Detalhe da pesquisa
1.
Metabolic dysfunction-associated steatotic liver disease and the heart.
Hepatology
; 2023 Dec 25.
Artigo
Inglês
| MEDLINE | ID: mdl-38147315
2.
Machine learning algorithm improves the detection of NASH (NAS-based) and at-risk NASH: A development and validation study.
Hepatology
; 78(1): 258-271, 2023 07 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36994719
3.
Diagnostic accuracy of non-invasive tests to screen for at-risk MASH-An individual participant data meta-analysis.
Liver Int
; 2024 Apr 04.
Artigo
Inglês
| MEDLINE | ID: mdl-38573034
4.
Anaerobutyricum soehngenii Reduces Hepatic Lipogenic Pathways and Increases Intestinal Gluconeogenic Gene Expression in Metabolic-Dysfunction-Associated Steatotic Liver Disease (MASLD) Mice.
Int J Mol Sci
; 25(6)2024 Mar 20.
Artigo
Inglês
| MEDLINE | ID: mdl-38542455
5.
Mutations in the V-ATPase Assembly Factor VMA21 Cause a Congenital Disorder of Glycosylation With Autophagic Liver Disease.
Hepatology
; 72(6): 1968-1986, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-32145091
6.
Assessment of Imaging Modalities Against Liver Biopsy in Nonalcoholic Fatty Liver Disease: The Amsterdam NAFLD-NASH Cohort.
J Magn Reson Imaging
; 54(6): 1937-1949, 2021 12.
Artigo
Inglês
| MEDLINE | ID: mdl-33991378
7.
Esterification of 4ß-hydroxycholesterol and other oxysterols in human plasma occurs independently of LCAT.
J Lipid Res
; 61(9): 1287-1299, 2020 09.
Artigo
Inglês
| MEDLINE | ID: mdl-32561542
8.
N-Glycosylation Defects in Humans Lower Low-Density Lipoprotein Cholesterol Through Increased Low-Density Lipoprotein Receptor Expression.
Circulation
; 140(4): 280-292, 2019 07 23.
Artigo
Inglês
| MEDLINE | ID: mdl-31117816
9.
Reduced CETP glycosylation and activity in patients with homozygous B4GALT1 mutations.
J Inherit Metab Dis
; 43(3): 611-617, 2020 05.
Artigo
Inglês
| MEDLINE | ID: mdl-31800099
10.
Moving Targets: Recent Advances in Lipid-Lowering Therapies
Arterioscler Thromb Vasc Biol
; 39(3): 349-359, 2019 03.
Artigo
Inglês
| MEDLINE | ID: mdl-30676072
11.
Lipidomics in Nonalcoholic Fatty Liver Disease: Exploring Serum Lipids as Biomarkers for Pediatric Nonalcoholic Fatty Liver Disease.
J Pediatr Gastroenterol Nutr
; 71(4): 433-439, 2020 10.
Artigo
Inglês
| MEDLINE | ID: mdl-32947564
12.
Complete and Partial Lecithin:Cholesterol Acyltransferase Deficiency Is Differentially Associated With Atherosclerosis.
Circulation
; 138(10): 1000-1007, 2018 09 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29748187
13.
TMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal Glycosylation.
Am J Hum Genet
; 98(2): 322-30, 2016 Feb 04.
Artigo
Inglês
| MEDLINE | ID: mdl-26833330
14.
CCDC115 Deficiency Causes a Disorder of Golgi Homeostasis with Abnormal Protein Glycosylation.
Am J Hum Genet
; 98(2): 310-21, 2016 Feb 04.
Artigo
Inglês
| MEDLINE | ID: mdl-26833332
15.
The P274S Mutation of Lecithin-Cholesterol Acyltransferase (LCAT) and Its Clinical Manifestations in a Large Kindred.
Am J Kidney Dis
; 74(4): 510-522, 2019 10.
Artigo
Inglês
| MEDLINE | ID: mdl-31103331
16.
New insights into the role of glycosylation in lipoprotein metabolism.
Curr Opin Lipidol
; 28(6): 502-506, 2017 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-28922188
17.
Lipoprotein profiles in human heterozygote carriers of a functional mutation P297S in scavenger receptor class B1.
Biochim Biophys Acta
; 1851(12): 1587-95, 2015 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-26454245
18.
Lipoprotein subfractions highly associated with renal damage in familial lecithin:cholesterol acyltransferase deficiency.
Arterioscler Thromb Vasc Biol
; 34(8): 1756-62, 2014 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-24876348
19.
Genetic variant of the scavenger receptor BI in humans.
N Engl J Med
; 364(2): 136-45, 2011 Jan 13.
Artigo
Inglês
| MEDLINE | ID: mdl-21226579
20.
ABCA1 mutation carriers with low high-density lipoprotein cholesterol are characterized by a larger atherosclerotic burden.
Eur Heart J
; 34(4): 286-91, 2013 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-23136402