User profiles for Linya You
Linya YouFudan University Verified email at fudan.edu.cn Cited by 921 |
Mice lacking α-tubulin acetyltransferase 1 are viable but display α-tubulin acetylation deficiency and dentate gyrus distortion
GW Kim, L Li, M Gorbani, L You, XJ Yang - Journal of Biological Chemistry, 2013 - jbc.org
α-Tubulin acetylation at Lys-40, located on the luminal side of microtubules, has been widely
studied and used as a marker for stable microtubules in the cilia and other subcellular …
studied and used as a marker for stable microtubules in the cilia and other subcellular …
[HTML][HTML] BRPF1-KAT6A/KAT6B complex: molecular structure, biological function and human disease
G Zu, Y Liu, J Cao, B Zhao, H Zhang, L You - Cancers, 2022 - mdpi.com
Simple Summary BRPF1 (also named as BR140) was identified 28 years ago, and it was
not until the past 5 years that its mutations in humans caught increasing attention. Those …
not until the past 5 years that its mutations in humans caught increasing attention. Those …
[HTML][HTML] The tumor suppressor kinase LKB1 activates the downstream kinases SIK2 and SIK3 to stimulate nuclear export of class IIa histone deacetylases
DR Walkinshaw, R Weist, GW Kim, L You, L Xiao… - Journal of Biological …, 2013 - Elsevier
Histone deacetylases 4 (HDAC4), -5, -7, and -9 form class IIa within the HDAC superfamily
and regulate diverse physiological and pathological cellular programs. With conserved motifs …
and regulate diverse physiological and pathological cellular programs. With conserved motifs …
Lysine acetylation: enzymes, bromodomains and links to different diseases
L You, J Nie, WJ Sun, ZQ Zheng… - Essays in …, 2012 - portlandpress.com
Lysine acetylation refers to transfer of the acetyl moiety from acetyl-CoA to the ε-amino
group of a lysine residue on a protein. This has recently emerged as a major covalent …
group of a lysine residue on a protein. This has recently emerged as a major covalent …
ICARUS, an interactive web server for single cell RNA-seq analysis
Here we present ICARUS, a web server to enable users without experience in R to undertake
single cell RNA-seq analysis. The focal point of ICARUS is its intuitive tutorial-style user …
single cell RNA-seq analysis. The focal point of ICARUS is its intuitive tutorial-style user …
[HTML][HTML] Deficiency of the chromatin regulator BRPF1 causes abnormal brain development
Epigenetic mechanisms are important in different neurological disorders, and one such
mechanism is histone acetylation. The multivalent chromatin regulator BRPF1 (bromodomain- …
mechanism is histone acetylation. The multivalent chromatin regulator BRPF1 (bromodomain- …
The lysine acetyltransferase activator Brpf1 governs dentate gyrus development through neural stem cells and progenitors
Lysine acetylation has recently emerged as an important post-translational modification in
diverse organisms, but relatively little is known about its roles in mammalian development and …
diverse organisms, but relatively little is known about its roles in mammalian development and …
Single nuclei RNA-seq reveals a medium spiny neuron glutamate excitotoxicity signature prior to the onset of neuronal death in an ovine Huntington's disease model
Huntington’s disease (HD) is a neurodegenerative genetic disorder caused by an expansion
in the CAG repeat tract of the huntingtin (HTT) gene resulting in behavioural, cognitive, and …
in the CAG repeat tract of the huntingtin (HTT) gene resulting in behavioural, cognitive, and …
BRPF1 is essential for development of fetal hematopoietic stem cells
Hematopoietic stem cells (HSCs) serve as a life-long reservoir for all blood cell types and
are clinically useful for a variety of HSC transplantation-based therapies. Understanding the …
are clinically useful for a variety of HSC transplantation-based therapies. Understanding the …
Spatial enrichment and genomic analyses reveal the link of NOMO1 with amyotrophic lateral sclerosis
J Guo, L You, Y Zhou, J Hu, J Li, W Yang, X Tang… - Brain, 2024 - academic.oup.com
Amyotrophic lateral sclerosis (ALS) is a severe motor neuron disease with uncertain genetic
predisposition in most sporadic cases. The spatial architecture of cell types and gene …
predisposition in most sporadic cases. The spatial architecture of cell types and gene …