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ULK4 gene

Known as: SERINE/THREONINE PROTEIN KINASE ULK4, FAM7C1, FLJ20574 
National Institutes of Health

Related topics

Related topics

1 relation
ULK3 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
High resolution structure and inhibition of the schizophrenia-linked pseudokinase ULK4.
The ULK (UNC51-like) enzymes are a family of mammalian kinases that have critical roles in autophagy and development. While ULK1… 
2018
2018
Ulk4 deficiency leads to hypomyelination in mice
Brain nerve fibers are insulated by myelin which is produced by oligodendrocytes. Defects in myelination are increasingly… 
2018
2018
Ulk4 regulates GABAergic signaling and anxiety-related behavior
Excitation/inhibition imbalance has been proposed as a fundamental mechanism in the pathogenesis of neuropsychiatric and… 
2018
2018
Intragenic Microdeletion of ULK4 and Partial Microduplication of BRWD3 in Siblings with Neuropsychiatric Features and Obesity
ULK4 and BRWD3 deletions have been identified in patients with developmental/language delay and intellectual disability. Both… 
2017
2017
Multiple roles of Ulk4 in neurogenesis and brain function
ABSTRACT Neurogenesis is essential for proper brain formation and function, and abnormal neural proliferation is an underlying… 
2016
2016
Control of cortex development by ULK4, a rare risk gene for mental disorders including schizophrenia
Schizophrenia is a debilitating familial neuropsychiatric disorder which affects 1% of people worldwide. Although the… 
2016
2016
Ulk4 Regulates Neural Stem Cell Pool
The size of neural stem cell (NSC) pool at birth determines the starting point of adult neurogenesis. Aberrant neurogenesis is… 
Review
2015
Review
2015
Cross-cancer profiling of molecular alterations within the human autophagy interaction network
Aberrant activation or disruption of autophagy promotes tumorigenesis in various preclinical models of cancer, but whether the… 
Highly Cited
2014
Highly Cited
2014
Recurrent deletions of ULK4 in schizophrenia: a gene crucial for neuritogenesis and neuronal motility
ABSTRACT Although many pathogenic copy number variations (CNVs) are associated with neuropsychiatric diseases, few of them have… 
2013
2013
Single-nucleotide polymorphism rs1052501 associated with monoclonal gammopathy of undetermined significance and multiple myeloma
Monoclonal gammopathy of undetermined significance (MGUS) is the most prevalent clonal plasma cell proliferative disorder… 
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