Matches in Nanopublications for { ?s ?p "[Mutations in serine-threonine kinase WNK4 with no lysine (K) at a key catalytic residue cause familial hypertension known as pseudohypoaldosteronism type II (PHAII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP792813.RAoSYjzWgx_r8Ep_HnMKNqXVazcI2UBvLIaT0wPm2_AVI130_assertion description "[Mutations in serine-threonine kinase WNK4 with no lysine (K) at a key catalytic residue cause familial hypertension known as pseudohypoaldosteronism type II (PHAII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792813.RAoSYjzWgx_r8Ep_HnMKNqXVazcI2UBvLIaT0wPm2_AVI130_provenance.
- NP807704.RAfBtgZpHIuPSNUnjjaArzj14RVr2x9acWWugynsOQxMY130_assertion description "[Mutations in serine-threonine kinase WNK4 with no lysine (K) at a key catalytic residue cause familial hypertension known as pseudohypoaldosteronism type II (PHAII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP807704.RAfBtgZpHIuPSNUnjjaArzj14RVr2x9acWWugynsOQxMY130_provenance.
- assertion description "[Mutations in serine-threonine kinase WNK4 with no lysine (K) at a key catalytic residue cause familial hypertension known as pseudohypoaldosteronism type II (PHAII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in serine-threonine kinase WNK4 with no lysine (K) at a key catalytic residue cause familial hypertension known as pseudohypoaldosteronism type II (PHAII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP374138.RAR3r6DxR_E1D7VXs3QJc9Bgjx4-cv_L81K_lJWrnwR8c130_assertion description "[Mutations in serine-threonine kinase WNK4 with no lysine (K) at a key catalytic residue cause familial hypertension known as pseudohypoaldosteronism type II (PHAII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374138.RAR3r6DxR_E1D7VXs3QJc9Bgjx4-cv_L81K_lJWrnwR8c130_provenance.
- assertion description "[Mutations in serine-threonine kinase WNK4 with no lysine (K) at a key catalytic residue cause familial hypertension known as pseudohypoaldosteronism type II (PHAII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP441560.RAeSXgaMB9rFNOVj2Szbs1RIJXiW82ebtAi-dSrnx7rxs130_assertion description "[Mutations in serine-threonine kinase WNK4 with no lysine (K) at a key catalytic residue cause familial hypertension known as pseudohypoaldosteronism type II (PHAII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441560.RAeSXgaMB9rFNOVj2Szbs1RIJXiW82ebtAi-dSrnx7rxs130_provenance.
- NP889781.RAHjO6Pza8qmp8dDc0xk3U2WVMmUPzVvt_PQjmrwjhdcU130_assertion description "[Mutations in serine-threonine kinase WNK4 with no lysine (K) at a key catalytic residue cause familial hypertension known as pseudohypoaldosteronism type II (PHAII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889781.RAHjO6Pza8qmp8dDc0xk3U2WVMmUPzVvt_PQjmrwjhdcU130_provenance.
- NP374189.RA_bnq915EAy4uCEH0xF4xetnFawdcDBNoVfHzS_O-Dng130_assertion description "[Mutations in serine-threonine kinase WNK4 with no lysine (K) at a key catalytic residue cause familial hypertension known as pseudohypoaldosteronism type II (PHAII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374189.RA_bnq915EAy4uCEH0xF4xetnFawdcDBNoVfHzS_O-Dng130_provenance.
- NP941552.RAMSio2EXH2V5_HtuAU8v-iMHYqvmU-PHeZdWU_nSas70130_assertion description "[Mutations in serine-threonine kinase WNK4 with no lysine (K) at a key catalytic residue cause familial hypertension known as pseudohypoaldosteronism type II (PHAII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP941552.RAMSio2EXH2V5_HtuAU8v-iMHYqvmU-PHeZdWU_nSas70130_provenance.
- NP441557.RAyuT_ZdqJUBqCUKeRgS_KAwBMwuWtAqsq1dqPZ3J16OE130_assertion description "[Mutations in serine-threonine kinase WNK4 with no lysine (K) at a key catalytic residue cause familial hypertension known as pseudohypoaldosteronism type II (PHAII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441557.RAyuT_ZdqJUBqCUKeRgS_KAwBMwuWtAqsq1dqPZ3J16OE130_provenance.
- NP441558.RA2ZI2BaAeUTIbUMfg2euOg33USVJn3X3U9JX6TBalbaI130_assertion description "[Mutations in serine-threonine kinase WNK4 with no lysine (K) at a key catalytic residue cause familial hypertension known as pseudohypoaldosteronism type II (PHAII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441558.RA2ZI2BaAeUTIbUMfg2euOg33USVJn3X3U9JX6TBalbaI130_provenance.