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- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Upregulation of the truncated basic hair keratin 1(hHb1‐ΔN) in carcinoma cells by Epstein‐Barr virus (EBV)
- Transcription Regulation and Protein Subcellular Localization of the Truncated Basic Hair Keratin hHb1-ΔN in Human Breast Cancer Cells
- Expression of a truncated form of hHb1 hair keratin in human breast carcinomas
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
- <i>De novo</i> mutations in monilethrix
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix
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