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Research 181–210 of 1000+
- SARS-CoV-2 Spike Protein S1-Mediated Endothelial Injury and Pro-Inflammatory State Is Amplified by Dihydrotestosterone and Prevented by Mineralocorticoid Antagonism
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Wound Healing Impairment in Type 2 Diabetes Model of Leptin-Deficient Mice—A Mechanistic Systematic Review
- Damage of hair follicle stem cells and alteration of keratin expression in external radiation-induced acute alopecia
- Understanding the Intricate Pathophysiology of Psoriasis and Related Skin Disorders
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- SEXUAL DIMORPHISM IN MAMMALS
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Bloom's syndrome–‐a first report from India
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- Transcriptome Analysis Reveals an Inhibitory Effect of Dihydrotestosterone-Treated 2D- and 3D-Cultured Dermal Papilla Cells on Hair Follicle Growth
- Combinatorial expression of cell cycle regulators is more suitable for immortalization than oncogenic methods in dermal papilla cells
- Case Report: Disorder of Sexual Development in a Chinese Crested Dog With XX/XY Leukocyte Chimerism and Mixed Cell Testicular Tumors
- Imprinted Dlk1-Gtl2 cluster miRNAs are potential epigenetic regulators of lamb fur quality
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Dermal papilla-induced hair differentiation of adult epithelial stem cells from human skin
- Sebaceous Gland Atrophy in Psoriasis: An Explanation for Psoriatic Alopecia?
- Current evidence for the involvement of sex steroid receptors and sex hormones in benign prostatic hyperplasia
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- From mechanisms to therapies: current advances breakthroughs in alopecia areata immunopathology
- Genetic and hormonal influence on SARS-CoV-2-infection susceptibility
- Netherton syndrome: effect on ichthyosis linearis circumflexa with dupilumab
- Inheritance-Specific Dysregulation of Th1- and Th17-Associated Cytokines in Alopecia Areata
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Effects of taxifolin from enzymatic hydrolysis of Rhododendron mucrotulatum on hair growth promotion
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene