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Research 211–240 of 1000+
- New Drugs for Leukæmia and Tumours
- NEW YORK ACADEMY OF MEDICINE, SECTION OF DERMATOLOGY AND SYPHILOLOGY
- NEW YORK ACADEMY OF MEDICINE, SECTION OF DERMATOLOGY AND SYPHILOLOGY
- NEW STRATEGIES FOR THE USE OF TOPICAL PRODUCTS IN THE TREATMENT OF ANDROGENETIC ALOPECIA
- New Nonsteroidal Molecules as Blockers of the Steroidogenic Pathway
- New product intros (finasteride/tadalafil (new combination); sutimlimab; human SARS-CoV-2 recombinant nanoparticle vaccine, adjuvanted with AS03; bupropion hydrochloride/dextromethorphan hydrobromide (new combination))
- New Perspectives on the Treatment of Androgenetic Alopecia
- ST008 Male androgenetic alopecia: A new treatment paradigm
- E.L.F. square waves: a new therapy for androgenetic alopecia?
- E.L.F. sqare waves: a new therapy for androgenetic alopecia?
- Ethosomes: New Prospects in Transdermal Delivery
- A new look into an old problem: keratins as tools to investigate determination, morphogenesis, and differentiation in skin.
- A New Look at the 5?-Reductase Inhibitor Finasteride
- A new classification of pattern hair loss that is universal for men and women: Basic and specific (BASP) classification
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- A new catalyst for organic synthesis: mercuric triflate
- A new path in defining light parameters for hair growth: Discovery and modulation of photoreceptors in human hair follicle
- A New Primary Wound Dressing Made of Polyethylene Oxide Gel
- Two New Unrelated Cases of Hereditary 1,25-Dihydroxyvitamin D-resistant Rickets with Alopecia resulting from the same Novel Nonsense Mutation in the Vitamin D Receptor Gene
- Organotypic culture of outer root sheath cells from human hair follicles using a new culture device
- Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5
- A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- A new hair follicle-derived human epidermal model for the evaluation of sunscreen genoprotection
- A New Case of Isolated Trichothiodystrophy
- A New Humanized Mouse Model for Alopecia Areata
- A new spectrophotometric method for the determination of finasteride in tablets
- A New Classification of Male Pattern Baldness and a Clinical Study of the Anterior Hairline
- Opening new horizons in regenerative dermatology using platelet‐based autologous therapies