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Research 181–210 of 1000+
- Compilation of a comprehensive gene panel for systematic assessment of genes that govern an individual’s drug responses
- Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Identification of the Ovine Keratin-Associated Protein 26-1 Gene and Its Association with Variation in Wool Traits
- Insights into Male Androgenetic Alopecia: Differential Gene Expression Profiling of Plucked Hair Follicles and Integration with Genetic Data
- Variation in the ovine keratin-associated protein 15-1 gene affects wool yield
- Ovine KRTAP36-2: A New Keratin-Associated Protein Gene Related to Variation in Wool Yield
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Identification of a Novel Missense Mutation in the Fibroblast Growth Factor 5 Gene Associated with Longhair in the Maine Coon Cat
- Autosomal Dominant Obstructive Sleep Apnea Syndrome Due to the New Variant c.980_984dup in COL1A2: A Case Report
- Finding bald spots on chromosome 20p11
- <i>WNT10A</i> , dermatology and dentistry
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
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- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- The impact of certain genetic variants (single nucleotide polymorphisms) on incidence and severity of COVID‐19
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Integrated single-cell chromatin and transcriptomic analyses of human scalp reveal etiological insights into genetic risk for hair and skin disease
- Unravelling the threads of central centrifugal cicatricial alopecia
- Spectrum of Phenotypes Associated with Human MC1R Variations
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- Sequence Variation in Caprine KRTAP6-2 Affects Cashmere Fiber Diameter
- Oral gabapentin for scalp pruritus in patients with lichen planopilaris: A case series
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype