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Research 781–810 of 1000+
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- The Genetics of Human Skin Disease
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- A cross-sectional study of clinical, dermoscopic, histopathological, and molecular patterns of scalp melanoma in patients with or without androgenetic alopecia
- Intratumoral <i>De Novo</i> Steroid Synthesis Activates Androgen Receptor in Castration-Resistant Prostate Cancer and Is Upregulated by Treatment with CYP17A1 Inhibitors
- Types I and II Keratin Intermediate Filaments
- Biotin and biotinidase deficiency
- Gene Array Profiling and Immunomodulation Studies Define a Cell-Mediated Immune Response Underlying the Pathogenesis of Alopecia Areata in a Mouse Model and Humans
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Characterization of Hair Follicle Development in Engineered Skin Substitutes
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- Proline-rich protein-like PRPL1 controls elongation of root hairs in Arabidopsis thaliana
- Identification of a preferred substrate peptide for transglutaminase 3 and detection of <i>in situ</i> activity in skin and hair follicles
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Human FOXN1-Deficiency Is Associated with αβ Double-Negative and FoxP3+ T-Cell Expansions That Are Distinctly Modulated upon Thymic Transplantation
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Milestones in Photocarcinogenesis
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- The Molecular Basis of Androgen Insensitivity
- New developments in the molecular treatment of ichthyosis: review of the literature
- DNA phenotyping: current application in forensic science
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Single-Cell Transcriptomics Reveals the Molecular Anatomy of Sheep Hair Follicle Heterogeneity and Wool Curvature
- Montagna Symposium 2014—Skin Aging: Molecular Mechanisms and Tissue Consequences
- Lgr6+ stem cells and their progeny in mouse epidermis under regimens of exogenous skin carcinogenesis, and their absence in ensuing skin tumors
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia