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Research 271–300 of 1000+
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- Hair follicle organoids: advances in construction, applications, and translational challenges
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- The Role of Extracellular Vesicles in Cutaneous Remodeling and Hair Follicle Dynamics
- Loose Anagen Hair Syndrome in Black‐Haired Indian Children
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Tissue resident and follicular Treg cell differentiation is regulated by CRAC channels
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Induction of Skin-Derived Precursor Cells from Human Induced Pluripotent Stem Cells
- Heterogeneity of Polymorphous Light Eruption: A Study of 105 Patients
- The involvement of androgens in human hair growth
- Autoimmune polyendocrine syndrome type 1 a case report from Bangladesh
- Autoimmune polyglandular syndrome type 4 – case report
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel
- Characterization and isolation of stem cell–enriched human hair follicle bulge cells
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Keratins: the hair shaft's backbone revealed
- Skin Pigmentation Types, Causes and Treatment—A Review
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Hair follicle stem cells:<i>In vitro</i>and<i>in vivo</i>neural differentiation
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles
- Resting no more: re‐defining telogen, the maintenance stage of the hair growth cycle