Search
for
Sort by
Research 30 of 1000+
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Edar Signaling in the Control of Hair Follicle Development
- Suppression of hair follicle development inhibits induction of sonic hedgehog, patched, and patched-2 in hair germs in mice
- The G60S Connexin43 Mutant Regulates Hair Growth and Hair Fiber Morphology in a Mouse Model of Human Oculodentodigital Dysplasia
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Hair shaft structures in EDAR induced ectodermal dysplasia
- A direct link between<i>Prss53</i>, hair curvature, and skeletal dysplasia
- Follicular dysplasia and hair loss in white-tailed deer (<i>Odocoileus virginianus</i>)
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Abstract LB-039: Chronic inflammation-mediated contribution of bone marrow-derived epithelial cells and hair follicle stem cells to development of cutaneous neoplasms
- Abstract LB-039: Chronic inflammation-mediated contribution of bone marrow-derived epithelial cells and hair follicle stem cells to development of cutaneous neoplasms
- Biology and Genetics of Hair
- Ectoderm-Targeted Overexpression of the Glucocorticoid Receptor Induces Hypohidrotic Ectodermal Dysplasia
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- Genetic hair and nail disorders
- Current Genetics in Hair Diseases
- Molecular Basis of Hereditary Hair Diseases
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Transcriptional activation of a subset of hair keratin genes by the NF-κB effector p65/RelA
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- N02. Hair and Nails
- Retinoids: Compounds important to hair growth
- Identification of Ectodysplasin Target Genes Reveals the Involvement of Chemokines in Hair Development
- Hypotrichosis and nail dysplasia: A novel hidrotic ectodermal dysplasia
- HAIR-ROOT ADAPTATION TO MARASMUS IN ANDEAN INDIAN CHILDREN
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- Black Hair Follicular Dysplasia in Black and White Saluki Dogs: Differentiation from Color Mutant Alopecia in the Doberman Pinscher by Microscopic Examination of Hairs
- Epidermal abnormalities and increased malignancy of skin tumors in human epidermal keratin 8‐expressing transgenic mice