Matches in Nanopublications for { ?s ?p "[Because hypermagnesuria and hypocalciuria accompanied the hypomagnesemia, we analyzed genes associated with hypermagnesuria and detected highly conserved HNF1 recognition sites in FXYD2, a gene that can cause autosomal dominant hypomagnesemia and hypocalciuria when mutated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP459491.RAtYa-zv7tSaMxnjNeIpicsEyK97TPDJVDd7ovIRQntiA130_assertion description "[Because hypermagnesuria and hypocalciuria accompanied the hypomagnesemia, we analyzed genes associated with hypermagnesuria and detected highly conserved HNF1 recognition sites in FXYD2, a gene that can cause autosomal dominant hypomagnesemia and hypocalciuria when mutated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP459491.RAtYa-zv7tSaMxnjNeIpicsEyK97TPDJVDd7ovIRQntiA130_provenance.
- assertion description "[Because hypermagnesuria and hypocalciuria accompanied the hypomagnesemia, we analyzed genes associated with hypermagnesuria and detected highly conserved HNF1 recognition sites in FXYD2, a gene that can cause autosomal dominant hypomagnesemia and hypocalciuria when mutated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP794947.RA9heLZIEQIul8lHGD7SSMCOsB1JAT3Cm83e-gxPjbLPQ130_assertion description "[Because hypermagnesuria and hypocalciuria accompanied the hypomagnesemia, we analyzed genes associated with hypermagnesuria and detected highly conserved HNF1 recognition sites in FXYD2, a gene that can cause autosomal dominant hypomagnesemia and hypocalciuria when mutated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794947.RA9heLZIEQIul8lHGD7SSMCOsB1JAT3Cm83e-gxPjbLPQ130_provenance.
- assertion description "[Because hypermagnesuria and hypocalciuria accompanied the hypomagnesemia, we analyzed genes associated with hypermagnesuria and detected highly conserved HNF1 recognition sites in FXYD2, a gene that can cause autosomal dominant hypomagnesemia and hypocalciuria when mutated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP256336.RAr8IfM64vPCnRlm4oG6WBesxPcnoe0NmpxgdOwIjWCbo130_assertion description "[Because hypermagnesuria and hypocalciuria accompanied the hypomagnesemia, we analyzed genes associated with hypermagnesuria and detected highly conserved HNF1 recognition sites in FXYD2, a gene that can cause autosomal dominant hypomagnesemia and hypocalciuria when mutated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256336.RAr8IfM64vPCnRlm4oG6WBesxPcnoe0NmpxgdOwIjWCbo130_provenance.
- NP734361.RAWEqLppw0x6obrUv2XyqynTce_NkGcUo1WzQFGXBjJXo130_assertion description "[Because hypermagnesuria and hypocalciuria accompanied the hypomagnesemia, we analyzed genes associated with hypermagnesuria and detected highly conserved HNF1 recognition sites in FXYD2, a gene that can cause autosomal dominant hypomagnesemia and hypocalciuria when mutated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734361.RAWEqLppw0x6obrUv2XyqynTce_NkGcUo1WzQFGXBjJXo130_provenance.
- NP734363.RAW4uaqTAksCkql6fKJ0uQ5nQR0PaRHTWSoHUKK5OsJdA130_assertion description "[Because hypermagnesuria and hypocalciuria accompanied the hypomagnesemia, we analyzed genes associated with hypermagnesuria and detected highly conserved HNF1 recognition sites in FXYD2, a gene that can cause autosomal dominant hypomagnesemia and hypocalciuria when mutated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734363.RAW4uaqTAksCkql6fKJ0uQ5nQR0PaRHTWSoHUKK5OsJdA130_provenance.
- NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_assertion description "[Because hypermagnesuria and hypocalciuria accompanied the hypomagnesemia, we analyzed genes associated with hypermagnesuria and detected highly conserved HNF1 recognition sites in FXYD2, a gene that can cause autosomal dominant hypomagnesemia and hypocalciuria when mutated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724779.RAOmsgwBIgbt8RY8-VsZevVA2MpLdkB35qcCC_QziCT_s130_provenance.