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Research 211–240 of 463
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Basement Membrane Zone Remodeling During Appendageal Development in Human Fetal Skin. The Absence of Type VII Collagen is Associated with Gelatinase-A (MMP2) Activity
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- A missense mutation in Lama3 causes androgen alopecia
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- Poster Presentations
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Molecular pathways involved in hair follicle tumor formation: all about mammalian target of rapamycin?
- Immunopathology and Immunotherapy of Inflammatory Skin Diseases
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Increasing GSH-Px Activity and Activating Wnt Pathway Promote Fine Wool Growth in FGF5-Edited Sheep
- Successful Treatment of Alopecia Areata with Topical Calcipotriol
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Ectopic olfactory receptors in human: New therapeutic possibilities
- <i>OsPHR2</i> Is Involved in Phosphate-Starvation Signaling and Excessive Phosphate Accumulation in Shoots of Plants
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Human Amniotic Fluid Stem Cell-Derived Exosomes as a Novel Cell-Free Therapy for Cutaneous Regeneration
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Sprouty/FGF signaling regulates the proximal–distal feather morphology and the size of dermal papillae
- An overview of the genetic aspects of hair loss and its connection with nutrition
- The nude gene and the skin