Buscar
Mostrando ítems 41-50 de 655
SLC anuncia aquisição de mais terras no Maranhão
(2008-09-04)
Novel pathogenic mechanism suggested by ex vivo analysis of MCT8 (SLC16A2) mutations
(2009)
Monocarboxylate transporter 8 (MCT8; approved symbol SLC16A2) facilitates cellular uptake and efflux of 3,3′,5-triiodothyronine (T3). Mutations in MCT8 are associated with severe psychomotor retardation, high serum T3 and ...
Genome-wide association studies identify DNA variants influencing eyebrow thickness variation in Europeans and across continental populations.
(Elsevier, 2023)
Ethics. Human subjects: All cohort participants gave written informed consent and consent to publish. Ethical approvals were provided for the Rotterdam Study according to the Population Study Act Rotterdam Study (Wet ...
Inhibition of cannabinoid CB1 receptor upregulates Slc2a4 expression via nuclear factor-kappa B and sterol regulatory element-binding protein-1 in adipocytes
(BIOSCIENTIFICA LTDBRISTOL, 2012)
Evidences have suggested that the endocannabinoid system is overactive in obesity, resulting in enhanced endocannabinoid levels in both circulation and visceral adipose tissue. The blockade of cannabinoid receptor type 1 ...
The clinical and biochemical hallmarks generally associated with GLUT1DS may be caused by defects in genes other than SLC2A1
(Wiley, 2022)
Glucose transporter 1 deficiency syndrome (GLUT1DS) is a neurometabolic disorder caused by haploinsufficiency of the GLUT1 glucose transporter (encoded by SLC2A1) leading to defective glucose transport across the blood-brain ...
Bases genéticas del autismoGenetic basis of autism
(Instituto Nacional de Pediatría, 2010)