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Research 121–150 of 1000+
- Mediator 1 ablation induces enamel-to-hair lineage conversion in mice through enhancer dynamics
- Keratin K15 as a Biomarker of Epidermal Stem Cells
- Epidermal Development in Mammals: Key Regulators, Signals from Beneath, and Stem Cells
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Hair loss in infancy and childhood
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- ALOPECIA AREATA-A CLINICAL ANALYSIS
- Abstracts from the Symposium on the Pathophysiology of Hair Growth Organized by the Institute of Dermatology at the Royal Society of Medicine, 29 October 1987
- Identification of key genes and signaling pathways related to Hetian sheep wool density by RNA-seq technology
- Signaling Involved in Hair Follicle Morphogenesis and Development
- British Society for Dermatopathology: Summaries of Papers
- Significance of iron status in hair loss in women
- The Spectrum of Skin Disease Among Indian Children
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Diagnosis and management of hair loss in children
- Acquired scalp alopecia. Part I: A review
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Clinical Case Notes. Malignant melanoma in eviscerated eyeball
- Micronutrients for Hair and Nails
- Combination of Transcriptomics and Proteomics Reveals Differentially Expressed Genes and Proteins in the Skin of EDAR Gene-Targeted and Wildtype Cashmere Goats
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Frequency of Types of Alopecia in a Single-centre Hair Referral Clinic Over a Ten Years Period
- Increasing GSH-Px Activity and Activating Wnt Pathway Promote Fine Wool Growth in FGF5-Edited Sheep
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.