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Research 301–330 of 1000+
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- Translational perspectives in HTRA1-associated disorders: biomarkers, gene therapy, and future directions
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Woolly Antics between the Sheaths
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Inflammatory and non-melanocytic tumoral pathology of the nail
- Finding models for skin diseases: successes and failures
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Genetic Disorders and Defects in Vitamin D Action
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- Skin diseases associated with atopic dermatitis
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Genetics of Structural Hair Disorders
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Connexin 26 (<i>GJB2</i>) mutations in keratitis–ichthyosis–deafness syndrome presenting with squamous cell carcinoma
- [Genetic expression and morphogenesis of the skin in vertebrates].
- Hypotrichosis with juvenile macular dystrophy
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Hypomorphic mutation in the hairless gene accelerates pruritic atopic skin caused by feeding a special diet to mice
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Nonclassical Congenital Adrenal Hyperplasia and Pregnancy
- Overlapping features of atopic dermatitis and alopecia areata: from pathogenesis to treatment
- Congenital Atrichia: A Case Report
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2