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Research 61–90 of 1000+
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- The Genetics of Human Skin Disease
- Alopecia in Epidermolysis Bullosa
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Expression Profiling Reveals Genes Involved in the Regulation of Wool Follicle Bulb Regression and Regeneration in Sheep
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- 9. Immunology and Genetics
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- The keratin 19 promoter is potent for cell-specific targeting of genes in transgenic mice
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Skin abnormalities generated by temporally controlled RXRα mutations in mouse epidermis
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- The Type I Keratin 19 Possesses Distinct and Context-dependent Assembly Properties
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- Interleukin-1 Induces Transcription of Keratin K6 in Human Epidermal Keratinocytes
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- iTRAQ-based quantitative proteomics revealing the therapeutic mechanism of a medicinal and edible formula YH0618 in reducing doxorubicin-induced alopecia by targeting keratins and TGF-β/Smad3 pathway
- Adsorption of Diclofenac and PFBS on a Hair Keratin Dimer
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease