| scholarly article | Q13442814 |
| P50 | author | Marian Groot Koerkamp | Q42356644 |
| Jeroen H F de Baaij | Q83593923 | ||
| P2093 | author name string | Joost G J Hoenderop | |
| René J M Bindels | |||
| Frank C P Holstege | |||
| Femke van Zeeland | |||
| Marla Lavrijsen | |||
| Hans Meijer | |||
| P2860 | cites work | CNNM2, encoding a basolateral protein required for renal Mg2+ handling, is mutated in dominant hypomagnesemia | Q24296446 |
| A missense mutation in the Kv1.1 voltage-gated potassium channel-encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia | Q24309111 | ||
| AS160, the Akt substrate regulating GLUT4 translocation, has a functional Rab GTPase-activating protein domain | Q24536241 | ||
| The bifunctional DCOH protein binds to HNF1 independently of its 4-alpha-carbinolamine dehydratase activity | Q24544517 | ||
| Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations | Q24631051 | ||
| Studies on the enzymatic and transcriptional activity of the dimerization cofactor for hepatocyte nuclear factor 1 | Q24633231 | ||
| Normalization for cDNA microarray data: a robust composite method addressing single and multiple slide systematic variation | Q27860759 | ||
| Characterization of a Cofactor That Regulates Dimerization of a Mammalian Homeodomain Protein | Q28115435 | ||
| SLC41A1 is a novel mammalian Mg2+ carrier | Q28116382 | ||
| Human gene SLC41A1 encodes for the Na+/Mg²+ exchanger | Q28118497 | ||
| Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family | Q28200813 | ||
| Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia | Q28200829 | ||
| AS160 modulates aldosterone-stimulated epithelial sodium channel forward trafficking | Q28588044 | ||
| Dissection of a metastatic gene expression signature into distinct components | Q33265960 | ||
| Atlas of gene expression in the mouse kidney: new features of glomerular parietal cells | Q33748384 | ||
| Dominant isolated renal magnesium loss is caused by misrouting of the Na(+),K(+)-ATPase gamma-subunit | Q33924163 | ||
| Monitoring global messenger RNA changes in externally controlled microarray experiments. | Q34236555 | ||
| AS160 Associates with the Na+,K+-ATPase and Mediates the Adenosine Monophosphate-stimulated Protein Kinase-dependent Regulation of Sodium Pump Surface Expression | Q34408505 | ||
| HNF1B mutations associate with hypomagnesemia and renal magnesium wasting | Q34658412 | ||
| Regulation of magnesium balance: lessons learned from human genetic disease | Q35683775 | ||
| Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia | Q35916097 | ||
| Magnesium deficiency and osteoporosis: animal and human observations | Q35988297 | ||
| Renal expression of parvalbumin is critical for NaCl handling and response to diuretics | Q35990289 | ||
| Electrolyte disturbances in the intensive care unit | Q36675537 | ||
| Molecular identification of ancient and modern mammalian magnesium transporters | Q37638953 | ||
| A comprehensive analysis of gene expression profiles in distal parts of the mouse renal tubule. | Q37777967 | ||
| Uromodulin Biology and Pathophysiology – An Update | Q37812546 | ||
| Drug-induced alterations in Mg2+ homoeostasis | Q37992700 | ||
| Sensing mechanisms involved in Ca2+ and Mg2+ homeostasis. | Q38012604 | ||
| 80K-H as a new Ca2+ sensor regulating the activity of the epithelial Ca2+ channel transient receptor potential cation channel V5 (TRPV5). | Q38342172 | ||
| Activation of the bumetanide-sensitive Na+,K+,2Cl- cotransporter (NKCC2) is facilitated by Tamm-Horsfall protein in a chloride-sensitive manner | Q38676686 | ||
| Regulation of multisite phosphorylation and 14-3-3 binding of AS160 in response to IGF-1, EGF, PMA and AICAR. | Q39252731 | ||
| SLC41A1 Mg(2+) transport is regulated via Mg(2+)-dependent endosomal recycling through its N-terminal cytoplasmic domain | Q39520156 | ||
| HNF-1B specifically regulates the transcription of the γa-subunit of the Na+/K+-ATPase | Q39624140 | ||
| Membrane topology and intracellular processing of cyclin M2 (CNNM2). | Q42102883 | ||
| Adaptable gene-specific dye bias correction for two-channel DNA microarrays | Q42145024 | ||
| EGF increases TRPM6 activity and surface expression | Q43210203 | ||
| The epithelial Mg2+ channel transient receptor potential melastatin 6 is regulated by dietary Mg2+ content and estrogens | Q46981321 | ||
| Thiazide-induced hypocalciuria is accompanied by a decreased expression of Ca2+ transport proteins in kidney | Q47778344 | ||
| Transcriptional and functional analyses of SLC12A3 mutations: new clues for the pathogenesis of Gitelman syndrome | Q48799866 | ||
| A primary culture of distal convoluted tubules expressing functional thiazide-sensitive NaCl transport. | Q50494139 | ||
| Emerging role of Akt substrate protein AS160 in the regulation of AQP2 translocation. | Q54376583 | ||
| Hypervitaminosis D mediates compensatory Ca2+ hyperabsorption in TRPV5 knockout mice. | Q54644767 | ||
| P433 | issue | 11 | |
| P921 | main subject | transcriptome | Q252857 |
| P304 | page(s) | F1563-73 | |
| P577 | publication date | 2013-10-02 | |
| P1433 | published in | American Journal of Physiology - Renal Physiology | Q2610177 |
| P1476 | title | Elucidation of the distal convoluted tubule transcriptome identifies new candidate genes involved in renal Mg(2+) handling. | |
| P478 | volume | 305 |
| Q35833468 | Antagonistic Regulation of Parvalbumin Expression and Mitochondrial Calcium Handling Capacity in Renal Epithelial Cells |
| Q27316532 | CNNM2 mutations cause impaired brain development and seizures in patients with hypomagnesemia |
| Q35784892 | Dietary Inulin Fibers Prevent Proton-Pump Inhibitor (PPI)-Induced Hypocalcemia in Mice. |
| Q35182091 | Flavaglines Stimulate Transient Receptor Potential Melastatin Type 6 (TRPM6) Channel Activity |
| Q35658770 | Genetic loci for serum magnesium among African-Americans and gene-environment interaction at MUC1 and TRPM6 in European-Americans: the Atherosclerosis Risk in Communities (ARIC) study |
| Q47726302 | Genetics of Magnesium Disorders |
| Q33870797 | HMGCS2 is a key ketogenic enzyme potentially involved in type 1 diabetes with high cardiovascular risk |
| Q37044436 | Identification of SLC41A3 as a novel player in magnesium homeostasis. |
| Q41524357 | Identification of adenylyl cyclase isoforms mediating parathyroid hormone- and calcitonin-stimulated cyclic AMP accumulation in distal tubule cells. |
| Q88791463 | Magnesium Handling in the Kidney |
| Q87077916 | P2X4 receptor regulation of transient receptor potential melastatin type 6 (TRPM6) Mg2+ channels |
| Q27341945 | P2X6 Knockout Mice Exhibit Normal Electrolyte Homeostasis |
| Q38654032 | Regulation of Mg2+ Reabsorption and Transient Receptor Potential Melastatin Type 6 Activity by cAMP Signaling |
| Q38638219 | Uromodulin: from physiology to rare and complex kidney disorders |
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