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Research 331–360 of 1000+
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Viewpoint 1
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Postzygotic Mutations in Beta-Actin Are Associated with Becker’s Nevus and Becker’s Nevus Syndrome
- Zinc Oxide Nanoparticles Fortified Biscuits as a Nutritional Supplement for Zinc Deficient Rats
- Androgen Receptor–Mediated Paracrine Signaling Induces Regression of Blood Vessels in the Dermal Papilla in Androgenetic Alopecia
- Morphological analyses in fragility of pili torti with Björnstad syndrome
- Viewpoint 4
- CD44 signaling in skin wound healing and regeneration
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Pathogenesis of pili annulati
- Circle Hairs in a Patient with Multiple Myeloma
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Combinatorial expression of cell cycle regulators is more suitable for immortalization than oncogenic methods in dermal papilla cells
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- The Yin and Yang of Integrin Function in Re-Epithelialization During Wound Healing
- The involvement of Elf5 in regulating keratinocyte proliferation and differentiation processes in skin
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- <i>WNT10A</i> , dermatology and dentistry
- Tissue Repair Mechanisms of Dental Pulp Stem Cells: A Comprehensive Review from Cutaneous Regeneration to Mucosal Healing
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Abstract 1835: Development of mammary hyperplasia, dysplasia, and invasive ductal carcinoma in transgenic mice expressing the 8p11 amplicon oncogene NSD3 (WHSC1L1)
- Rapunzel Syndrome as a Rare Presentation of Trichobezoar
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Hypotrichosis with juvenile macular dystrophy
- IgG/IgA pemphigus with differing regional presentations