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Research 631–660 of 1000+
- Main Plenary Sessions: Summaries of Papers
- Dermatology
- Abstracts
- British Society for Dermatopathology: Summaries of Papers
- Letters to the Editor
- Quantitation of Hepatitis C Virus RNA
- Diagnosing Vascular Causes of Renal Failure
- Liver Cirrhosis and Circadian Rhythm
- Cutaneous manifestations of systemic infection in children
- Generation of an integration-free human induced pluripotent stem cell line MUSIi010-A from occipital scalp fibroblasts of a male patient with androgenetic alopecia
- Severe cardiac conduction abnormalities associated with atypical toxic shock syndrome
- Plasma Zinc Levels in Males with Androgenetic Alopecia as Possible Predictors of the Subsequent Conservative Therapy’s Effectiveness
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Idiopathic CD4+ T-lymphocytopenia
- Stem cell rejuvenation and the role of autophagy in age retardation by caloric restriction: An update
- In vitro and In vivo Hair Growth Promotion Effects of Lactobacillus plantarum-Fermented Plant Extracts (MBN)
- In Vivo Evaluation of<i>Eclipta alba</i>Extract as Anticancer and Multidrug Resistance Reversal Agent
- The role of androgens in hormone replacement therapy
- ATP-dependent chromatin remodeling during mammalian development
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Targeting lymphoid-derived IL-17 signaling to delay skin aging
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Experimental and Clinical Pharmacology of<i>Ziziphus jujuba</i>Mills
- Novel agents for the treatment of alopecia
- Current Perspectives on the Physiological Activities of Fermented Soybean-Derived Cheonggukjang
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Retinoid-mediated stimulation of steroid sulfatase activity in myeloid leukemic cell lines requires RARα and RXR and involves the phosphoinositide 3-kinase and ERK-MAP kinase pathways
- Newborn infant skin gene expression: Remarkable differences versus adults