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Research 691–720 of 812
- Hair toxic and essential trace elements in children with autism spectrum disorder
- When whorls collide: the development of hair patterns in frizzled 6 mutant mice
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Immune-Epithelial Cross Talk in Regeneration and Repair
- Efficient In Vivo Targeting of Epidermal Stem Cells by Early Gestational Intraamniotic Injection of Lentiviral Vector Driven by the Keratin 5 Promoter
- Hair, Wool, Quill, Nail, Claw, Hoof, and Horn
- Pericyte Plasticity in the Brain
- Hair Shaft Abnormalities – Clues to Diagnosis and Treatment
- RANKL Induces Organized Lymph Node Growth by Stromal Cell Proliferation
- Myotonic Dystrophy—A Progeroid Disease?
- Comprehensive analysis of circRNAs from cashmere goat skin by next generation RNA sequencing (RNA-seq)
- NG2 Proteoglycan Expression in Mouse Skin: Altered Postnatal Skin Development in the NG2 Null Mouse
- Neuregulin3 alters cell fate in the epidermis and mammary gland
- Transcriptome Reveals Long Non-coding RNAs and mRNAs Involved in Primary Wool Follicle Induction in Carpet Sheep Fetal Skin
- Ichthyosis with confetti: clinics, molecular genetics and management
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- FOXN1 deficient nude severe combined immunodeficiency
- Identification of skin-expressed genes possibly associated with wool growth regulation of Aohan fine wool sheep
- Wound healing in development
- Activated Kras Alters Epidermal Homeostasis of Mouse Skin, Resulting in Redundant Skin and Defective Hair Cycling
- Neonatal finasteride induces anxiogenic-like profile and deteriorates passive avoidance in adulthood after intrahippocampal neurosteroid administration
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Developmental genetics of color pattern establishment in cats
- Teratogenic effect of isotretinoin in both fertile females and males (Review)
- The role of metabolism in cellular quiescence