Hypomagnesemia with secondary hypocalcemia due to a missense mutation in the putative pore-forming region of TRPM6

Journal of Biological Chemistry

Volumn 282, Issue 10, 2007, Pages 7656-7667

  Chubanov, Vladimir ^a   Schlingmann, Karl P ^a   Wäring, Janine ^a   Heinzinger, Jolanta ^a   Kaske, Silke ^a   Waldegger, Siegfried ^a   Schnitzler, Michael Mederos ^a   Gudermann, Thomas ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CELL SURFACE; FLUORESCENCE RESONANCE ENERGY TRANSFER; MAGNESIUM HOMEOSTASIS; MUTATIONS;

AMINO ACIDS; CONFOCAL MICROSCOPY; GENE EXPRESSION; MAGNESIUM;

MEDICAL PROBLEMS;

MAGNESIUM; MELASTATIN RELATED TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL 6; MELASTATIN RELATED TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL 7; MEMBRANE PROTEIN; UNCLASSIFIED DRUG; TRANSIENT RECEPTOR POTENTIAL CHANNEL M; TRPM6 PROTEIN, HUMAN; TRPM7 PROTEIN, HUMAN;

AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; CELL STRAIN HEK293; CELL SURFACE; CONTROLLED STUDY; ELECTRIC CURRENT; EMBRYO; FEMALE; FLUORESCENCE RESONANCE ENERGY TRANSFER; GENE EXPRESSION; GENE FUNCTION; HETEROZYGOSITY; HOMEOSTASIS; HUMAN; HUMAN CELL; HYPOCALCEMIA; HYPOMAGNESEMIA; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NONHUMAN; NUCLEOTIDE SEQUENCE; OOCYTE; PRIORITY JOURNAL; RNA SPLICING; VOLTAGE CLAMP; WILD TYPE; XENOPUS; AMINO ACID SEQUENCE; ANIMAL; BLOOD; CELL CULTURE; CHEMISTRY; GENETICS; MAGNESIUM DEFICIENCY; MOLECULAR GENETICS; PHYSIOLOGY;

AMINO ACID SEQUENCE; ANIMALS; CELLS, CULTURED; HUMANS; HYPOCALCEMIA; MAGNESIUM; MAGNESIUM DEFICIENCY; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; TRPM CATION CHANNELS; XENOPUS;

EID: 34147109145     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M611117200     Document Type: Article

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