Zobrazeno 1 - 3
of 3
pro vyhledávání: '"L J Stoltzfus"'
Autor:
J K Bielicki, T M Forte, M R McCall, L J Stoltzfus, G Chiesa, C R Sirtori, G Franceschini, E M Rubin
Publikováno v:
Journal of Lipid Research, Vol 38, Iss 11, Pp 2314-2321 (1997)
Human carriers of apolipoprotein A-I(Milano) (Arg173 –> Cys substitution in apolipoprotein A-I) are characterized by an HDL deficiency in which small, dense HDL accumulate in plasma. Because affected individuals are heterozygous for this mutation,
Externí odkaz:
https://doaj.org/article/d5ace512eee243eaa4b49d2f0477d099
Autor:
L J Stoltzfus, Giulia Chiesa, C R Sirtori, G Franceschini, Trudy M. Forte, John K. Bielicki, Mark R. McCall, Edward M. Rubin
Publikováno v:
Journal of Lipid Research, Vol 38, Iss 11, Pp 2314-2321 (1997)
Human carriers of apolipoprotein A-I(Milano) (Arg173 --> Cys substitution in apolipoprotein A-I) are characterized by an HDL deficiency in which small, dense HDL accumulate in plasma. Because affected individuals are heterozygous for this mutation, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2324fcbed9de3da55f99d19aa9d23df5
http://www.sciencedirect.com/science/article/pii/S0022227520349452
http://www.sciencedirect.com/science/article/pii/S0022227520349452
Autor:
L J, Stoltzfus, B, Sosa-Pineda, S M, Moskowitz, K P, Menon, B, Dlott, L, Hooper, D B, Teplow, R M, Shull, E F, Neufeld
Publikováno v:
The Journal of biological chemistry. 267(10)
alpha-L-Iduronidase is a lysosomal enzyme, the deficiency of which causes mucopolysaccharidosis I (MPS I); a canine MPS I colony has been bred to test therapeutic intervention. The enzyme was purified to apparent homogeneity from canine testis and fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d751fa44daa6b4104d11faa0956837a0
https://pubmed.ncbi.nlm.nih.gov/1551868
https://pubmed.ncbi.nlm.nih.gov/1551868