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Research 331–360 of 1000+
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Pediatric adrenocortical carcinoma complicated by uric acid nephrolithiasis: a unique case report
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Editors' Picks
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- <i>AXR3</i>and<i>SHY2</i>interact to regulate root hair development
- Targeted Disruption of Stat3 Reveals a Major Role for Follicular Stem Cells in Skin Tumor Initiation
- Membrane androgen receptors may mediate androgen reinforcement
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Hair Graying: Mechanisms, Prevention, and Innovative Treatment Strategies – literature review
- Dissecting the boundary of quiescence and activation of murine melanocyte stem cells in the hair follicle niche
- PCSK9: From Nature’s Loss to Patient’s Gain
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Real-world safety of Tepotinib: Insights from the Food and Drug Administration Adverse Event Reporting System
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Seasonal Variability in Transcript Expression of Type I and Type II Keratins in Wool Follicles of Lustrous Fleece-Producing Magra Sheep
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- <i>Hoxc13</i> mutant mice lack external hair
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Hair Loss in Children
- Epimorphic regeneration in mice is p53-independent
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- Metabolism and skin diseases
- Nuclear Topology, Epigenetics, and Keratinocyte Differentiation
- WNT10B (wingless-type MMTV integration site family)