Detalhe da pesquisa
1.
Obesity-induced metabolic imbalance allosterically modulates CtBP2 to inhibit PPAR-alpha transcriptional activity.
J Biol Chem
; 299(7): 104890, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37286039
2.
CtBP2 confers protection against oxidative stress through interactions with NRF1 and NRF2.
Biochem Biophys Res Commun
; 562: 146-153, 2021 07 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34052660
3.
Hepatocyte ELOVL Fatty Acid Elongase 6 Determines Ceramide Acyl-Chain Length and Hepatic Insulin Sensitivity in Mice.
Hepatology
; 71(5): 1609-1625, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31529722
4.
Transcriptional co-repressor CtBP2 orchestrates epithelial-mesenchymal transition through a novel transcriptional holocomplex with OCT1.
Biochem Biophys Res Commun
; 523(2): 354-360, 2020 03 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31866012
5.
Skeletal muscle-specific HMG-CoA reductase knockout mice exhibit rhabdomyolysis: A model for statin-induced myopathy.
Biochem Biophys Res Commun
; 466(3): 536-40, 2015 Oct 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-26381177
6.
Genetic and Functional Analyses of Patients with Marked Hypo-High-Density Lipoprotein Cholesterolemia.
J Atheroscler Thromb
; 2024 Mar 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38538338
7.
Takotsubo cardiomyopathy with left ventricle thrombus caused by subacute thyroiditis.
BMJ Case Rep
; 16(3)2023 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-36918211
8.
Loss of CtBP2 may be a mechanistic link between metabolic derangements and progressive impairment of pancreatic ß cell function.
Cell Rep
; 42(8): 112914, 2023 08 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37557182
9.
Identification of key microRNAs regulating ELOVL6 and glioblastoma tumorigenesis.
BBA Adv
; 3: 100078, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37082255
10.
Rhomboid protease RHBDL4/RHBDD1 cleaves SREBP-1c at endoplasmic reticulum monitoring and regulating fatty acids.
PNAS Nexus
; 2(11): pgad351, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37954160
11.
Prediction of late (24-hour) radioactive iodine uptake using early (3-hour) uptake values in Japanese patients with Graves' disease.
Endocr J
; 59(2): 173-7, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22095001
12.
A case of early-onset diabetes with impaired insulin secretion carrying a PAX6 gene Gln135* mutation.
Endocrinol Diabetes Metab Case Rep
; 20222022 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35979842
13.
Effects of Branched-Chain Amino Acids on Skeletal Muscle, Glycemic Control, and Neuropsychological Performance in Elderly Persons with Type 2 Diabetes Mellitus: An Exploratory Randomized Controlled Trial.
Nutrients
; 14(19)2022 Sep 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36235570
14.
Morphological and functional adaptation of pancreatic islet blood vessels to insulin resistance is impaired in diabetic db/db mice.
Biochim Biophys Acta Mol Basis Dis
; 1868(4): 166339, 2022 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35017029
15.
A case of NASH with genetic predisposition successfully treated with an SGLT2 inhibitor: a possible involvement of mitochondrial dysfunction.
Endocrinol Diabetes Metab Case Rep
; 20222022 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36571472
16.
ACTH response to desmopressin in a patient with acromegaly; expression of corticotropin-releasing factor, urocortins and vasopressin V1b receptor in GH-producing pituitary adenoma.
Endocr J
; 58(12): 1029-36, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21908929
17.
Enterohepatic Transcription Factor CREB3L3 Protects Atherosclerosis via SREBP Competitive Inhibition.
Cell Mol Gastroenterol Hepatol
; 11(4): 949-971, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33246135
18.
CREBH Improves Diet-Induced Obesity, Insulin Resistance, and Metabolic Disturbances by FGF21-Dependent and FGF21-Independent Mechanisms.
iScience
; 23(3): 100930, 2020 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-32151974
19.
Selective peroxisome proliferator-activated receptor-α modulator K-877 efficiently activates the peroxisome proliferator-activated receptor-α pathway and improves lipid metabolism in mice.
J Diabetes Investig
; 8(4): 446-452, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28084058
20.
Familial Dysalbuminemic Hyperthyroxinemia in a Japanese Man Caused by a Point Albumin Gene Mutation (R218P).
Jpn Clin Med
; 7: 9-13, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27081329