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Research 241–270 of 1000+
- PCSK9: From Nature’s Loss to Patient’s Gain
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Birt–Hogg–Dubé syndrome
- Structural perspectives on the androgen receptor, the elusive shape-shifter
- Significance of stress keratin expression in normal and diseased epithelia
- When bugs and drugs conspire: driving acneiform skin toxicity
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Clinical, pathological, and molecular features of classical and L-type atypical-BSE in goats
- One Transgene: Two Outcomes
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Specific receptor detection by a functional keratinocyte growth factor-immunoglobulin chimera.
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Intramembrane Proteolysis of Astrotactins
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Variation in the ovine trichohyalin gene and its association with wool curvature
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Author response: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- Decision letter: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- Identification and Analysis of MYB Gene Family for Discovering Potential Regulators Responding to Abiotic Stresses in Curcuma wenyujin
- Analysis of Apoptotic Cell Death in Human Hair Follicles In Vivo andIn Vitro
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Single injection of very mild dose botulinum toxin in the vastus lateralis improves testicular spermatogenesis and sperm motility in ageing experimental mice
- Dermoscopic features of follicular mycosis fungoides of nonscalp areas: Report of 11 cases and literature review
- Calreticulin: non‐endoplasmic reticulum functions in physiology and disease
- Epidermal Notch signalling: differentiation, cancer and adhesion