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Research 151–180 of 730
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- A novel human type I hair keratin gene: evidence for two keratin hHa3 isoforms
- 197 A novel splice site mutation in LIPH identified in a Japanese patient with autosomal recessive woolly hair
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Transcription Regulation and Protein Subcellular Localization of the Truncated Basic Hair Keratin hHb1-ΔN in Human Breast Cancer Cells
- Hoxc13 Expression Pattern in Cashmere Goat Skin During Hair Follicle Development
- Lipin 1 Gene Polymorphisms in Polycystic Ovary Syndrome
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- ЭКСПЕРИМЕНТАЛЬНОЕ ОБОСНОВАНИЕ ПРИМЕНЕНИЯ ШОВНЫХ МАТЕРИАЛОВ ПРИ ОПЕРАЦИИ “УДАЛЕНИЕ ЗУБА”
- Pmg-1 and Pmg-2 constitute a novel family of KAP genes differentially expressed during skin and mammary gland development
- Evolution of Trichocyte Keratins
- Variation in the ovine trichohyalin gene and its association with wool curvature
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Skin regional specification and higher-order <i>HoxC</i> regulation
- Structure of human type II 5 alpha-reductase gene.
- Structure of human type II 5 alpha-reductase gene
- Hair follicle differentiation: expression, structure and evolutionary conservation of the hair type II keratin intermediate filament gene family
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- A Girl with a Novel Splice Site Mutation in <i>VDR</i> Supports the Role of a Ligand-Independent VDR Function on Hair Cycling
- Structure and expression of the ovine Hoxc-13 gene
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Updated mutational spectrum and genotype-phenotype correlations in ichthyosis patients with ABCA12 pathogenic variants
- Is polymorphism of the STK11 gene a predictor of response to metformin in polycystic ovarian syndrome?
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Some Tensile Properties of Specialty Hair Fibers
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Telogen Effluvium due to Recombinant Interferon α-2b
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- CUTANEOUS T-CELL LYMPHOMA