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Research 361–390 of 1000+
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- The Mean Staple Length of Wool Fibre Is Associated with Variation in the Ovine Keratin-Associated Protein 21-2 Gene
- Pseudallescheria boydii infection associated with IgG4-related disease
- Polymorphism of keratin-associated protein (KAP) 7 gene and its association with wool traits in Rambouillet sheep
- Abstracts
- Post SARS-CoV-2 vaccination effluvium
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Why were Sardinians the shortest Europeans? A journey through genes, infections, nutrition, and sex
- Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
- Australasian Society for Dermatology Research Meeting, May 2006
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Ugreelig hår
- Alopecias: Practical Tips for the Management of Biopsies and Main Diagnostic Clues for General Pathologists and Dermatopathologists
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Senescence-accelerated Mouse (SAM): With Special Reference to Development and Pathobiological Phenotypes
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- Different Patterns of Lichen Planus in Three Members of One Family
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- An Updated Nomenclature for Keratin-Associated Proteins (KAPs)
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes
- Therapeutics of premature hair graying: A long journey ahead
- ACE1 rs1799752 polymorphism is not associated with long-COVID symptomatology in previously hospitalized COVID-19 survivors
- A Powerful Method for Pleiotropic Analysis under Composite Null Hypothesis Identifies Novel Shared Loci Between Type 2 Diabetes and Prostate Cancer