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Research 421–450 of 1000+
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Genetic Disorders and Defects in Vitamin D Action
- The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Targeting Superficial or Nodular Basal Cell Carcinoma with Topically Formulated Small Molecule Inhibitor of Smoothened
- The nude gene and the skin
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Nutritional Disorders of the Hair and Their Management
- HtrA1L364P leads to cognitive dysfunction and vascular destruction through TGF‐β/Smad signaling pathway in CARASIL model mice
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Ernährungsstörungen des Haares und deren Management
- Monilethrix – Case report of a rare disease
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- Two-ligand priming mechanism for potentiated phosphoinositide synthesis is an evolutionarily conserved feature of Sec14-like phosphatidylinositol and phosphatidylcholine exchange proteins
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- The stem cell quiescence and niche signaling is disturbed in the hair follicle of the hairpoor mouse, an MUHH model mouse
- Unravelling the molecular basis for symbiotic signal transduction in legumes
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Heterozygous deletion of the <i>NSDHL</i> gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic nevi
- Heterozygous 21‐hydroxylasedeficiency as a cause of hyperandrogenism
- Heterozygous <i>KRT32</i> variant is responsible for autosomal dominant loose anagen hair syndrome
- Heterozygous <i>COL5A1</i> deletion in a cat with classical Ehlers–Danlos syndrome