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pro vyhledávání: '"Revekka L. Boguslavsky"'
Publikováno v:
Human Molecular Genetics. 15:653-663
Mutations in the LMNA gene encoding A-type lamins cause several diseases, including Emery-Dreifuss muscular dystrophy and Dunnigan-type familial partial lipodystrophy (FPLD). We analyzed differentiation of 3T3-L1 preadipocytes to adipocytes in cells
Autor:
Karima Djabali, Christina Pedicelli, Dayle McClintock, Mauro Paradisi, Revekka L. Boguslavsky, Howard J. Worman
Publikováno v:
BMC Cell Biology. 6:27
Hutchinson-Gilford progeria syndrome (HGPS, OMIM 176670) is a rare sporadic disorder with an incidence of approximately 1 per 8 million live births. The phenotypic appearance consists of short stature, sculptured nose, alopecia, prominent scalp veins