Matches in Nanopublications for { ?s ?p "[We found that in a mouse model of the human lysosomal storage disease GM1-gangliosidosis, GM1-ganglioside accumulates in the glycosphingolipid-enriched microdomain (GEM) fractions of MAMs, where it interacts with the phosphorylated form of IP3 receptor-1, influencing the activity of this channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP340858.RAue82Ews68KGIN5ksrtvDBMhHybXI5XwL-Rgk-DZ64Vk130_assertion description "[We found that in a mouse model of the human lysosomal storage disease GM1-gangliosidosis, GM1-ganglioside accumulates in the glycosphingolipid-enriched microdomain (GEM) fractions of MAMs, where it interacts with the phosphorylated form of IP3 receptor-1, influencing the activity of this channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP340858.RAue82Ews68KGIN5ksrtvDBMhHybXI5XwL-Rgk-DZ64Vk130_provenance.
- NP524268.RADHy1ZKxJ9XF_iKHVia0K2f8qywdl8TMXUXNSfjlo2IM130_assertion description "[We found that in a mouse model of the human lysosomal storage disease GM1-gangliosidosis, GM1-ganglioside accumulates in the glycosphingolipid-enriched microdomain (GEM) fractions of MAMs, where it interacts with the phosphorylated form of IP3 receptor-1, influencing the activity of this channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524268.RADHy1ZKxJ9XF_iKHVia0K2f8qywdl8TMXUXNSfjlo2IM130_provenance.
- NP749492.RAmOvSOsefs7k0pgWXufABOds_N-GGJJ1J9Mi-aQVyCIM130_assertion description "[We found that in a mouse model of the human lysosomal storage disease GM1-gangliosidosis, GM1-ganglioside accumulates in the glycosphingolipid-enriched microdomain (GEM) fractions of MAMs, where it interacts with the phosphorylated form of IP3 receptor-1, influencing the activity of this channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749492.RAmOvSOsefs7k0pgWXufABOds_N-GGJJ1J9Mi-aQVyCIM130_provenance.
- NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_assertion description "[We found that in a mouse model of the human lysosomal storage disease GM1-gangliosidosis, GM1-ganglioside accumulates in the glycosphingolipid-enriched microdomain (GEM) fractions of MAMs, where it interacts with the phosphorylated form of IP3 receptor-1, influencing the activity of this channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP813873.RAnWISAalNpK-QiYFEh6BiFomVwUoirkolrFKgw2afUWI130_provenance.
- NP833008.RAhu7a1QYVlnG9xpEqfX5qjHIB3iObyhquA0kx_kI92FE130_assertion description "[We found that in a mouse model of the human lysosomal storage disease GM1-gangliosidosis, GM1-ganglioside accumulates in the glycosphingolipid-enriched microdomain (GEM) fractions of MAMs, where it interacts with the phosphorylated form of IP3 receptor-1, influencing the activity of this channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833008.RAhu7a1QYVlnG9xpEqfX5qjHIB3iObyhquA0kx_kI92FE130_provenance.
- NP499112.RAQsWJ3hlUM0KNhcD9cA_j4WepdTGDOSEoqvtQqXin6kQ130_assertion description "[We found that in a mouse model of the human lysosomal storage disease GM1-gangliosidosis, GM1-ganglioside accumulates in the glycosphingolipid-enriched microdomain (GEM) fractions of MAMs, where it interacts with the phosphorylated form of IP3 receptor-1, influencing the activity of this channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499112.RAQsWJ3hlUM0KNhcD9cA_j4WepdTGDOSEoqvtQqXin6kQ130_provenance.
- NP583505.RAaGgNrM9MFftoWnmApP2VXwN0LcirVRphTjw2sIWIBZk130_assertion description "[We found that in a mouse model of the human lysosomal storage disease GM1-gangliosidosis, GM1-ganglioside accumulates in the glycosphingolipid-enriched microdomain (GEM) fractions of MAMs, where it interacts with the phosphorylated form of IP3 receptor-1, influencing the activity of this channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583505.RAaGgNrM9MFftoWnmApP2VXwN0LcirVRphTjw2sIWIBZk130_provenance.
- NP435641.RAwH3gRpGXAqS4tHYelZFXVrDmyAY651dpEfQiU_MpNbM130_assertion description "[We found that in a mouse model of the human lysosomal storage disease GM1-gangliosidosis, GM1-ganglioside accumulates in the glycosphingolipid-enriched microdomain (GEM) fractions of MAMs, where it interacts with the phosphorylated form of IP3 receptor-1, influencing the activity of this channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435641.RAwH3gRpGXAqS4tHYelZFXVrDmyAY651dpEfQiU_MpNbM130_provenance.
- NP608441.RA9sVbXFvsaNzNqTSUV9eE1t7xA4y73pmou01doFrQ9M0130_assertion description "[We found that in a mouse model of the human lysosomal storage disease GM1-gangliosidosis, GM1-ganglioside accumulates in the glycosphingolipid-enriched microdomain (GEM) fractions of MAMs, where it interacts with the phosphorylated form of IP3 receptor-1, influencing the activity of this channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP608441.RA9sVbXFvsaNzNqTSUV9eE1t7xA4y73pmou01doFrQ9M0130_provenance.
- NP576184.RAKD4mDZUsw9GdsjT9bbhx9W2YJynSR7-xxpRQjI34Xlg130_assertion description "[We found that in a mouse model of the human lysosomal storage disease GM1-gangliosidosis, GM1-ganglioside accumulates in the glycosphingolipid-enriched microdomain (GEM) fractions of MAMs, where it interacts with the phosphorylated form of IP3 receptor-1, influencing the activity of this channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576184.RAKD4mDZUsw9GdsjT9bbhx9W2YJynSR7-xxpRQjI34Xlg130_provenance.
- assertion description "[We found that in a mouse model of the human lysosomal storage disease GM1-gangliosidosis, GM1-ganglioside accumulates in the glycosphingolipid-enriched microdomain (GEM) fractions of MAMs, where it interacts with the phosphorylated form of IP3 receptor-1, influencing the activity of this channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[We found that in a mouse model of the human lysosomal storage disease GM1-gangliosidosis, GM1-ganglioside accumulates in the glycosphingolipid-enriched microdomain (GEM) fractions of MAMs, where it interacts with the phosphorylated form of IP3 receptor-1, influencing the activity of this channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.