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Automatic registration of mass spectrometry imaging data sets to the Allen brain atlas. [electronic resource] by
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- van den Maagdenberg, Arn M J M
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Renal phospholipidosis and impaired magnesium handling in high-fat-diet-fed mice. [electronic resource] by
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- Tack, Cees J J
- Hoenderop, Joost G J
- de Baaij, Jeroen H F
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Mutations in PCBD1 cause hypomagnesemia and renal magnesium wasting. [electronic resource] by
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- Venselaar, Hanka
- Kluijtmans, Leo A J
- Hoenderop, Joost G J
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TRP channel-associated factors are a novel protein family that regulates TRPM8 trafficking and activity. [electronic resource] by
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- Bidaux, Gabriel
- Degerny, Cindy
- Verreman, Kathye
- Guarmit, Basma
- Benahmed, Mohamed
- de Launoit, Yvan
- Bindels, Rene J M
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Calcitriol controls the epithelial calcium channel in kidney. [electronic resource] by
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- Sweep, Fred
- Willems, Peter H G M
- Os, Carel H VAN
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Mismatch repair status in the prediction of benefit from adjuvant fluorouracil chemotherapy in colorectal cancer. [electronic resource] by
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- Reñé, J M
- Clofent, J
- Bessa, X
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Early development of hyperparathyroidism due to loss of PTH transcriptional repression in patients with HNF1β mutations? [electronic resource] by
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- Cornelissen, Elisabeth A M
- van der Vlag, Johan
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- Wetzels, Jack F M
- Hoenderop, Joost G J
- Bindels, René J M
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Producer: 20131210
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High incidence of large deletions in the PMS2 gene in Spanish Lynch syndrome families. [electronic resource] by
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- Anido, U
- Milá, M
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NaCl cotransporter abundance in urinary vesicles is increased by calcineurin inhibitors and predicts thiazide sensitivity. [electronic resource] by
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- Zietse, Robert
- Hoenderop, Joost G J
- Hoorn, Ewout J
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Lipid and protein maps defining arterial layers in atherosclerotic aorta. [electronic resource] by
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- de la Cuesta, Fernando
- Barderas, Maria G
- Lopez-Almodovar, Luis F
- Padial, Luis R
- McDonnell, Liam A
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- Alvarez-Llamas, Gloria
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Molecular anatomy of ascending aorta in atherosclerosis by MS Imaging: Specific lipid and protein patterns reflect pathology. [electronic resource] by
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- van Zeijl, Rene J M
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- de la Cuesta, Fernando
- Barderas, Maria G
- Lopez-Almodovar, Luis F
- Padial, Luis R
- McDonnell, Liam A
- Vivanco, Fernando
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In:
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CNNM2 mutations cause impaired brain development and seizures in patients with hypomagnesemia. [electronic resource] by
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- Regele, Sabrina
- Korenke, G Christoph
- Neophytou, Birgit
- Rust, Stephan
- Reintjes, Nadine
- Konrad, Martin
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ISAG/IUIS-VIC Comparative MHC Nomenclature Committee report, 2005. [electronic resource] by
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- Kaufman, Jim
- Kennedy, Lorna J
- Robinson, James
- Smith, Douglas M
- Stear, Michael J
- Stet, Rene J M
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- Walter, Lutz
- Marsh, Steven G E
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In:
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Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia. [electronic resource] by
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- Muller, Michelle
- van den Dorpel, Marinus A
- Bindels, René J M
- Hoenderop, Joost G J
- Devuyst, Olivier
- Knoers, Nine V A M
Producer: 20151020
In:
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Common single nucleotide polymorphisms in transient receptor potential melastatin type 6 increase the risk for proton pump inhibitor-induced hypomagnesemia: a case-control study. [electronic resource] by
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- Broekman, Mark M T J
- Bisseling, Tanya M
- Haarhuis, Bertram J T
- Tan, Adriaan C I T L
- Te Morsche, René H M
- Hoenderop, Joost G J
- Bindels, René J M
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Producer: 20171010
In:
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Imaging mass spectrometry-based molecular histology differentiates microscopically identical and heterogeneous tumors. [electronic resource] by
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- van Remoortere, Alexandra
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- Heck, Albert J R
- Hogendoorn, Pancras C W
- Deelder, André M
- Altelaar, A F Maarten
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Producer: 20141028
In:
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De novo gain-of-function and loss-of-function mutations of SCN8A in patients with intellectual disabilities and epilepsy. [electronic resource] by
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- Dib-Hajj, Sulayman D
- Waxman, Stephen G
- Jongmans, Marjolijn C J
- Kleefstra, Tjitske
- van de Warrenburg, Bart P
- Praamstra, Peter
- Nicolai, Joost
- Yntema, Helger G
- Bindels, René J M
- Meisler, Miriam H
- Kamsteeg, Erik-Jan
Producer: 20160106
In:
Journal of medical genetics vol. 52
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