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Research 661–690 of 1000+
- KIF18B is a cell-type specific regulator of spindle orientation in the epidermis
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- A perspective on predictive markers of alopecia
- LB1077 Cutaneous responses to systemic iron: A potential role for epidermal turnover in mammalian iron excretion
- Stem Cells Sheltered from Air-Raids Repair Airways
- Australasian Society for Dermatology Research Meeting, May 2006
- British Society for Dermatopathology: Summaries of Papers
- A genetic test for androgenetic alopecia: polymorphisms in the androgen receptor gene provide a genetic screening test for androgenetic alopecia and earlier medical intervention
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Ovine KRTAP36-2: A New Keratin-Associated Protein Gene Related to Variation in Wool Yield
- An Update of Congenital Adrenal Hyperplasia
- What causes hidradenitis suppurativa ?—15 years after
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Madarosis: A marker of many Maladies
- Diagnostic approach to low‐renin hypertension
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Interaction between stem cell factor and endothelin-1: effects on melanogenesis in human skin xenografts
- The dermatological consequences of obesity
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- In Vivo Evaluation of<i>Eclipta alba</i>Extract as Anticancer and Multidrug Resistance Reversal Agent
- Hair shaft structures in EDAR induced ectodermal dysplasia
- TRPV3 Ion Channel: From Gene to Pharmacology
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Staphylococcus aureus accessory gene regulator quorum-sensing system inhibits keratinocyte lipid enzymes and delays wound repair
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- Genotyping of the rs1800440 Polymorphism in CYP1B1 Gene and the rs9258883 Polymorphism in HLA-B Gene in a Spanish Cohort of 223 Patients with Frontal Fibrosing Alopecia
- Genome-wide DNA methylation and transcriptome analyses reveal the key gene for wool type variation in sheep