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Research 541–570 of 1000+
- 1032 Characterization of the human scalp hair follicle microbiome reveals differential spatial distribution, abundance and viability of intrafollicular microbiota and modulation of hair growth and metabolism by staphylococcus epidermidis
- Defining compartmentalized stem and progenitor populations with distinct cell division frequency in the ocular surface epithelium
- Single-cell sequencing reveals the intermediate cell state and function of dermal papilla cells in the hair follicle cycle of cashmere goats
- Decision letter: Sphingosine 1-phosphate-regulated transcriptomes in heterogenous arterial and lymphatic endothelium of the aorta
- The post-terminal differentiation fate of RNAs revealed by next-generation sequencing
- Hair Straightening
- EZH1 and EZH2 cogovern histone H3K27 trimethylation and are essential for hair follicle homeostasis and wound repair
- Clinical Findings, Cutaneous Pathology, and Response to Therapy in 21 Patients With Keratosis Pilaris Atrophicans
- Characterizing Wool Keratin
- The Enzymic Derivation of Citrulline Residues from Arginine Residues In Situ during the Biosynthesis of Hair Proteins that are Cross-Linked by Isopeptide Bonds
- HAIR KERATINIZATION IN HEALTH AND DISEASE
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Changes in the Molecular Structure of Hair in Insulin-Dependent Diabetes
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Finasteride administration potentiates the disruption of prepulse inhibition induced by forced swim stress
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- Exploring imputation performance of phenotype-associated SNPs for forensic prediction models
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- Deciphering gene regulatory programs in mouse embryonic skin through single-cell multiomics analysis
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Deciphering the function of canonical Wnt signals in development and disease: conditional loss- and gain-of-function mutations of β-catenin in mice
- Skin shedding and tissue regeneration in African spiny mice (Acomys)
- Defining stem cell dynamics and migration during wound healing in mouse skin epidermis
- Fibroblast heterogeneity: implications for human disease
- Tracking adult stem cells
- Epigenetic control of adult stem cell function
- Epithelial stem cells and implications for wound repair