User profiles for Ayyappan Anitha
Ayyappan AnithaAssociate Professor, Dept. of Neurogenetics, ICCONS, Shoranur, Palakkad, Kerala, India Verified email at iccons.co.in Cited by 2110 |
miRNAs as biomarkers of neurodegenerative disorders
…, MM Vasu, SA Poovathinal, A Anitha - Biomarkers in …, 2017 - Future Medicine
Neurodegenerative diseases (NDDs) are the result of progressive deterioration of neurons,
ultimately leading to disabilities. There is no effective cure for NDDs at present; ongoing …
ultimately leading to disabilities. There is no effective cure for NDDs at present; ongoing …
Two genetic variants of CD38 in subjects with autism spectrum disorder and controls
T Munesue, S Yokoyama, K Nakamura, A Anitha… - Neuroscience …, 2010 - Elsevier
The neurobiological basis of autism spectrum disorder (ASD) remains poorly understood.
Given the role of CD38 in social recognition through oxytocin (OT) release, we hypothesized …
Given the role of CD38 in social recognition through oxytocin (OT) release, we hypothesized …
[HTML][HTML] Serum microRNA profiles in children with autism
M Mundalil Vasu, A Anitha, I Thanseem, K Suzuki… - Molecular autism, 2014 - Springer
Background As regulators of gene expression, microRNAs (miRNAs) play a key role in the
transcriptional networks of the developing human brain. Circulating miRNAs in the serum and …
transcriptional networks of the developing human brain. Circulating miRNAs in the serum and …
Telomeres in neurological disorders
A Anitha, I Thanseem, MM Vasu… - Advances in Clinical …, 2019 - Elsevier
Ever since their discovery, the telomeres and the telomerase have been topics of intensive
research, first as a mechanism of cellular aging and later as an indicator of health and …
research, first as a mechanism of cellular aging and later as an indicator of health and …
[HTML][HTML] Brain region-specific altered expression and association of mitochondria-related genes in autism
A Anitha, K Nakamura, I Thanseem, K Yamada… - Molecular autism, 2012 - Springer
Background Mitochondrial dysfunction (MtD) has been observed in approximately five
percent of children with autism spectrum disorders (ASD). MtD could impair highly energy-…
percent of children with autism spectrum disorders (ASD). MtD could impair highly energy-…
Downregulation of the expression of mitochondrial electron transport complex genes in autism brains
A Anitha, K Nakamura, I Thanseem… - Brain …, 2013 - Wiley Online Library
Mitochondrial dysfunction ( MtD ) and abnormal brain bioenergetics have been implicated
in autism, suggesting possible candidate genes in the electron transport chain ( ETC ). We …
in autism, suggesting possible candidate genes in the electron transport chain ( ETC ). We …
Mitochondrial dysfunction in cognitive neurodevelopmental disorders: Cause or effect?
A Anitha, I Thanseem, M Iype, SV Thomas - Mitochondrion, 2023 - Elsevier
Mitochondria have a crucial role in brain development and neurogenesis, both in embryonic
and adult brains. Since the brain is the highest energy consuming organ, it is highly …
and adult brains. Since the brain is the highest energy consuming organ, it is highly …
[HTML][HTML] Decreased expression of axon-guidance receptors in the anterior cingulate cortex in autism
S Suda, K Iwata, C Shimmura, Y Kameno, A Anitha… - Molecular autism, 2011 - Springer
Background Axon-guidance proteins play a crucial role in brain development. As the dysfunction
of axon-guidance signaling is thought to underlie the microstructural abnormalities of …
of axon-guidance signaling is thought to underlie the microstructural abnormalities of …
Genetic and expression analyses reveal elevated expression of syntaxin 1A (STX1A) in high functioning autism
K Nakamura, A Anitha, K Yamada… - International Journal …, 2008 - academic.oup.com
Autism is a pervasive developmental disorder diagnosed in early childhood. Abnormalities
of serotonergic neurotransmission have been reported in autism. Serotonin transporter (5-…
of serotonergic neurotransmission have been reported in autism. Serotonin transporter (5-…
Protocadherin α (PCDHA) as a novel susceptibility gene for autism
A Anitha, I Thanseem, K Nakamura, K Yamada… - Journal of Psychiatry and …, 2013 - jpn.ca
Background: Synaptic dysfunction has been shown to be involved in the pathogenesis of
autism. We hypothesized that the protocadherin α gene cluster (PCDHA), which is involved in …
autism. We hypothesized that the protocadherin α gene cluster (PCDHA), which is involved in …