Matches in Nanopublications for { ?s ?p "[Despite a growing body of evidence concerning the gene structures responsible for genetically heterogenous CMT2B and other CMT2 neuropathies, little is known about the in vitro neuropathy model and how CMT2B-associated mutation-caused aberrant neuritogenesis is properly reversed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP199227.RAAyMMsahgwJDcR09SFvvMNjM2b37-R-ib_2FUGgW2AwY130_assertion description "[Despite a growing body of evidence concerning the gene structures responsible for genetically heterogenous CMT2B and other CMT2 neuropathies, little is known about the in vitro neuropathy model and how CMT2B-associated mutation-caused aberrant neuritogenesis is properly reversed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199227.RAAyMMsahgwJDcR09SFvvMNjM2b37-R-ib_2FUGgW2AwY130_provenance.
- NP275520.RABQPWMlSP4lX-Ektv-o15mp5gM1y50aCaNHVN193rLXw130_assertion description "[Despite a growing body of evidence concerning the gene structures responsible for genetically heterogenous CMT2B and other CMT2 neuropathies, little is known about the in vitro neuropathy model and how CMT2B-associated mutation-caused aberrant neuritogenesis is properly reversed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP275520.RABQPWMlSP4lX-Ektv-o15mp5gM1y50aCaNHVN193rLXw130_provenance.
- NP756384.RAYpn8dERsdfImMqyGEDcHIVnIPCn0xQGc7gs6oUYKJyQ130_assertion description "[Despite a growing body of evidence concerning the gene structures responsible for genetically heterogenous CMT2B and other CMT2 neuropathies, little is known about the in vitro neuropathy model and how CMT2B-associated mutation-caused aberrant neuritogenesis is properly reversed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756384.RAYpn8dERsdfImMqyGEDcHIVnIPCn0xQGc7gs6oUYKJyQ130_provenance.
- assertion description "[Despite a growing body of evidence concerning the gene structures responsible for genetically heterogenous CMT2B and other CMT2 neuropathies, little is known about the in vitro neuropathy model and how CMT2B-associated mutation-caused aberrant neuritogenesis is properly reversed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Despite a growing body of evidence concerning the gene structures responsible for genetically heterogenous CMT2B and other CMT2 neuropathies, little is known about the in vitro neuropathy model and how CMT2B-associated mutation-caused aberrant neuritogenesis is properly reversed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP827270.RAomx4JIqd3JHLHH5zgL4WuwWOOFueiBTaYp7qiakoPsc130_assertion description "[Despite a growing body of evidence concerning the gene structures responsible for genetically heterogenous CMT2B and other CMT2 neuropathies, little is known about the in vitro neuropathy model and how CMT2B-associated mutation-caused aberrant neuritogenesis is properly reversed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP827270.RAomx4JIqd3JHLHH5zgL4WuwWOOFueiBTaYp7qiakoPsc130_provenance.
- NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_assertion description "[Despite a growing body of evidence concerning the gene structures responsible for genetically heterogenous CMT2B and other CMT2 neuropathies, little is known about the in vitro neuropathy model and how CMT2B-associated mutation-caused aberrant neuritogenesis is properly reversed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP827170.RAKnW6AbUSUgELqJQ7SB1w1cP8sY6rUlSoHH94nUXSNG0130_provenance.
- NP827172.RA7jW2gUcXyh6rfnFKb2OklJHlsvoRVIh_gL6l3GKuzCc130_assertion description "[Despite a growing body of evidence concerning the gene structures responsible for genetically heterogenous CMT2B and other CMT2 neuropathies, little is known about the in vitro neuropathy model and how CMT2B-associated mutation-caused aberrant neuritogenesis is properly reversed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP827172.RA7jW2gUcXyh6rfnFKb2OklJHlsvoRVIh_gL6l3GKuzCc130_provenance.
- NP868163.RA2H4ZTdH_lkzWlljVK_yOhCtvyw3Rk4g_ypa9gEXUo-A130_assertion description "[Despite a growing body of evidence concerning the gene structures responsible for genetically heterogenous CMT2B and other CMT2 neuropathies, little is known about the in vitro neuropathy model and how CMT2B-associated mutation-caused aberrant neuritogenesis is properly reversed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868163.RA2H4ZTdH_lkzWlljVK_yOhCtvyw3Rk4g_ypa9gEXUo-A130_provenance.