Molecular Genetics of Human Hair Diseases
June 2008
Not medical advice or a treatment recommendation. Read the original study, and consult a qualified healthcare professional before changing treatment. Full disclaimer
Research cited in this study 34
- Disruption of P2RY5, an Orphan G Protein–Coupled Receptor, Underlies Autosomal Recessive Woolly Hair
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene LIPH
- Connexin 30, A New Marker Of Hyperproliferative Epidermis
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-Like Congenital Hypotrichosis
- Characterization and Isolation of Stem Cell-Enriched Human Hair Follicle Bulge Cells
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- A Missense Mutation in the Type II Hair Keratin hHb3 Is Associated with Monilethrix
- Characterization of New Members of the Human Type II Keratin Gene Family and a General Evaluation of the Keratin Gene Domain on Chromosome 12q13.13
- Keratins of the Human Hair Follicle
- Molecular Principles of Hair Follicle Induction and Morphogenesis
- Ligand-Independent Actions of the Vitamin D Receptor Maintain Hair Follicle Homeostasis
- The Human Type I Keratin Gene Family: Characterization of New Hair Follicle Specific Members and Evaluation of the Chromosome 17q21.2 Gene Domain
- Intragenic Deletion in the Desmoglein 4 Gene Underlies the Skin Phenotype in the Iffa Credo Hairless Rat
- Expression of Hair Keratins in the Adult Nail Unit: An Immunohistochemical Analysis of Onychogenesis in the Proximal Nail Fold, Matrix, and Nail Bed
- The Lanceolate Hair Rat Phenotype Results from a Missense Mutation in a Calcium Coordinating Site of the Desmoglein 4 Gene
- Physical And Functional Interaction Between The Vitamin D Receptor And Hairless Corepressor, Two Proteins Required For Hair Cycling
- Stimulation of Ectodermal Organ Development by Ectodysplasin-A1
- Molecular Mechanisms Regulating Hair Follicle Development
- The Hairless Gene Mutated in Congenital Hair Loss Disorders Encodes a Novel Nuclear Receptor Corepressor
- The Catalog of Human Hair Keratins
- Morphogenesis and Renewal of Hair Follicles from Adult Multipotent Stem Cells
- Involvement of Follicular Stem Cells in Forming Not Only the Follicle but Also the Epidermis
- Lanceolate Hair-J (LahJ): A Mouse Model for Human Hair Disorders
- Forkhead/Winged-Helix Transcription Factor Whn Regulates Hair Keratin Gene Expression: Molecular Analysis of the Nude Skin Phenotype
- Whn and mHa3 Are Components of the Genetic Hierarchy Controlling Hair Follicle Differentiation
- The Role of the Hairless (Hr) Gene in the Regulation of Hair Follicle Catagen Transformation
- The Catalog of Human Hair Keratins
- Alopecia Universalis Associated With a Mutation in the Human Hairless Gene
- Mutations in the Hair Cortex Keratin HHB6 Cause the Inherited Hair Disease Monilethrix
- 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) Affects Keratin 1 and Keratin 17 Gene Expression and Differentially Induces Keratinization in Hairless Mouse Skin
- Lanceolate Hair (Lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair
Related research 4
- A Review of Hair Anatomy and Animal Models for Alopecia
- Electron Paramagnetic Resonance Spectroscopy for Investigating Murine Telogen Skin After Spontaneous or Depilation-Induced Hair Growth
- Cyclic Alopecia in Msx2 Mutants: Defects in Hair Cycling and Hair Shaft Differentiation
- Congenital Hypotrichosis Due to Short Anagen Phase