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Research 451–480 of 1000+
- Characterization of the Human Hair Shaft Cuticle–Specific Keratin-Associated Protein 10 Family
- Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- ROBERTSONIAN TRANSLOCATION PATIENT WITH RECURRENT MISCARRIAGE
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Immune mechanisms associated with sex-based differences in severe COVID-19 clinical outcomes
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- Sex- or Gender-specific Differences in the Clinical Presentation, Outcome, and Treatment of SARS-CoV-2
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Dermatologic care of patients with differences of sex development
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- Improving human forensics through advances in genetics, genomics and molecular biology
- Molecular basis of androgen insensitivity
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Androgens and hair loss
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis
- Gene Expression of Mouse S100A3, a Cysteine-Rich Calcium-Binding Protein, in Developing Hair Follicle
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Clinical Case Notes. Tamoxifen optic neuropathy
- Pallister-Killian Syndrome
- SUN-069 A 14 Year Old Female with Primary Amenorrhea
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- Human Hair Keratin‐Associated Proteins (KAPs)