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Research 151–180 of 162
- Recent Insights in Multi‐Target Drugs in Pharmacology and Medicinal Chemistry
- Multi-omics revealed that the postbiotic of hawthorn-probiotic alleviated constipation caused by loperamide in elderly mice
- Global trends in tertiary lymphoid structures: a bibliometric analysis from 2014 to 2023
- A bibliometric analysis of endoplasmic reticulum stress and atherosclerosis
- Outcomes of paediatric patients with chronic liver disease in early adulthood: A heterogeneous, but representative, regional cohort study
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Oral Combination Treatment of Gefitinib (IressaTM) and Sasam-Kyeongokgo: Synergistic Effects on the NCI-H520 Tumor Cell Line
- Unlocking the versatile potential: Adipose-derived mesenchymal stem cells in ocular surface reconstruction and oculoplastics
- Integrating levels of bone growth control: From stem cells to body proportions
- Gender Surgery Beyond Chest and Genitals: Current Insurance Landscape
- A Multidimensional Study Integrating Traditional Chinese Medicine and Network Pharmacology: Exploring the Skin Repair and Anti-Aging Effects of a Specific Combination of Five-Colored Plants
- Drug Survival and Long-term Outcome of Tofacitinib in Patients with Alopecia Areata: A Retrospective Study
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Why Do Not All Chemotherapy Patients Lose Their Hair? Answering an Intriguing Question
- Chemotherapy-Induced Alopecia by Docetaxel: Prevalence, Treatment and Prevention
- Diffuse hair loss in Addison disease: A reason for X-linked adrenoleukodystrophy screening
- An unusual presentation of X-linked adrenoleukodystrophy
- Jieduquyuziyin prescription alleviates SLE complicated by atherosclerosis via promoting cholesterol efflux and suppressing TLR9/MyD88 activation
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Zebrafish Model of Hereditary Pigmentary Disorders
- No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia
- An analysis of gene expression data involving examination of signaling pathways activation reveals new insights into the mechanism of action of minoxidil topical foam in men with androgenetic alopecia
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Differential expression and functionality of ATP-binding cassette transporters in the human hair follicle
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells