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Research 30 of 32
- Whn and mHa3 are components of the genetic hierarchy controlling hair follicle differentiation
- A novel human type I hair keratin gene: evidence for two keratin hHa3 isoforms
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- Genetically separable determinants of hair keratin gene expression
- Sequence of a Cashmere goat type I hair keratin gene and its expression in skin
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Different gene expression profile observed in dermal papilla cells related to androgenic alopecia by DNA macroarray analysis
- Ultrastructural Localization of Hair Keratins in Human Scalp Hair Shafts as Revealed by Rapid-Freezing Immunocytochemistry.
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Learning from nudity: lessons from the nude phenotype
- <i>Hoxc13</i> mutant mice lack external hair
- Towards a molecular understanding of hair loss and its treatment
- Regeneration of skin appendages and nerves: current status and further challenges
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- The Catalog of Human Hair Keratins
- Genetically null mice reveal a central role for epidermal growth factor receptor in the differentiation of the hair follicle and normal hair development.
- Molecular Genetics of Human Hair Diseases
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- Molecular Mechanisms Regulating Hair Follicle Development
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- Embryonic hair follicle fate change by augmented β-catenin through Shh and Bmp signaling
- Sequence and Expression of Murine Type I Hair Keratins mHa2 and mHa3
- FOXN1 deficient nude severe combined immunodeficiency