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27 matching publication(s)

Publication	Journal	Year	Score	Verdict
The TREM2-APOE Pathway Drives the Transcriptional Phenotype of Dysfunctional Microglia in Neurodegenerative Diseases. PMID 28930663	Immunity	2017	67	L1 67/100
Endogenous retroviral elements LTR8B and MER65 rewire PSG9 regulation to control trophoblast syncytialization and pre-eclampsia risk. PMID 41796334	Genome Biol	2026	68	L1 68/100
Distinct sympathetic projections to brown fat regulate thermogenesis and glucose tolerance. PMID 41559445	Nat Metab	2026	85	L1 85/100
Single-nucleus mRNA-sequencing reveals dynamics of lipogenic and thermogenic adipocyte populations in murine brown adipose tissue in response to cold exposure. PMID 40945691	Mol Metab	2025	93	L1 93/100
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings PMID 40555819	Nature Genetics (Author Correction 2025; orig 2024;56:1644)	2025	76	L1 76/100
Covalent binding of thioredoxin to TXNIP is required for diet-induced insulin resistance in the liver. PMID 40345590	J Biol Chem	2025	87	L1 87/100
NK2R control of energy expenditure and feeding to treat metabolic diseases. PMID 39537932	Nature	2024	87	L1 87/100
Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviors PMID 39256359	—	2024	87	L1 87/100
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findi PMID 39039281	Nat Genet	2024	87	L1 87/100
Fatty acid synthesis suppresses dietary polyunsaturated fatty acid use PMID 38167725	Nature Communications	2024	94	L1 94/100
Prediction of Antibiotic Susceptibility Profiles of Vibrio cholerae Isolates From Whole Genome Illumina and Nanopore Sequencing Data: CholerAegon. PMID 35814690	Front Microbiol	2022	86	L1 86/100
Apoptotic brown adipocytes enhance energy expenditure via extracellular inosine PMID 35790189	—	2022	57	L1 57/100
TFEB deficiency attenuates mitochondrial degradation upon brown adipose tissue whitening at thermoneutrality PMID 33516944	Molecular Metabolism 47:101173	2021	—	L1 No computation
Endogenous Fatty Acid Synthesis Drives Brown Adipose Tissue Involution PMID 33440156	—	2021	—	L1 No data access
The novel duplication HRAS c.186_206dup p.(Glu62_Arg68dup): clinical and functional aspects. PMID 32499600	—	2020	—	L1 No computation
PID1 regulates insulin-dependent glucose uptake by controlling intracellular sorting of GLUT4-storage vesicles PMID 30904610	—	2019	—	L1 No computation
Lipolysis Triggers a Systemic Insulin Response Essential for Efficient Energy Replenishment of Activated Brown Adipose Tissue in Mice PMID 30033199	—	2018	—	L1 No computation
FoxO transcription factors are required for hepatic HDL cholesterol clearance PMID 29408809	—	2018	49	L1 49/100
Cold-induced conversion of cholesterol to bile acids in mice shapes the gut microbiome and promotes adaptive thermogenesis PMID 28604703	—	2017	—	No data access
Thermogenic adipocytes promote HDL turnover and reverse cholesterol transport PMID 28422089	Nature Communications	2017	—	L1 No computation
The role of the multidisciplinary health care team in the management of patients with Marfan syndrome. PMID 27843325	—	2016	—	L1 No computation
FGF21 Lowers Plasma Triglycerides by Accelerating Lipoprotein Catabolism in White and Brown Adipose Tissues PMID 26853749	—	2016	—	L1 No computation
An attenuated phenotype of Costello syndrome in three unrelated individuals with a HRAS c.179G>A (p.Gly60Asp) mutation correlates with uncommon functional consequences. PMID 25914166	—	2015	—	L1 No computation
Brown fat activation reduces hypercholesterolaemia and protects from atherosclerosis development PMID 25754609	—	2015	—	L1 No computation
A novel HRAS substitution (c.266C>G; p.S89C) resulting in decreased downstream signaling suggests a new dimension of RAS pathway dysregulation in human development. PMID 22821884	—	2012	88	L1 88/100
WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. PMID 20887964	—	2010	—	L1 No computation
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. PMID 18834967	—	2008	70	L1 70/100