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Research 691–720 of 1000+
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Targeting the Hippo/YAP/TAZ signalling pathway: Novel opportunities for therapeutic interventions into skin cancers
- URB expression in human dermal papilla cells
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Hedgehog Signaling in Papillary Fibroblasts Is Essential for Hair Follicle Regeneration during Wound Healing
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Analogs of human genetic skin disease in domesticated animals
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Acne Syndromes and Mosaicism
- Antioxidant and Antiproliferative Activity of Finasteride against Glioblastoma Cells
- Current Genetics in Hair Diseases
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- Revolutionary Approaches to Hair Regrowth: Follicle Neogenesis, Wnt/ß-Catenin Signaling, and Emerging Therapies
- The Opioid Receptor Influences Circadian Rhythms in Human Keratinocytes through the β-Arrestin Pathway
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Oral Presentation Abstracts
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- HSD3B1 Genotypes Conferring Adrenal-Restrictive and Adrenal-Permissive Phenotypes in Prostate Cancer and Beyond