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Research 631–660 of 1000+
- Factors Associated with Severity of Alopecia Areata
- Anagen effluvium
- The role of lymphocytes in the development and treatment of alopecia areata
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Alopecia areata: a review on diagnosis, immunological etiopathogenesis and treatment options
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Plasticity and Cytokinetic Dynamics of the Hair Follicle Mesenchyme During the Hair Growth Cycle: Implications for Growth Control and Hair Follicle Transformations
- Modulating hair follicle size with <i>Wnt10b/DKK1</i> during hair regeneration
- An Overview of Alopecias
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Idiopathic Hirsutism*
- Practical Guidelines for Evaluation of Loose Anagen Hair Syndrome
- Cicatricial (Scarring) Alopecias
- Acquired scalp alopecia. Part I: A review
- Tissue resident and follicular Treg cell differentiation is regulated by CRAC channels
- Introducing Platelet-Rich Stroma: Platelet-Rich Plasma (PRP) and Stromal Vascular Fraction (SVF) Combined for the Treatment of Androgenetic Alopecia
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Loose anagen hair syndrome
- Morphological Approach to Hair Disorders
- Identification of potential key genes and pathways associated with the Pashmina fiber initiation using RNA-Seq and integrated bioinformatics analysis
- Label Retaining Cells (LRCs) with Myoepithelial Characteristic from the Proximal Acinar Region Define Stem Cells in the Sweat Gland
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Cellular senescence in tissue repair: every cloud has a silver lining
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Madarosis
- Dermatoses of pregnancy
- Comparative Transcriptome Analysis Reveals that a Ubiquitin-Mediated Proteolysis Pathway Is Important for Primary and Secondary Hair Follicle Development in Cashmere Goats
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- What does acne genetics teach us about disease pathogenesis?