Inventaire - arkadaşlarınız ve topluluklarınız en iyi kitaplığınızdır

Contribution of SLC22A12 on hypouricemia and its clinical significance for screening purposes

yazar

Heon Yung Gee

Daeui Park

Sung Kweon Cho

Cheryl A Winkler

Sun Ha Jee

1963 -

yayınlandığı: Bilimsel Raporlar

yayımlanma tarihi: 2019-10-07

Cites articles 41

Date

Başlık

Yazarlar

2018-10-10

Evaluation of the diet wide contribution to serum urate levels: meta-analysis of population based cohorts

Tanya Flynn, Ruth Topless, Nicola Dalbeth, Tony Merriman
2018-10-12

Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels

Adrienne Tin, Yong Li, Jennifer Body, Teresa Nutile, Qiong Yang, Cassianne Robinson-Cohen, Jun Liu, Ayşe Demirkan, Alexander Teumer, Marina Ciullo, Zoltán Kutalik, Owen M Woodward, Anna Köttgen, Cornelia M. van Duijn, Caroline S Fox
2017-04-27

Prevalence and complications of hypouricemia in a general population: A large-scale cross-sectional study in Japan

Masanari Kuwabara
2017-08-01

Cohort Profile: The Korean Genome and Epidemiology Study (KoGES) Consortium
2016-04-27

A Novel Homozygous SLC2A9 Mutation Associated with Renal-Induced Hypouricemia

Marco Ritelli
2016-03-12

Rare case of nephrocalcinosis in the distal tubules caused by hereditary renal hypouricaemia 3 months after kidney transplantation
2015-02-23

Depletion of Uric Acid Due to SLC22A12 (URAT1) Loss-of-Function Mutation Causes Endothelial Dysfunction in Hypouricemia.

Masanari Kuwabara, Yukihito Higashi
2015-11-24

Discovery of URAT1 SNPs and association between serum uric acid levels and URAT1

Sun Ha Jee, Soriul Kim
2015-10-15

Molecular basis of ligand recognition and transport by glucose transporters

Meng Ke, Masaki Yamamoto, Nieng Yan
2015-09-30

Structure and mechanism of the mammalian fructose transporter GLUT5

Takatoshi Arakawa, Grégory Verdon, David Drew, Takeshi Murata
2015-01-01

The I-TASSER Suite: protein structure and function prediction.

Jianyi Yang
2014-10-06

Expression, purification, and structural insights for the human uric acid transporter, GLUT9, using the Xenopus laevis oocytes system

Olivier Bonny, Matthias A Hediger
2014-03-19

A novel homozygous GLUT9 mutation cause recurrent exercise-induced acute renal failure and posterior reversible encephalopathy syndrome
2014-04-01

MutationTaster2: mutation prediction for the deep-sequencing age.

David N. Cooper, Dominik Seelow
2013-02

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

Christian Hengstenberg, Peter Vollenweider, Christian Gieger, Henry Völzke, Alexander Teumer, Fernando Rivadeneira, Hugh Christian Watkins, Ulf Gyllensten, Igor Rudan, Serena Sanna, Veronique Vitart, Markus Perola, Massimo Mangino, Asa Johansson, Murielle Bochud, Vilmundur Gudnason, Luigi Ferrucci, Veikko Salomaa, Nicole Soranzo, Inga Prokopenko, Eric Boerwinkle, Philippe Froguel, Cornelia M. van Duijn, Heinz Erich Wichmann, Caroline Hayward, Claudia Langenberg, Anke Tönjes, Daniela Toniolo, Marina Ciullo, Sheila Ulivi, Claudia Schurmann, Abbas Dehghan, Andres Metspalu, Tõnu Esko, Mika Kähönen, Terho Lehtimäki, Samuli Ripatti, Melanie Waldenberger, Naoyuki Kamatani, André Uitterlinden, Tanja Zeller, Winfried März, Tatijana Zemunik, Maksim Struchalin, Olli Raitakari, Albert Tenesa, Pio D'Adamo, Jorma Viikari, Antti Jula, Beverley Balkau, Nabila Bouatia-Naji, Albert Hofman, Bruce M. Psaty, Helena Schmidt, Michael Stumvoll, Zoltán Kutalik, Anna Köttgen, Matthias Nauck, Josef Coresh, Myriam Fornage, Harold Snieder, Gerjan Navis, Evropi Theodoratou, Maria Grazia Piras, Francesco Cucca, Darina Czamara, Angela Döring, Marcel Bruinenberg, Arnold von Eckardstein, Nicole Probst-Hensch, Medea Imboden, Olivier Devuyst, Gérard Waeber, Ozren Polašek, Gian Andri Thun, Maristella Steri, Halit Ongen, Loic Yengo, Stefan Kloiber, Nicola Pirastu, Giovanni Malerba, Lorna M. Lopez, Pau Navarro, Maris Laan, Marcus E Kleber, Andrew A Hicks, Toshihiro Tanaka, Andres Salumets, Alan J. Gow, Malcolm G. Dunlop, Albert V. Smith, Fabian J. Theis, John Attia, Ronald P. Stolk, Alan R. Shuldiner, Wiek H van Gilst, Nick Martin, Ivana Kolcic, Mark Caulfield, Daniela Ruggiero, Grant W. Montgomery, Ian Deary, Jerome I Rotter, Elin Org, Christopher P Nelson, Christopher Oldmeadow, Tamara B. Harris, Brenda Penninx, Ayşe Demirkan, Nilesh Samani, Nicholas J. Wareham, Ruth J. Loos, Lenore J Launer, Andrew Singleton, Pim van der Harst, Federico Murgia, Mary Feitosa, Kay-Tee Khaw, Konstantin Strauch, David S Siscovick, Norman Klopp, Ingrid B Borecki, Paul Ridker, Daniel I Chasman, Patricia B Munroe, Lynda M Rose, Jacqueline C M Witteman, Jaspal Kooner, James F. Wilson, Harry Campbell, Tim Spector, Caroline S Fox, Toshiko Tanaka, Anuj Goel, Hans L Hillege, James F Meschia, Michiaki Kubo, Jennifer E Huffman, Ilja M Nolte, Sarah H Wild, Nicholas D Hastie, Peter P. Pramstaller, John G Peden, W. H. Linda Kao, Bruce H Wolffenbuttel, Owen M Woodward, Michael Marmot, John B Whitfield, Poorva Mudgal, Vasiliki Lagou, Irene Mateo Leach, Perttu Salo, Aaron Isaacs, Ramaiah Nagaraja, Giovanni Gambaro, Adrienne Tin, Afshin Parsa, Jeffrey E Metter, Philipp S Wild, Gary Curhan, Patrick McArdle, Bernhard R. Winkelmann, Aldi Kraja, Claudia Hundertmark, Conall M O'Seaghdha, Elizabeth Holliday, Rossella Sorice, Giorgio Pistis, Sala Cinzia Felicita, Mario Pirastu, Mirna Kirin, Sabine Schipf, Toomas Haller, Susanne Lucae, Rita P Middelberg, Antonio Lupo, Ivana Persico, Johannes H Smit, Susan M Farrington, Jan Krumsiek, Margus Viigimaa, Kathrin Budde, Kiang Liu, Margus Putku, Robert M Plenge, Gauti Kjartan Gislason, Alan F Wright, David R. Jacobs, Eva Albrecht, Yūsuke Nakamura, Bernhard Otto Boehm, Peter Kraft
2013-02-06

Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis

Vladimir Krylov, Blanka Stibůrková, Ivan Sebesta
2013-11-19

Hereditary renal hypouricemia: a new role for allopurinol?

Blanka Stibůrková, Joann N Bodurtha
2012-04-21

Acute kidney injury in two children caused by renal hypouricaemia type 2.
2011-12-01

Diagnostic tests for primary renal hypouricemia

Ivan Sebesta, Blanka Stibůrková, Josef Bártl
2011-07-16

In addition to malnutrition and renal function impairment, anemia is associated with hyponatremia in the elderly
2011

Clinical and functional characterization of URAT1 variants

John A. Sayer, Naohiko Anzai
2011-03-31

Improving the assessment of the outcome of nonsynonymous SNVs with a consensus deleteriousness score, Condel

Núria López-Bigas, Abel Gonzalez-Perez
2010-12-09

URAT1 mutations cause renal hypouricemia type 1 in Iraqi Jews.
2010-06-30

Variation in the Uric Acid Transporter Gene SLC2A9 and Its Association with AAO of Parkinson’s Disease

Caroline Hayward, Christine Klein, Andrew A Hicks, Cosetta Minelli, Vladimir Kostić
2010-04

A method and server for predicting damaging missense mutations

Peer Bork, Leonid Peshkin
2010-12-05

Toward the estimation of the absolute quality of individual protein structure models

Torsten Schwede
2009-10-01

Recent insights into the pathogenesis of hyperuricaemia and gout

Stuart H Ralston
2009

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
2008-09

Age and origin of the G774A mutation in SLC22A12 causing renal hypouricemia in Japanese
2007-03-01

New insights into renal transport of urate

Naohiko Anzai
2006-05-05

Hereditary renal hypouricemia
2005-05-24

Mutational analysis of idiopathic renal hypouricemia in Korea

Suhnggwon Kim

Makale - wd:Q90575612

Welcome to Inventaire

arkadaşlarınızın ve topluluklarınızın kütüphanesi

daha fazlasını öğrenin