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Research 991–1000 of 1000+
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Characterization of a Cluster of Human High/Ultrahigh Sulfur Keratin-associated Protein Genes Embedded in the Type I Keratin Gene Domain on Chromosome 17q12-21
- Hyperandrogenism and Polycystic Ovary Syndrome in Women with Type 1 Diabetes Mellitus
- Nonsteroidal inhibitors of human type I steroid 5-.alpha.-reductase
- Type II Keratins Are Phosphorylated on a Unique Motif during Stress and Mitosis in Tissues and Cultured Cells
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Structure of human type II 5 alpha-reductase gene
- Characterization of a 190-Kilobase Pair Domain of Human Type I Hair Keratin Genes
- Novel Type I Hair Keratins K39 and K40 Are the Last to be Expressed in Differentiation of the Hair: Completion of the Human Hair Keratin Catalog