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Research 151–180 of 1000+
- Skin aging: mechanisms, evaluation, and rejuvenation
- Molecular Mechanisms Affecting Development of Animal Fibers and Some Studies on Goats
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Biology of Human Hair: Know Your Hair to Control It
- HAIR KERATINIZATION IN HEALTH AND DISEASE
- Transcriptomics sequencing reveals Qu-shi-yu-fa Decoction promotes hair cycle and keratinization by upregulating FOXN1 and TGM3 to treat androgenetic alopecia
- Role of Sulfur Metabolism Gene and High-Sulfur Gene Expression in Wool Growth Regulation in the Cashmere Goat
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- An analysis of gene expression data involving examination of signaling pathways activation reveals new insights into the mechanism of action of minoxidil topical foam in men with androgenetic alopecia
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Drug eruptions in dermatology
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Presence of Uterine Leiomyomas Has No Significant Impact on Gene Expression Profile in the Scalp of Patients with Central Centrifugal Cicatricial Alopecia
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- Correlation Analysis of CXCL10, FOS, HOXC13, and WNT4 Gene Polymorphisms with Key Economic Traits—Initial Population Screening for Jiangnan Cashmere Goats
- Understanding the Intricate Pathophysiology of Psoriasis and Related Skin Disorders
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Extracellular vesicles in age-related diseases: disease pathogenesis, intervention, and biomarker
- Screening of Protein Related to Wool Development and Fineness in Gansu Alpine Fine-Wool Sheep