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- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions
- A frameshift mutation in the TRPS1 gene showing a mild phenotype of trichorhinophalangeal syndrome type 1
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Molecular basis of congenital atrichia in humans and mice.
- The abnormal, mis-localizated HR bmh protein associates with members of the protein processing machinery in the cytoplasm
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Comparison of comedolytic effect of benzoyl peroxide and adapalene in rhino mice
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