A5041426594- Genetics and Neurodevelopmental Disorders
- Autism Spectrum Disorder Research
- Family and Disability Support Research
- Medicinal Plants and Neuroprotection
- CRISPR and Genetic Engineering
- Genetic factors in colorectal cancer
- Genomic variations and chromosomal abnormalities
- RNA modifications and cancer
- Pluripotent Stem Cells Research
- Dermatological and Skeletal Disorders
- Medicinal Plant Research
- Network Security and Intrusion Detection
- Potassium and Related Disorders
- Radiation Therapy and Dosimetry
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Wireless Body Area Networks
- Cholinesterase and Neurodegenerative Diseases
- Gastric Cancer Management and Outcomes
- Ubiquitin and proteasome pathways
- Genetics, Aging, and Longevity in Model Organisms
- Muscle Physiology and Disorders
- Carcinogens and Genotoxicity Assessment
- Oral and gingival health research
- COVID-19 Clinical Research Studies
- Neurogenetic and Muscular Disorders Research
Karpagam Academy of Higher Education
2023-2024
Bharathiar University
2013-2023
Radiotherapy (RT) is the chief nonsurgical method to control malignant tumors. RT has advanced in both methodological and biological aspects over past few decades. Though a momentous adjuvant non-invasive technique, it leaves behind some unsympathetic effects. Research going on surmount these pessimistic sides of RT. We made mini review recent articles from period 2000 2017 regarding radiotherapy its side effects various types cancers. The literature was done by searching PUBMED, MEDLINE,...
Abstract The current study aimed to investigate the drug delivery potential of chitosan‐conjugated Spondias pinnata phytocompounds for anticancer and antibacterial applications. phytochemical composition aqueous extract S. plant leaves revealed seven major compounds, including stearic acid, 2H‐Indol‐2‐one, beta amyrin, oleic octadecanoic 7‐hexadecenoic phytol. Additionally, five minor compounds were identified through GC–MS analysis. SEM analysis amorphous particles. This demonstrates...
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Duchenne muscular dystrophy (DMD) is an X-linked neuromuscular degenerative disorder initiated by mutation in the dystrophin gene that located on chromosome Xp21.The present case a novel report of DMD with co-occurrence Autism associated disorder, which has similar genetic component. In this report, researchers family based study 17 year old male who been diagnosed DMD. The objective to identify abnormalities and neuro behavioral disabilities. methodology followed classical cytogenetic...
Abstract Goldberg–Shprintzen Syndrome (GOSHS, OMIM# 182212) is a rare autosomal dominant disorder with the characteristic features of craniosynostosis, developmental delays, intellectual disability, hypotonia, joint laxity, respiratory dysfunction, cardiovascular abnormalities, and abdominal hernias. Here we presented case 5‐years old male child facial dysmorphism, global delay, microcephaly, infection, breathing hematochezia, meconium ileus. Whole exome sequencing revealed novel homozygous...
The Glass syndrome is a rare genetic disorder that associated with multisystem due to SATB2 gene mutation. intellectual development delay and the in speech are predominant characteristics of disorder. reports on very few have not been reported India. In present study, we report an Indian mother her child, both affected by same likely pathogenic mutation c.1741-2A>C intronic variant at intron 11 gene. was observed as heterozygous autosomal dominant missense through focused exome sequencing...
Abstract: Coronavirus Disease 2019 (COVID-19) is a pandemic disease caused by novel virus, SARS-CoV-2. COVID-19-infected people have high chance of altered microbiota in various regions the human body, such as gut, oral, and respiratory pathways. In one case, gastrointestinal symptoms are mostly disturbances gut microbiota. The shows magnificent changes response to SARS-CoV-2 infection. impairment levels humans can lead neurological diseases. Here, present chapter, we discussed probable...