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Research 30 of 1000+
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- Severe form of keratitis–ichthyosis–deafness (KID) syndrome associated with septic complications
- Porokeratotic Eccrine Duct and Hair Follicle Nevus (PEHFN) Associated with Keratitis-Ichthyosis-Deafness (KID) Syndrome
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Connexin 26 (<i>GJB2</i>) mutations in keratitis–ichthyosis–deafness syndrome presenting with squamous cell carcinoma
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- Episodes of Keratitis during Treatment with Baricitinib for Alopecia Areata
- Overexpression of HE4/WFDC2 gene in mice leads to keratitis and corneal opacity
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Outer root sheath keratinization in anagen and catagen of the mammalian hair follicle. A seventh distinct type of keratinization in the hair follicle: trichilemmal keratinization.
- Keratinisation status and cytokeratins of the human Meibomian gland epithelium
- Keratinization and its Disorders
- Increased expression of keratin 16 causes anomalies in cytoarchitecture and keratinization in transgenic mouse skin.
- Patterns of epithelial expression of Fos protein suggest important role in the transition from viable to cornified cell during keratinization
- Structural and Immunocytochemical Characterization of Keratinization in Vertebrate Epidermis and Epidermal Derivatives
- The Process of Cornification Evolved From the Initial Keratinization in the Epidermis and Epidermal Derivatives of Vertebrates: A New Synthesis and the Case of Sauropsids
- Embryonic keratinization in vertebrates in relation to land colonization
- Disorders of Keratinization
- Retinoids and Keratinization
- Spiny keratoderma ‐ a demonstration of hair keratin and hair type keratinization
- Study of the keratinization process in human hair follicle by X-ray microdiffraction.
- Keratinization of sheath and calamus cells in developing and regenerating feathers
- Structural changes in trichocyte keratin intermediate filaments during keratinization
- Effects of cepharanthine and minoxidil on proliferation, differentiation and keratinization of cultured cells from the murine hair apparatus
- HAIR KERATINIZATION IN HEALTH AND DISEASE
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- Glycoconjugate expression of cells of human anagen hair follicles during keratinization
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers