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Research 30 of 1000+
- The abnormal skin structure of newly born Wistar rat maternally-treated with aspartame: histological and immunohistochemical study
- Mice with a null mutation of the TGFα gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation
- The character “hairless” in the mouse
- Cyclic Alopecia and Abnormal Epidermal Cornification in Zdhhc13 -Deficient Mice Reveal the Importance of Palmitoylation in Hair and Skin Differentiation
- Growth of the Mouse Coat VII. Hair Cycles and Sebaceous Glands in Homozygous and Heterozygous Naked Mice
- Diseases of the Hair and Scalp
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- 1330 Flexible fate determination ensures robust differentiation in the skin hair follicle
- Gene-knockout mice with abnormal epidermal and hair follicular development
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- [Construction and identification of mouse model with conditional knockout of p75 neurotrophin receptor gene in epidermal cells by Cre-loxP system].
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- The scope of the dermoscope
- 745 Full thickness wound healing in the Lanyu pig
- A novel fracture lattice in spiny mouse skin facilitates tissue autotomy and regeneration
- Glandular metaplasia of hair follicles and other responses to vitamin A excess in cultures of rodent skin
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole‐body energy expenditure
- Preliminary investigations of rat skin after topical application of optical clearing agent
- Overexpression of human keratin 16 produces a distinct skin phenotype in transgenic mouse skin
- Targeted expression of activated erbB-2 to the epidermis of transgenic mice elicits striking developmental abnormalities in the epidermis and hair follicles.
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Anti-inflammatory role of 15-lipoxygenase contributes to the maintenance of skin integrity in mice
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- A hair abnormality in Abyssinian cats
- 190 Deficiency of the Human Cysteine Protease Inhibitor Cystatin M/E Causes Hypotrichosis and Dry Skin
- CUBIC Protocol Visualizes Protein Expression at Single Cell Resolution in Whole Mount Skin Preparations
- Concise Review: Wnt Signaling Pathways in Skin Development and Epidermal Stem Cells
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines