Search
for
Sort by
Research 631–660 of 1000+
- Platelet-derived growth factor signaling modulates adult hair follicle dermal stem cell maintenance and self-renewal
- Prediction of male-pattern baldness from genotypes
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Vitamin D receptor polymorphisms and the polycystic ovary syndrome: A systematic review
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- Human TSC2-null fibroblast-like cells induce hair follicle neogenesis and hamartoma morphogenesis
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- The Mesenchymal Niche of the Hair Follicle Induces Regeneration by Releasing Primed Progenitors from Inhibitory Effects of Quiescent Stem Cells
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- Assessment of the usefulness of dihydrotestosterone in the diagnostics of patients with androgenetic alopecia
- Skin and hair: models for exploring organ regeneration
- Regulation of VDR by ΔNp63α is associated with inhibition of cell invasion
- Treatment strategies for alopecia
- Lichen planus and other cutaneous manifestations in chronic hepatitis C: pre- and post-interferon-based treatment prevalence vary in a cohort of patients from low hepatitis C virus endemic area
- Planar cell polarity-dependent and independent functions in the emergence of tissue-scale hair follicle patterns
- Parathyroid Hormone Hormone-Related Protein and the PTH Receptor Regulate Angiogenesis of the Skin
- Oncogenic senescence: a multi-functional perspective
- Fate of Prominin-1 Expressing Dermal Papilla Cells during Homeostasis, Wound Healing and Wnt Activation
- Organ Specificity in Autoimmune Diseases: Thyroid and Islet Autoimmunity in Alopecia Areata
- Loss of Keratin K2 Expression Causes Aberrant Aggregation of K10, Hyperkeratosis, and Inflammation
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- A Clinical Approach to Severe Insulin Resistance
- Smad1 and 5 but Not Smad8 Establish Stem Cell Quiescence Which Is Critical to Transform the Premature Hair Follicle During Morphogenesis Toward the Postnatal State
- Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism*
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- An Ovol2‐Zeb1 transcriptional circuit regulates epithelial directional migration and proliferation
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Removing all obstacles: A critical role for p53 in promoting tissue renewal
- Hairless is a nuclear receptor corepressor essential for skin function