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- Molecular genetics of androgen insensitivity
- Adrenal 21-hydroxylase gene mutations in Slovenian hyperandrogenic women: evaluation of corticotrophin stimulation and HLA polymorphisms in screening for carrier status
- Identification of Drug-Disease Associations Using Information of Molecular Structures and Clinical Symptoms via Deep Convolutional Neural Network
- The legacy of Bruce Ames and mitochondrial DNA mutagenicity: integrating oxidative stress, aging, and modern perspectives
- A Thallium-Based Screening Procedure to Identify Molecules That Modulate the Activity of Ca2+-Activated Monovalent Cation-Selective Channels
- Development of a 3D In Vitro Model of Dupuytren’s Disease as a Platform for Drug Screening
- Characterisation of Myotonic Dystrophy type I cell models and drug evaluation by a cell- based quantification platform.
- In silico screening of bioactive compounds derived from Polyherbal Oil against Seborrhea dermatitis.
- Screening for diabetes in women with polycystic ovary syndrome
- Congenital adrenal hyperplasia
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