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Research 451–480 of 1000+
- Gsdma3 is required for hair follicle differentiation in mice
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Biochemistry of epidermal stem cells
- Functional redundancy of <i>Frizzled 3</i> and <i>Frizzled 6</i> in planar cell polarity control of mouse hair follicles
- Identification of a novel<i>PNPLA1</i>mutation in a Spanish family with autosomal recessive congenital ichthyosis
- HAIR KERATINIZATION IN HEALTH AND DISEASE
- Characterization of Human Keratin-Associated Protein 1 Family Members
- β1 Integrins with Individually Disrupted Cytoplasmic NPxY Motifs Are Embryonic Lethal but Partially Active in the Epidermis
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- Stem Cell Competition for Niche Occupancy: Emerging Themes and Mechanisms
- Molecular Analysis of a Series of Israeli Families with Comèl-Netherton Syndrome
- Genetic Basis of Pigmentation and Its Disorders
- Disease causing homozygous variants in the human hairless gene
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- High-resolution structures of mutants of residues that affect access to the ligand-binding cavity of human lipocalin-type prostaglandin D synthase
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Tradescantia-Based Test Systems Can Be Used for the Evaluation of the Toxic Potential of Harmful Algal Blooms
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Vitiligo – Study In view of familial occurence
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
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- Exploiting molecular genetic diagnoses of polycystic ovary syndrome to achieve better patient outcome
- Inherited Disorders of the Hair
- Research on Keratins Reveals Unexpected Link Between Hair Disorders and Dental Decay
- Modulation of Androgen Receptor Transcriptional Activity
- Molecular genetics of androgen insensitivity
- Discussion: Themes in the Molecular Structure of Hair
- Molecular Genetics of Inherited Disorders of Epidermal Keratins
- To be hairless or wise?
- <i>CCDC47</i> gene and trichohepatoneurodevelopmental syndrome: Report of the fifth and sixth cases from Saudi Arabia