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- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- The KRAB domain zinc finger protein, Zfp157, is expressed in multiple tissues during mouse embryogenesis and in specific cells in adult mammary gland and skin
- Atrichia with papular lesions
- Atrichia With Papular Lesions Confirmed via Genetic Testing: A Case Report
- Snail2: Estudios estructura-función y análisis in vivo de su papel en el desarrollo del folícullo piloso y la carcinogénesis química de la piel
- Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene
- Dynamic expression of the zinc-finger transcription factor Trps1 during hair follicle morphogenesis and cycling
- The zinc finger protein 3 of Arabidopsis thaliana regulates vegetative growth and root hair development
- Arabidopsis ZINC FINGER PROTEIN1 Acts Downstream of GL2 to Repress Root Hair Initiation and Elongation by Directly Suppressing bHLH Genes
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Large Scale Gene Expression Profiles of Regenerating Inner Ear Sensory Epithelia
- Inhibiting the cytosolic function of CXXC5 accelerates diabetic wound healing by enhancing angiogenesis and skin repair
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Zfp462 deficiency causes anxiety‐like behaviors with excessive self‐grooming in mice
- The function of TRPS1 in the development and differentiation of bone, kidney, and hair follicles.
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Distinct transcriptomic landscapes of cutaneous basal cell carcinomas and squamous cell carcinomas
- Signal integrator function of CXXC5 in Cancer
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- The Negative Regulator CXXC5: Making WNT Look a Little Less Dishevelled
- GLI2-specific Transcriptional Activation of the Bone Morphogenetic Protein/Activin Antagonist Follistatin in Human Epidermal Cells
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Role of Zinc in Mucosal Health and Disease: A Review of Physiological, Biochemical, and Molecular Processes
- Zinc as an ambivalent but potent modulator of murine hair growth in vivo- preliminary observations
- The Function of Zinc in Animal, Plant, and Human Nutrition
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- Lymphoid Enhancer-binding Factor-1 (LEF1) Interacts with the DNA-binding Domain of the Vitamin D Receptor