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Research 91–120 of 1000+
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Molecular Genetics of Human Hair Diseases
- TONGUE, RED
- The molecular basis of human keratin disorders
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Immunostaining study of cytokeratins in human hair follicle development
- Steatocystoma Multiplex
- Oral Presentations
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- ST14 interacts with TMEFF1 and is a predictor of poor prognosis in ovarian cancer
- Eyebrow and Eyelash Alopecia: A Clinical Review
- Alopecia in Children
- Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis
- Madarosis: A marker of many Maladies
- Hair shaft disorders in children – An update
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Identification of a novel<i>PNPLA1</i>mutation in a Spanish family with autosomal recessive congenital ichthyosis
- Autosomal recessive congenital ichthyosis due to <i>PNPLA1</i> mutation in a golden retriever–poodle cross‐bred dog and the effect of topical therapy
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Topical polyhydroxy acid treatment for autosomal recessive congenital ichthyosis in the golden retriever: a prospective pilot study
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- 152 Alopecia patterns in patients with autosomal receesive congenital ichthyosis
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Genetics of Inherited Ichthyoses and Related Diseases