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forResearch 10 of 1000+
- <i>WNT10A</i> , dermatology and dentistry
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Cantú Syndrome Is Caused by Mutations in ABCC9
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Structure-guided manipulation of the regioselectivity of the cyclosporine A hydroxylase CYP-sb21 from Sebekia benihana
- Repurposing FDA approved drugs for psoriasis indications through integrated molecular docking, one-SVM algorithm, and molecular dynamics simulation approaches
- Exploring the effects of wetting and free fatty acid deposition on an atomistic hair fiber surface model incorporating Keratin Associated Protein 5-1
- Identification of a Cyclosporine-Specific P450 Hydroxylase Gene through Targeted Cytochrome P450 Complement (CYPome) Disruption in Sebekia benihana
Community 4 of 10
- Topical finasteride (P-3074) inhibits scalp DHT up to 70%
- P-1075: a BETTER version of Minoxidil
- How does Pedro P have a full head of hear. I'm losing mine and will be bald within 1 year. I'm not even 30yo.
- Still losing on fin 5x & dut 2x p/w (1.5 years in) - next steps advice