Search Results - "Algothmi, K"
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DNA Methylation Level of Transcription Factor Binding Site in the Promoter Region of Acyl-CoA Synthetase Family Member 3 (ACSF3) in Saudi Autistic Children [Corrigendum]
Published in Pharmacogenomics and personalized medicine (01-01-2023)“…Algothmi K, Alqurashi A, Alrofaidi A, et al. Pharmgenomics Pers Med. 2022;15:131-142. The authors have advised affiliation 4 on page 131 is incorrect. The…”
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The correlation between copy number variation in Chromosome 14 and DNA methylation in Saudi autistic children
Published in European review for medical and pharmacological sciences (01-11-2022)“…Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder that represents a range of aberrant behaviour symptoms such as repetitive behaviours and…”
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Multiple Recurrent Copy Number Variations (CNVs) in Chromosome 22 Including 22q11.2 Associated with Autism Spectrum Disorder
Published in Pharmacogenomics and personalized medicine (01-01-2022)“…Introduction: Autism spectrum disorder (ASD) is a developmental disorder that can cause substantial social, communication, and behavioral challenges. Genetic…”
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DNA Methylation Level of Transcription Factor Binding Site in the Promoter Region of Acyl-CoA Synthetase Family Member 3
Published in Pharmacogenomics and personalized medicine (31-01-2023)Get full text
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DNA Methylation Level of Transcription Factor Binding Site in the Promoter Region of Acyl-CoA Synthetase Family Member 3 ( ACSF3 ) in Saudi Autistic Children
Published in Pharmacogenomics and personalized medicine (01-01-2022)“…DNA methylation (DNAm) is one of the main epigenetic mechanisms that affects gene expression without changing the underlying DNA sequence. Aberrant DNAm has an…”
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