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Research 61–90 of 866
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Signaling Involved in Hair Follicle Morphogenesis and Development
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Hairless down-regulates expression of Msx2 and its related target genes in hair follicles
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Integrative skin phenotypic and transcriptomic analyses reveal candidate genes for coat color and fiber length in four Chinese goat breeds (<i>Capra hircus</i>)
- Network analysis reveals potential mechanisms that determine the cellular identity of keratinocytes and corneal epithelial cells through the Hox/Gtl2-Dio3 miRNA axis
- Expression of fox-related genes in the skin follicles of Inner Mongolia cashmere goat
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Screened of long non-coding RNA related to wool development and fineness in Gansu alpine fine-wool sheep
- Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak
- Structure and expression of the ovine Hoxc-13 gene
- miR-150 regulates endothelial progenitor cell differentiation via Akt and promotes thrombus resolution
- Molecular Mechanisms Regulating Hair Follicle Development
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Current Genetics in Hair Diseases
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- Epstein-Barr virus associated with high-grade B-cell lymphoma in nude severe combined immunodeficiency
- Pathogenesis and management of TRPV3-related Olmsted syndrome