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Research 301–330 of 1000+
- Interpretation of the Yak Skin Single-Cell Transcriptome Landscape
- Multi-omics analysis of functional substances and expression verification in cashmere fineness
- A missense mutation in Lama3 causes androgen alopecia
- Keratinocytes of the Upper Epidermis and Isthmus of Hair Follicles Express Hemoglobin mRNA and Protein
- The Rho GTPase exchange factor Vav2 promotes extensive age-dependent rewiring of the hair follicle stem cell transcriptome
- Novel Insights to Assess Climate Resilience in Goats Using a Holistic Approach of Skin-Based Advanced NGS Technologies
- Transcriptomic Analysis Reveals Candidate Ligand-Receptor Pairs and Signaling Networks Mediating Intercellular Communication between Hair Matrix Cells and Dermal Papilla Cells from Cashmere Goats
- Nanotechnology-Based Strategies for Hair Follicle Regeneration in Androgenetic Alopecia
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- Fibrotic enzymes modulate wound‐induced skin tumorigenesis
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Prevention of Male Late-Onset Hypogonadism by Natural Polyphenolic Antioxidants
- UDP-GlcNAc-1-Phosphotransferase Is a Clinically Important Regulator of Human and Mouse Hair Pigmentation
- Hair follicles modulate skin barrier function
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Examination of epigenetic inhibitor zebularine in treatment of skin wounds in healthy and diabetic mice
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Hedgehog Signaling in Papillary Fibroblasts Is Essential for Hair Follicle Regeneration during Wound Healing
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction
- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- Skin regional specification and higher-order <i>HoxC</i> regulation
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Combined Systemic and Cutaneous Ovalbumin–Aluminum Sensitization Triggers Thermal Hyperalgesia, Spinal Gliosis, and Nociceptive Nerve Fibers Sprouting in Mice