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Research 661–690 of 1000+
- Ectodermal Dysplasia: Variable Expressions
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- Genetics of Diabetes in Childhood
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.
- Terrestrial vertebrates have two keratin gene clusters; striking differences in teleost fish
- Epidermal Differentiation Complex: A Review on Its Epigenetic Regulation and Potential Drug Targets.
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Resequencing and Signatures of Selective Scans Point to Candidate Genetic Variants for Hair Length Traits in Long-Haired and Normal-Haired Tianzhu White Yak
- Transcriptome Profiling of Human Follicle Dermal Papilla Cells in response to Porphyra-334 Treatment by RNA-Seq
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- Viewpoint 6
- p63 expression in normal skin and usual cutaneous carcinomas
- Endocrine intervention for transsexuals
- Role of the Autoimmune Regulator (<i>AIRE</i>) gene in alopecia areata: Strong association of a potentially functional <i>AIRE</i> polymorphism with alopecia universalis
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals