Year |
Citation |
Score |
2024 |
Finch RH, Vitry G, Siew K, Walsh SB, Behesti A, Hardiman G, da Silveira WA. Spaceflight causes strain-dependent gene expression changes associated with lipid and extracellular matrix dysregulation in the mouse kidney in vivo. Biorxiv : the Preprint Server For Biology. PMID 38559158 DOI: 10.1101/2024.03.13.584781 |
0.672 |
|
2023 |
Manzano A, Weging S, Bezdan D, Borg J, Cahill T, Carnero-Diaz E, Cope H, Deane CS, Etheridge T, Giacomello S, Hardiman G, Leys N, Madrigal P, Mastroleo F, Medina FJ, ... ... Siew K, et al. Enhancing European capabilities for application of multi-omics studies in biology and biomedicine space research. Iscience. 26: 107289. PMID 37636054 DOI: 10.1016/j.isci.2023.107289 |
0.622 |
|
2023 |
Olde Engberink RHG, van Oosten PJ, Weber T, Tabury K, Baatout S, Siew K, Walsh SB, Valenti G, Chouker A, Boutouyrie P, Heer M, Jordan J, Goswami N. Author Correction: The kidney, volume homeostasis and osmoregulation in space: current perspective and knowledge gaps. Npj Microgravity. 9: 60. PMID 37528092 DOI: 10.1038/s41526-023-00307-x |
0.638 |
|
2023 |
D'Ambrosio V, Wan ER, Hawkins-van der Cingel G, Siew K, Hawthorne M, Crawford C, Walsh SB. Hyperoxaluric acute kidney injury and frontotemporal dementia. Lancet (London, England). 401: 1530. PMID 37149308 DOI: 10.1016/S0140-6736(22)02601-0 |
0.625 |
|
2023 |
Zhang J, Siew K, Sun D. Editorial: Targeting pumps, channels and transporters for the treatments of vascular, cardiovascular and kidney diseases. Frontiers in Pharmacology. 14: 1130882. PMID 36817130 DOI: 10.3389/fphar.2023.1130882 |
0.402 |
|
2022 |
Wan ER, Iancu D, Ashton E, Siew K, Mohidin B, Sung CC, Nagano C, Bockenhauer D, Lin SH, Nozu K, Walsh SB. Machine Learning to Identify Genetic Salt-Losing Tubulopathies in Hypokalemic Patients. Kidney International Reports. 8: 556-565. PMID 36938092 DOI: 10.1016/j.ekir.2022.12.008 |
0.635 |
|
2021 |
Wan ER, Siew K, Heptinstall L, Walsh SB. Fumaric acid ester-induced renal Fanconi syndrome: evidence of mitochondrial toxicity. Clinical Kidney Journal. 14: 2085-2089. PMID 35261762 DOI: 10.1093/ckj/sfaa270 |
0.643 |
|
2021 |
Patel V, Klootwijk E, Whiting G, Bockenhauer D, Siew K, Walsh S, Bleich M, Himmerkus N, Jaureguiberry G, Issler N, Godovac-Zimmermann J, Kleta R, Wheeler J. Quantification of FAM20A in human milk and identification of calcium metabolism proteins. Physiological Reports. 9: e15150. PMID 34957696 DOI: 10.14814/phy2.15150 |
0.669 |
|
2021 |
Rezk T, Salota R, Gan JJ, Lachmann HJ, Fontana M, Siew K, Martinez-Naharro A, Guillotte C, Bass P, Sachchithanantham S, Mahmood S, Petrie A, Whelan CJ, Pinney JH, Dockrell M, et al. Urinary retinol binding protein predicts renal outcome in systemic immunoglobulin light-chain (AL) amyloidosis. British Journal of Haematology. PMID 34374069 DOI: 10.1111/bjh.17706 |
0.642 |
|
2018 |
Maskari RA, Hardege I, Cleary S, Figg N, Li Y, Siew K, Khir A, Yu Y, Liu P, Wilkinson I, O'Shaughnessy K, Yasmin. Functional characterization of common BCL11B gene desert variants suggests a lymphocyte-mediated association of BCL11B with aortic stiffness. European Journal of Human Genetics : Ejhg. 26: 1648-1657. PMID 30089823 DOI: 10.1038/s41431-018-0226-z |
0.615 |
|
2018 |
Yasmin, Maskari RA, McEniery CM, Cleary SE, Li Y, Siew K, Figg NL, Khir AW, Cockcroft JR, Wilkinson IB, O'Shaughnessy KM. The matrix proteins aggrecan and fibulin-1 play a key role in determining aortic stiffness. Scientific Reports. 8: 8550. PMID 29867203 DOI: 10.1038/s41598-018-25851-5 |
0.678 |
|
2017 |
Ware JS, Wain LV, Channavajjhala SK, Jackson VE, Edwards E, Lu R, Siew K, Jia W, Shrine N, Kinnear S, Jalland M, Henry AP, Clayton J, O'Shaughnessy KM, Tobin MD, et al. Phenotypic and pharmacogenetic evaluation of patients with thiazide-induced hyponatremia. The Journal of Clinical Investigation. 127: 3367-3374. PMID 28783044 DOI: 10.1172/JCI89812 |
0.701 |
|
2015 |
Schumacher FR, Siew K, Zhang J, Johnson C, Wood N, Cleary SE, Al Maskari RS, Ferryman JT, Hardege I, Yasmin, Figg NL, Enchev R, Knebel A, O'Shaughnessy KM, Kurz T. Characterisation of the Cullin-3 mutation that causes a severe form of familial hypertension and hyperkalaemia. Embo Molecular Medicine. 7: 1285-306. PMID 26286618 DOI: 10.15252/emmm.201505444 |
0.706 |
|
2015 |
Zhang J, Siew K, Macartney T, O'Shaughnessy KM, Alessi DR. Critical role of the SPAK protein kinase CCT domain in controlling blood pressure. Human Molecular Genetics. 24: 4545-58. PMID 25994507 DOI: 10.1093/hmg/ddv185 |
0.713 |
|
2014 |
Siew K, de los Heros P, Alessi DR, O'Shaughnessy KM. Erratum: PD.1. Blood pressure maintenance in MO25β has no physiological role in electrolyte homeostasis or systemic blood pressure maintenance in the mouse Journal of Human Hypertension. 28: 342-342. DOI: 10.1038/Jhh.2013.120 |
0.536 |
|
2013 |
Siew K, O'Shaughnessy KM. Extrarenal roles of the with-no-lysine[K] kinases (WNKs). Clinical and Experimental Pharmacology & Physiology. 40: 885-94. PMID 23662678 DOI: 10.1111/1440-1681.12108 |
0.611 |
|
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