Search
for
Sort by
Research 631–660 of 1000+
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses
- Safety of Whole-Body Abrogation of the TRF1 Shelterin Protein in Wild-Type and Cancer-Prone Mouse Models
- The Mean Staple Length of Wool Fibre Is Associated with Variation in the Ovine Keratin-Associated Protein 21-2 Gene
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodeling
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i>
- Algorithms For Preventive Measures For Disease Prevention And Antioxidant Protection
- Iron Deficiency-Induced Hair Loss Is Associated with ROS-Mediated Disruption of Wnt/β-Catenin Signaling
- Causal relationship between gut microbiota and androgenetic alopecia: A Mendelian randomization study
- Genome-Wide Association Studies of Hair Whorl in Pigs
- Effects of KRTAP20-1 Gene Variation on Wool Traits in Chinese Tan Sheep
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- Association between Family History and Male Androgenetic Alopecia with Female Pattern Hair Loss
- Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31
- Fabrication of Bilayer Nanofibrous-Hydrogel Scaffold from <i>Bacterial Cellulose</i>, <i>PVA</i>, and <i>Gelatin</i> as Advanced Dressing for Wound Healing and Soft Tissue Engineering