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Research 121–150 of 1000+
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Overactive Wnt5a signaling disrupts hair follicle polarity during mouse skin development
- Genome-wide p63-Target Gene Analyses Reveal TAp63/NRF2-Dependent Oxidative Stress Responses
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Ossifying pilomatrixoma with marrow formation of the left cheek region – Case report with review of literature
- Aberrant Wnt Signaling Induces Comedo-Like Changes in the Murine Upper Hair Follicle
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal–Epidermal Junction of Mouse Skin
- Temporal Triangular Alopecia – A Diagnostic Dilemma: Case Series of Six Patients
- Research progress in the treatment of non-scarring alopecia: mechanism and treatment
- Subject Index
- TONGUE, RED
- Author Index
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- The Dickkopf Protein Family in Non-Neoplastic Disorders: Emerging Roles and Therapeutic Targeting
- Unraveling Translational Insights into Systemic Multi-Organ Toxicity of Cytosine Arabinoside (Ara-C): A Systematic Review of Preclinical Animal Evidence
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- Hox genes in development and beyond
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Genetic Tools for Cell Lineage Tracing and Profiling Developmental Trajectories in the Skin
- Developmentally regulated expression of integrin alpha-6 distinguishes neural crest derivatives in the skin
- E-Poster
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Early inductive events in ectodermal appendage morphogenesis
- Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes