The bromodomain and extra-terminal domain (BET) family: functional anatomy of BET paralogous proteins
Y Taniguchi - International journal of molecular sciences, 2016 - mdpi.com
The Bromodomain and Extra-Terminal Domain (BET) family of proteins is characterized by
the presence of two tandem bromodomains and an extra-terminal domain. The mammalian …
the presence of two tandem bromodomains and an extra-terminal domain. The mammalian …
Genetic landscape of common epilepsies: advancing towards precision in treatment
Epilepsy, a neurological disease characterized by recurrent seizures, is highly
heterogeneous in nature. Based on the prevalence, epilepsy is classified into two types …
heterogeneous in nature. Based on the prevalence, epilepsy is classified into two types …
Sex differences in the epilepsies and associated comorbidities: implications for use and development of pharmacotherapies
The epilepsies are common neurologic disorders characterized by spontaneous recurrent
seizures. Boys, girls, men, and women of all ages are affected by epilepsy and, in many …
seizures. Boys, girls, men, and women of all ages are affected by epilepsy and, in many …
Place your BETs: the therapeutic potential of bromodomains
RK Prinjha, J Witherington, K Lee - Trends in pharmacological sciences, 2012 - cell.com
Therapeutic targeting of the processes that regulate histone modification is a growing area
of scientific exploration. Although most interest has concentrated on the various families of …
of scientific exploration. Although most interest has concentrated on the various families of …
Genetic and epigenetic mechanisms of epilepsy: a review
T Chen, M Giri, Z Xia, YN Subedi… - … disease and treatment, 2017 - Taylor & Francis
Epilepsy is a common episodic neurological disorder or condition characterized by recurrent
epileptic seizures, and genetics seems to play a key role in its etiology. Early linkage studies …
epileptic seizures, and genetics seems to play a key role in its etiology. Early linkage studies …
Bromodomains and their pharmacological inhibitors
D Gallenkamp, KA Gelato, B Haendler… - …, 2014 - Wiley Online Library
Over 60 bromodomains belonging to proteins with very different functions have been
identified in humans. Several of them interact with acetylated lysine residues, leading to the …
identified in humans. Several of them interact with acetylated lysine residues, leading to the …
Bromodomain and extra-terminal (BET) family proteins: New therapeutic targets in major diseases
B Padmanabhan, S Mathur, R Manjula, S Tripathi - Journal of biosciences, 2016 - Springer
The bromodomains and extra-terminal domain (BET) family proteins recognize acetylated
chromatin through their bromodomains (BDs) and help in regulating gene expression. BDs …
chromatin through their bromodomains (BDs) and help in regulating gene expression. BDs …
A review of the differences in developmental, psychiatric, and medical endophenotypes between males and females with autism spectrum disorder
E Rubenstein, LD Wiggins, LC Lee - Journal of Developmental and …, 2015 - Springer
Autism spectrum disorder (ASD) is over four times more prevalent in males compared to
females. Increased understanding of sex differences in ASD endophenotypes could add …
females. Increased understanding of sex differences in ASD endophenotypes could add …
[HTML][HTML] Domain-selective targeting of BET proteins in cancer and immunological diseases
M Petretich, EH Demont, P Grandi - Current Opinion in Chemical Biology, 2020 - Elsevier
Cancer and inflammation are strongly interconnected processes. Chronic inflammatory
pathologies can be at the heart of tumor development; similarly, tumor-elicited inflammation …
pathologies can be at the heart of tumor development; similarly, tumor-elicited inflammation …
Impaired regulation of KCC2 phosphorylation leads to neuronal network dysfunction and neurodevelopmental pathology
KCC2 is a vital neuronal K+/Cl− cotransporter that is implicated in the etiology of numerous
neurological diseases. In normal cells, KCC2 undergoes developmental dephosphorylation …
neurological diseases. In normal cells, KCC2 undergoes developmental dephosphorylation …