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Research 421–450 of 1000+
- Human Fetal Scalp Dermal Papilla Enriched Genes and the Role of R-Spondin-1 in the Restoration of Hair Neogenesis in Adult Mouse Cells
- Concomitant presentation of alopecia areata in siblings: A rare occurrence
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Le gène<i>hairless</i>de la souris
- Differential activity of 2-methylene-19-nor vitamin D analogs on growth factor gene expression in rhino mouse skin and comparison to all-trans retinoic acid
- Standardizing the Nomenclature of Grafts
- Association of Cyp11a Gene with Polycystic Ovarian Syndrome Patients in Lahore, Pakistan
- A Role for Steroid 5 alpha-reductase 1 in Vascular Remodelling During Endometrial Decidualisation
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- 公表学術論文等リスト 2018
- Follikelhormone
- Natural Killer Group 2 Type D (NKG2D) Gene Polymorphism in Systemic Lupus Erythematosus-Suez Canal Region - Egypt
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Antioxidants in dermatology
- New lifestyle drugs and somatoform disorders in dermatology
- Hyperadrenocorticism in Ferrets
- Modulating testosterone pathway: a new strategy to tackle male skin aging?
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- Side Effects and Adverse Events After Treatment With Teprotumumab for Thyroid Eye Disease: A Retrospective Observational Case Series
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- 316 Specialized ribosomes in human dermal fibroblast senescence
- 313 Different polyamine levels in the vertex and occipital hair of pattern hair loss patients
- Clinical Management in Psychodermatology
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study
- The evaluation of IL-4 intron 3 VNTR and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with Alopecia Areata: a case-control study
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- A functional polymorphism in interleukin-1α (IL1A) gene is associated with risk of alopecia areata in Chinese populations