Matches in Nanopublications for { ?s ?p "[Gain-of-function mutations in TRPC6 cause hereditary focal segmental glomerulosclerosis (FSGS), and several human acquired proteinuric diseases show increased glomerular TRPC6 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP36717.RA5vNih-pAPLNFDCHNMgkLViVpydGMMxx4pNvH1sonryM130_assertion description "[Gain-of-function mutations in TRPC6 cause hereditary focal segmental glomerulosclerosis (FSGS), and several human acquired proteinuric diseases show increased glomerular TRPC6 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP36717.RA5vNih-pAPLNFDCHNMgkLViVpydGMMxx4pNvH1sonryM130_provenance.
- NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_assertion description "[Gain-of-function mutations in TRPC6 cause hereditary focal segmental glomerulosclerosis (FSGS), and several human acquired proteinuric diseases show increased glomerular TRPC6 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43016.RAhjF57apo64p8day6Jc3fuLvoKunPyhLvi_EveYXrd5c130_provenance.
- NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_assertion description "[Gain-of-function mutations in TRPC6 cause hereditary focal segmental glomerulosclerosis (FSGS), and several human acquired proteinuric diseases show increased glomerular TRPC6 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_provenance.
- NP758324.RAgpn4Uz_QGrKq3EQyAhM5Ow_MtVDelNN43xGcvSuwqy4130_assertion description "[Gain-of-function mutations in TRPC6 cause hereditary focal segmental glomerulosclerosis (FSGS), and several human acquired proteinuric diseases show increased glomerular TRPC6 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP758324.RAgpn4Uz_QGrKq3EQyAhM5Ow_MtVDelNN43xGcvSuwqy4130_provenance.