Search
for
Sort by
Research 181–210 of 563
- Ultrastructural Resemblance of Basal Cell Epithelioma to Primary Epithelial Germ
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Congenital hair loss disorders: Rare, but not too rare
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Genetics of Structural Hair Disorders
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Bikunin, a Serine Protease Inhibitor, is Present on the Cell Boundary of Epidermis
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- Molecular Genetics of Alopecias
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Biomechanics of hair fibre growth: A multi-scale modeling approach
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Intercellular junctions in normal epidermis
- Inherited Disorders of the Hair
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Ectopic Expression of a Truncated Isoform of Hair Keratin 81 in Breast Cancer Alters Biophysical Characteristics to Promote Metastatic Propensity
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Patterns of desmocollin synthesis in human epithelia: immunolocalization of desmocollins 1 and 3 in special epithelia and in cultured cells.
- Increased expression of keratin 16 causes anomalies in cytoarchitecture and keratinization in transgenic mouse skin.
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Against the Rules: Human Keratin K80
- Ichthyosis follicularis with alopecia and photophobia in a mother and daughter
- Growth of human hair follicle keratinocytes in vitro
- A case of monilethrix caused by novel compound heterozygous mutations in the desmoglein 4 (DSG4) gene
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function
- Hereditary mucoepithelial dysplasia: unique histopathological findings in skin lesions
- Novel compound heterozygous mutations in the<i>desmoplakin</i>gene cause hair shaft abnormalities and culminate in lethal cardiomyopathy
- No difference in the proteome of racially and geometrically classified scalp hair sample from a South African cohort: Preliminary findings
- Formation of the cornified envelope
- 127 Long-term remission of Hailey-Hailey disease by Er:YAG ablative laser therapy