Search
for
Sort by
Research 601–630 of 1000+
- Symptomatic zinc deficiency in a full-term breast-fed infant
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- Gray Hair: From Preventive to Treatment
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Rothmund Thomson syndrome with late onset and good preventive control of non-melanoma cancer with acitretin: case report
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- The Mechanisms of Fur Development and Color Formation in American Mink Revealed Using Comparative Transcriptomics
- Efficient In Vitro Transfection of Human Keratinocytes with an Adenovirus-Enhanced Receptor-Mediated System
- An Infant with Worsening Rash
- Molecular Mechanisms Regulating Hair Follicle Development
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Lysophospholipid Mediators in Health and Disease
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- The secret identities of TMPRSS2: Fertility factor, virus trafficker, inflammation moderator, prostate protector and tumor suppressor
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice