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Research 451–480 of 1000+
- The Rotterdam Study: 2018 update on objectives, design and main results
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- In vivo transcriptional governance of hair follicle stem cells by canonical Wnt regulators
- Decreased Serum Ferritin is Associated With Alopecia in Women
- Tissue regenerative delays and synthetic lethality in adult mice after combined deletion of Atr and Trp53
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Ferreting out stem cells from their niches
- YAP and TAZ are essential for basal and squamous cell carcinoma initiation
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Alopecia areata: An update
- Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for <i>In Vivo</i> CRISPR/Cas-Based Genome Editing
- Review article: dermatological complications of immunosuppressive and anti-TNF therapy in inflammatory bowel disease
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Cutaneous and Mucosal Manifestations Associated with Celiac Disease
- Nonclassic adrenal hyperplasia
- Differential Expression of miR-93 and miR-21 in Granulosa Cells and Follicular Fluid of Polycystic Ovary Syndrome Associating with Different Phenotypes
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- High proliferation and delamination during skin epidermal stratification
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Nonclassic Congenital Adrenal Hyperplasia
- JunB defines functional and structural integrity of the epidermo-pilosebaceous unit in the skin
- Gender aspects in skin diseases
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- A preliminary study of finasteride in Tourette syndrome
- Types of Hair Loss and Treatment Options, Including the Novel Low-Level Light Therapy and Its Proposed Mechanism
- Androgen receptor gene polymorphism and polycystic ovary syndrome
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Roles of tumor suppressors in regulating tumor-associated inflammation