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Research 601–630 of 1000+
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Mitochondrial DNA Variation in Human Hair Shafts Influenced by Physical Characteristics: A Massively Parallel Sequencing Analysis
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- APECED: JAK Inhibition in an Adult Case with Long-Term Follow-up
- Genetic Insights into Acne, Androgenetic Alopecia, and Alopecia Areata: Implications for Mechanisms and Precision Dermatology
- The Impact of Vitamin D Receptor Gene Polymorphisms (FokI, ApaI, TaqI) in Correlation with Oxidative Stress and Hormonal and Dermatologic Manifestations in Polycystic Ovary Syndrome
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- C‐reactive protein as a novel biomarker for vitamin D deficiency in alopecia areata
- Dissecting the genetic variations associated with response to first-line chemotherapy in patients with small cell lung cancer: a retrospective cohort study
- The Genomic Variation in Textured Hair: Implications in Developing a Holistic Hair Care Routine
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- The malignant capacity of skin tumours induced by expression of a mutant H-ras transgene depends on the cell type targeted
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- Targeted Disruption of Stat3 Reveals a Major Role for Follicular Stem Cells in Skin Tumor Initiation
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- The common regulatory pathway of COVID-19 and multiple inflammatory diseases and the molecular mechanism of cepharanthine in the treatment of COVID-19
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- Auditory Threshold Variability in the SAMP8 Mouse Model of Age-Related Hearing Loss: Functional Loss and Phenotypic Change Precede Outer Hair Cell Loss
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Evaluation of Personalized Skincare Through in-silico Gene Interactive Networks and Cellular Responses to UVR and Oxidative Stress
- Homozygous whole body <i>Cbs</i> knockout in adult mice features minimal pathology during ageing despite severe homocysteinemia
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Association of JAK 1 and JAK 2 gene polymorphism with alopecia areata risk: a case–control genetic study
- 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
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Dietary and Genetic Aspects of Polycystic Ovary Syndrome (PCOS) in Polish Women-Part II: Association of