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Research 601–630 of 1000+
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- ATP6AP1‐CDG: Follow‐up and female phenotype
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Shedding light on the FDA’s 510(k) approvals process: low-level laser therapy devices used in the treatment of androgenetic alopecia
- A translational approach to improve therapeutics in atopic dermatitis and beyond
- Tracing the Change and Contribution of Subcutaneous Adipose to Skin Expansion Using a Luciferase-Transgenic Fat Transplantation Model
- Congenital cutaneous lymphadenoma
- Effect of gelatin nanoparticles’ size and charge on iontophoretic targeted deposition to the hair follicles
- Follicular unit extraction [FUE] – One procedure, many uses
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Biological therapy in the treatment of melanoma
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Inborn Errors of Metabolism
- A Profile of Advertising in China’s “Socialist-Market Economy”
- Multiscale spatial mapping of cell populations across anatomical sites in healthy human skin and basal cell carcinoma
- Rare Gli1+ perivascular fibroblasts promote skin wound repair
- Editorial: Progress and Prospects on Skin Imaging Technology, Teledermatology and Artificial Intelligence in Dermatology
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Faces of the Face
- Trichosporon asteroides: A novel ethiological agent of Kerion celsi in a child
- Lipedematous alopecia with mucinosis: report of the first case in Taiwan
- Australian Medicines Handbook 2003
- Multi-scale spatial mapping of cell populations across anatomical sites in healthy human skin and basal cell carcinoma
- 69 Follicular Unit Excision to Harvest Body Hair
- Remarks on the Hormonal Background of the Male Equivalent of Polycystic Ovary Syndrome
- Platelet-rich plasma has a place in the treatment of androgenetic alopecia
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- Dynamic interactions of lymphatic vessels at the hair follicle stem cell niche during hair regeneration
- 455 Molecular correlation with clinical outcomes in an open label clinical trial of oral tofacitinib in patients with alopecia areata