Search
for
Sort by
Research 721–750 of 1000+
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Genomic Analysis of Trichotillomania
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Phytochemicals of Alpinia zerumbet: A Review
- Pigmentary mosaicism: An update
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Genome-wide association study reveals candidate genes associated with body weight and wool traits in Ordos fine-wool sheep
- miR-200a Targets PITX2 to Mediate Goose Fibroblast Proliferation Through the Wnt Pathway
- Molecular mechanisms underlying cashmere quality differences between Jiangnan cashmere goats and Changthangi pashmina goats
- Light-Emitting Hair Follicles: Studying Skin Regeneration With In Vivo Imaging
- Cyberspace Chat
- Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Metformin therapy for the reproductive and metabolic consequences of polycystic ovary syndrome
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Chronic Overlapping Pain Conditions and Nociplastic Pain
- Algorithms For Preventive Measures For Disease Prevention And Antioxidant Protection
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- FOXN1 deficient nude severe combined immunodeficiency
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Predicting Human Appearance from DNA for Forensic Investigations
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits