Search Results - "Guadaño‐Ferraz, Ana"
-
1
Thyroid hormone transporters—functions and clinical implications
Published in Nature reviews. Endocrinology (01-07-2015)“…Key Points Many proteins can mediate thyroid hormone transport, but only mutations in genes encoding MCT8, MCT10 and OATP1C1 have pathophysiological effects…”
Get full text
Journal Article -
2
Generation and Characterization of dickkopf3 Mutant Mice
Published in Molecular and Cellular Biology (01-03-2006)“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
Get full text
Journal Article -
3
Expression of the cold thermoreceptor TRPM8 in rodent brain thermoregulatory circuits
Published in Journal of comparative neurology (1911) (01-01-2021)“…The cold‐ and menthol‐activated ion channel transient receptor potential channel subfamily M member 8 (TRPM8) is the principal detector of environmental cold…”
Get full text
Journal Article -
4
Thyroid Hormone Transporters MCT8 and OATP1C1 Are Expressed in Pyramidal Neurons and Interneurons in the Adult Motor Cortex of Human and Macaque Brain
Published in International journal of molecular sciences (01-02-2023)“…Monocarboxylate transporter 8 (MCT8) and organic anion transporter polypeptide 1C1 (OATP1C1) are thyroid hormone (TH) transmembrane transporters that play an…”
Get full text
Journal Article -
5
Combined deletion of Mct8 and Dio2 impairs SVZ neurogliogenesis and olfactory function in adult mice
Published in Neurobiology of disease (01-09-2024)“…Within the adult mouse subventricular zone (SVZ), neural stem cells (NSCs) produce neuroblasts and oligodendrocyte precursor cells (OPCs). T3, the active…”
Get full text
Journal Article -
6
Mutations of the Thyroid Hormone Transporter MCT8 Cause Prenatal Brain Damage and Persistent Hypomyelination
Published in The journal of clinical endocrinology and metabolism (01-12-2014)“…Context: Mutations in the MCT8 (SLC16A2) gene, encoding a specific thyroid hormone transporter, cause an X-linked disease with profound psychomotor…”
Get full text
Journal Article -
7
Adult Mice Lacking Mct8 and Dio2 Proteins Present Alterations in Peripheral Thyroid Hormone Levels and Severe Brain and Motor Skill Impairments
Published in Thyroid (New York, N.Y.) (01-11-2019)“…Mutations in the thyroid hormone (TH) transporter monocarboxylate transporter 8 (MCT8) lead to peripheral hyperthyroidism and profound psychomotor alterations…”
Get more information
Journal Article -
8
Increased anxiety and fear memory in adult mice lacking type 2 deiodinase
Published in Psychoneuroendocrinology (01-10-2017)“…•Deiodinase type 2 (D2) deficiency leads to emotional alterations in adult mice.•D2 deficiency decreases T3 content in hippocampus and most probably in…”
Get full text
Journal Article -
9
Thyroid hormone availability in the human fetal brain: novel entry pathways and role of radial glia
Published in Brain Structure and Function (01-07-2019)“…Thyroid hormones (TH) are crucial for brain development; their deficiency during neurodevelopment impairs neural cell differentiation and causes irreversible…”
Get full text
Journal Article -
10
Thyroid Hormone Transporters MCT8 and OATP1C1 Are Expressed in Projection Neurons and Interneurons of Basal Ganglia and Motor Thalamus in the Adult Human and Macaque Brains
Published in International journal of molecular sciences (01-06-2023)“…Monocarboxylate transporter 8 (MCT8) and organic anion-transporting polypeptide 1C1 (OATP1C1) are thyroid hormone (TH) transmembrane transporters relevant for…”
Get full text
Journal Article -
11
Thyroid Hormone Availability and Action during Brain Development in Rodents
Published in Frontiers in cellular neuroscience (14-08-2017)“…Thyroid hormones (THs) play an essential role in the development of all vertebrates; in particular adequate TH content is crucial for proper neurodevelopment…”
Get full text
Journal Article -
12
Thyroid hormone action in adult neurogliogenic niches: the known and unknown
Published in Frontiers in endocrinology (Lausanne) (07-03-2024)“…Over the last decades, thyroid hormones (THs) signaling has been established as a key signaling cue for the proper maintenance of brain functions in adult…”
Get full text
Journal Article -
13
MCT8 Deficiency: The Road to Therapies for a Rare Disease
Published in Frontiers in neuroscience (28-04-2020)“…Allan-Herndon-Dudley syndrome is a rare disease caused by inactivating mutations in the gene, which encodes the monocarboxylate transporter 8 (MCT8), a…”
Get full text
Journal Article -
14
REGULATION OF THE TRANSCRIPTIONAL AND CELLULAR LANDSCAPE OF THE ADULT MOUSE SUBVENTRICULAR ZONE BY THYROID HORMONE SIGNALING
Published in IBRO neuroscience reports (01-10-2023)Get full text
Journal Article -
15
Type 3 Iodothyronine Deiodinase Is Selectively Expressed in Areas Related to Sexual Differentiation in the Newborn Rat Brain
Published in Endocrinology (Philadelphia) (01-11-1999)“…Thyroid hormone (T4 and T3) concentrations in target tissues are greatly influenced by the activity of iodothyronine deiodinases. Type 1 and 2 deiodinases…”
Get full text
Journal Article -
16
Deficient thyroid hormone transport to the brain leads to impairments in axonal caliber and oligodendroglial development
Published in Neurobiology of disease (01-01-2022)“…Mutations in the thyroid hormone transporter monocarboxylate transporter 8 (MCT8) lead to profound brain alterations, including myelination impairments, in…”
Get full text
Journal Article -
17
A CRISPR/Cas9-engineered avatar mouse model of monocarboxylate transporter 8 deficiency displays distinct neurological alterations
Published in Neurobiology of disease (01-11-2022)“…Inactivating mutations in the specific thyroid hormone transporter monocarboxylate transporter 8 (MCT8) lead to an X-linked rare disease named MCT8 deficiency…”
Get full text
Journal Article -
18
Defective thyroid hormone transport to the brain leads to astroglial alterations
Published in Neurobiology of disease (01-10-2024)“…Allan-Herndon-Dudley syndrome (AHDS) is a rare X-linked disorder that causes severe neurological damage, for which there is no effective treatment. AHDS is due…”
Get full text
Journal Article -
19
Intranasal delivery of Thyroid hormones in MCT8 deficiency
Published in PloS one (20-07-2020)“…Loss of function mutations in the gene encoding the thyroid hormone transporter monocarboxylate transporter 8 (MCT8) lead to severe neurodevelopmental defects…”
Get full text
Journal Article -
20
STRUCTURAL AND FUNCTIONAL ALTERATIONS AT THE BLOOD-BRAIN BARRIER IN A MOUSE MODEL FOR MCT8 DEFICIENCY
Published in IBRO neuroscience reports (01-10-2023)Get full text
Journal Article