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- Structure of human steroid 5α-reductase 2 with the anti-androgen drug finasteride
- Cloning and Expression of Cellular Retinoic Acid Binding Protein I Gene in Inner Mongolian Cashmere Goats
- Cloning, computational analysis and expression profiling of steroid 5 alpha-reductase 1 (SRD5A1) gene during reproductive phases and ovatide stimulation in endangered catfish, Clarias magur
- Structural basis for the catalysis and inhibition of human steroid 5α‐reductase 2
- Roles of existing drug and drug targets for COVID-19 management
- Molecular mechanism of ligand recognition and activation of lysophosphatidic acid receptor LPAR6
- The Emerging Structural Pharmacology of ATP-Sensitive Potassium Channels
- Targeting integrin pathways: mechanisms and advances in therapy
- Insights learned from L457(3.43)R, an activating mutant of the human lutropin receptor
- Functional identification of the phosphorylation sites of Arabidopsis PIN-FORMED3 for its subcellular localization and biological role
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- Spontaneous fertility in a male patient with testotoxicosis despite suppression of FSH levels
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Differential Auxin-Transporting Activities of PIN-FORMED Proteins in Arabidopsis Root Hair Cells
- Comparative transcriptomic analysis of dermal wound healing reveals de novo skeletal muscle regeneration in Acomys cahirinus
- Hyperadrenocorticism in Ferrets
- ER-located Ca2+ ATPase ACA2 regulates Ca2+ cytoplasmic pool linked to root hair growth in Arabidopsis thaliana
- Melatonin membrane receptors in peripheral tissues: Distribution and functions
- Steroid Sulfatase: Molecular Biology, Regulation, and Inhibition
- K channel therapeutics at the bedside
- Sulfatase inhibitors: a patent review
- Applications and Risks of Nanomaterials Used in Regenerative Medicine, Delivery Systems, Theranostics, and Therapy
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- From a stem-cell–centered to a niche-centered view: the core role of collagen networks in hair loss and hair follicle miniaturization
- General Dermatology
- Hair, Cutaneous Homeostasis and Stem Cell Functions
- Highway Deconstruction
- Four Closure