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Research 391–420 of 1000+
- Congenital atrichia associated with nevus flammeus: A rare association
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- SOX9 in organogenesis: shared and unique transcriptional functions
- Targeting the Hippo/YAP/TAZ signalling pathway: Novel opportunities for therapeutic interventions into skin cancers
- Highly Upregulated Lhx2 in the Foxn1−/− Nude Mouse Phenotype Reflects a Dysregulated and Expanded Epidermal Stem Cell Niche
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- MmuPV1-Induced Cutaneous Squamous Cell Carcinoma Arises Preferentially from Lgr5+ Epithelial Progenitor Cells
- Whole blood transcriptome profiling identifies candidate genes associated with alopecia in male giant pandas (Ailuropoda melanoleuca)
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Surgical Management of Scarring Alopecia
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- Potential Treatment of Steroid‐Resistant Alopecia Areata Using Allogeneic Exosomes Derived From Adipose Tissue Mesenchymal Stromal Cells: A Case Report
- Immune therapies for alopecia areata: evidence and new perspectives
- Unusual progression of renal cell carcinoma with carcinomatosis peritoneii and Krukenberg tumour and alopecia with sunitinib therapy in young female
- Cyclin D3 deficiency inhibits skin tumor development, but does not affect normal keratinocyte proliferation
- Tissue engineering of skin and regenerative medicine for wound care
- Matriptase: Potent Proteolysis on the Cell Surface
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development