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The Journal of Biological Chemistry|May 26, 2018
The transcription factor Vezf1 represses the expression of the antiangiogenic factor Cited2 in endothelial cellsLama AlAbdi, Ming He, Qianyi Yang, et al.
Human Genetics|September 27, 2022
PMEL is mutated in oculocutaneous albinismLama AlAbdi, Muneera Alshammari, Rana Helaby, et al.
Biochemistry|October 22, 2016
Dnmt3b Methylates DNA by a Noncooperative Mechanism, and Its Activity Is Unaffected by Manipulations at the Predicted Dimer InterfaceAllison B Norvil, Christopher J Petell, Lama Alabdi, et al.
Nucleic Acids Research|May 15, 2016
An epigenetic switch regulates de novo DNA methylation at a subset of pluripotency gene enhancers during embryonic stem cell differentiationChristopher J Petell, Lama Alabdi, Ming He, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2021
Residual risk for additional recessive diseases in consanguineous couplesLama AlAbdi, Shatha Alrashseed, Ahood Alsulaiman, et al.
Human Genetics|May 14, 2024
Human ABL1 deficiency syndrome (HADS) is a recognizable syndrome distinct from ABL1-related congenital heart defects and skeletal malformations syndromeLama AlAbdi, Teresa Neuhann, Eva-Christina Prott, et al.
Ophthalmology. Retina|September 7, 2023
Early-Onset Myopia and Retinal Detachment without Typical Microcoria or Severe Proteinuria due to a Novel LAMB2 VariantAbdulaziz A Alshamrani, Moustafa Magliyah, Fowzan S Alkuraya, et al.
NAR Cancer|December 6, 2021
Misregulation of the expression and activity of DNA methyltransferases in cancerIsaiah K Mensah, Allison B Norvil, Lama AlAbdi, et al.
Scientific Reports|July 11, 2023
Cone dystrophy associated with autoimmune polyglandular syndrome type 1Abdulrahman Badawi, Moustafa Magliyah, Omar Alabbasi, et al.
Molecular Genetics & Genomic Medicine|May 5, 2021
Genetic testing results of children suspected to have Stickler syndrome type collagenopathy after ocular examinationArif O Khan, Lama AlAbdi, Nisha Patel, et al.
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