Search
for
Sort by
Research 61–90 of 1000+
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- The nude gene and the skin
- Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak
- Short-term Efficacy of Tofacitinib, a JAK Inhibitor, in IFIH1-related Aicardi-Goutières Syndrome
- Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Fidelity of the Human Mitochondrial DNA Polymerase
- Stem cell rejuvenation and the role of autophagy in age retardation by caloric restriction: An update
- Distinct Conditions Support a Novel Classification for Bradykinin-Mediated Angio-Oedema
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- Regulatory T Cells: the Many Faces of Foxp3
- Androgen receptors and their biology
- 507 Trial to investigate the role of ATP-sensitive potassium channels (KATPc) in dermal papilla cells (DPCs)
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Analogs of human genetic skin disease in domesticated animals
- Impact of estrogens in males and androgens in females
- Bridging Personal and Population in Excitability Diseases: Will Studies of Rare Diseases Bring Generalizable Mechanisms From Monogenic Channelopathies?
- Structure and Function of the Skin
- Negative Impact of Testosterone Deficiency and 5α-Reductase Inhibitors Therapy on Metabolic and Sexual Function in Men
- New insights into the functions of Cox-2 in skin and esophageal malignancies
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Physiologic functions of PP2A: Lessons from genetically modified mice
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- The urine as a diagnostic key for a homozygous EGFR mutation
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- 1339 Mature adipocytes inhibit the antimicrobial function of dermal adipogenic stem cells: An explanation for impaired cutaneous defense in obesity
- Beyond acne: Current aspects of sebaceous gland biology and function
- Epigenetic control of adult stem cell function
- Function and underlying mechanisms of seasonal colour moulting in mammals and birds: what keeps them changing in a warming world?