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Research 31–60 of 542
- Biomechanics of hair fibre growth: A multi-scale modeling approach
- 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
- Inherited Disorders of the Hair
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Dysfunction of keratinocyte adhesion
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Intercellular junctions in normal epidermis
- 127 Long-term remission of Hailey-Hailey disease by Er:YAG ablative laser therapy
- A Monoclonal Antibody Established from the Immunization of Basal Cell Carcinoma (BCC) Tissues Reacts to the Intercellular Space of BCC and Hair Follicles
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- PA05 A rare case of cardiocutaneous syndrome in a young child
- 875 A novel animal model of Desmoglein 1 (Dsg1) deficiency reveals an essential role for Dsg1 in epidermal barrier formation
- 피부 발육과정에서 데스모콜린 1의 발현에 관한 면역조직화학적 연구
- Electron microscopic observation of skin and hair on a case of Netherton syndrome
- <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
- Transcriptome Profiling of Pilosebaceous Units in Male Androgenetic Alopecia Reveals Altered Junctional Networks
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Congenital hair loss disorders: Rare, but not too rare
- Genetics of Structural Hair Disorders
- A function for Rac1 in the terminal differentiation and pigmentation of hair
- Recent advances in congenital ichthyoses
- Pili Trianguli et Canaliculi Is a Defect of Inner Root Sheath Keratinization
- A case of cicatricial alopecia associated with pemphigus: a case report
- Male sex hormone and reduced plakoglobin jointly impair atrial conduction and cardiac sodium currents
- 1433 Role of BNC1 in keratinocytes proliferation and migration: A critical regulator of wound healing?