검색결과 : 18건
| No. | Article |
|---|---|
| 1 |
A polylysine-polyhistidine fusion peptide for lysosome-targeted protein delivery Iwasaki T, Murakami N, Kawano T Biochemical and Biophysical Research Communications, 533(4), 905, 2020 |
| 2 |
Lysosomal integral membrane protein type-2 (LIMP-2/SCARB2) is a substrate of cathepsin-F, a cysteine protease mutated in type-B-Kufs-disease Peters J, Rittger A, Weisner R, Knabbe J, Zunke F, Rothaug M, Damme M, Berkovic SF, Blanz J, Saftig P, Schwake M Biochemical and Biophysical Research Communications, 457(3), 334, 2015 |
| 3 |
Does Lysosomial Acid Lipase Reduction Play a Role in Adult Non-Alcoholic Fatty Liver Disease? Baratta F, Pastori D, Polimeni L, Tozzi G, Violi F, Angelico F, Del Ben M International Journal of Molecular Sciences, 16(12), 28014, 2015 |
| 4 |
Expression and functional characterization of human lysosomal acid lipase gene (LIPA) mutation responsible for cholesteryl ester storage disease (CESD) phenotype Rajamohan F, Reyes AR, Ruangsiriluk W, Hoth LR, Han S, Caspers N, Tu MH, Ward J, Kurumbail RG Protein Expression and Purification, 110, 22, 2015 |
| 5 |
Deletion of sterol O-acyltransferase 2 (SOAT2) function in mice deficient in lysosomal acid lipase (LAL) dramatically reduces esterified cholesterol sequestration in the small intestine and liver Lopez AM, Posey KS, Turley SD Biochemical and Biophysical Research Communications, 454(1), 162, 2014 |
| 6 |
Inherent lipid metabolic dysfunction in glycogen storage disease IIIa Li XH, Gong QM, Ling Y, Huang C, Yu DM, Gu LL, Liao XW, Zhang DH, Hu XQ, Han Y, Kong XF, Zhang XX Biochemical and Biophysical Research Communications, 455(1-2), 90, 2014 |
| 7 |
Subclinical myopathy in a child with neutral lipid storage disease and mutations in the PNPLA2 gene Fiorillo C, Brisca G, Cassandrini D, Scapolan S, Astrea G, Valle M, Scuderi F, Trucco F, Natali A, Magnano G, Gazzerro E, Minetti C, Arca M, Santorelli FM, Bruno C Biochemical and Biophysical Research Communications, 430(1), 241, 2013 |
| 8 |
The adult polyglucosan body disease mutation GBE1 c.1076A > C occurs at high frequency in persons of Ashkenazi Jewish background Hussain A, Armistead J, Gushulak L, Kruck C, Pind S, Triggs-Raine B, Natowicz MR Biochemical and Biophysical Research Communications, 426(2), 286, 2012 |
| 9 |
Immortalization of murine muscle cells from lysosomal alpha-glucosidase deficient mice: A new tool to study pathophysiology and assess therapeutic strategies for Pompe disease Douillard-Guilloux G, Mouly V, Caillaud C, Richard E Biochemical and Biophysical Research Communications, 388(2), 333, 2009 |
| 10 |
Clinical and genetic characterization of Chanarin-Dorfman syndrome Bruno C, Bertini E, Di Rocco M, Cassandrini D, Ruffa G, De Toni T, Seri M, Spada M, Volti GL, D'Amico A, Trucco F, Arca M, Casali C, Angelini C, DiMauro S, Minetti C Biochemical and Biophysical Research Communications, 369(4), 1125, 2008 |