Matches in Nanopublications for { ?s ?p "[Hutchinson-Gilford Progeria Syndrome (HGPS) is a premature aging disorder caused by mutations in LMNA, which encodes the nuclear scaffold proteins lamin A and C. In HGPS and related progerias, processing of prelamin A is blocked at a critical step mediated by the zinc metalloprotease ZMPSTE24.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP336486.RA3x_nj_SjeFK4yzqN2RG-7sy-hAO2xMnR1yyKWfE-aiY130_assertion description "[Hutchinson-Gilford Progeria Syndrome (HGPS) is a premature aging disorder caused by mutations in LMNA, which encodes the nuclear scaffold proteins lamin A and C. In HGPS and related progerias, processing of prelamin A is blocked at a critical step mediated by the zinc metalloprotease ZMPSTE24.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP336486.RA3x_nj_SjeFK4yzqN2RG-7sy-hAO2xMnR1yyKWfE-aiY130_provenance.
- NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_assertion description "[Hutchinson-Gilford Progeria Syndrome (HGPS) is a premature aging disorder caused by mutations in LMNA, which encodes the nuclear scaffold proteins lamin A and C. In HGPS and related progerias, processing of prelamin A is blocked at a critical step mediated by the zinc metalloprotease ZMPSTE24.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_provenance.
- NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_assertion description "[Hutchinson-Gilford Progeria Syndrome (HGPS) is a premature aging disorder caused by mutations in LMNA, which encodes the nuclear scaffold proteins lamin A and C. In HGPS and related progerias, processing of prelamin A is blocked at a critical step mediated by the zinc metalloprotease ZMPSTE24.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_provenance.
- NP1077146.RAiNQbWxO8GelGfe6qVtYQy-1fi556a3rUp1ziZypEEVg130_assertion description "[Hutchinson-Gilford Progeria Syndrome (HGPS) is a premature aging disorder caused by mutations in LMNA, which encodes the nuclear scaffold proteins lamin A and C. In HGPS and related progerias, processing of prelamin A is blocked at a critical step mediated by the zinc metalloprotease ZMPSTE24.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1077146.RAiNQbWxO8GelGfe6qVtYQy-1fi556a3rUp1ziZypEEVg130_provenance.