Search
for
Sort by
Research 811–840 of 1000+
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- 304 Sephardic Ancestry in Recessive Dystrophic Epidermolysis Bullosa Individuals Carrying the Prevalent c.6527insC Mutation
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Effect of a transcriptional inactive or absent vitamin D receptor on beta-cell function and glucose homeostasis in mice
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Structure and function of skin, hair and nails
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Mitochondrial Function in Murine Skin Epithelium Is Crucial for Hair Follicle Morphogenesis and Epithelial–Mesenchymal Interactions
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Epithelial loss of mitochondrial oxidative phosphorylation leads to disturbed enamel and impaired dentin matrix formation in postnatal developed mouse incisor
- Cantú Syndrome Is Caused by Mutations in ABCC9
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- Androgen Receptor Mutations and Polymorphisms in African American Prostate Cancer
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Tissue regenerative delays and synthetic lethality in adult mice after combined deletion of Atr and Trp53
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Distinct Developmental Functions of Prostasin (CAP1/PRSS8) Zymogen and Activated Prostasin
- Loss of ‘Epidermal Melanin Unit’ Integrity in Human Skin During Melanoma-Genesis