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Research 751–780 of 1000+
- Human stratum corneum proteomics reveals cross‐linking of a broad spectrum of proteins in cornified envelopes
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- A case of monilethrix caused by novel compound heterozygous mutations in the desmoglein 4 (DSG4) gene
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- New familial association between ocular coloboma and loose anagen syndrome
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Sjogren-Larsson syndrome
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- Congenital atrichia with papular lesions
- Topical minoxidil improves congenital hypotrichosis caused by <i>LIPH</i> mutations
- The medusa head: Dermoscopic diagnosis of woolly hair syndrome
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- Congenital atrichia with papular lesions
- Monilethrix
- Hypotrichosis with Juvenile Macular Dystrophy in Saudi Arabia: A Case Report
- Woolly Antics between the Sheaths
- Reply
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- Neonatal ichthyosis-sclerosing cholangitis syndrome caused by a novel CLDN1 mutation: a case report and literature review
- Unusual Dermatologic Findings in an Extremely Low Birthweight Infant: The Genetic Diagnosis
- Reviewer #3 (Public Review): CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells
- Syndromic or non-syndromic congenital ichthyosis? A case report of two brothers with ichthyosis but microphthalmia and blindness in only one brother
- Congenital Atrichia: A Case Report
- Molecular Basis of Hereditary Hair Diseases
- Evaluation of hair structural abnormalities in children with different neurological diseases