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Research 91–120 of 1000+
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- Variation in the ovine trichohyalin gene and its association with wool curvature
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Identification of the Ovine Keratin-Associated Protein 26-1 Gene and Its Association with Variation in Wool Traits
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Exploring Variation in Ovine KRTAP19-5 and Its Effect on Fine Wool Fibre Curvature in Chinese Tan Sheep
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- BJD Editor's Choice
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Coming of Age of Melanogenesis-Related Proteins
- Ovine KRTAP36-2: A New Keratin-Associated Protein Gene Related to Variation in Wool Yield
- Genetic, hormonal and metabolic aspects of PCOS: an update
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Australasian Society for Dermatology Research Meeting, May 2006
- What does acne genetics teach us about disease pathogenesis?
- [The effect of cgVEGF164 on the growth of murine hair follicles].
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Nucleic acid-induced chemokine expression in keratinocytes: Implications for skin inflammation
- Expression of vascular endothelial growth factor (VEGF) in various compartments of the human hair follicle
- Strategies for High-Efficiency Mutation Using the CRISPR/Cas System