Results 11 to 20 of about 13,855 (152)

Rare cause of ketolysis: Monocarboxylate transporter 1 deficiency

open access: yesThe Turkish Journal of Pediatrics, 2022
Background. Monocarboxylate transporter 1 (MCT1) deficiency (MIM #616095) is a relatively new identified cause of recurrent ketoacidosis triggered by fasting or infections. MCT1 was first described in 2014 by van Hasselt et al. to result from both
Ayşe Ergül Bozacı   +1 more
doaj   +1 more source

Monocarboxylate transporter and lactate metabolism

open access: yesJournal of Physical Fitness and Sports Medicine, 2012
For many years, lactate was considered as a metabolic waste product, and a cause of fatigue during exercise. However, lactate is now known as a carbohydrate fuel source, shuttled between cells and tissues.
Yu Kitaoka, Daisuke Hoshino, Hideo Hatta
doaj   +1 more source

Monocarboxylate Transporter 8 Deficiency: Delayed or Permanent Hypomyelination?

open access: yesFrontiers in Endocrinology, 2020
Monocarboxylate transporter 8 (MCT8) deficiency or the Allan-Herndon-Dudley Syndrome (AHDS) is an X-linked psychomotor disability syndrome with around 320 clinical cases described worldwide.
Pieter Vancamp   +2 more
doaj   +1 more source

Uptake and Advanced Therapy of Butyrate in Inflammatory Bowel Disease

open access: yesImmuno, 2022
The pathogenesis and refractory nature of inflammatory bowel disease (IBD) are related to multiple factors, including genetic factors, environmental factors, and abnormalities in gut microbial diversity, which lead to decreased levels of short-chain ...
Shinji Ota, Hirotake Sakuraba
doaj   +1 more source

Monocarboxylate transporter functions and neuroprotective effects of valproic acid in experimental models of amyotrophic lateral sclerosis

open access: yesJournal of Biomedical Science, 2022
Background Amyotrophic lateral sclerosis (ALS) is a devasting neurodegenerative disorder for which no successful therapeutics are available. Valproic acid (VPA), a monocarboxylate derivative, is a known antiepileptic drug and a histone deacetylase ...
Asmita Gyawali   +5 more
doaj   +1 more source

IMMUNOHISTOCHEMICAL EXPRESSION OF MONOCARBOXYLATE TRANSPORTER 1&4 IN TANYCYTE–LIKE CELLS OF THE SULCUS MEDIANUS ORGANUM

open access: yesThe Iraqi Journal of Medical Sciences, 2019
Background: Circumventricular organs (CVOs) are specialized structures border the brain ventricles and lack the blood-brain barrier. These CVOs are lined by specialized ependymal cells (ECs) called tanycyte.
Haider F. Jawad   +2 more
doaj   +6 more sources

Adipocytes promote malignant growth of breast tumours with monocarboxylate transporter 2 expression via β-hydroxybutyrate

open access: yesNature Communications, 2017
Invasion of the adipose tissue correlates with poor prognosis in breast cancer. Here, the authors show that mammary gland adipocytes promote malignancy via β-hydroxybutyrate, which acts on cancer cells through the monocarboxylate transporter MCT2 ...
Chun-Kai Huang   +8 more
doaj   +1 more source

Intestinal OCTN2- and MCT1-targeted drug delivery to improve oral bioavailability

open access: yesAsian Journal of Pharmaceutical Sciences, 2020
Various drug transporters are widely expressed throughout the intestine and play important roles in absorbing nutrients and drugs, thus providing high quality targets for the design of prodrugs or nanoparticles to facilitate oral drug delivery.
Gang Wang   +8 more
doaj   +1 more source

Exercise-induced hyperinsulinism: genetic basis and clinical management

open access: yes中国当代儿科杂志
Exercise-induced hyperinsulinism, also known as monocarboxylate transporter 1 hyperinsulinemia, is a rare subtype of congenital hyperinsulinism caused by gain-of-function variants in the SLC16A1 gene, which encodes monocarboxylate transporter 1.
ZHANG Qi-Ting, HOU Ling
doaj   +1 more source

Generation of iPSC lines with SLC16A2:G401R or SLC16A2 knock out

open access: yesStem Cell Research, 2023
The X-linked Allan-Herndon-Dudley syndrome (AHDS) is characterized by severely impaired psychomotor development and is caused by mutations in the SLC16A2 gene encoding the thyroid hormone transporter MCT8 (monocarboxylate transporter 8).
Katarzyna Anna Ludwik   +7 more
doaj   +1 more source

Home - About - Disclaimer - Privacy