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Research 961–990 of 1000+
- IL-17a induces age-related olfactory dysfunction by impairing regeneration and promoting respiratory metaplasia in mice
- Proportional Prevalence of Bovine Parasitic Diseases at Mymensingh District of Bangladesh
- DHEA and TNF-α: Key Factors in Managing Polycystic Ovary Syndrome in Iraqi Females
- Estimation of Dehydroepiandrosterone (DHEA) and Tumor Necrosis Factor–Alpha (TNF-α) Levels Women Diagnosed with Polycystic Syndrome
- Morphological, molecular and histopathological identification of Sarcoptes scabieiinfection in a goat herd at Goa, India
- Optimized Methodology to Produce Platelet-Rich Plasma and Perform Platelet Aggregation in Patients With Coronary Artery Disease
- Identifying causal genes in alopecia areata using integrative analysis of differential expression and Mendelian randomization
- Association Between Natural Hair Color, Race, and Alopecia
- Arabidopsis retromer subunit AtVPS29 is involved in SLY1-mediated gibberellin signaling
- Herbal insights into melanin synthesis: Enhancing hair health naturally
- Molecular heterogeneity of quiescent melanocyte stem cells revealed by single-cell RNA-sequencing
- Molecular Mechanisms Affecting Development of Animal Fibers and Some Studies on Goats
- Clinical Findings, Response to Steroid Treatment, and Recurrence Rate in Alopecia Areata Patients with or without a Nonsynonymous Variant of Coiled-Coil Alpha-Helical Rod Protein 1
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- KIF18B is a cell-type specific regulator of spindle orientation in the epidermis
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Dermal EZH2 simultaneously orchestrates dermal differentiation and epidermal proliferation during murine skin development
- 863 Central centrifugal cicatricial alopecia gene expression analysis revealed cholesterol, fatty acid, and mast cell pathways
- Follikelhormone
- INVESTIGATING THE MECHANISMS UNDERLYING THE PATHOGENESIS OF ALOPECIA AREATA
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Lab Quality Management and Methodology
- B‐ RAF , naevi and melanoma: a complex relationship
- Epidermal Notch1 recruits innate lymphoid cells to orchestrate normal skin repair
- Selected Abstracts
- Contents
- Syndromes of Severe Insulin Resistance (SSIRs)
- 464 Phenotypic heterogeneity of epidermolysis bullosa associated with the recurrent pathogenic variant p.(Arg2000Trp) in plectin
- Genome-wide Target Enrichment-aided Chip Design: a 66 K SNP Chip for Cashmere Goat
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix