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Research 811–840 of 1000+
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Fibrotic enzymes modulate wound‐induced skin tumorigenesis
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Genetic Tools for Cell Lineage Tracing and Profiling Developmental Trajectories in the Skin
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Acne Syndromes and Mosaicism
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Adipose transcriptome in the scalp of androgenetic alopecia
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- LBODP010 A Case of Glucocorticoid Resistance Syndrome
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- 861 Frontal fibrosing alopecia (FFA) under dynamic optical coherence tomography (D-OCT)
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Bachmann–Bupp syndrome and treatment
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Pilot study: Autologous platelet‐rich plasma used in a topical cream for facial rejuvenation
- Developmental genetics of color pattern establishment in cats
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Skin transcriptome reveals the periodic changes in genes underlying cashmere (ground hair) follicle transition in cashmere goats
- Induction of the hair growth phase in postnatal mice by localized transient expression of Sonic hedgehog
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development