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Research 601–630 of 1000+
- Central centrifugal cicatricial alopecia: a subtype of lichen planopilaris in African descent?
- Developmental origin of polycystic ovary syndrome - a hypothesis
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Biology and Genetics of Hair
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders
- TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia
- 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
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Basal Cell Carcinoma, Hedgehog Signaling, and Targeted Therapeutics: The Long and Winding Road
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Dermatopathology and molecular genetics
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- A novel 22-bp InDel within <i>FGF7</i> gene is significantly associated with growth traits in goat
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- Genetic Susceptibility to Alopecia
- Hair shaft structures in EDAR induced ectodermal dysplasia
- 12-O-Tetradecanoylphorbol-13-acetate Induces Apoptosis in Renal Epithelial Cells through a Growth Signal Conflict Which Is Prevented by Activated ras1
- SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Production of a 135-residue long N-truncated human keratinocyte growth factor 1 in Escherichia coli