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Research 751–780 of 1000+
- Spotlight commentary: Navigating the cutaneous side effects of chemotherapy
- Evolution of long scalp hair in humans
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- Aesthetic Rehabilitation Medicine: Enhancing Wellbeing beyond Functional Recovery
- CXCL12 Neutralizing Antibody Promotes Hair Growth in Androgenic Alopecia and Alopecia Areata
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- E-Poster
- Diagnosis and Management of Alopecia Areata: A Saudi Expert Consensus Statement (2023)
- Review on Alopecia Areata in the Middle East and Africa: Landscape and Unmet Needs
- Hair & Cutaneous Development
- Molecular Genetics of Human Hair Diseases
- Female pattern hair loss: therapeutic update
- Trichohyalin-Like Proteins Have Evolutionarily Conserved Roles in the Morphogenesis of Skin Appendages
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles
- The Pharmacology of Regenerative Medicine
- Sebaceous immunobiology - skin homeostasis, pathophysiology, coordination of innate immunity and inflammatory response and disease associations
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- The Roles of Non-coding RNA in the Development and Regeneration of Hair Follicles: Current Status and Further Perspectives
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Pentacyclic Triterpenoid Maslinic Acid Promotes Hair Growth Comparable to Minoxidil: A New Insight on the Potential Involvement of Cilia Activity
- Treg–tissue cell interactions in repair and regeneration
- Understanding Type 3 Innate Lymphoid Cells and Crosstalk with the Microbiota: A Skin Connection
- Treatments for alopecia areata: a network meta-analysis
- Localized in vivo genotypic and phenotypic correction of the albino mutation in skin by RNA-DNA oligonucleotide
- Treatment of localized scleroderma and lichen sclerosus with etretinate
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Localized syringolymphoid hyperplasia with alopecia and anhidrosis
- Reversible Alopecia with Localized Scalp Necrosis After Accidental Embolization of the Parietal Artery with Hyaluronic Acid
- Localized Autosomal Recessive Hypotrichosis Due to a Frameshift Mutation in the Desmoglein 4 Gene Exhibits Extensive Phenotypic Variability within a Pakistani Family
- A case of localized follicular hamartoma: an ultrastructural and immunohistochemical study