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Research 241–270 of 1000+
- Genetics
- Marie-unna hereditary hypotrichosis
- Diagnosis of Hair Loss: Clinical features of common causes of hair loss.
- A case of loose anagen hair syndrome associated with trichotillomania in a 14-year-old girl
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Cicatricial (Scarring) Alopecias
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- The Basic Science of Hair Biology
- Diseases of Periocular Hair
- Cysteine and Glutamine level in hair shaft fractures patients
- Fibroproliferative genes are preferentially expressed in central centrifugal cicatricial alopecia
- 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
- 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
- The involvement of androgens in human hair growth
- 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
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update