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Research 571–600 of 1000+
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Differential Expression of miR-93 and miR-21 in Granulosa Cells and Follicular Fluid of Polycystic Ovary Syndrome Associating with Different Phenotypes
- Inducing hair follicle neogenesis with secreted proteins enriched in embryonic skin
- A multi-omic single-cell landscape of perinatal mouse skin maps lineage specification and reveals shared dynamics in human fetal skin
- Comprehensive Program Planning for the Integration of 21st Century Learning Center After-School Programs with Regular Day Programs and Community Partners.
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- 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
- A novel mouse model demonstrates that oncogenic melanocyte stem cells engender melanoma resembling human disease
- Identification of potential key genes and pathways associated with the Pashmina fiber initiation using RNA-Seq and integrated bioinformatics analysis
- Development and Molecular Characterization of Human Placental Mesenchymal Stem Cells from Human Aborted Fetal Tissue as a Model to Study Mechanism of Spontaneous Abortion
- Industry update: the latest developments in the field of therapeutic delivery, July 2018
- Deciphering the cellular landscape and genetic underpinnings of fiber diameter determined by dermal papilla cells in fine-wool sheep
- Amelioration of psoriasis-like skin lesions by human amniotic mesenchymal stem cells: insights from multiomics profiling in mice
- The role of lipids in promoting hair growth through HIF-1 signaling pathway
- Pathway enrichment and network analysis of differentially expressed genes in pashmina goat
- Identification of Distinct Immune Signatures and Chemokine Networks in Scalp Inflammatory Diseases
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- FGF5 is a crucial regulator of hair length in humans
- Identification of Differentially Expressed Genes During a Wool Follicle Growth Cycle Induced by Prolactin
- Transcriptional profiling of putative human epithelial stem cells
- Tissue-Specific Multi-Omics Integration Demonstrates Molecular Signatures Connecting Obesity to Immune Vulnerability
- Transcriptome Sequencing Reveals Differences between Primary and Secondary Hair Follicle-derived Dermal Papilla Cells of the Cashmere Goat (Capra hircus)
- Transcriptomic regulation of seasonal coat color change in hares
- Single-cell transcriptomics defines keratinocyte differentiation in avian scutate scales
- Transcriptome sequencing reveals the key genes associated with hair follicle development in Qianhua Mutton Merino
- Exploring the role of CYP19A1 single nucleotide polymorphisms in the pathogenesis of female pattern hair loss
- Dissecting the genetic variations associated with response to first-line chemotherapy in patients with small cell lung cancer: a retrospective cohort study
- PSXIV-17 Examining Mammary Gland Transcriptomic Profiles Using Rna-Seq in Slick and Wild-Type Haired Holstein Cattle Under Tropical Conditions
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria