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Research 31–60 of 1000+
- Molecular genetics of androgen insensitivity
- Diagnostic approach to low‐renin hypertension
- Expression of an Olfactomedin-Related Gene in Rat Hair Follicular Papilla Cells
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Multiple cyclic nucleotide‐gated channels coordinate calcium oscillations and polar growth of root hairs
- A novel calmodulin‐interacting Domain of Unknown Function 506 protein represses root hair elongation in <i>Arabidopsis</i>
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Signal Peptide-CUB-EGF-like Domain-Containing Protein 3 (SCUBE3): From Molecule to Therapy
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Intra-host SARS-CoV-2 single-nucleotide variants emerged during the early stage of COVID-19 pandemic forecast population fixing mutations
- Human Peptidylarginine Deiminase Type III: Molecular Cloning and Nucleotide Sequence of the cDNA, Properties of the Recombinant Enzyme, and Immunohistochemical Localization in Human Skin
- Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS
- GLI2 Is Expressed in Normal Human Epidermis and BCC and Induces GLI1 Expression by Binding to its Promoter
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Spatiotemporal dynamics of mammalian wound healing
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- Molecular characterization of caprine<i>KRTAP13-3</i>in Liaoning cashmere goat in China
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- 17β-estradiol Inhibits the Production of RANTES in Human Keratinocytes
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia