Related references
Note: Only part of the references are listed.Thyroid hormone regulation of neural stem cell fate: From development to ageing
Jean-David Gothie et al.
ACTA PHYSIOLOGICA (2020)
Thyroid Hormone Transporters
Stefan Groeneweg et al.
ENDOCRINE REVIEWS (2020)
Tissue-Specific Function of Thyroid Hormone Transporters: New Insights from Mouse Models
Eva Salveridou et al.
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES (2020)
Thyroid hormone influences brain gene expression programs and behaviors in later generations by altering germ line epigenetic information
M. Elena Martinez et al.
MOLECULAR PSYCHIATRY (2020)
Spatiotemporal Changes of Cerebral Monocarboxylate Transporter 8 Expression
Nina-Maria Wilpert et al.
THYROID (2020)
Insights from zebrafish deficiency models to understand the impact of local thyroid hormone regulator action on early development
Pieter Vancamp et al.
GENERAL AND COMPARATIVE ENDOCRINOLOGY (2019)
Adult hippocampal neurogenesis is abundant in neurologically healthy subjects and drops sharply in patients with Alzheimer's disease
Elena P. Moreno-Jimenez et al.
NATURE MEDICINE (2019)
Oligodendroglial Lineage Cells in Thyroid Hormone-Deprived Conditions
Min Joung Kim et al.
STEM CELLS INTERNATIONAL (2019)
Thyroid hormone availability in the human fetal brain: novel entry pathways and role of radial glia
Daniela Lopez-Espindola et al.
BRAIN STRUCTURE & FUNCTION (2019)
Novel mutations in SLC16A2 associated with a less severe phenotype of MCT8 deficiency
Silvia Masnada et al.
METABOLIC BRAIN DISEASE (2019)
Adult Mice Lacking Mct8 and Dio2 Proteins Present Alterations in Peripheral Thyroid Hormone Levels and Severe Brain and Motor Skill Impairments
Soledad Barez-Lopez et al.
THYROID (2019)
Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial
Stefan Groeneweg et al.
LANCET DIABETES & ENDOCRINOLOGY (2019)
Expanding the phenotypic spectrum of Allan-Herndon-Dudley syndrome in patients with SLC16A2 mutations
Ganaelle Remeran et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2019)
Ontogenetic expression of thyroid hormone signaling genes: An in vitro and in vivo species comparison
Kyla M. Walter et al.
PLOS ONE (2019)
In Vitro Characterization of Human, Mouse, and Zebrafish MCT8 Orthologues
Stefan Groeneweg et al.
THYROID (2019)
Oligodendrocyte Progenitor Cells Become Regionally Diverse and Heterogeneous with Age
Sonia Olivia Spitzer et al.
NEURON (2019)
Structure-Activity Relationships of Central Nervous System Penetration by Fatty Acid Amide Hydrolase (FAAH)-Targeted Thyromimetic Prodrugs
J. Matthew Meinig et al.
ACS MEDICINAL CHEMISTRY LETTERS (2019)
Myelin repair stimulated by CNS-selective thyroid hormone action
Meredith D. Hartley et al.
JCI INSIGHT (2019)
White matter microstructural abnormalities in children with severe congenital hypothyroidism
Hannah E. Cooper et al.
NEUROIMAGE-CLINICAL (2019)
From zebrafish to human: A comparative approach to elucidate the role of the thyroid hormone transporter MCT8 during brain development
Pieter Vancamp et al.
GENERAL AND COMPARATIVE ENDOCRINOLOGY (2018)
Origin and dynamics of oligodendrocytes in the developing brain: Implications for perinatal white matter injury
Erik van Tilborg et al.
GLIA (2018)
Sobetirome and its Amide Prodrug Sob-AM2 Exert Thyromimetic Actions in Mct8-Deficient Brain
Soledad Barez-Lopez et al.
THYROID (2018)
Transient Hypothyroidism During Lactation Arrests Myelination in the Anterior Commissure of Rats. A Magnetic Resonance Image and Electron Microscope Study
Federico S. Lucia et al.
FRONTIERS IN NEUROANATOMY (2018)
The Axon-Myelin Unit in Development and Degenerative Disease
Ruth M. Stassart et al.
FRONTIERS IN NEUROSCIENCE (2018)
Regulation of T3 Availability in the Developing Brain: The Mouse Genetics Contribution
Sabine Richard et al.
FRONTIERS IN ENDOCRINOLOGY (2018)
Leukodystrophies - much more than just diseases of myelin
Marjo S. van der Knaap et al.
NATURE REVIEWS NEUROLOGY (2018)
The Chemical Chaperone Phenylbutyrate Rescues MCT8 Mutations Associated With Milder Phenotypes in Patients With Allan-Herndon-Dudley Syndrome
Doreen Braun et al.
ENDOCRINOLOGY (2017)
Thyroid hormone regulated genes in cerebral cortex development
Juan Bernal
JOURNAL OF ENDOCRINOLOGY (2017)
Concise Review: Stem Cell-Based Treatment of Pelizaeus-Merzbacher Disease
M. Joana Osorio et al.
STEM CELLS (2017)
Severe neurological abnormalities in a young boy with impaired thyroid hormone sensitivity due to a novel mutation in the MCT8 gene
Teresa Rego et al.
HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM (2017)
Clinical and Molecular Characteristics of SLC16A2 (MCT8) Mutations in Three Families with the Allan-Herndon-Dudley Syndrome
Francesca Novara et al.
HUMAN MUTATION (2017)
Triiodothyroacetic acid in health and disease
Stefan Groeneweg et al.
JOURNAL OF ENDOCRINOLOGY (2017)
INFLUENCE OF MATERNAL THYROID HORMONES DURING GESTATION ON FETAL BRAIN DEVELOPMENT
N. K. Moog et al.
NEUROSCIENCE (2017)
Remyelinating Pharmacotherapies in Multiple Sclerosis
Riley M. Bove et al.
NEUROTHERAPEUTICS (2017)
Transient hypothyroidism favors oligodendrocyte generation providing functional remyelination in the adult mouse brain
Sylvie Remaud et al.
eLife (2017)
Differentiation of oligodendrocyte progenitor cells from dissociated monolayer and feeder free cultured pluripotent stem cells
Tomoko Yamashita et al.
PLOS ONE (2017)
Leukodystrophies: a proposed classification system based on pathological changes and pathogenetic mechanisms
Marjo S. van der Knaap et al.
ACTA NEUROPATHOLOGICA (2017)
Disorder of thyroid hormone transport into the tissues
Stefan Groeneweg et al.
BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM (2017)
Modeling Psychomotor Retardation using iPSCs from MCT8-Deficient Patients Indicates a Prominent Role for the Blood-Brain Barrier
Gad D. Vatine et al.
CELL STEM CELL (2017)
Ester-to-amide rearrangement of ethanolamine-derived prodrugs of sobetirome with increased blood-brain barrier penetration
Skylar J. Ferrara et al.
BIOORGANIC & MEDICINAL CHEMISTRY (2017)
The Value of Comprehensive Thyroid Function Testing and Family History for Early Diagnosis of MCT8 Deficiency
Jirair K. Bedoyan et al.
CLINICAL PEDIATRICS (2016)
Sobetirome: the past, present and questions about the future
Jan Lammel Lindemann et al.
EXPERT OPINION ON THERAPEUTIC TARGETS (2016)
Dynamic Imaging of Individual Remyelination Profiles in Multiple Sclerosis
Benedetta Bodini et al.
ANNALS OF NEUROLOGY (2016)
Hypomyelinating leukodystrophies a molecular insight into the white matter pathology
A. Charzewska et al.
CLINICAL GENETICS (2016)
Pharmacological treatment and BBB-targeted genetic therapy for MCT8-dependent hypomyelination in zebrafish
David Zada et al.
DISEASE MODELS & MECHANISMS (2016)
Thyroid Hormone Signaling in Oligodendrocytes: from Extracellular Transport to Intracellular Signal
Jae Young Lee et al.
MOLECULAR NEUROBIOLOGY (2016)
Hypomyelinating disorders: An MRI approach
A. James Barkovich et al.
NEUROBIOLOGY OF DISEASE (2016)
Purification and Characterization of Progenitor and Mature Human Astrocytes Reveals Transcriptional and Functional Differences with Mouse
Ye Zhang et al.
NEURON (2016)
86thAnnual Meeting of the American Thyroid Association
THYROID (2016)
Association of maternal thyroid function during early pregnancy with offspring IQ and brain morphology in childhood: a population-based prospective cohort study
Tim I. M. Korevaar et al.
LANCET DIABETES & ENDOCRINOLOGY (2016)
Novel SLC16A2 mutations in patients with Allan-Herndon-Dudley syndrome
Keiko Shimojima et al.
INTRACTABLE & RARE DISEASES RESEARCH (2016)
Three novel mutations of the MCT8 (SLC16A2) gene: individual and temporal variations of endocrinological and radiological features
Erina Ono et al.
CLINICAL PEDIATRIC ENDOCRINOLOGY (2016)
Allan-Herndon-Dudley Syndrome with Unusual Profound Sensorineural Hearing Loss
Lucia Gagliardi et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2015)
Intracellular thyroid hormone metabolism as a local regulator of nuclear thyroid hormone receptor-mediated impact on vertebrate development
Veerle M. Darras et al.
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS (2015)
A temporary compendium of thyroid hormone target genes in brain
F. Chatonnet et al.
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS (2015)
The Thyroid Hormone Analog DITPA Ameliorates Metabolic Parameters of Male Mice With Mct8 Deficiency
Alfonso Massimiliano Ferrara et al.
ENDOCRINOLOGY (2015)
Efficient Activation of Pathogenic ΔPhe501 Mutation in Monocarboxylate Transporter 8 by Chemical and Pharmacological Chaperones
Doreen Braun et al.
ENDOCRINOLOGY (2015)
Clinical and Endocrine Features of Two Allan-Herndon-Dudley Syndrome Patients with Monocarboxylate Transporter 8 Mutations
Ja Hye Kim et al.
HORMONE RESEARCH IN PAEDIATRICS (2015)
Redefining the Pediatric Phenotype of X-Linked Monocarboxylate Transporter 8 (MCT8) Deficiency: Implications for Diagnosis and Therapies
Maria Gisele Matheus et al.
JOURNAL OF CHILD NEUROLOGY (2015)
A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies
Sumit Parikh et al.
MOLECULAR GENETICS AND METABOLISM (2015)
Case definition and classification of leukodystrophies and leukoencephalopathies
Adeline Vanderver et al.
MOLECULAR GENETICS AND METABOLISM (2015)
Promoting remyelination in multiple sclerosis: Current drugs and future prospects
David Kremer et al.
MULTIPLE SCLEROSIS JOURNAL (2015)
Thyroid hormone transporters-functions and clinical implications
Juan Bernal et al.
NATURE REVIEWS ENDOCRINOLOGY (2015)
Further Insights into the Allan-Herndon-Dudley Syndrome: Clinical and Functional Characterization of a Novel MCT8 Mutation
Christine M. Armour et al.
PLOS ONE (2015)
Children Born to Women Treated for Hypothyroidism During Pregnancy Show Abnormal Corpus Callosum Development
Arash Samadi et al.
THYROID (2015)
Transcriptional activation by the thyroid hormone receptor through ligand-dependent receptor recruitment and chromatin remodelling
Lars Grontved et al.
NATURE COMMUNICATIONS (2015)
Promoting remyelination in multiple sclerosis: Current drugs and future prospects
David Kremer et al.
MULTIPLE SCLEROSIS JOURNAL (2015)
Myelin damage and repair in pathologic CNS: challenges and prospects
Arsalan Alizadeh et al.
FRONTIERS IN MOLECULAR NEUROSCIENCE (2015)
Zebrafish as a Model to Investigate CNS Myelination
Marnie A. Preston et al.
GLIA (2015)
Myelination Delay and Allan-Herndon-Dudley Syndrome Caused by a Novel Mutation in the SLC16A2 Gene
Roberta La Piana et al.
JOURNAL OF CHILD NEUROLOGY (2015)
Role of the Thyroid System in Myelination and Neural Connectivity
Laura Calza et al.
COMPREHENSIVE PHYSIOLOGY (2015)
Hypomyelinating Leukodystrophies: Translational Research Progress and Prospects
Petra J. W. Pouwels et al.
ANNALS OF NEUROLOGY (2014)
Hypotonic male infant and MCT8 deficiency - a diagnosis to think about
Filipa Rodrigues et al.
BMC PEDIATRICS (2014)
Delayed myelination is not a constant feature of Allan-Herndon-Dudley syndrome: Report of a new case and review of the literature
Sara Azzolini et al.
BRAIN & DEVELOPMENT (2014)
Neurogenesis in the Striatum of the Adult Human Brain
Aurelie Ernst et al.
CELL (2014)
Remyelination and Multiple Sclerosis: Therapeutic Approaches and Challenges
Meredith D. Hartley et al.
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS (2014)
The Role of Arg445 and Asp498 in the Human Thyroid Hormone Transporter MCT8
Stefan Groeneweg et al.
ENDOCRINOLOGY (2014)
Placenta Passage of the Thyroid Hormone Analog DITPA to Male Wild-Type and Mct8-Deficient Mice
Alfonso Massimiliano Ferrara et al.
ENDOCRINOLOGY (2014)
A Selective Thyroid Hormone β Receptor Agonist Enhances Human and Rodent Oligodendrocyte Differentiation
Emily G. Baxi et al.
GLIA (2014)
Psychomotor Retardation Caused by a Defective Thyroid Hormone Transporter: Report of Two Families with Different MCT8 Mutations
Ahmet Anik et al.
HORMONE RESEARCH IN PAEDIATRICS (2014)
Mutations of the Thyroid Hormone Transporter MCT8 Cause Prenatal Brain Damage and Persistent Hypomyelination
Daniela Lopez-Espindola et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2014)
Transporters MCT8 and OATP1C1 maintain murine brain thyroid hormone homeostasis
Steffen Mayer et al.
JOURNAL OF CLINICAL INVESTIGATION (2014)
In Vitro and Mouse Studies Supporting Therapeutic Utility of Triiodothyroacetic Acid in MCT8 Deficiency
Simone Kersseboom et al.
MOLECULAR ENDOCRINOLOGY (2014)
Clinical Course and Images of Four Familial Cases of Allan-Herndon-Dudley Syndrome With a Novel Monocarboxylate Transporter 8 Gene Mutation
Satoru Kobayashi et al.
PEDIATRIC NEUROLOGY (2014)
Altered Behavioral Performance and Live Imaging of Circuit-Specific Neural Deficiencies in a Zebrafish Model for Psychomotor Retardation
David Zada et al.
PLOS GENETICS (2014)
Thyroid hormone action: astrocyte-neuron communication
Beatriz Morte et al.
FRONTIERS IN ENDOCRINOLOGY (2014)
Expression pattern of thyroid hormone transporters in the postnatal mouse brain
Julia Mueller et al.
FRONTIERS IN ENDOCRINOLOGY (2014)
Thyroid hormone signaling and adult neurogenesis in mammals
Sylvie Remaud et al.
FRONTIERS IN ENDOCRINOLOGY (2014)
Dynamics of Hippocampal Neurogenesis in Adult Humans
Kirsty L. Spalding et al.
CELL (2013)
Human iPSC-Derived Oligodendrocyte Progenitor Cells Can Myelinate and Rescue a Mouse Model of Congenital Hypomyelination
Su Wang et al.
CELL STEM CELL (2013)
Identification, functional analysis, prevalence and treatment of monocarboxylate transporter 8 (MCT8) mutations in a cohort of adult patients with mental retardation
W. Edward Visser et al.
CLINICAL ENDOCRINOLOGY (2013)
Tetrac Can Replace Thyroid Hormone During Brain Development in Mouse Mutants Deficient in the Thyroid Hormone Transporter Mct8
Sigrun Horn et al.
ENDOCRINOLOGY (2013)
Allane-Herndone-Dudley syndrome (AHDS) in two consecutive generations caused by a missense MCT8 gene mutation. Phenotypic variability with the presence of normal serum T3 levels
Loredana Boccone et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2013)
Zebrafish as a Model for Monocarboxyl Transporter 8-Deficiency
Gad David Vatine et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2013)
MCT8 Deficiency: Extrapyramidal Symptoms and Delayed Myelination as Prominent Features
Davide Tonduti et al.
JOURNAL OF CHILD NEUROLOGY (2013)
The zebrafish reference genome sequence and its relationship to the human genome
Kerstin Howe et al.
NATURE (2013)
Functional Characterisation of the Maturation of the Blood-Brain Barrier in Larval Zebrafish
Angeleen Fleming et al.
PLOS ONE (2013)
Impact of Oatp1c1 Deficiency on Thyroid Hormone Metabolism and Action in the Mouse Brain
Steffen Mayerl et al.
ENDOCRINOLOGY (2012)
Finding the Way into the Brain without MCT8
W. Edward Visser et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2012)
Diiodothyropropionic Acid (DITPA) in the Treatment of MCT8 Deficiency
Charles F. Verge et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2012)
The T3-induced gene KLF9 regulates oligodendrocyte differentiation and myelin regeneration
Jason C. Dugas et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2012)
A culture system to study oligodendrocyte myelination processes using engineered nanofibers
Seonok Lee et al.
NATURE METHODS (2012)
Prolonged myelination in human neocortical evolution
Daniel J. Miller et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Pelizaeus-Merzbacher Disease, Pelizaeus-Merzbacher-Like Disease 1, and Related Hypomyelinating Disorders
Grace M. Hobson et al.
SEMINARS IN NEUROLOGY (2012)
Long-Term 3,5,3′- Triiodothyroacetic Acid Therapy in a Child with Hyperthyroidism Caused by Thyroid Hormone Resistance: Pharmacological Study and Therapeutic Recommendations
Rie Anzai et al.
THYROID (2012)
A child with a deletion in the monocarboxylate transporter 8 gene: 7-year follow-up and effects of thyroid hormone treatment
Amnon Zung et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY (2011)
Expression of Thyroid Hormone Transporters in the Human Hypothalamus
Anneke Alkemade et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2011)
Rapid detection of a mutation causing X-linked leucoencephalopathy by exome sequencing
Yoshinori Tsurusaki et al.
JOURNAL OF MEDICAL GENETICS (2011)
The expression of thyroid hormone transporters in the human fetal cerebral cortex during early development and in N-Tera-2 neurodifferentiation
S. -Y. Chan et al.
JOURNAL OF PHYSIOLOGY-LONDON (2011)
Hypomyelination Versus Delayed Myelination
Marjo S. van der Knaap et al.
ANNALS OF NEUROLOGY (2010)
White matter abnormalities and dystonic motor disorder associated with mutations in the SLC16A2 gene
Artemis D. Gika et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2010)
Thyroid Hormone-Regulated Mouse Cerebral Cortex Genes Are Differentially Dependent on the Source of the Hormone: A Study in Monocarboxylate Transporter-8-and Deiodinase-2-Deficient Mice
Beatriz Morte et al.
ENDOCRINOLOGY (2010)
Allan-Herndon-Dudley syndrome (AHDS) caused by a novel SLC16A2 gene mutation showing severe neurologic features and unexpectedly low TRH-stimulated serum TSH
Loredana Boccone et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2010)
Elevated TSH levels in a mentally retarded boy
Ellen Crushell et al.
EUROPEAN JOURNAL OF PEDIATRICS (2010)
Pelizaeus-Merzbacher-Like Disease Presentation of MCT8 Mutated Male Subjects
Catherine Vaurs-Barriere et al.
ANNALS OF NEUROLOGY (2009)
Elevated serum triiodothyronine and intellectual and motor disability with paroxysmal dyskinesia caused by a monocarboxylate transporter 8 gene mutation
Oliver Fuchs et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2009)
A Thyroid Hormone Analog with Reduced Dependence on the Monocarboxylate Transporter 8 for Tissue Transport
Caterina Di Cosmo et al.
ENDOCRINOLOGY (2009)
Importance of Monocarboxylate Transporter 8 for the Blood-Brain Barrier-Dependent Availability of 3,5,3′-Triiodo-L-Thyronine
Ainhoa Ceballos et al.
ENDOCRINOLOGY (2009)
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
Eva K. Wirth et al.
JOURNAL OF NEUROSCIENCE (2009)
Invited Article: An MRI-based approach to the diagnosis of white matter disorders
Raphael Schiffmann et al.
NEUROLOGY (2009)
The origin of the myelination program in vertebrates
B. Zalc et al.
CURRENT BIOLOGY (2008)
Genotype-phenotype relationship in patients with mutations in thyroid hormone transporter MCT8
Jurgen Jansen et al.
ENDOCRINOLOGY (2008)
Expression of the Thyroid Hormone Transporters Monocarboxylate Transporter-8 (SLC16A2) and Organic Ion Transporter-14 (SLCO1C1) at the Blood-Brain Barrier
Lori M. Roberts et al.
ENDOCRINOLOGY (2008)
1H magnetic resonance spectroscopy in monocarboxylate transporter 8 gene deficiency
Paul E. Sijens et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2008)
A novel monocarboxylate transporter 8 gene mutation as a cause of severe neonatal hypotonia and developmental delay
Anastasios Papadimitriou et al.
PEDIATRICS (2008)
Activation and inactivation of thyroid hormone by deiodinases:: Local action with general consequences
B. Gereben et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2008)
Clinical phenotype and endocrinological investigations in a patient with a mutation in the MCT8 thyroid hormone transporter
Noriyuki Namba et al.
EUROPEAN JOURNAL OF PEDIATRICS (2008)
The MCT8 thyroid hormone transporter and Allan-Herndon-Dudley syndrome
Charles E. Schwartz et al.
BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM (2007)
Abnormal thyroid hormone metabolism in mice lacking the monocarboxylate transporter 8
Marija Trajkovic et al.
JOURNAL OF CLINICAL INVESTIGATION (2007)
Thyroid hormone receptors in brain development and function
Juan Bernal
NATURE CLINICAL PRACTICE ENDOCRINOLOGY & METABOLISM (2007)
Thyroid hormone deficiency changes the distribution of oligodendrocyte/myelin markers during oligodendroglial differentiation in vitro
V. Younes-Rapozo et al.
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE (2006)
Medical progress: Multiple sclerosis - The plaque and its pathogenesis
EM Frohman et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (Mct) 8-deficient mice
Alexandra M. Dumitrescu et al.
ENDOCRINOLOGY (2006)
A novel mutation in the monocarboxylate transporter 8 gene in a boy with putamen lesions and low free T4 levels in cerebrospinal fluid
H Kakinuma et al.
JOURNAL OF PEDIATRICS (2005)
X-linked MCT8 gene mutations:: Characterization of the pediatric neurologic phenotype
KR Holden et al.
JOURNAL OF CHILD NEUROLOGY (2005)
Endocrine and neuropsychological assessment in a child with a novel mutation of thyroid hormone receptor: Response to 12-month triiodothyroacetic acid (TRIAC) therapy
P Torre et al.
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION (2005)
Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene
CE Schwartz et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
Unique astrocyte ribbon in adult human brain contains neural stem cells but lacks chain migration
N Sanai et al.
NATURE (2004)
A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene
AM Dumitrescu et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Thyroid hormone regulates oligodendrocyte accumulation in developing rat brain white matter tracts
CM Schoonover et al.
ENDOCRINOLOGY (2004)
Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation
ECH Friesema et al.
LANCET (2004)
Timing of thyroid hormone action in the developing brain: Clinical observations and experimental findings
RT Zoeller et al.
JOURNAL OF NEUROENDOCRINOLOGY (2004)
Thyroid hormone signaling is highly heterogeneous during pre- and postnatal brain development
L Quignodon et al.
JOURNAL OF MOLECULAR ENDOCRINOLOGY (2004)
Identification of monocarboxylate transporter 8 as a specific thyroid hormone transporter
ECH Friesema et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Normal timing of oligodendrocyte development depends on thyroid hormone receptor alpha 1 (TRα1)
N Billon et al.
EMBO JOURNAL (2002)
Role of thyroid hormone receptors in timing oligodendrocyte differentiation
N Billon et al.
DEVELOPMENTAL BIOLOGY (2001)
Share Paper
