KCTD10 regulates brain development by destabilizing brain disorder–associated protein KCTD13

J Cheng, Z Wang, M Tang, W Zhang… - Proceedings of the …, 2024 - National Acad Sciences
KCTD10 belongs to the KCTD (potassiumchannel tetramerization domain) family, many
members of which are associated with neuropsychiatric disorders. However, the biological …

Kctd7 deficiency induces myoclonic seizures associated with Purkinje cell death and microvascular defects

JH Liang, J Alevy, V Akhanov, R Seo… - Disease Models & …, 2022 - journals.biologists.com
Mutations in the potassium channel tetramerization domain-containing 7 (KCTD7) gene are
associated with a severe neurodegenerative phenotype characterized by childhood onset of …

[HTML][HTML] KCTD5 Forms Hetero-Oligomeric Complexes with Various Members of the KCTD Protein Family

Y Liao, DC Sloan, JH Widjaja, BS Muntean - International journal of …, 2023 - mdpi.com
Potassium Channel Tetramerization Domain 5 (KCTD5) regulates diverse aspects of
physiology, ranging from neuronal signaling to colorectal cancer. A key feature of KCTD5 is …

Pathogenic variants in KCTD7 perturb neuronal K+ fluxes and glutamine transport

MN Moen, R Fjær, EH Hamdani, JK Laerdahl… - Brain, 2016 - academic.oup.com
Progressive myoclonus epilepsy is a heterogeneous group of disorders characterized by
myoclonic and tonic-clonic seizures, ataxia and cognitive decline. We here present two …

[HTML][HTML] The oncosuppressive properties of KCTD1: its role in cell growth and mobility

G Smaldone, G Pecoraro, K Pane, M Franzese… - Biology, 2023 - mdpi.com
Simple Summary Members of the KCTD protein family play major roles in numerous
physiopathological functions. Although they are traditionally considered to be involved in …

KCTD: A new gene family involved in neurodevelopmental and neuropsychiatric disorders

X Teng, A Aouacheria, L Lionnard… - CNS neuroscience & …, 2019 - Wiley Online Library
The underlying molecular basis for neurodevelopmental or neuropsychiatric disorders is not
known. In contrast, mechanistic understanding of other brain disorders including …

Protein partners of KCTD proteins provide insights about their functional roles in cell differentiation and vertebrate development

M Skoblov, A Marakhonov, E Marakasova… - …, 2013 - Wiley Online Library
The KCTD family includes tetramerization (T1) domain containing proteins with diverse
biological effects. We identified a novel member of the KCTD family, BTBD10. A …

[HTML][HTML] KCTD15 deregulation is associated with alterations of the NF-κB signaling in both pathological and physiological model systems

G Smaldone, L Coppola, K Pane, M Franzese… - Scientific Reports, 2021 - nature.com
Like other KCTD proteins, KCTD15 is involved in important albeit distinct biological
processes as cancer, neural crest formation, and obesity. Here, we characterized the role of …

Compound heterozygous KCTD7 variants in progressive myoclonus epilepsy

EA Burke, M Sturgeon, DB Zastrow… - Journal of …, 2021 - Taylor & Francis
KCTD7 is a member of the potassium channel tetramerization domain-containing protein
family and has been associated with progressive myoclonic epilepsy (PME), characterized …

Kctd13 deletion reduces synaptic transmission via increased RhoA

CO Escamilla, I Filonova, AK Walker, ZX Xuan… - Nature, 2017 - nature.com
Copy-number variants of chromosome 16 region 16p11. 2 are linked to neuropsychiatric
disorders,,,,, and are among the most prevalent in autism spectrum disorders,,. Of many …