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Research 91–120 of 1000+
- Molecular Dissection of Mesenchymal–Epithelial Interactions in the Hair Follicle
- Adverse effects of common medications on male fertility
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Steroidogenic Isoenzymes in Human Hair and Their Potential Role in Androgenetic Alopecia
- What does acne genetics teach us about disease pathogenesis?
- Diagnostic approach to low‐renin hypertension
- Predicting Human Appearance from DNA for Forensic Investigations
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- Les hormones sexuelles et la peau : questionnaire à l'attention des vétérinaires praticiens. Mise à jour bibliographique et synthèse
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- ‘Hard’ and ‘soft’ principles defining the structure, function and regulation of keratin intermediate filaments
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Generation of the Krt24-CreERT2 Mouse Line Targeting Outer Bulge Hair Follicle Cells
- Characterization of Human KAP24.1, A Cuticular Hair Keratin-Associated Protein with Unusual Amino-Acid Composition and Repeat Structure
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Functional Food Nutrients, Redox Resilience Signaling and Neurosteroids for Brain Health
- Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss
- From Follicle Cell Differentiation and Structure to Chorion Biogenesis in Insects: Cellular Mechanisms, Gene Regulation, Biochemical Composition and Structural Diversity
- Hair Keratins and Hair Follicle–Specific Epithelial Keratins
- Variation in Ovine KRTAP13-3 and Its Association with Wool Characteristics in Chinese Tan Sheep
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients