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- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- [Genetic dissection of retinoic acid function in epidermis physiology].
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- cis-Element- and Transcriptome-Based Screening of Root Hair-Specific Genes and Their Functional Characterization in Arabidopsis
- Ligand-Independent Actions of the Vitamin D Receptor Maintain Hair Follicle Homeostasis
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- A function for Rac1 in the terminal differentiation and pigmentation of hair
- The role of Glucosylceramides in Keratinocyte Differentiation and Epidermal Barrier Function
- 889 Trpv3 gain-of-function mutation impairs differentiation of hair follicle inner root sheath
- Expression of a dominant negative mutant of epidermal growth factor receptor in the epidermis of transgenic mice elicits striking alterations in hair follicle development and skin structure.
- Hairless is a nuclear receptor corepressor essential for skin function
- Hairless: A nuclear receptor corepressor essential for skin function
- Inducible deletion of epidermal <i>Dicer</i> and <i>Drosha</i> reveals multiple functions for miRNAs in postnatal skin
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish
- The TFIID subunit TAF4 regulates keratinocyte proliferation and has cell-autonomous and non-cell-autonomous tumour suppressor activity in mouse epidermis
- Functional analysis of collagen XVII in epithelial cancers and a mouse model
- Ptch2 is a Potential Regulator of Mesenchymal Stem Cells
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- 361 p120-catenin regulates epidermal inflammation in a cadherin-dependent manner
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Remodelling of cytoskeleton and plasma membrane proteins contributes to drought sensitivity of Arabidopsis<i>rhd2</i>mutant
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- A function for Rac1 in the terminal differentiation and pigmentation of hair
- Inducible deletion of Dicer or Drosha reveals multiple functions for miRNAs in postnatal epidermis and hair follicles
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- Interaction of the vacuolar H+-pyrophosphatase AVP1 with the secondary transporters AtNHX1 and SOS1 in Arabidopsis thaliana: Implications in salt tolerance and mineral nutrition
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis