Search
for
Sort by
Research 391–420 of 498
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Endogenous Skin Fluorescence is a Good Marker for Objective Evaluation of Comedolysis
- HIV Symptom Clusters are Similar Using the Dimensions of Symptom Occurrence and Distress
- Assessment of prescribing information for generic drugs manufactured in the Middle East and marketed in Saudi Arabia
- Exosomes derived from umbilical cord mesenchymal stem cells promote healing of complex perianal fistulas in rats
- Vitamin B<sub>3</sub> (niacin), B<sub>6</sub>, C, and iron intake are associated with the free androgen index, especially in normoandrogenic polycystic ovary syndrome
- Intestinal Lymphatic Biology, Drug Delivery, and Therapeutics: Current Status and Future Directions
- Analyzing the role of ACE2, AR, MX1 and TMPRSS2 genetic markers for COVID-19 severity
- Phytochemical Constitution, Anti-Inflammation, Anti-Androgen, and Hair Growth-Promoting Potential of Shallot (Allium ascalonicum L.) Extract
- Low-Molecular-Weight Synthetic Antioxidants: Classification, Pharmacological Profile, Effectiveness and Trends
- Tissue Resident Foxp3+ Regulatory T Cells: Sentinels and Saboteurs in Health and Disease
- Melatonin Regulates the Periodic Growth of Cashmere by Upregulating the Expression of Wnt10b and β-catenin in Inner Mongolia Cashmere Goats
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- A trichobezoar in a child with undiagnosed celiac disease: A case report
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- The Efficacy and Psychoneuroimmunology Mechanism of Camouflage Combined With Psychotherapy in Vitiligo Treatment
- The Silent Syndrome of Long COVID and Gaps in Scientific Knowledge: A Narrative Review
- A synbiotic preparation (SIM01) for post-acute COVID-19 syndrome in Hong Kong (RECOVERY): a randomised, double-blind, placebo-controlled trial
- Ischemia-Modified Albumin—A Potential New Marker of Oxidative Stress in Dermatological Diseases
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Simultaneous Determination of Selected Steroids with Neuroactive Effects in Human Serum by Ultrahigh-Performance Liquid Chromatography–Tandem Mass Spectrometry
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Nutritional Disorders of the Hair and Their Management
- Effects of bright light exposure during daytime on peripheral clock gene expression in humans
- Transcription Factor DLX5 Promotes Hair Follicle Stem Cell Differentiation by Regulating the c-MYC/microRNA-29c-3p/NSD1 Axis
- Impacts of iron on phosphate starvation-induced root hair growth in Arabidopsis
- Confocal Laser Scanning Microscopy as a Tool for the Investigation of Skin Drug Delivery Systems and Diagnosis of Skin Disorders
- Measurement of Acne Severity, Dietary Habits, and Blood Zonulin Levels in Acne Patients