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Research 91–120 of 419
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- Main Plenary Sessions: Summaries of Papers
- Multiple Roles of Integrin-Linked Kinase in Epidermal Development, Maturation and Pigmentation Revealed by Molecular Profiling
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- LB1081 Three-dimensional imaging of tight junction-network across multiple layers of human epidermis by array tomography using backscattered electron-mode scanning electron microscopy
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Exploring the “Thyroid–Skin Connection”: Concepts, Questions, and Clinical Relevance
- Alopecia in Epidermolysis Bullosa
- The seasonal development dynamics of the yak hair cycle transcriptome
- Biology of the Hair Follicle: The Basics
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Hair physiology and its disorders
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Hair follicles, their disorders and their opportunities
- Advances in Hair Diseases
- Paternal Finasteride Treatment Can Influence the Testicular Transcriptome Profile of Male Offspring—Preliminary Study
- Trichodystrophies: A hair-raising differential diagnosis
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- The Basic Science of Hair Biology
- Genetic Hair Disorders: A Review
- Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep
- Faculty Opinions recommendation of Loss of desmocollin 3 in mice leads to epidermal blistering.
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Microarray Gene Expression Analysis of Lesional Skin in Canine Pemphigus Foliaceus
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds