Search Results - "Kopplin, Kathrin"

CNNM2, Encoding a Basolateral Protein Required for Renal Mg2+ Handling, Is Mutated in Dominant Hypomagnesemia by STUIVER, Marchel, LAINEZ, Sergio, QUERFELD, Uwe, WILLNOW, Thomas E, NEMEC, Vladimir, WAGNER, Carsten A, HOENDEROP, Joost G, DEVUYST, Olivier, KNOERS, Nine V. A. M, BINDELS, René J, MEIJ, Iwan C, MÜLLER, Dominik, WILL, Constanze, TERRYN, Sara, GÜNZEL, Dorothee, DEBAIX, Huguette, SOMMER, Kerstin, KOPPLIN, Kathrin, THUMFART, Julia, KAMPIK, Nicole B

“…Familial hypomagnesemia is a rare human disorder caused by renal or intestinal magnesium (Mg(2+)) wasting, which may lead to symptoms of Mg(2+) depletion such…”
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Membrane Topology and Intracellular Processing of Cyclin M2 (CNNM2) by de Baaij, Jeroen H.F., Stuiver, Marchel, Meij, Iwan C., Lainez, Sergio, Kopplin, Kathrin, Venselaar, Hanka, Müller, Dominik, Bindels, René J.M., Hoenderop, Joost G.J.

“…Recently, mutations in the cyclin M2 (CNNM2) gene were identified to be causative for severe hypomagnesemia. In kidney, CNNM2 is a basolaterally expressed…”
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Disturbed function of the blood–cerebrospinal fluid barrier aggravates neuro-inflammation by Kooij, Gijs, Kopplin, Kathrin, Blasig, Rosel, Stuiver, Marchel, Koning, Nathalie, Goverse, Gera, van der Pol, Susanne M. A., van het Hof, Bert, Gollasch, Maik, Drexhage, Joost A. R., Reijerkerk, Arie, Meij, Iwan C., Mebius, Reina, Willnow, Thomas E., Müller, Dominik, Blasig, Ingolf E., de Vries, Helga E.

“…Multiple sclerosis (MS) is a chronic neuro-inflammatory disorder, which is marked by the invasion of the central nervous system by monocyte-derived macrophages…”
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Targeted deletion of murine Cldn16 identifies extra- and intrarenal compensatory mechanisms of Ca2+ and Mg2+ wasting by Will, Constanze, Breiderhoff, Tilman, Thumfart, Julia, Stuiver, Marchel, Kopplin, Kathrin, Sommer, Kerstin, Günzel, Dorothee, Querfeld, Uwe, Meij, Iwan C, Shan, Qixian, Bleich, Markus, Willnow, Thomas E, Müller, Dominik

“…Claudin-16 (CLDN16) is critical for renal paracellular epithelial transport of Ca(2+) and Mg(2+) in the thick ascending loop of Henle. To gain novel insights…”
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CNNM2, Encoding a Basolateral Protein Required for Renal Mg^sup 2+^ Handling, Is Mutated in Dominant Hypomagnesemia by Stuiver, Marchel, Lainez, Sergio, Will, Constanze, Terryn, Sara, Günzel, Dorothee, Debaix, Huguette, Sommer, Kerstin, Kopplin, Kathrin, Thumfart, Julia, Kampik, Nicole B, Querfeld, Uwe, Willnow, Thomas E, N-mec, Vladimír, Wagner, Carsten A, Hoenderop, Joost G, Devuyst, Olivier, Knoers, Nine VAM, Bindels, René J, Meij, Iwan C, Müller, Dominik

“…Familial hypomagnesemia is a rare human disorder caused by renal or intestinal magnesium (Mg...) wasting, which may lead to symptoms of Mg... depletion such as…”
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CNNM2, Encoding a Basolateral Protein Required for Renal Mg super(2+) Handling, Is Mutated in Dominant Hypomagnesemia by Stuiver, Marchel, Lainez, Sergio, Will, Constanze, Terryn, Sara, Guenzel, Dorothee, Debaix, Huguette, Sommer, Kerstin, Kopplin, Kathrin, Thumfart, Julia, Kampik, Nicole B, Querfeld, Uwe, Willnow, Thomas E, Nemec, Vladimir, Wagner, Carsten A, Hoenderop, Joost G, Devuyst, Olivier, Knoers, Nine VAM, Bindels, Rene J, Meij, Iwan C, Mueller, Dominik

“…Familial hypomagnesemia is a rare human disorder caused by renal or intestinal magnesium (Mg super(2+)) wasting, which may lead to symptoms of Mg super(2+)…”
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CNNM2, Encoding a Basolateral Protein Required for Renal Mg 2+ Handling, Is Mutated in Dominant Hypomagnesemia by Stuiver, Marchel, Lainez, Sergio, Will, Constanze, Terryn, Sara, Günzel, Dorothee, Debaix, Huguette, Sommer, Kerstin, Kopplin, Kathrin, Thumfart, Julia, Kampik, Nicole B., Querfeld, Uwe, Willnow, Thomas E., Němec, Vladimír, Wagner, Carsten A., Hoenderop, Joost G., Devuyst, Olivier, Knoers, Nine V.A.M., Bindels, René J., Meij, Iwan C., Müller, Dominik

“…Familial hypomagnesemia is a rare human disorder caused by renal or intestinal magnesium (Mg 2+) wasting, which may lead to symptoms of Mg 2+ depletion such as…”
Get full text