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Research 61–90 of 1000+
- Clinical Findings, Cutaneous Pathology, and Response to Therapy in 21 Patients With Keratosis Pilaris Atrophicans
- Diffuse partial woolly hair in a patient with epidermolysis bullosa simplex with mottled pigmentation
- Retinoids and Keratinization
- Ulerythema ophryogenes (keratosis pilaris atrophicans faciei).
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Hair casts: Classification, staining characteristics, and differential diagnosis
- Immunostaining study of cytokeratins in human hair follicle development
- Generation of folliculogenic human epithelial stem cells from induced pluripotent stem cells
- The proteomic profile of hair damage
- Localized trichorrhexis nodosa
- Hypotrichosis and Hair Loss on the Occipital Scalp
- LB1019 The early region of trichodysplasia spinulosa polyomavirus drives proliferation, altered differentiation, and ectopic expression of hair follicle differentiation markers in interfollicular tail epidermis
- Hair Anomalies in a 6-Year-Old Girl
- Monilethrix
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- The hair shaft: normality, abnormality, and genetics
- Self-Activated Electrical Stimulation for Effective Hair Regeneration <i>via</i> a Wearable Omnidirectional Pulse Generator
- <i>De novo</i> mutations in monilethrix
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- Masquerading of trichotillomania in a family with monilethrix
- Monilethrix in three generations
- Monilethrix
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Monilethrix: Beaded hair and hypotrichosis in a child
- Keratins: the hair shaft's backbone revealed
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles
- Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix
- Hair follicle-specific keratins and their diseases
- Neuroendocrine Controls of Keratin Expression in Human Skin