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Research 181–210 of 1000+
- Low level of maternal biotin intake changes the expression of biotin transporter in dams and fetuses in mice
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Irradiation-induced hair graying in mice: an experimental model to evaluate the effectiveness of interventions targeting oxidative stress, DNA damage prevention, and cellular senescence
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Pubic to Scalp F.U.E. Hair Transplant for Transgender
- Genetic Defects of Female Sexual Differentiation
- Syndromes of Severe Insulin Resistance (SSIRs)
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Premature graying of hair
- Psychodermatology
- WISP-1 induced by mechanical stress contributes to fibrosis and hypertrophy of the ligamentum flavum through Hedgehog-Gli1 signaling
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Current standards in the diagnostics and therapy of hair diseases - hair consultation
- Improvement in Hair Loss and Better Hair Quality with Vitamin Therapy in Monilethrix
- Characterization of Primary Cilia and Intraflagellar Transport 20 in the Epidermis
- Treatment of acne vulgaris: a literature review / Lečenje običnih akni (acne vulgaris) – pregled literature
- Precision-Based Management of Chronic Hair Fall: A Genomic-Guided Trichology Approach - A Case Analysis from Qatar
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Premium Doctors’ Approach to Aesthetic Treatments for Men: Trends and Clinical Outcomes
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Idiopathic hypoparathyroidism with extensive intracranial calcification in children
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Mechanical and Immunological Regulation in Wound Healing and Skin Reconstruction
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- Bubble hair and other acquired hair shaft anomalies due to hot ironing on wet hair
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome