^c DARTMOUTH MEDICAL SCHOOL   (United States)

^d MINNESOTA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

THYROID HORMONE; THYROID HORMONE INACTIVATING TYPE 3 DEIODINASE; THYROID HORMONE RECEPTOR; THYROID HORMONE RECEPTOR ALPHA1; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BRAIN DEVELOPMENT; CELL MIGRATION; CEREBELLUM DISEASE; DEVELOPMENTAL DISORDER; EMBRYO DEVELOPMENT; ENZYME ACTIVATION; FEMALE; HEARING; HEARING IMPAIRMENT; HISTOPATHOLOGY; IMMUNOHISTOCHEMISTRY; LOCOMOTION; MOTOR PERFORMANCE; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PERINATAL DEVELOPMENT; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION;

ANIMALS; CEREBELLUM; FEMALE; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; IODIDE PEROXIDASE; MALE; MICE; MICE, KNOCKOUT; MOTOR ACTIVITY; THYROID HORMONE RECEPTORS ALPHA; THYROID HORMONES;

EID: 84871682430     PISSN: 00137227     EISSN: 19457170     Source Type: Journal    
DOI: 10.1210/en.2012-1738     Document Type: Article

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