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Research 751–780 of 1000+
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Forensic DNA Phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Case report: NUDT15 polymorphism and severe azathioprine-induced myelosuppression in a young Chinese female with systematic lupus erythematosus: a case analysis and literature review
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- RNA-seq analysis identifies key genes enhancing hoof strength to withstand barefoot racing in Standardbred trotters
- Molecular monitoring of short- and long-term transcriptional effects of hair growth stimulating agents
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Gene-Environment Interaction Between <i>CYP1B1</i> and Oral Contraception on Frontal Fibrosing Alopecia
- Risk factors for the development of and outcomes after diagnosis of autoimmune alopecia areata in patients with inflammatory bowel diseases
- Enhancing diagnostic yield of monogenic diabetes through phenotypic and molecular reanalysis of 128 individuals with young onset hyperglycemia: highlighting the significance of accurate case characterization
- A missense mutation in Lama3 causes androgen alopecia
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Myotonic dystrophy type 1
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Peroxisome Proliferator Activated Receptors Gamma Serum levels and Gene Polymorphism in Frontal Fibrosing Alopecia: A Case Control Study
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Male pattern baldness
- 10-Year-Old Female with an Irregularly Shaped Patch of Hair Loss
- Melasma and Endocrine Disorders
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Identification of the cell lineage at the origin of basal cell carcinoma
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- What’s Sex Got to Do With COVID-19? Gender-Based Differences in the Host Immune Response to Coronaviruses
- Fluorescence Microscopy—An Outline of Hardware, Biological Handling, and Fluorophore Considerations
- Obesity and polycystic ovary syndrome
- Androgenetic alopecia: An update
- Anabolic androgenic steroids and carcinogenicity focusing on Leydig cell: a literature review
- Alopecia areata update
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA