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Research 691–720 of 1000+
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Behavioural characterization of Vitamin D receptor knockout mice
- Integument pattern formation involves genetic and epigenetic controls: feather arrays simulated by digital hormone models.
- Phospholipase C 1 is required for skin stem cell lineage commitment
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- Endocrine intervention for transsexuals
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Defining the Cellular Environment in the Organ of Corti following Extensive Hair Cell Loss: A Basis for Future Sensory Cell Replacement in the Cochlea
- The Skin and Inflamm-Aging
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Medicinal Chemistry of Drugs with <i>N</i>-Oxide Functionalities
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- No Evidence that 2D:4D is Related to the Number of CAG Repeats in the Androgen Receptor Gene
- Society for Endocrinology guidelines for testosterone replacement therapy in male hypogonadism
- ACE2 and TMPRSS2 Potential Involvement in Genetic Susceptibility to SARS-COV-2 in Cancer Patients
- Protein and sulphur amino acid nutrition of hair fibre-producing Angora and Cashmere goats
- Coming of Age of Melanogenesis-Related Proteins
- Understanding Melanocyte Stem Cells for Disease Modeling and Regenerative Medicine Applications
- Identification of the keratin-associated protein 13-3 (KAP13-3) gene in sheep
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Bone vs. fat: Embryonic origin of progenitors determines response to androgen in adipocytes and osteoblasts
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- Predictive factors for adverse dermatological events during pegylated/interferon alpha and ribavirin treatment for hepatitis C
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles
- Analyzing the role of ACE2, AR, MX1 and TMPRSS2 genetic markers for COVID-19 severity
- LGR5 is a conserved marker of hair follicle stem cells in multiple species and is present early and throughout follicle morphogenesis