The complexity and multiplicity of the specific cAMP phosphodiesterase family: PDE4, open new adapted therapeutic approaches

C Lugnier - International Journal of Molecular Sciences, 2022 - mdpi.com
Cyclic nucleotides (cAMP, cGMP) play a major role in normal and pathologic signaling.
Beyond receptors, cyclic nucleotide phosphodiesterases;(PDEs) rapidly convert the cyclic …

PRDM16 regulating adipocyte transformation and thermogenesis: a promising therapeutic target for obesity and diabetes

N Jiang, M Yang, Y Han, H Zhao, L Sun - Frontiers in pharmacology, 2022 - frontiersin.org
Given that obesity and diabetes have been major public health concerns and that disease
morbidities have been rising continuously, effective treatment for these diseases is urgently …

Maternal glycemia in pregnancy is longitudinally associated with blood DNAm variation at the FSD1L gene from birth to 5 years of age

A Taschereau, K Thibeault, C Allard… - Clinical …, 2023 - Springer
Background In utero exposure to maternal hyperglycemia has been associated with an
increased risk for the development of chronic diseases in later life. These predispositions …

Genetic polymorphisms associated with obesity in the Arab world: a systematic review

S Younes, A Ibrahim, R Al-Jurf, H Zayed - International Journal of …, 2021 - nature.com
Background Obesity, one of the most common chronic health conditions worldwide, is a
multifactorial disease caused by complex genetic and environmental interactions. Several …

Genome-wide DNA methylation profiling in blood reveals epigenetic signature of incident acute coronary syndrome

P Long, J Si, Z Zhu, Y Jiang, Y Wang, Q Jiang… - Nature …, 2024 - nature.com
DNA methylation (DNAm) has been implicated in acute coronary syndrome (ACS), but the
causality remains unclear in cross-sectional studies. Here, we conduct a prospective …

Genetic variants in migraine: A field synopsis and systematic re-analysis of meta-analyses

Y Zhao, R Zhu, T Xiao, X Liu - The Journal of Headache and Pain, 2020 - Springer
Objective Numerous genetic variants from meta-analyses of observational studies and
GWAS were reported to be associated with migraine susceptibility. However, due to the …

Association of rs2651899 Polymorphism in the Positive Regulatory Domain 16 and Common Migraine Subtypes: A Meta‐Analysis

HH Lee, CC Chen, JR Ong, YF Lin… - … : The Journal of …, 2020 - Wiley Online Library
Background Migraine is a neurovascular disease with recurrent headache attacks. A
polymorphism (rs2651899) of the PRDM16 gene, which is associated with migraine, was …

PRDM16 Represses the Pig White Lipogenesis through Promoting Lipolysis Activity

T Gu, G Xu, C Jiang, L Hou, Z Wu… - BioMed Research …, 2019 - Wiley Online Library
The positive regulatory domain containing 16 (PRDM16) gene is a dominant transcriptional
regulator that favors the “browning” of white adipocytes in rodents. Since the “browning” of …

Association of PRDM16 rs12409277 and CtBP2 rs1561589 gene polymorphisms with lipid profile of adolescents

N Maksimovic, V Vidovic… - Archives of Medical …, 2021 - pmc.ncbi.nlm.nih.gov
Introduction Positive regulatory domain containing 16 (PRDM16) protein represents the key
regulator of brown adipose tissue (BAT) development. It induces brown fat phenotype and …

Role of Single Nucleotide Polymorphisms (SNPs) in Common Migraine

SS Aga, MZ Banday, S Nissar, K Akhtar… - Genetic …, 2022 - taylorfrancis.com
Migraine is regarded as the most common disease affecting human functioning. Migraine is
classified as the common type of primary headache disorder characterized by the “episodic …