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Research 151–180 of 798
- Peer Review #2 of "Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis (v0.1)"
- Learning from nudity: lessons from the nude phenotype
- Skin changes in pediatric transplant patients
- Analysis of the abnormal human hair keratins by two-dimensional polyacrylamide gel electrophoresis
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Immunostaining study of cytokeratins in human hair follicle development
- Madarosis and facial keratinaceous spines
- Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis
- Skin Appendage Proteins of Tetrapods: Building Blocks of Claws, Feathers, Hair and Other Cornified Epithelial Structures
- Ichthyosis
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Ichthyosis Follicularis With Alopecia and Photophobia
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Genetics of Inherited Ichthyoses and Related Diseases
- Care of the newborn with ichthyosis
- Inherited ichthyosis: Syndromic forms
- Neonatal Ichthyosis and Sclerosing Cholangitis Syndrome
- Ichthyosis follicularis, alopecia and photophobia (IFAP) syndrome treated with acitretin
- Ichthyosis follicularis with alopecia and photophobia in a mother and daughter
- 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
- Nutritional Status and Gastrointestinal Structure and Function in Children With Ichthyosis and Growth Failure
- New developments in the molecular treatment of ichthyosis: review of the literature
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- Follicular ichthyosis
- Netherton's syndrome and ichthyosis linearis circumflexa.
- A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation
- Clearance of ichthyosis linearis circumflexa with balneophototherapy
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome