Search
for
Sort by
Research 271–300 of 1000+
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- 332 OTULIN maintains skin homeostasis by controlling keratinocyte death and stem cell identity
- Increased PHGDH expression uncouples hair follicle cycle progression and promotes inappropriate melanin accumulation
- Increased PHGDH expression promotes aberrant melanin accumulation
- The role of functional variants in the aetiology of polycystic ovary syndrome
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- ERG induces androgen receptor-mediated regulation of SOX9 in prostate cancer
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Pharmacological Mobilization of Endogenous Stem Cells Significantly Promotes Skin Regeneration after Full-Thickness Excision: The Synergistic Activity of AMD3100 and Tacrolimus
- Increased lactate dehydrogenase activity is dispensable in squamous carcinoma cells of origin
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- Age-Related Changes in Hair Shaft Protein Profiling and Genetically Variant Peptides
- Male Androgenetic Alopecia
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- Clinicopathologic Characteristics and Response to Treatment of Persistent Chemotherapy-Induced Alopecia in Breast Cancer Survivors
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- The Roles of EDA2R in Ageing and Disease
- Genome-wide association study of atopic and autoimmune comorbidities in alopecia areata
- <i>PIK3CA</i> gain-of-function mutation in Schwann cells leads to severe neuropathy and aerobic glycolysis through a non-cell autonomous effect
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Primärprävention urologischer Tumore: Prostatakarzinom
- The Off-Label Use of Selective Serotonin Reuptake Inhibitors for Sexual Behavior Management: Risks and Considerations
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- The Rotterdam Study: objectives and design update
- Defective trophoblast function in mice with a targeted mutation of Ets2
- Integrin signalling regulates YAP/TAZ to control skin homeostasis
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder