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Research 271–300 of 1000+
- A Current Diagnostic and Therapeutic Challenge: Tinea Capitis
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- The role of ingrown hairs in persistent kerion of children: A clinical study
- Dermal Papilla Cells: From Basic Research to Translational Applications
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- <i>Hoxc13</i> mutant mice lack external hair
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- Functional identification of the phosphorylation sites of Arabidopsis PIN-FORMED3 for its subcellular localization and biological role
- LAMELLAR ICHTHYOSIS: ONE CASE REPORT
- TERT/BMI1-transgenic human dermal papilla cells enhance murine hair follicle formation in vivo
- Comorbidities in alopecia areata: A systematic review and meta-analysis
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- Roles of GasderminA3 in Catagen–Telogen Transition During Hair Cycling
- Analyzing the innate immunity of NIH hairless mice and the impact of gut microbial polymorphisms on<i>Listeria monocytogenes</i>infection
- Inherited Epidermolysis Bullosa: A Clinical Case
- The antiandrogen enzalutamide downregulates TMPRSS2 and reduces cellular entry of SARS-CoV-2 in human lung cells
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Spironolactone and XPB: An Old Drug with a New Molecular Target
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Syphilis: today
- News in brief
- Exploring the Drug Repurposing Versatility of Valproic Acid as a Multifunctional Regulator of Innate and Adaptive Immune Cells
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- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Disorganization of Transcriptional Regulation and Alteration of Keratin Family Gene Expression in Hairy Ear Mice
- CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Towards Defining the Pathogenesis of the Hairless Phenotype