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Research 391–420 of 1000+
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- The nude gene and the skin
- The character “hairless” in the mouse
- Ectodysplasin research—Where to next?
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Effectiveness of Anastrozole and Cyproterone Acetate in Two Brothers with Familial Male Precocious Puberty
- β1 Integrins with Individually Disrupted Cytoplasmic NPxY Motifs Are Embryonic Lethal but Partially Active in the Epidermis
- Stem cell identification-<i>in vivo</i> lineage analysis versus <i>in vitro</i> isolation and clonal expansion
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- An adult case of suspected A20 haploinsufficiency mimicking polyarteritis nodosa
- Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Becker's Nevus Syndrome
- At the Root: Cutaneous Langerhans Cell Histiocytosis
- Value of dermoscopy for the diagnosis of monilethrix
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- 199 Impairment of notch 1 signaling is a common defect in lesions from patients with hidradenitis suppurativa
- Subchronic study of sperm morphology, genotoxic and mutagenic effect of Lepidium sativum seeds aqueous extract in vivo
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies
- Heterozygous deletion of the <i>NSDHL</i> gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic nevi
- Netherton Syndrome: A Case-Based Review of Diagnosis, Management, and Emerging Treatments.
- Data from Activator Protein-1 Activity Regulates Epithelial Tumor Cell Identity
- Data from Activator Protein-1 Activity Regulates Epithelial Tumor Cell Identity
- Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Hypotrichosis in a child with olmsted syndrome
- A 9-month-old infant with severe scalp dermatosis
- To be hairless or wise?