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Research 91–120 of 1000+
- Effects of Restraint Stress and Allopregnanolone Inhibition on Amphetamine Locomotor Sensitivity
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- A Theoretical Model for the Treatment of Androgenetic Alopecia Using the STEAP3 Protein, and the Genetic Challenges of Treating AGA
- The Opioid Receptor Influences Circadian Rhythms in Human Keratinocytes through the β-Arrestin Pathway
- Justicia procumbens prevents hair loss in androgenic alopecia mice
- 1332 Janus kinase inhibitor increases hair growth by increasing beta-catenin activity in outer root sheath cells
- Short Peptides Induce Development of Root Hair Nicotiana tabacum
- Rare Diagnosis of a Proliferating Pilar Tumor in a Facial Hairline Cryst
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- MECHANISM OF ACTION OF AVICENNIA MARINA HEARTWOOD EXTRACT AND AVICEQUINONE C ON HUMAN DERMAL PAPILLA CELLS ISOLATED FROM ANDROGENIC ALOPECIA PATIENTS
- Generalised Glucocorticoid Resistance
- Identification of Pygopus 2 as a component of the ribosomal RNA transcription complex in cancer
- Minireview: vitamin D receptor: new assignments for an already busy receptor. - eScholarship
- Influence of dietary linoleic acid (18:2, n6) on the effects of hyperthyroidism in Mus musculus
- Faculty Opinions recommendation of Live imaging of stem cell and progeny behaviour in physiological hair-follicle regeneration.
- 12 Treatment of hirsutism with 5α-reductase inhibitors
- 9 Role of 5α-reductase in health and disease
- Steroid Hormones
- Neuroactive Steroids and Ethanol Exposure: Relevance to Ethanol Sensitivity and Alcohol Use Disorders Risk
- Perspectives on Dermatopathology
- 086 Evaluation of hair re-growth by cyclosporine and minoxidil using C3H mouse model
- Molecular genetics of androgen insensitivity
- Finasteride-related Leydig cell tumour: report of a case and literature review
- Embryology, Histology, and Physiology of the Hair Follicle
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- The human keratins: biology and pathology
- Tcf3 and Lef1 regulate lineage differentiation of multipotent stem cells in skin
- Timing of expression of the core clock gene <i>Bmal1</i> influences its effects on aging and survival
- The 5 Alpha-Reductase Isozyme Family: A Review of Basic Biology and Their Role in Human Diseases