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Research 91–120 of 117
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- Regulation of Hair Shedding by the Type 3 IP3 Receptor
- Genetics of Structural Hair Disorders
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- Role of skin enzymes in metabolism of topical drugs
- Structure and Function of the Skin
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- 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
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Morphological characteristics and notes of the skin in preclinical toxicity assessment
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- Immunolocalization of junctional proteins in human hairs indicates that the membrane complex stabilizes the inner root sheath while desmosomes contact the companion layer through specific keratins
- Desmogleins: Hair perspective
- Proteome Analysis of Human Hair Shaft
- Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis
- Desmosomes in Developing Human Epidermis
- IgG/IgA pemphigus with differing regional presentations
- X-linked Recessive Ectodysplasin A Mutations Induced Hypohidrotic Ectodermal Dysplasia and Severe Atopic Dermatitis Successfully Treated with Dupilumab
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- The role of hair follicles and Edar signalling in cutaneous wound healing
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Patterns of desmocollin synthesis in human epithelia: immunolocalization of desmocollins 1 and 3 in special epithelia and in cultured cells.
- 피부 발육과정에서 데스모콜린 1의 발현에 관한 면역조직화학적 연구