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486 related items for PubMed ID: 33491567

  • 1. Generation and characterization of a novel rat model of primary hyperoxaluria type 1 with a nonsense mutation in alanine-glyoxylate aminotransferase gene.
    Li Y, Zheng R, Xu G, Huang Y, Li Y, Li D, Geng H.
    Am J Physiol Renal Physiol; 2021 Mar 01; 320(3):F475-F484. PubMed ID: 33491567
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  • 2. Generation of a Primary Hyperoxaluria Type 1 Disease Model Via CRISPR/Cas9 System in Rats.
    Zheng R, Fang X, He L, Shao Y, Guo N, Wang L, Liu M, Li D, Geng H.
    Curr Mol Med; 2018 Mar 01; 18(7):436-447. PubMed ID: 30539697
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  • 3. Hydroxyproline metabolism in mouse models of primary hyperoxaluria.
    Knight J, Holmes RP, Cramer SD, Takayama T, Salido E.
    Am J Physiol Renal Physiol; 2012 Mar 15; 302(6):F688-93. PubMed ID: 22189945
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  • 4. In vivo base editing rescues primary hyperoxaluria type 1 in rats.
    Chen Z, Zhang D, Zheng R, Yang L, Huo Y, Zhang D, Fang X, Li Y, Xu G, Li D, Geng H.
    Kidney Int; 2024 Mar 15; 105(3):496-507. PubMed ID: 38142039
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  • 8. Primary hyperoxaluria type 1 in children: clinical and laboratory manifestations and outcome.
    Wannous H.
    Pediatr Nephrol; 2023 Aug 15; 38(8):2643-2648. PubMed ID: 36917293
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  • 10. [From gene to disease; primary hyperoxaluria type I caused by mutations in the AGXT gene].
    van Woerden CS, Groothof JW, Wanders RJ, Waterham HR, Wijburg FR.
    Ned Tijdschr Geneeskd; 2006 Jul 29; 150(30):1669-72. PubMed ID: 16922352
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  • 11. Enteric oxalate elimination is induced and oxalate is normalized in a mouse model of primary hyperoxaluria following intestinal colonization with Oxalobacter.
    Hatch M, Gjymishka A, Salido EC, Allison MJ, Freel RW.
    Am J Physiol Gastrointest Liver Physiol; 2011 Mar 29; 300(3):G461-9. PubMed ID: 21163900
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  • 12. A Putative Mutation Hotspot of the AGXT Gene Associated with Primary Hyperoxaluria Type 1 in the Chinese Population.
    Li X, Gu J, Yang Y, Li J, Li Y.
    Tohoku J Exp Med; 2018 Dec 29; 246(4):233-241. PubMed ID: 30541997
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  • 13. Systemic Alanine Glyoxylate Aminotransferase mRNA Improves Glyoxylate Metabolism in a Mouse Model of Primary Hyperoxaluria Type 1.
    Kukreja A, Lasaro M, Cobaugh C, Forbes C, Tang JP, Gao X, Martin-Higueras C, Pey AL, Salido E, Sobolov S, Subramanian RR.
    Nucleic Acid Ther; 2019 Apr 29; 29(2):104-113. PubMed ID: 30676254
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  • 14. Identification of compound heterozygous patients with primary hyperoxaluria type 1: clinical evaluations and in silico investigations.
    Kanoun H, Jarraya F, Maalej B, Lahiani A, Mahfoudh H, Makni F, Hachicha J, Fakhfakh F.
    BMC Nephrol; 2017 Oct 02; 18(1):303. PubMed ID: 28969594
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  • 15. Mutation spectrum of primary hyperoxaluria type 1 in Tunisia: implication for diagnosis in North Africa.
    Nagara M, Tiar A, Ben Halim N, Ben Rhouma F, Messaoud O, Bouyacoub Y, Kefi R, Hassayoun S, Zouari N, Ben Ammar MS, Abdelhak S, Chemli J.
    Gene; 2013 Sep 15; 527(1):316-20. PubMed ID: 23810941
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  • 16. Novel mutations of the AGXT gene causing primary hyperoxaluria type 1.
    Yuen YP, Lai CK, Tong GM, Wong PN, Wong FK, Mak SK, Lo KY, Wong AK, Tong SF, Chan YW, Lam CW.
    J Nephrol; 2004 Sep 15; 17(3):436-40. PubMed ID: 15365967
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  • 18. Human MiR-4660 regulates the expression of alanine-glyoxylate aminotransferase and may be a biomarker for idiopathic oxalosis.
    Tu X, Zhao Y, Li Q, Yu X, Yang Y, Shi S, Ding Z, Miao Y, Zou Z, Wang X, Jiang J, Du D.
    Clin Exp Nephrol; 2019 Jul 15; 23(7):890-897. PubMed ID: 30852714
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  • 19. Infant primary hyperoxaluria type 1: A case report and literature review.
    Zheng Y, Li Q, Liang S.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2024 Jun 28; 49(6):856-862. PubMed ID: 39311781
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  • 20. Targeting kidney inflammation as a new therapy for primary hyperoxaluria?
    Martin-Higueras C, Ludwig-Portugall I, Hoppe B, Kurts C.
    Nephrol Dial Transplant; 2019 Jun 01; 34(6):908-914. PubMed ID: 30169827
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