Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Dent's disease, an X-linked disorder characterized by low molecular weight proteinuria, hypercalciuria and nephrolithiasis, is due to mutations of the chloride/proton antiporter 5, CLC-5; ADHH is associated with activating mutations of the CaSR, which is a G-protein-coupled receptor; hypophosphatemic hypercalciuric nephrolithiasis associated with rickets is due to mutations in the type 2c sodium-phosphate co-transporter (NPT2c); and familial hypomagnesemia with hypercalciuria is due to mutations of paracellin-1, which is a member of the claudin family of membrane proteins that form the intercellular tight junction barrier in a variety of epithelia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP668578.RATzEuKKAbblQQNwy63GgL1DeU958o2Zg8BeHs3LOJIxU130_assertion description "[Dent's disease, an X-linked disorder characterized by low molecular weight proteinuria, hypercalciuria and nephrolithiasis, is due to mutations of the chloride/proton antiporter 5, CLC-5; ADHH is associated with activating mutations of the CaSR, which is a G-protein-coupled receptor; hypophosphatemic hypercalciuric nephrolithiasis associated with rickets is due to mutations in the type 2c sodium-phosphate co-transporter (NPT2c); and familial hypomagnesemia with hypercalciuria is due to mutations of paracellin-1, which is a member of the claudin family of membrane proteins that form the intercellular tight junction barrier in a variety of epithelia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668578.RATzEuKKAbblQQNwy63GgL1DeU958o2Zg8BeHs3LOJIxU130_provenance.
• NP668585.RAfeDEt1EllemT0-hbzuTASTWNs6046sh90-Rm4EX6ytA130_assertion description "[Dent's disease, an X-linked disorder characterized by low molecular weight proteinuria, hypercalciuria and nephrolithiasis, is due to mutations of the chloride/proton antiporter 5, CLC-5; ADHH is associated with activating mutations of the CaSR, which is a G-protein-coupled receptor; hypophosphatemic hypercalciuric nephrolithiasis associated with rickets is due to mutations in the type 2c sodium-phosphate co-transporter (NPT2c); and familial hypomagnesemia with hypercalciuria is due to mutations of paracellin-1, which is a member of the claudin family of membrane proteins that form the intercellular tight junction barrier in a variety of epithelia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668585.RAfeDEt1EllemT0-hbzuTASTWNs6046sh90-Rm4EX6ytA130_provenance.
• NP668576.RACW60OCcvowVCfsQSZKmJ-I6Ae8it8C60FNJ0GvRsqH4130_assertion description "[Dent's disease, an X-linked disorder characterized by low molecular weight proteinuria, hypercalciuria and nephrolithiasis, is due to mutations of the chloride/proton antiporter 5, CLC-5; ADHH is associated with activating mutations of the CaSR, which is a G-protein-coupled receptor; hypophosphatemic hypercalciuric nephrolithiasis associated with rickets is due to mutations in the type 2c sodium-phosphate co-transporter (NPT2c); and familial hypomagnesemia with hypercalciuria is due to mutations of paracellin-1, which is a member of the claudin family of membrane proteins that form the intercellular tight junction barrier in a variety of epithelia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668576.RACW60OCcvowVCfsQSZKmJ-I6Ae8it8C60FNJ0GvRsqH4130_provenance.
• NP668577.RAr3MFqZzgHIw0bCs2UPHWPm_D5UrjsBpmQbDkipwdD1Q130_assertion description "[Dent's disease, an X-linked disorder characterized by low molecular weight proteinuria, hypercalciuria and nephrolithiasis, is due to mutations of the chloride/proton antiporter 5, CLC-5; ADHH is associated with activating mutations of the CaSR, which is a G-protein-coupled receptor; hypophosphatemic hypercalciuric nephrolithiasis associated with rickets is due to mutations in the type 2c sodium-phosphate co-transporter (NPT2c); and familial hypomagnesemia with hypercalciuria is due to mutations of paracellin-1, which is a member of the claudin family of membrane proteins that form the intercellular tight junction barrier in a variety of epithelia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668577.RAr3MFqZzgHIw0bCs2UPHWPm_D5UrjsBpmQbDkipwdD1Q130_provenance.
• NP668579.RAvzYjYS0i5vJpnyQbZLQpo4Zb4_V4c4jkA0JFa1c1L-k130_assertion description "[Dent's disease, an X-linked disorder characterized by low molecular weight proteinuria, hypercalciuria and nephrolithiasis, is due to mutations of the chloride/proton antiporter 5, CLC-5; ADHH is associated with activating mutations of the CaSR, which is a G-protein-coupled receptor; hypophosphatemic hypercalciuric nephrolithiasis associated with rickets is due to mutations in the type 2c sodium-phosphate co-transporter (NPT2c); and familial hypomagnesemia with hypercalciuria is due to mutations of paracellin-1, which is a member of the claudin family of membrane proteins that form the intercellular tight junction barrier in a variety of epithelia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668579.RAvzYjYS0i5vJpnyQbZLQpo4Zb4_V4c4jkA0JFa1c1L-k130_provenance.
• NP668581.RAv-zCZ9nziprQfjFi_w1ij3bUs00fgb9-tUoDVaGA2ZE130_assertion description "[Dent's disease, an X-linked disorder characterized by low molecular weight proteinuria, hypercalciuria and nephrolithiasis, is due to mutations of the chloride/proton antiporter 5, CLC-5; ADHH is associated with activating mutations of the CaSR, which is a G-protein-coupled receptor; hypophosphatemic hypercalciuric nephrolithiasis associated with rickets is due to mutations in the type 2c sodium-phosphate co-transporter (NPT2c); and familial hypomagnesemia with hypercalciuria is due to mutations of paracellin-1, which is a member of the claudin family of membrane proteins that form the intercellular tight junction barrier in a variety of epithelia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668581.RAv-zCZ9nziprQfjFi_w1ij3bUs00fgb9-tUoDVaGA2ZE130_provenance.
• NP668580.RAEsIc71ov_pFQ_X_3G4J-saGrIlGwRjj_luMlDhMIkmU130_assertion description "[Dent's disease, an X-linked disorder characterized by low molecular weight proteinuria, hypercalciuria and nephrolithiasis, is due to mutations of the chloride/proton antiporter 5, CLC-5; ADHH is associated with activating mutations of the CaSR, which is a G-protein-coupled receptor; hypophosphatemic hypercalciuric nephrolithiasis associated with rickets is due to mutations in the type 2c sodium-phosphate co-transporter (NPT2c); and familial hypomagnesemia with hypercalciuria is due to mutations of paracellin-1, which is a member of the claudin family of membrane proteins that form the intercellular tight junction barrier in a variety of epithelia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668580.RAEsIc71ov_pFQ_X_3G4J-saGrIlGwRjj_luMlDhMIkmU130_provenance.
• NP668584.RAHmfcB-s0VEoufRfGwLZ2wBU4G7yCng4LQXbre-rPO6Y130_assertion description "[Dent's disease, an X-linked disorder characterized by low molecular weight proteinuria, hypercalciuria and nephrolithiasis, is due to mutations of the chloride/proton antiporter 5, CLC-5; ADHH is associated with activating mutations of the CaSR, which is a G-protein-coupled receptor; hypophosphatemic hypercalciuric nephrolithiasis associated with rickets is due to mutations in the type 2c sodium-phosphate co-transporter (NPT2c); and familial hypomagnesemia with hypercalciuria is due to mutations of paracellin-1, which is a member of the claudin family of membrane proteins that form the intercellular tight junction barrier in a variety of epithelia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668584.RAHmfcB-s0VEoufRfGwLZ2wBU4G7yCng4LQXbre-rPO6Y130_provenance.
• NP668582.RAwrha7MJo4bNh78DcSjPacRXAezkiJu4700TBnZvqiCw130_assertion description "[Dent's disease, an X-linked disorder characterized by low molecular weight proteinuria, hypercalciuria and nephrolithiasis, is due to mutations of the chloride/proton antiporter 5, CLC-5; ADHH is associated with activating mutations of the CaSR, which is a G-protein-coupled receptor; hypophosphatemic hypercalciuric nephrolithiasis associated with rickets is due to mutations in the type 2c sodium-phosphate co-transporter (NPT2c); and familial hypomagnesemia with hypercalciuria is due to mutations of paracellin-1, which is a member of the claudin family of membrane proteins that form the intercellular tight junction barrier in a variety of epithelia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668582.RAwrha7MJo4bNh78DcSjPacRXAezkiJu4700TBnZvqiCw130_provenance.
• NP668583.RA4cZyTl3cfSjaxhMvLGZYNR2BnczYUxhvqjlr6iV7m04130_assertion description "[Dent's disease, an X-linked disorder characterized by low molecular weight proteinuria, hypercalciuria and nephrolithiasis, is due to mutations of the chloride/proton antiporter 5, CLC-5; ADHH is associated with activating mutations of the CaSR, which is a G-protein-coupled receptor; hypophosphatemic hypercalciuric nephrolithiasis associated with rickets is due to mutations in the type 2c sodium-phosphate co-transporter (NPT2c); and familial hypomagnesemia with hypercalciuria is due to mutations of paracellin-1, which is a member of the claudin family of membrane proteins that form the intercellular tight junction barrier in a variety of epithelia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668583.RA4cZyTl3cfSjaxhMvLGZYNR2BnczYUxhvqjlr6iV7m04130_provenance.