نتائج البحث - Stibůrková, Blanka

Metabolic Syndrome, Alcohol Consumption and Genetic Factors Are Associated with Serum Uric Acid Concentration حسب Stibůrková, Blanka, Pavlíková, Markéta, Sokolová, Jitka, Kožich, Viktor

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Circulating microRNA alternations in primary hyperuricemia and gout حسب Bohatá, Jana, Horváthová, Veronika, Pavlíková, Markéta, Stibůrková, Blanka

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A heterozygous variant in the SLC22A12 gene in a Sri Lanka family associated with mild renal hypouricemia حسب Vidanapathirana, Dinesha Maduri, Jayasena, Subashinie, Jasinge, Eresha, Stiburkova, Blanka

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The impact of dysfunctional variants of ABCG2 on hyperuricemia and gout in pediatric-onset patients حسب Stiburkova, Blanka, Pavelcova, Katerina, Pavlikova, Marketa, Ješina, Pavel, Pavelka, Karel

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Complex Analysis of Urate Transporters SLC2A9, SLC22A12 and Functional Characterization of Non-Synonymous Allelic Variants of GLUT9 in the Czech Population: No Evidence of Effect o... حسب Hurba, Olha, Mancikova, Andrea, Krylov, Vladimir, Pavlikova, Marketa, Pavelka, Karel, Stibůrková, Blanka

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Familial early-onset hyperuricemia and gout associated with a newly identified dysfunctional variant in urate transporter ABCG2 حسب Toyoda, Yu, Pavelcová, Kateřina, Klein, Martin, Suzuki, Hiroshi, Takada, Tappei, Stiburkova, Blanka

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Evaluation of the Influence of Genetic Variants of SLC2A9 (GLUT9) and SLC22A12 (URAT1) on the Development of Hyperuricemia and Gout حسب Pavelcova, Katerina, Bohata, Jana, Pavlikova, Marketa, Bubenikova, Eliska, Pavelka, Karel, Stiburkova, Blanka

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Functional Characterization of Rare Variants in OAT1/SLC22A6 and OAT3/SLC22A8 Urate Transporters Identified in a Gout and Hyperuricemia Cohort حسب Vávra, Jiří, Mančíková, Andrea, Pavelcová, Kateřina, Hasíková, Lenka, Bohatá, Jana, Stibůrková, Blanka

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Interaction of the p.Q141K Variant of the ABCG2 Gene with Clinical Data and Cytokine Levels in Primary Hyperuricemia and Gout حسب Horváthová, Veronika, Bohatá, Jana, Pavlíková, Markéta, Pavelcová, Kateřina, Pavelka, Karel, Šenolt, Ladislav, Stibůrková, Blanka

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Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis حسب Stiburkova, Blanka, Sebesta, Ivan, Ichida, Kimiyoshi, Nakamura, Makiko, Hulkova, Helena, Krylov, Vladimir, Kryspinova, Lenka, Jahnova, Helena

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Identification of Two Dysfunctional Variants in the ABCG2 Urate Transporter Associated with Pediatric-Onset of Familial Hyperuricemia and Early-Onset Gout حسب Toyoda, Yu, Pavelcová, Kateřina, Bohatá, Jana, Ješina, Pavel, Kubota, Yu, Suzuki, Hiroshi, Takada, Tappei, Stiburkova, Blanka

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Renal Hypouricemia 1: Rare Disorder as Common Disease in Eastern Slovakia Roma Population حسب Stiburkova, Blanka, Bohatá, Jana, Pavelcová, Kateřina, Tasic, Velibor, Plaseska-Karanfilska, Dijana, Cho, Sung-Kweon, Potočnaková, Ludmila, Šaligová, Jana

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Analysis of Purine Metabolism to Elucidate the Pathogenesis of Acute Kidney Injury in Renal Hypouricemia حسب Miyamoto, Daisuke, Sato, Nana, Nagata, Koji, Sakai, Yukinao, Sugihara, Hitoshi, Ohashi, Yuki, Stiburkova, Blanka, Sebesta, Ivan, Ichida, Kimiyoshi, Okamoto, Ken

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Functional Characterization of Clinically-Relevant Rare Variants in ABCG2 Identified in a Gout and Hyperuricemia Cohort حسب Toyoda, Yu, Mančíková, Andrea, Krylov, Vladimír, Morimoto, Keito, Pavelcová, Kateřina, Bohatá, Jana, Pavelka, Karel, Pavlíková, Markéta, Suzuki, Hiroshi, Matsuo, Hirotaka, Takada, Tappei, Stiburkova, Blanka

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Clinical manifestations and molecular aspects of phosphoribosylpyrophosphate synthetase superactivity in females حسب Zikánová, Marie, Wahezi, Dawn, Hay, Arielle, Stibůrková, Blanka, Pitts, Charles, Mušálková, Dita, Škopová, Václava, Barešová, Veronika, Součková, Olga, Hodaňová, Kateřina, Živná, Martina, Stránecký, Viktor, Hartmannová, Hana, Hnízda, Ales, Bleyer, Anthony J, Kmoch, Stanislav

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Uric acid, an important screening tool to detect inborn errors of metabolism: a case series حسب Jasinge, Eresha, Kularatnam, Grace Angeline Malarnangai, Dilanthi, Hewa Warawitage, Vidanapathirana, Dinesha Maduri, Jayasena, Kandana Liyanage Subhashinie Priyadarshika Kapilani Menike, Chandrasiri, Nambage Dona Priyani Dhammika, Indika, Neluwa Liyanage Ruwan, Ratnayake, Pyara Dilani, Gunasekara, Vindya Nandani, Fairbanks, Lynette Dianne, Stiburkova, Blanka

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A homozygous deletion in the SLC19A1 gene as a cause of folate-dependent recurrent megaloblastic anemia حسب Svaton, Michael, Skvarova Kramarzova, Karolina, Kanderova, Veronika, Mancikova, Andrea, Smisek, Petr, Jesina, Pavel, Krijt, Jakub, Stiburkova, Blanka, Dobrovolny, Robert, Sokolova, Jitka, Bakardjieva-Mihaylova, Violeta, Vodickova, Elena, Rackova, Marketa, Stuchly, Jan, Kalina, Tomas, Stary, Jan, Trka, Jan, Fronkova, Eva, Kozich, Viktor

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Multiple common and rare variants of ABCG2 cause gout حسب Higashino, Toshihide, Takada, Tappei, Nakaoka, Hirofumi, Toyoda, Yu, Stiburkova, Blanka, Miyata, Hiroshi, Ikebuchi, Yuki, Nakashima, Hiroshi, Shimizu, Seiko, Kawaguchi, Makoto, Sakiyama, Masayuki, Nakayama, Akiyoshi, Akashi, Airi, Tanahashi, Yuki, Kawamura, Yusuke, Nakamura, Takahiro, Wakai, Kenji, Okada, Rieko, Yamamoto, Ken, Hosomichi, Kazuyoshi, Hosoya, Tatsuo, Ichida, Kimiyoshi, Ooyama, Hiroshi, Suzuki, Hiroshi, Inoue, Ituro, Merriman, Tony R, Shinomiya, Nariyoshi, Matsuo, Hirotaka

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GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes حسب Nakayama, Akiyoshi, Nakaoka, Hirofumi, Yamamoto, Ken, Sakiyama, Masayuki, Shaukat, Amara, Toyoda, Yu, Okada, Yukinori, Kamatani, Yoichiro, Nakamura, Takahiro, Takada, Tappei, Inoue, Katsuhisa, Yasujima, Tomoya, Yuasa, Hiroaki, Shirahama, Yuko, Nakashima, Hiroshi, Shimizu, Seiko, Higashino, Toshihide, Kawamura, Yusuke, Ogata, Hiraku, Kawaguchi, Makoto, Ohkawa, Yasuyuki, Danjoh, Inaho, Tokumasu, Atsumi, Ooyama, Keiko, Ito, Toshimitsu, Kondo, Takaaki, Wakai, Kenji, Stiburkova, Blanka, Pavelka, Karel, Stamp, Lisa K, Dalbeth, Nicola, Sakurai, Yutaka, Suzuki, Hiroshi, Hosoyamada, Makoto, Fujimori, Shin, Yokoo, Takashi, Hosoya, Tatsuo, Inoue, Ituro, Takahashi, Atsushi, Kubo, Michiaki, Ooyama, Hiroshi, Shimizu, Toru, Ichida, Kimiyoshi, Shinomiya, Nariyoshi, Merriman, Tony R, Matsuo, Hirotaka

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Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into gout حسب Kawamura, Yusuke, Nakaoka, Hirofumi, Nakayama, Akiyoshi, Okada, Yukinori, Yamamoto, Ken, Higashino, Toshihide, Sakiyama, Masayuki, Shimizu, Toru, Ooyama, Hiroshi, Ooyama, Keiko, Nagase, Mitsuo, Hidaka, Yuji, Shirahama, Yuko, Hosomichi, Kazuyoshi, Nishida, Yuichiro, Shimoshikiryo, Ippei, Hishida, Asahi, Katsuura-Kamano, Sakurako, Shimizu, Seiko, Kawaguchi, Makoto, Uemura, Hirokazu, Ibusuki, Rie, Hara, Megumi, Naito, Mariko, Takao, Mikiya, Nakajima, Mayuko, Iwasawa, Satoko, Nakashima, Hiroshi, Ohnaka, Keizo, Nakamura, Takahiro, Stiburkova, Blanka, Merriman, Tony R, Nakatochi, Masahiro, Ichihara, Sahoko, Yokota, Mitsuhiro, Takada, Tappei, Saitoh, Tatsuya, Kamatani, Yoichiro, Takahashi, Atsushi, Arisawa, Kokichi, Takezaki, Toshiro, Tanaka, Keitaro, Wakai, Kenji, Kubo, Michiaki, Hosoya, Tatsuo, Ichida, Kimiyoshi, Inoue, Ituro, Shinomiya, Nariyoshi, Matsuo, Hirotaka

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