Works matching DE "XANTHINURIA"

Results: 19

Modern diagnostic approach to hereditary xanthinuria.

Published in:

Urolithiasis, 2015, v. 43, n. 1, p. 61, doi. 10.1007/s00240-014-0734-4

By:

Mraz, Martin;
Hurba, Olha;
Bartl, Josef;
Dolezel, Zdenek;
Marinaki, Anthony;
Fairbanks, Lynette;
Stiburkova, Blanka

Publication type:

Article

Classical xanthinuria: a rare cause of pediatric urolithiasis.

Published in:

Turkish Journal of Urology, 2013, v. 39, n. 4, p. 274, doi. 10.5152/tud.2013.066

By:

Akıncı, Nurver;
Çakıl, Adviye;
Öner, Ayşe

Publication type:

Article

A Mouse Model of Early-Onset Renal Failure Due to a Xanthine Dehydrogenase Nonsense Mutation.

Published in:

PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0045217

By:

Piret, Sian E.;
Esapa, Christopher T.;
Gorvin, Caroline M.;
Head, Rosie;
Loh, Nellie Y.;
Devuyst, Olivier;
Thomas, Gethin;
Brown, Steve D. M.;
Brown, Matthew;
Croucher, Peter;
Cox, Roger;
Thakker, Rajesh V.;
Shree Ram Singh

Publication type:

Article

Screening inhibitors of xanthine oxidase from natural products using enzyme immobilized magnetic beads by high-performance liquid chromatography coupled with tandem mass spectrometry.

Published in:

Journal of Separation Science, 2017, v. 40, n. 9, p. 1877, doi. 10.1002/jssc.201601438

By:

Wang, Ting;
Li, Dapeng;
Yu, Boyang;
Qi, Jin

Publication type:

Article

Using Next-Generation Sequencing to Identify a Mutation in Human MCSU that is Responsible for Type II Xanthinuria.

Published in:

Cellular Physiology & Biochemistry (Karger AG), 2015, v. 35, n. 6, p. 2412, doi. 10.1159/000374042

By:

Zhou, Yunan;
Zhang, Xueguang;
Ding, Rui;
Li, Zuoxiang;
Hong, Quan;
Wang, Yan;
Zheng, Wei;
Geng, Xiaodong;
Fan, Meng;
Cai, Guangyan;
Chen, Xiangmei;
Wu, Di

Publication type:

Article

Urine metabolomics reveals novel physiologic functions of human aldehyde oxidase and provides biomarkers for typing xanthinuria.

Published in:

Metabolomics, 2012, v. 8, n. 5, p. 951, doi. 10.1007/s11306-011-0391-3

By:

Peretz, Hava;
Watson, David;
Blackburn, Gavin;
Zhang, Tong;
Lagziel, Ayala;
Shtauber-Naamati, Meirav;
Morad, Tova;
Keren-Tardai, Elena;
Greenshpun, Victoria;
Usher, Sali;
Shalev, Hanna;
Landau, Daniel;
Levartovsky, David

Publication type:

Article

Xanthine oxidase inhibition alleviates the cardiac complications of insulin resistance: effect on low grade inflammation and the angiotensin system.

Published in:

Journal of Translational Medicine, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s12967-015-0445-9

By:

El-Bassossy, Hany M.;
Watson, Malcolm L.

Publication type:

Article

Hereditary xanthinuria in a goat.

Published in:

Journal of Veterinary Internal Medicine, 2019, v. 33, n. 2, p. 1009, doi. 10.1111/jvim.15431

By:

Vail, Krystal J.;
Tate, Nicole M.;
Likavec, Tasha;
Minor, Katie M.;
Gibbons, Philippa M.;
Rech, Raquel R.;
Furrow, Eva

Publication type:

Article

Human Xanthine Oxidase Changes its Substrate Specificity to Aldehyde Oxidase Type upon Mutation of Amino Acid Residues in the Active Site: Roles of Active Site Residues in Binding and Activation of Purine Substrate.

Published in:

Journal of Biochemistry, 2007, v. 141, n. 4, p. 513, doi. 10.1093/jb/mvm053

By:

Yamaguchi, Yuichiro;
Matsumura, Tomohiro;
Ichida, Kimiyoshi;
Okamoto, Ken;
Nishino, Takeshi

Publication type:

Article

Xanthine Stone in the Urinary Bladder of a Male Child.

Published in:

Urologia Internationalis, 1999, v. 63, n. 4, p. 242, doi. 10.1159/000030458

By:

Kiss, András;
Berényi, Mihály;
Csontai, Ágoston

Publication type:

Article

Xanthinuria type I: a rare cause of urolithiasis.

Published in:

Pediatric Nephrology, 2007, v. 22, n. 2, p. 310, doi. 10.1007/s00467-006-0267-3

By:

Arikyants, Nina;
Sarkissian, Ashot;
Hesse, Albrecht;
Eggermann, Thomas;
Leumann, Ernst;
Steinmann, Beat

Publication type:

Article

Acute renal failure due to bilateral xanthine urolithiasis in a boy with Lesch-Nyhan syndrome.

Published in:

Pediatric Nephrology, 2006, v. 21, n. 7, p. 1045, doi. 10.1007/s00467-006-0149-8

By:

Sikora, Przemysław;
Pijanowska, Monika;
Majewski, Marek;
Bieniaś, Beata;
Borzęcka, Halina;
Zajczkowska, Małgorzata

Publication type:

Article

Hereditary xanthinuria is not so rare disorder of purine metabolism.

Published in:

Nucleosides, Nucleotides & Nucleic Acids, 2018, v. 37, n. 6, p. 324, doi. 10.1080/15257770.2018.1460478

By:

Sebesta, I.;
Stiburkova, B.;
Krijt, J.

Publication type:

Article

PURINE DISORDERS WITH HYPOURICEMIA.

Published in:

Contributions / Prilozi (1857-9345), 2014, v. 35, n. 1, p. 87

By:

Sebesta, Ivan;
Stiburkova, Blanka

Publication type:

Article

XDH gene mutation is the underlying cause of classical xanthinuria: A second report.

Published in:

Kidney International, 2000, v. 57, n. 6, p. 2215, doi. 10.1046/j.1523-1755.2000.00082.x

By:

Levartovsky, David;
Lagziel, Ayala;
Sperling, Oded;
Liberman, Uri;
Yaron, Michael;
Hosoya, Tatsuo;
Ichida, Kimiyoshi;
Peretz, Hava

Publication type:

Article

Mutations Associated with Functional Disorder of Xanthine Oxidoreductase and Hereditary Xanthinuria in Humans.

Published in:

International Journal of Molecular Sciences, 2012, v. 13, n. 11, p. 15475, doi. 10.3390/ijms131115475

By:

Ichida, Kimiyoshi;
Amaya, Yoshihiro;
Okamoto, Ken;
Nishino, Takeshi

Publication type:

Article

Hyperuricaemia, Xanthine Oxidoreductase and Ribosome-Inactivating Proteins from Plants: The Contributions of Fiorenzo Stirpe to Frontline Research.

Published in:

Molecules, 2017, v. 22, n. 2, p. 206, doi. 10.3390/molecules22020206

By:

Bolognesi, Andrea;
Bortolotti, Massimo;
Battelli, Maria Giulia;
Polito, Letizia

Publication type:

Article

Xanthine urolithiasis in a Cavalier King Charles spaniel.

Published in:

Veterinary Record: Journal of the British Veterinary Association, 2011, v. 169, n. 8, p. 209, doi. 10.1136/vr.d3932

By:

Gow, A. G.;
Fairbanks, L. D.;
Simpson, J. W.;
Jacinto, A. M. L.;
Ridyard, A. E.

Publication type:

Article

Xanthinuria in a domestic shorthair cat.

Published in:

2009

By:

Schweighauser, A.;
Howard, J.;
Malik, Y.;
Francey, T.

Publication type:

Case Study