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Research 121–150 of 254
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- Inducing hair follicle neogenesis with secreted proteins enriched in embryonic skin
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Symmetry breaking of tissue mechanics in wound induced hair follicle regeneration of laboratory and spiny mice
- Defining the identity of mouse embryonic dermal fibroblasts
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Morpho‐regulation in diverse chicken feather formation: Integrating branching modules and sex hormone‐dependent morpho‐regulatory modules
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Demethylation of ITGAV accelerates osteogenic differentiation in a blast-induced heterotopic ossification in vitro cell culture model
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Human Fetal Scalp Dermal Papilla Enriched Genes and the Role of R-Spondin-1 in the Restoration of Hair Neogenesis in Adult Mouse Cells
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- The pioneer factor SOX9 competes for epigenetic factors to switch stem cell fates
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- A Tale of Two Haplotypes: The EDA2R/AR Intergenic Region is the Most Divergent Genomic Segment between Africans and East Asians in the Human Genome
- Genetic determinants of skin ageing: a systematic review and meta-analysis of genome-wide association studies and candidate genes
- Distinct mechanisms for sebaceous gland self-renewal and regeneration provide durability in response to injury
- Identification of a Novel Missense Mutation in the Fibroblast Growth Factor 5 Gene Associated with Longhair in the Maine Coon Cat
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- Bioelectric state transitions enable <i>de novo</i> feather bud formation in developing skin
- Somatic mutations distinguish melanocyte subpopulations in human skin
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Nucleic acid-induced chemokine expression in keratinocytes: Implications for skin inflammation