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Research 361–390 of 1000+
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Differential expression of steroid 5α-reductase isozymes and association with disease severity and angiogenic genes predict their biological role in prostate cancer
- Identification and dissection of an enhancer controlling epithelial gene expression in skin
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Candidate genes of SARS-CoV-2 gender susceptibility
- Analysis of Sequences Controlling Tissue-Specific and Hyperproliferation-Related Keratin 6 Gene Expression in Transgenic Mice
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Fibroproliferative genes are preferentially expressed in central centrifugal cicatricial alopecia
- Human gene correlation analysis (HGCA): A tool for the identification of transcriptionally co-expressed genes
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Evaluation of androgen receptor gene as a candidate gene in female androgenetic alopecia
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Signaling and Gene Expression for Water-Tolerant Legume Nodulation
- Pmg-1 and Pmg-2 constitute a novel family of KAP genes differentially expressed during skin and mammary gland development
- A novel human type I hair keratin gene: evidence for two keratin hHa3 isoforms
- A curated catalog of canine and equine keratin genes
- Planar cell polarity effector gene Intu regulates cell fate-specific differentiation of keratinocytes through the primary cilia
- Identification of novel glucocorticoid receptor-regulated genes involved in epidermal homeostasis and hair follicle differentiation
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Effect of the FA2H Gene on cashmere fineness of Jiangnan cashmere goats based on transcriptome sequencing
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Production of artificial synthetic spidroin gene 4S-transgenic cloned sheep embryos using somatic cell nuclear transfer
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Hidradenitis Suppurativa and Comorbid Disorder Biomarkers, Druggable Genes, New Drugs and Drug Repurposing—A Molecular Meta-Analysis
- The Genetics of Seborrheic Dermatitis: A Candidate Gene Approach and Pilot Genome-Wide Association Study
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- Androgen Receptor (<i>AR</i>) Gene (CAG)n and (GGN)n Length Polymorphisms and Symptoms in Young Males With Long-Lasting Adverse Effects After Finasteride Use Against Androgenic Alopecia
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia