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Research 691–720 of 1000+
- Differences in reproductive toxicology between alopecia drugs: an analysis on adverse events among female and male cases
- Alopecia Areata
- Epigenetic regulation in adult stem cells and cancers
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Effects of the selective TrkA agonist gambogic amide on pigmentation and growth of human hair follicles in vitro
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation
- Beyond Clinical Efficacy: A Literature Review on the Safety Challenges of Isotretinoin Therapy
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Nonalcoholic fatty liver disease and polycystic ovary syndrome
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Design of a RADA16-based self-assembling peptide nanofiber scaffold for biomedical applications
- 5-Alpha reductase deficiency
- Morphological Approach to Hair Disorders
- Genetic basis of polycystic ovary syndrome
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- 795 Bacteria induce skin regeneration
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Australasian Society for Dermatology Research Meeting, May 2006
- Apoptosis in human skin development: Morphogenesis, periderm, and stem cells
- Wound Induced Hair Neogenesis – A Novel Paradigm for Studying Regeneration and Aging