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Research 361–390 of 1000+
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Cutaneous manifestations associated with COVID-19 infection at a university hospital in eastern China
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Efficacy of modern methods for assessing the severity of alopecia areata
- Identification and expression of the target gene SLC24A2 of oar-miR-377 and its novel SNPs effects on wool traits in sheep
- Androgen receptor gene polymorphism and biological age markers in men
- Integrative Whole-Transcriptome Sequencing Analysis of Skin Tissues with Different Coat Types in Cashmere Goats Across Stages of Hair Follicle Development
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- 313 Different polyamine levels in the vertex and occipital hair of pattern hair loss patients
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- miR-200a Targets PITX2 to Mediate Goose Fibroblast Proliferation Through the Wnt Pathway
- Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Keratin disorders: from gene to therapy
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- 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
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus