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Research 511–540 of 1000+
- Single-cell chromatin landscapes of mouse skin development
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Nuclear Topology, Epigenetics, and Keratinocyte Differentiation
- Early prediction of alopecia areata using machine learning modeling of neuro stress immune signatures from multi datasets
- Genome-wide DNA methylation and transcriptome analyses reveal the key gene for wool type variation in sheep
- Combination of Transcriptomics and Proteomics Reveals Differentially Expressed Genes and Proteins in the Skin of EDAR Gene-Targeted and Wildtype Cashmere Goats
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Diversity of Adult Stem Cell Niches in the Dermal Compartment of Skin
- Enhanced Differentiation Potential of Pigmented Human Epidermal Equivalents
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions
- Photo-downregulation of SIRT4 mitigates aging in mice by enhancing H3K9ac via fatty acid metabolism
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Tangled Causes, Targeted Solutions: A Comprehensive Review of Alopecia.
- Gene expression of FOXA1 and CCL2 in different phenotypes of infertile women with polycystic ovarian syndrome
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- 165 Single-cell RNA sequencing analysis unveils highly active yet diminished CD14+CD16- circulating monocytes, independent of alopecia areata severity
- TNC+ fibroblasts involve in skin inflammation via neuro-immune and interacting with T cells
- Molecular Mechanisms Affecting Development of Animal Fibers and Some Studies on Goats
- PA15 Becker naevus syndrome associated with a mosaic pathogenic variant in <i>ACTB</i>
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Recent advances in neuropeptide-related omics and gene editing: Spotlight on NPY and somatostatin and their roles in growth and food intake of fish
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation