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August 2006 / J Clin Endocrinol Metab Unusual clinical presentation and possible rescue of a novel Claudin-16 mutation D. Mueller P.J. Kausalya D. Bockenhauer J. Tumfart I.C. Meij M.J. Dillon W. van't Hoff W. Hunziker 01. April 2006 / Hum Mol Genet Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: blocking endocytosis restores surface expression of a novel Claudin-16 mutant that lacks the entire C-terminal cytosolic tail D. Mueller P.J. Kausalya I.C. Meij W. Hunziker 01. April 2005 / Organogenesis The European Renal Genome Project: An integrated approach towards understanding the genetics of kidney development and disease T.E. Willnow C. Antignac A.W. Braendli E.I. Christensen R.D. Cox D. Davidson J.A. Davies O. Devuyst G. Eichele N.D. Hastie P.J. Verroust A. Schedl I.C. Meij 28. August 2012 / Proc Natl Acad Sci U S A Deletion of claudin-10 (Cldn10) in the thick ascending limb impairs paracellular sodium permeability and leads to hypermagnesemia and nephrocalcinosis T. Breiderhoff N. Himmerkus M. Stuiver K. Mutig C. Will I.C. Meij S. Bachmann M. Bleich T.E. Willnow D. Mueller 01. August 2014 / Acta Neuropathol Disturbed function of the blood-cerebrospinal fluid barrier aggravates neuro-inflammation G. Kooij K. Kopplin R. Blasig M. Stuiver N. Koning G. Goverse S.M.A. van der Pol B. van het Hof M. Gollasch J.A.R. Drexhage A. Reijerkerk I.C. Meij R. Mebius T.E. Willnow D. Müller I.E. Blasig H.E. de Vries 20. April 2012 / J Biol Chem Membrane topology and intracellular processing of cyclin M2 (CNNM2) J.H.F. de Baaij M. Stuiver I.C. Meij S. Lainez K. Kopplin H. Venselaar D. Mueller R.J.M. Bindels J.G.J. Hoenderop 01. Mai 2010 / Am J Physiol Renal Physiol Targeted deletion of murine Cldn16 identifies extra- and intrarenal compensatory mechanisms of Ca2+ and Mg2+ wasting C. Will T. Breiderhoff J. Thumfart M. Stuiver K. Kopplin K. Sommer D. Guenzel U. Querfeld I.C. Meij Q. Shan M. Bleich T.E. Willnow D. Mueller 01. Juli 2007 / Hum Mol Genet L1 retrotransposition can occur early in human embryonic development J.A. van den Hurk I.C. Meij M.C. Seleme H. Kano K. Nikopoulos L.H. Hoefsloot E.A. Sistermans I.J. de Wijs A. Mukhopadhyay A.S. Plomp P.T. de Jong H.H. Kazazian F.P. Cremers 11. März 2011 / Am J Hum Genet CNNM2, encoding a basolateral protein required for renal Mg(2+) handling, is mutated in dominant hypomagnesemia M. Stuiver S. Lainez C. Will S. Terryn D. Guenzel H. Debaix K. Sommer K. Kopplin J. Thumfart N.B. Kampik U. Querfeld T.E. Willnow V. Nemec C.A. Wagner J.G. Hoenderop O. Devuyst N.V. Knoers R.J. Bindels I.C. Meij D. Mueller 01. Juli 2009 / Nephrol Dial Transplant EUNEFRON, the European Network for the Study of Orphan Nephropathies O. Devuyst I. Meij X. Jeunemaitre P. Ronco C. Antignac E.I. Christensen N.V. Knoers E.N. Levtchenko P.M. Deen D. Mueller C.A. Wagner L. Rampoldi W.G. van't Hoff Seitennummerierung Aktuelle Seite 1 Seite 2 Nächste Seite Next › Letzte Seite Last »
01. August 2006 / J Clin Endocrinol Metab Unusual clinical presentation and possible rescue of a novel Claudin-16 mutation D. Mueller P.J. Kausalya D. Bockenhauer J. Tumfart I.C. Meij M.J. Dillon W. van't Hoff W. Hunziker
01. April 2006 / Hum Mol Genet Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: blocking endocytosis restores surface expression of a novel Claudin-16 mutant that lacks the entire C-terminal cytosolic tail D. Mueller P.J. Kausalya I.C. Meij W. Hunziker
01. April 2005 / Organogenesis The European Renal Genome Project: An integrated approach towards understanding the genetics of kidney development and disease T.E. Willnow C. Antignac A.W. Braendli E.I. Christensen R.D. Cox D. Davidson J.A. Davies O. Devuyst G. Eichele N.D. Hastie P.J. Verroust A. Schedl I.C. Meij
28. August 2012 / Proc Natl Acad Sci U S A Deletion of claudin-10 (Cldn10) in the thick ascending limb impairs paracellular sodium permeability and leads to hypermagnesemia and nephrocalcinosis T. Breiderhoff N. Himmerkus M. Stuiver K. Mutig C. Will I.C. Meij S. Bachmann M. Bleich T.E. Willnow D. Mueller
01. August 2014 / Acta Neuropathol Disturbed function of the blood-cerebrospinal fluid barrier aggravates neuro-inflammation G. Kooij K. Kopplin R. Blasig M. Stuiver N. Koning G. Goverse S.M.A. van der Pol B. van het Hof M. Gollasch J.A.R. Drexhage A. Reijerkerk I.C. Meij R. Mebius T.E. Willnow D. Müller I.E. Blasig H.E. de Vries
20. April 2012 / J Biol Chem Membrane topology and intracellular processing of cyclin M2 (CNNM2) J.H.F. de Baaij M. Stuiver I.C. Meij S. Lainez K. Kopplin H. Venselaar D. Mueller R.J.M. Bindels J.G.J. Hoenderop
01. Mai 2010 / Am J Physiol Renal Physiol Targeted deletion of murine Cldn16 identifies extra- and intrarenal compensatory mechanisms of Ca2+ and Mg2+ wasting C. Will T. Breiderhoff J. Thumfart M. Stuiver K. Kopplin K. Sommer D. Guenzel U. Querfeld I.C. Meij Q. Shan M. Bleich T.E. Willnow D. Mueller
01. Juli 2007 / Hum Mol Genet L1 retrotransposition can occur early in human embryonic development J.A. van den Hurk I.C. Meij M.C. Seleme H. Kano K. Nikopoulos L.H. Hoefsloot E.A. Sistermans I.J. de Wijs A. Mukhopadhyay A.S. Plomp P.T. de Jong H.H. Kazazian F.P. Cremers
11. März 2011 / Am J Hum Genet CNNM2, encoding a basolateral protein required for renal Mg(2+) handling, is mutated in dominant hypomagnesemia M. Stuiver S. Lainez C. Will S. Terryn D. Guenzel H. Debaix K. Sommer K. Kopplin J. Thumfart N.B. Kampik U. Querfeld T.E. Willnow V. Nemec C.A. Wagner J.G. Hoenderop O. Devuyst N.V. Knoers R.J. Bindels I.C. Meij D. Mueller
01. Juli 2009 / Nephrol Dial Transplant EUNEFRON, the European Network for the Study of Orphan Nephropathies O. Devuyst I. Meij X. Jeunemaitre P. Ronco C. Antignac E.I. Christensen N.V. Knoers E.N. Levtchenko P.M. Deen D. Mueller C.A. Wagner L. Rampoldi W.G. van't Hoff