Search
for
Sort by
Research 571–600 of 1000+
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- Genome wide association analysis of root hair traits in rice reveals novel genomic regions controlling epidermal cell differentiation
- Trapa bispinosa Roxb. Pericarp Extract Exerts 5α-Reductase Inhibitory Activity in Castrated Benign Prostatic Hyperplasia Model Mice
- Inconsistent effects of surgical and chemical castration on arterial baroreceptor dysfunction and cardiac and brainstem inflammation in endotoxic rats
- Clinical Snippets
- Androgenic alopecia in men: the significance of genetic, hormonal and metabolic factors (prospective cohort comparative study)
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
- Synergistic Antibacterial Activity and Wound Healing Properties of Selenium-Chitosan-Mupirocin Nanohybrid System: An in Vivo Study on Rat Diabetic Staphylococcus aureus Wound Infection Model
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Molecular characterization of HOXC8 gene and methylation status analysis of its exon 1 associated with the length of cashmere fiber in Liaoning cashmere goat
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- A Short Report on Melanocyte/Melanoma Culture, Senescence, and Reproducibility
- Interleukin 15 Gene Polymorphism in patients with Alopecia Areata
- 0441 Systemic autoimmune comorbidity in alopecia totalis and universalis compared with patchy alopecia areata: A retrospective cohort study
- Adipose‐Derived Stem Cells for Tissue Engineering and Regenerative Medicine Applications
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- Emerging roles of Sox6 in the renal and cardiovascular system
- Sex-limited chromosomes and non-reproductive traits
- Stimuli-responsive nanoformulations for CRISPR-Cas9 genome editing
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Narrowband UVB treatment induces expression of WNT7B, WNT10B and TCF7L2 in psoriasis skin
- Associations between type 1 diabetes and autoimmune skin diseases: Mendelian randomization analysis
- Association between genetically predicted leukocyte telomere length and non-scarring alopecia: A two-sample Mendelian randomization study
- RETRACTED: Genetic association between asthma and alopecia areata: A two‐sample Mendelian randomization study