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Research 751–780 of 1000+
- Efektivitas Terapi Minoksidil pada Alopesia Androgenetik: Studi in Vivo
- Do you know this syndrome? * Você conhece esta síndrome? *
- New drugs under investigation for the treatment of alopecias
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- <i>WNT10A</i> , dermatology and dentistry
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- An updated review of the sebaceous gland and its role in health and diseases Part 2: Pathophysiological clinical disorders of sebaceous glands
- Disease causing homozygous variants in the human hairless gene
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- p53‐dependent transcriptional regulation of EDA2R and its involvement in chemotherapy‐induced hair loss
- The Potential Role of Minoxidil in the Hair Transplantation Setting
- [4-t-Butylphenyl]-N-(4-imidazol-1-yl phenyl)sulfonamide (ISCK03) inhibits SCF/c-kit signaling in 501mel human melanoma cells and abolishes melanin production in mice and brownish guinea pigs
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Polycystic Ovarian Syndrome: Exploring Hypertension and Cardiometabolic Implications
- Next-Generation Skin Regeneration: Multicellular 3D Bioprinting and Biomimetic Bioinks for Advanced Cutaneous Reconstruction
- Treatment of Hair Loss
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- Aging and Immortality: Quasi-Programmed Senescence and Its Pharmacologic Inhibition
- Genetic, hormonal and metabolic aspects of PCOS: an update
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Androgenetic alopecia: pathogenesis and potential for therapy
- The prevalence and types of androgenetic alopecia in Korean men and women