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Research 871–900 of 1000+
- Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers
- Pseudofolliculitis barbae; current treatment options
- New approach to the understanding of keloid: psychoneuroimmune–endocrine aspects
- Alopecia in Epidermolysis Bullosa
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- The Contribution of Endogenous and Exogenous Factors to Female Alopecia
- A Comprehensive Review of Mammalian Pigmentation: Paving the Way for Innovative Hair Colour-Changing Cosmetics
- Rare Germline Pathogenic Variants Identified by Multigene Panel Testing and the Risk of Aggressive Prostate Cancer
- Molecular characterization of HOXC8 gene and methylation status analysis of its exon 1 associated with the length of cashmere fiber in Liaoning cashmere goat
- An epidemiological study of androgenic alopecia in 3114 Korean patients
- Pemphigus vulgaris in only one of two monozygotic twins
- HAIR MATRIX CELL KINETICS: A SELECTIVE REVIEW
- Are sex hormones promising candidates to explain sex disparities in the COVID-19 pandemic?
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Adrenal 21-hydroxylase gene mutations in Slovenian hyperandrogenic women: evaluation of corticotrophin stimulation and HLA polymorphisms in screening for carrier status
- Uncovering the complex relationship between balding, testosterone and skin cancers in men
- The disrupted balance between hair follicles and sebaceous glands in<i>Hoxc13</i>‐ablated rabbits
- The twisting tale of woolly hair: a trait with many causes
- Efficient expansion of human keratinocyte stem/progenitor cells carrying a transgene with lentiviral vector
- Hair Loss in Patients with Inflammatory Bowel Disease
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Making Waves with Hairs
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Managing hair loss in midlife women
- Stem cell identification-<i>in vivo</i> lineage analysis versus <i>in vitro</i> isolation and clonal expansion
- The aetiology and pathogenesis of alopecia areata
- COLOCOLIZATION OF VITILIGO AND ALOPECIA AREATA
- Skin cancer: understanding the journey of transformation from conventional to advanced treatment approaches