Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Nelli Markova"'
Publikováno v:
Journal of Biological Chemistry. 271:4561-4568
The transglutaminase 3 enzyme is expressed during the late stages of the terminal differentiation of the epidermis and in certain cell types of the hair follicle. The enzyme is thought to be critically involved in the cross-linking of structural prot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c602235e10de5e591cacbfc2c5d208d2
https://doi.org/10.1074/jbc.271.8.4561
https://doi.org/10.1074/jbc.271.8.4561
Autor:
David J. Hamrock, Peter M. Steinert, Lyuben N. Marekov, Vincenzo De Laurenzi, Geraldine R. Rogers, William B. Rizzo, Nelli Markova, John G. Compton
Publikováno v:
Nature Genetics. 12:52-57
Sjögren-Larsson syndrome (SLS) is an inherited neurocutaneous disorder characterized by mental retardation, spasticity and ichthyosis. SLS patients have a profound deficiency in fatty aldehyde dehydrogenase (FALDH) activity. We have now cloned the h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cd4f52ca2df852f940ea763959d0a87
https://doi.org/10.1038/ng0196-52
https://doi.org/10.1038/ng0196-52
Autor:
Constantin C. Chipev, Song-Qing Gan, Lyuben N. Marekov, Nelli Markova, William W. Idler, Peter M. Steinert
Publikováno v:
Molecular and cellular biology. 13(1)
Profilaggrin is a major highly phosphorylated protein component of the keratohyalin granules of mammalian epidermis. It contains 10 to 12 tandemly repeated filaggrin units and is processed into the intermediate filament-associated protein filaggrin b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14cc1a4b5d2400e115d113eee64bf2ba
https://pubmed.ncbi.nlm.nih.gov/8417356
https://pubmed.ncbi.nlm.nih.gov/8417356
Autor:
Nelli Markova, Gael Carney, William B. Rizzo, Peter M. Steinert, Edit Tarcsa, John G. Compton, Sherri J. Bale, Lyuben N. Marekov, Vincenzo De Laurenzi, Geraldine R. Rogers
Publikováno v:
Journal of Investigative Dermatology. (1):79-83
Sjogren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by congenital ichthyosis, mental retardation, and spastic diplegia or tetraplegia. Patients with SLS have deficient activity of fatty aldehyde dehydrogenase (FALDH), an e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8387f6a6a62b230a56b79506cf925779
Publikováno v:
In Journal of the American Academy of Dermatology 2009 60(3) Supplement 1:AB156-AB156
Publikováno v:
In Journal of the American Academy of Dermatology 2009 60(3) Supplement 1:AB152-AB152
Publikováno v:
In Journal of the American Academy of Dermatology 2009 60(3) Supplement 1:AB79-AB79
Publikováno v:
In Journal of the American Academy of Dermatology 2008 58(2) Supplement 2:AB110-AB110
Publikováno v:
In Journal of the American Academy of Dermatology 2008 58(2) Supplement 2:AB64-AB64