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Research 121–150 of 1000+
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Unlocking finasteride's potential via carboxymethyl-β-cyclodextrin inclusion complex for androgenic alopecia
- Exploring the Gut Microbiome and Metabolome in Individuals with Alopecia Areata Disease
- Forehead Anthropometrics of Jazan Population, Saudi Arabia: A Prospective Analytical Study
- <i>PIK3CA</i> gain-of-function mutation in Schwann cells leads to severe neuropathy and aerobic glycolysis through a non-cell autonomous effect
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- Thou shall not heal: Overcoming the non-healing behaviour of diabetic foot ulcers by engineering the inflammatory microenvironment
- Aging of the hair follicle pigmentation system
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- The Hair Follicle: An Underutilized Source of Cells and Materials for Regenerative Medicine
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- Recent Progress in the Understanding of the Effect of Sympathetic Nerves on Hair Follicle Growth
- Human Liver MSCs Retain Their Basic Cellular Properties in Chronically Inflamed Liver Tissue
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Evaluation and Treatment of Hirsutism in Premenopausal Women: An Endocrine Society Clinical Practice Guideline
- The Biological Actions of Dehydroepiandrosterone Involves Multiple Receptors
- Post-COVID-19 Syndrome: The Persistent Symptoms at the Post-viral Stage of the Disease. A Systematic Review of the Current Data
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Sostdc1 defines the size and number of skin appendage placodes
- Immune Privilege Collapse and Alopecia Development: Is Stress a Factor
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles
- Resistance to the Insulin and Elevated Level of Androgen: A Major Cause of Polycystic Ovary Syndrome
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- Palatogenesis and cutaneous repair: A two‐headed coin