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Research 151–180 of 1000+
- Heterozygous deletion of the <i>NSDHL</i> gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic nevi
- Molecular Mechanisms Regulating Hair Follicle Development
- Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Gsdma3 is required for hair follicle differentiation in mice
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Stem cell identification-<i>in vivo</i> lineage analysis versus <i>in vitro</i> isolation and clonal expansion
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Vitiligo – Study In view of familial occurence
- Multiple facial atrophic scars in childhood
- Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- Two females with hair loss
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Letter from Brisbane [Letters to editor]
- Hair Today
- Discussion: Themes in the Molecular Structure of Hair
- The character “hairless” in the mouse
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- A combination of low-dose systemic etretinate and topical calcipotriol/betamethasone dipropionate treatment for hyperkeratosis and itching in Olmsted syndrome associated with a TRPV3 mutation
- Muir-torre syndrome in two families in Leicestershire, United Kingdom
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay