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Research 271–300 of 1000+
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- Pallister-Killian Syndrome
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- Sex Reversal in Birds
- Androgens and hair loss
- SUN-069 A 14 Year Old Female with Primary Amenorrhea
- Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with <i>MCHR2</i>
- Two parietal cephaloceles in a female neonate
- Human Hair Keratin‐Associated Proteins (KAPs)
- Increased copy number of the TERT and TERC telomerase subunit genes in cancer cells
- Hair follicle-specific keratins and their diseases
- Handbook of Mouse Mutations with Skin and Hair Abnormalities: Animal Models and Biomedical Tools
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- 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
- Androgen receptors and their biology
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep
- Organization and Expression of Hair Follicle Genes.
- 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.
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Lithium alters mitotic progression in stamen hair cells of Tradescantia in a time-dependent and reversible fashion.
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Expression of a truncated form of hHb1 hair keratin in human breast carcinomas