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Research 691–720 of 1000+
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Congenital atrichia associated with nevus flammeus: A rare association
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Psychological Stress-Induced Pathogenesis of Alopecia Areata: Autoimmune and Apoptotic Pathways
- Ophthalmologic Comorbidities in Alopecia Areata
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Androgenetic Alopecia: a Review and Emerging Treatments
- Optimizing Scalp Cooling: (Ultra)Structural Follicular Characteristic and Restorative Advances
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Keratins and disease at a glance
- Runx Family Genes in Tissue Stem Cell Dynamics
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Androgenetic Alopecia: Therapy Update
- The potential of androgenic alopecia management from plant derivatives
- Androgenetic alopecia: pathogenesis and potential for therapy
- Effects on Steroid 5-Alpha Reductase Gene Expression of Thai Rice Bran Extracts and Molecular Dynamics Study on SRD5A2
- Association of Androgenetic Alopecia with Metabolic Syndrome
- Free Androgen Index (FAI): Marker of Premature Androgenetic Alopecia in Men
- Finasteride-induced recurrent aphthous ulceration–like lesions: a case report with dechallenge–rechallenge confirmation
- Androgenetic alopecia: evaluation of hormonal profile and its systemic implications
- Advances in Topical Therapies for Clinically Relevant and Prevalent Forms of Alopecia
- Role of Dermal Melanocytes in Cutaneous Pigmentation of Stasis Dermatitis
- Severe Unilateral Alopecia in a Long-Term Surviving Male Adolescent Glioblastoma Multiforme Patient
- Hirsutism: diagnosis and treatment
- The Role of the VEGF, KGF, EGF, and TGF-β1 Growth Factors in the Pathogenesis of Telogen Effluvium in Women
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- European Society of Endocrinology Clinical Practice Guideline: Endocrine work-up in obesity