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Research 61–90 of 1000+
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Transcriptomics analysis reveals molecular alterations underpinning spaceflight dermatology
- Surface modification and endothelialization of biomaterials as potential scaffolds for vascular tissue engineering applications
- Skin aging: mechanisms, evaluation, and rejuvenation
- Investigating the Genetic Association of Selected Candidate Loci with Alopecia Areata Susceptibility in Jordanian Patients
- Causal Relationship Between Blood Metabolomics and Female Pattern Hair Loss: A Bidirectional Mendelian Randomization Study
- Causal effects of omega‐6 and LDL‐C on androgenetic alopecia: A Mendelian randomization study
- The Basic Science of Hair Biology
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Integrated multiple machine learning and Mendelian randomization reveal LTF gene as a prognostic biomarker for nonspecific orbital inflammation
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- Genome-Wide Identification and Characterization of the Wnt Gene Family in Donkey (Equus asinus): Phylogenetic Analysis and Expression Profiling
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Predictive Metagenomic Profiling, Urine Metabolomics, and Human Marker Gene Expression as an Integrated Approach to Study Alopecia Areata
- Vitamin D Receptor gene polymorphisms taq-1 and cdx-1 in female pattern hair loss
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Gene Array Profiling and Immunomodulation Studies Define a Cell-Mediated Immune Response Underlying the Pathogenesis of Alopecia Areata in a Mouse Model and Humans
- Gene expression profiling of intestinal regeneration in the sea cucumber
- Phospholipase A2 in skin biology: new insights from gene-manipulated mice and lipidomics
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Association between SQSTM1 dysregulation and risk in alopecia areata: a Mendelian randomization study
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- Titanium dioxide nanoparticles: a promising candidate for wound healing applications
- Integrated single-cell chromatin and transcriptomic analyses of human scalp identify gene-regulatory programs and critical cell types for hair and skin diseases
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- From Follicle Cell Differentiation and Structure to Chorion Biogenesis in Insects: Cellular Mechanisms, Gene Regulation, Biochemical Composition and Structural Diversity