Search
for
Sort by
Research 241–270 of 1000+
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Diseases of the Canine Prostate Gland
- Antioxidant and Antiproliferative Activity of Finasteride against Glioblastoma Cells
- GTL1 is required for a robust root hair growth response to avoid nutrient overloading
- Prolonged use of finasteride-induced gonadal sex steroids alterations, DNA damage and menstrual bleeding in women
- Sex Differences in Physiological Hair Cycling and Adhesive Material-Induced Hair Regeneration in Mice
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Transcriptomic Analysis Provides Molecular Insights into Skin Development in Dezhou Donkey Foals
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Revolutionary Approaches to Hair Regrowth: Follicle Neogenesis, Wnt/ß-Catenin Signaling, and Emerging Therapies
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- New Target for Minoxidil in the Treatment of Androgenetic Alopecia
- A 3D microtumour system that faithfully represents ovarian cancer minimal residual disease
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Short Peptides Induce Development of Root Hair Nicotiana tabacum
- A direct link between<i>Prss53</i>, hair curvature, and skeletal dysplasia
- The peach RGF/GLV signalling peptide pCTG134 is involved in a regulatory circuit that sustains auxin and ethylene actions
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Developmental Genetics of Color Pattern Establishment in Cats
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Chemotherapy-Induced Alopecia by Docetaxel: Prevalence, Treatment and Prevention
- CRISPR/Cas9-mediated Generation of<i>COL7A1</i>-deficient Keratinocyte Model of Recessive Dystrophic Epidermolysis Bullosa
- Mediator 1 ablation induces enamel-to-hair lineage conversion through enhancer dynamics
- Male sex hormone and reduced plakoglobin jointly impair atrial conduction and cardiac sodium currents
- Fundamental hair follicle biology and fine fibre production in animals
- Multi-layered environmental regulation on the homeostasis of stem cells: The saga of hair growth and alopecia