Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP529296.RA9Wg9nvfPJgSpqg3oNS48xUtniV26tczwLlHhpzs_Ms0130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP529296.RA9Wg9nvfPJgSpqg3oNS48xUtniV26tczwLlHhpzs_Ms0130_provenance.
• NP575776.RA8kiMJJFY8H3VptFswp_7PzQVxY731K-5RbMBUKcCNZw130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575776.RA8kiMJJFY8H3VptFswp_7PzQVxY731K-5RbMBUKcCNZw130_provenance.
• assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP670783.RA8c4TKD0i5NfnH8qpr4qhZmLG4GwvKjbB81uqvZLXyXc130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670783.RA8c4TKD0i5NfnH8qpr4qhZmLG4GwvKjbB81uqvZLXyXc130_provenance.
• NP371471.RAXNO7M9TB7JY73iKjlenar42nrUBUFusuiG9qSuGbiyQ130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371471.RAXNO7M9TB7JY73iKjlenar42nrUBUFusuiG9qSuGbiyQ130_provenance.
• NP810416.RARQ0xAAELpANji1rUqpQl27U-fT7YRbo3SZJ6Y20vGw0130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810416.RARQ0xAAELpANji1rUqpQl27U-fT7YRbo3SZJ6Y20vGw0130_provenance.
• assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP519298.RARtf76xk6YcQbFWL8qba6ZI0kT_2PRk9u464rcOcjHP0130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519298.RARtf76xk6YcQbFWL8qba6ZI0kT_2PRk9u464rcOcjHP0130_provenance.
• NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519301.RAR4I_MTcJnar_QLyXSrZlo_XWe2EITBBTcj-FrTVUgqs130_provenance.
• NP519305.RAZKtppXCLldJ2gRteskDzbSjDJSQOnnJ3maFDz5lP800130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519305.RAZKtppXCLldJ2gRteskDzbSjDJSQOnnJ3maFDz5lP800130_provenance.
• NP519307.RAcRg4nUr9fFhAsd6FTUHnMTEoqcfuMbgMBKSwHvMdtN8130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519307.RAcRg4nUr9fFhAsd6FTUHnMTEoqcfuMbgMBKSwHvMdtN8130_provenance.
• NP810402.RAmVBWFMLjJeQPxDfC7jkI_UgxpqjIjwJgFsuwZsNwauI130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810402.RAmVBWFMLjJeQPxDfC7jkI_UgxpqjIjwJgFsuwZsNwauI130_provenance.
• NP810575.RArIQGIssMobMoaJaQlJA5Qb0ekN8ufiOV1NQR2H3zZWk130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810575.RArIQGIssMobMoaJaQlJA5Qb0ekN8ufiOV1NQR2H3zZWk130_provenance.
• NP810592.RAkTbC9lhe5DIpwLpLSTIVdVEJ3ZZ_4KvF4N2omnFcH8Q130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810592.RAkTbC9lhe5DIpwLpLSTIVdVEJ3ZZ_4KvF4N2omnFcH8Q130_provenance.
• NP519296.RAhMDK8q4mXPNaPQHCNOlbQRIwfpEaH6O21P9ocy6Rg6Q130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519296.RAhMDK8q4mXPNaPQHCNOlbQRIwfpEaH6O21P9ocy6Rg6Q130_provenance.
• NP519299.RAiK_rgYc78VQtEGqUhrq4Q8AIXs1qQvDTIuhct36hwbc130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519299.RAiK_rgYc78VQtEGqUhrq4Q8AIXs1qQvDTIuhct36hwbc130_provenance.
• NP921270.RAMwydnlzOLkbs_tY0bpK9KBjr1cY_l1hJx1-dQDf2b9g130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921270.RAMwydnlzOLkbs_tY0bpK9KBjr1cY_l1hJx1-dQDf2b9g130_provenance.
• NP519300.RAoPQokMDp_J5AcOZHNmJBVv28eLvnUSaMXc4tkYZM3mM130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519300.RAoPQokMDp_J5AcOZHNmJBVv28eLvnUSaMXc4tkYZM3mM130_provenance.
• NP519304.RAnRG_ZeacxVMJrPEWyAnTSeGigEqxf6MKjL1KlvYG2Ek130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519304.RAnRG_ZeacxVMJrPEWyAnTSeGigEqxf6MKjL1KlvYG2Ek130_provenance.
• NP371459.RAxeiqswa1c9WegIR9yFDRVoeWereVZ3_ZcPFiziR6rPY130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371459.RAxeiqswa1c9WegIR9yFDRVoeWereVZ3_ZcPFiziR6rPY130_provenance.
• NP371571.RA1FOGR5d50Ga497g1QDSXdKSnjuEvnYqTe8D2kEJMX0Y130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371571.RA1FOGR5d50Ga497g1QDSXdKSnjuEvnYqTe8D2kEJMX0Y130_provenance.
• NP371576.RA7kWLKtEVSanYeSEOpgcwjKrRm3_O6DxP5GsedSRRfvM130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371576.RA7kWLKtEVSanYeSEOpgcwjKrRm3_O6DxP5GsedSRRfvM130_provenance.
• NP810473.RAI76HXEEznc28miozqinToaWjxxwB7cZ2sEfKb4raO4o130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810473.RAI76HXEEznc28miozqinToaWjxxwB7cZ2sEfKb4raO4o130_provenance.
• NP810487.RAGQV_CEjYeYczRTTrcKTGTT_K-vB6BKW4DzJZ-Asuxcw130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810487.RAGQV_CEjYeYczRTTrcKTGTT_K-vB6BKW4DzJZ-Asuxcw130_provenance.
• NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371513.RAOwNgQNwN2bP4Dxl9UjnPS4F3WTskFR6ygSvzADg0RSs130_provenance.
• NP371528.RAI0xezP1HIxH6jmqGBMZhqFgtu5x5WTw_njdeZuxXd18130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371528.RAI0xezP1HIxH6jmqGBMZhqFgtu5x5WTw_njdeZuxXd18130_provenance.
• NP519297.RAPsUHmNO7ehFqDdIrTrC6qTY_HV6TBu57wXu-Pz3puMk130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519297.RAPsUHmNO7ehFqDdIrTrC6qTY_HV6TBu57wXu-Pz3puMk130_provenance.
• NP519302.RAJQzIPCQ9BCpco_NbT_rjVp4haposWaX211h3wBVPuFE130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519302.RAJQzIPCQ9BCpco_NbT_rjVp4haposWaX211h3wBVPuFE130_provenance.
• NP519303.RA4HDob8MZc4_ZobNlRR_it9p37JDjmdoB8B2WazuaJkg130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519303.RA4HDob8MZc4_ZobNlRR_it9p37JDjmdoB8B2WazuaJkg130_provenance.
• NP519306.RA3b4TZZ3PO-1J-bF-qb53s6VGhmNRyiKUaddl9HjLXFA130_assertion description "[The importance of correct control of eIF2 and eIF2B for normal physiology is underlined by the recent involvement of the five genes that encode the five eIF2B subunits in a severe autosomal recessive neurodegenerative disease, described in young children as CACH (childhood ataxia with central nervous system hypomyelination)/VWM (leukoencephalopathy with vanishing white matter) syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519306.RA3b4TZZ3PO-1J-bF-qb53s6VGhmNRyiKUaddl9HjLXFA130_provenance.