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Research 511–540 of 1000+
- COX2-ATP Synthase Regulates Spine Follicle Size in Hedgehogs
- 547 CDK9 Kinase Activation in Association with AFF1-SEC Initiate Epidermal Progenitor differentiation
- 591 Chromatin architectural protein CTCF regulates terminal keratinocyte differentiation in the developing epidermis and hair follicles
- Inherited Epidermolysis Bullosa: A Clinical Case
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa
- 1325 Age-dependent loss of the stemness and antimicrobial defense function of dermal fibroblasts is mediated by TGFbeta
- Hair, Cutaneous Homeostasis and Stem Cell Functions
- 277 An open label pilot clinical trial of the JAK inhibitor tofacitinib for alopecia areata
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Melanogenesis Is Coupled to Murine Anagen: Toward New Concepts for the Role of Melanocytes and the Regulation of Melanogenesis in Hair Growth.
- Somatosensory organization and behavior in naked mole‐rats: II. Peripheral structures, innervation, and selective lack of neuropeptides associated with thermoregulation and pain
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Phenotypic variability associated with<i>WNT10A</i>nonsense mutations
- Inactivation of autophagy leads to changes in sebaceous gland morphology and function
- Promotion of Insulin-Like Growth Factor-I Production by Sensory Neuron Stimulation; Molecular Mechanism(s) and Therapeutic Implications
- Pseudofolliculitis barbae; current treatment options
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Birt–Hogg–Dubé syndrome
- Severe metabolic disorders coexisting with Werner syndrome: a case report
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Werner′s syndrome
- Diagnosis and Management of Melanoma of the Scalp: A Review of the Literature
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Deimination in epidermal barrier and hair formation
- Isolating subpopulations of human epidermal basal cells based on polyclonal serum against trypsin-resistant CSPG4 epitopes
- An unusual presentation of X-linked adrenoleukodystrophy
- Growth of the Mouse Coat VII. Hair Cycles and Sebaceous Glands in Homozygous and Heterozygous Naked Mice