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Research 781–810 of 1000+
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Renal tubular dysfunction presenting as recurrent hypokalemic periodic quadriparesis in systemic lupus erythematosus
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Ulerythema Ophryogenes in a Saudi Male: A Case Report
- Quantification of mast cells in central centrifugal cicatricial alopecia
- Granulomatous skin involvement in a patient with an unusual <i>NOD2</i> mutation
- Xiaozhi Yufa decoction ameliorates androgenetic alopecia through inhibition of MAPK signaling and regulation of lipid metabolism
- Can We Use Laser Hair Removal to Prevent the Formation of Trichoepithelioma Lesions?
- Pediatric adrenocortical carcinoma complicated by uric acid nephrolithiasis: a unique case report
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- 481 Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- A review of isotretinoin in the treatment of frontal fibrosing alopecia
- 1429 Proteomic analysis of cultured dermal papilla, dermal sheath and dermal fibroblast cells from female scalp highlights alterations in the cell populations with increasing age
- 567 Skin aging and carcinogenesis mechanisms by focusing on the stem cell competitive dynamics
- 565 hiPSC-derived skin organoids as tools for disease modelling: characterization of the epidermal-dermal junction
- 569 Hypoxic response of the expression of TGF-β2 and BMP4 in human dermal papilla cells
- Lichen Planopilaris
- A randomized double blind study of the effect of finasteride on hair growth in male patients of androgenetic alopecia
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Triangular temporal alopecia: a rare case in adulthood
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Characterization of Hydrogels of Gelatin/O-Carboxymethyl Chitosan in Ovule Form with Curcumin and Retinyl Palmitate as a Treatment for Cervical Cancer
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Targeting of Smoothened for therapeutic gain
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Bone morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: alternative mode for Dlx3 induction in mouse keratinocytes