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Research 631–660 of 1000+
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Who Am I? Eyebrow Follicles Minimize Donor-Derived DNA for Germline Testing After Hematopoietic Stem Cell Transplantation
- Editorial: Animal fibers
- Melanocytes: The new Black
- Skin diseases in consequence of endocrine alterations
- Androgenetic alopecia: pathogenesis and potential for therapy
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Pathways to inflammation: acne pathophysiology
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- The quantification of reproductive hormones in the hair of captive adult brown bears and their application as indicators of sex and reproductive state
- Hair shaft disorders
- Hair Re-Pigmentation After Nilotinib
- Australasian Society for Dermatology Research Meeting, May 2006
- Alopecia and its medical management
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Alopecia androgénica femenina: nuevos factores fisiopatológicos y futuras tendencias para un abordaje clínico más integral
- Light-Emitting Hair Follicles: Studying Skin Regeneration With In Vivo Imaging
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Congenital atrichia and hypotrichosis
- Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome
- Polycystic Ovary Syndrome: A Complex Interplay of Hormones and Metabolism
- Identification of Familial Infections Using Multilocus Microsatellite Typing in Tinea Corporis due to <i>Microsporum canis</i>
- 1375 Cutaneous adnexal cysts revisited: A novel classification based on morphological and molecular features
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1