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Adenine phosphoribosyltransferase isoforms of Arabidopsis and their potential contributions to adenine and cytokinin metabolism.

Physiologia plantarum

Allen M, Qin W, Moreau F, Moffatt B.
PMID: 12010467
Physiol Plant. 2002 May;115(1):56-68. doi: 10.1034/j.1399-3054.2002.1150106.x.

Adenine phosphoribosyltransferase (APT; EC 2.4.2.7) is a constitutively expressed enzyme involved in the one-step salvage of adenine to AMP. The Arabidopsis thaliana genome contains five sequences annotated as encoding APT or APT-like enzymes. Three of these have now been...

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Allen M, Qin W, Moreau F, et al. Adenine phosphoribosyltransferase isoforms of Arabidopsis and their potential contributions to adenine and cytokinin metabolism. Physiol Plant. 2002;115(1):56-68doi: 10.1034/j.1399-3054.2002.1150106.x.
Allen, M., Qin, W., Moreau, F., & Moffatt, B. (2002). Adenine phosphoribosyltransferase isoforms of Arabidopsis and their potential contributions to adenine and cytokinin metabolism. Physiologia plantarum, 115(1), 56-68. https://doi.org/10.1034/j.1399-3054.2002.1150106.x
Allen, Michael, et al. "Adenine phosphoribosyltransferase isoforms of Arabidopsis and their potential contributions to adenine and cytokinin metabolism." Physiologia plantarum vol. 115,1 (2002): 56-68. doi: https://doi.org/10.1034/j.1399-3054.2002.1150106.x
Allen M, Qin W, Moreau F, Moffatt B. Adenine phosphoribosyltransferase isoforms of Arabidopsis and their potential contributions to adenine and cytokinin metabolism. Physiol Plant. 2002 May;115(1):56-68. doi: 10.1034/j.1399-3054.2002.1150106.x. PMID: 12010467.
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Purine-phosphoribosyltransferase activities in rat and mouse tissues and in Ehrlich ascites-tumour cells.

The Biochemical journal

Murray AW.
PMID: 16742414
Biochem J. 1966 Sep;100(3):664-70. doi: 10.1042/bj1000664.

1. The activities of adenine phosphoribosyltransferase and hypoxanthine phosphoribosyltransferase in extracts of rat and mouse liver, brain, spleen, heart and kidney, of rat bone marrow and of Ehrlich ascites-tumour cells have been measured. The specific activity of adenine phosphoribosyltransferase...

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Murray AW. Purine-phosphoribosyltransferase activities in rat and mouse tissues and in Ehrlich ascites-tumour cells. Biochem J. 1966;100(3):664-70doi: 10.1042/bj1000664.
Murray, A. W. (1966). Purine-phosphoribosyltransferase activities in rat and mouse tissues and in Ehrlich ascites-tumour cells. The Biochemical journal, 100(3), 664-70. https://doi.org/10.1042/bj1000664
Murray, A W. "Purine-phosphoribosyltransferase activities in rat and mouse tissues and in Ehrlich ascites-tumour cells." The Biochemical journal vol. 100,3 (1966): 664-70. doi: https://doi.org/10.1042/bj1000664
Murray AW. Purine-phosphoribosyltransferase activities in rat and mouse tissues and in Ehrlich ascites-tumour cells. Biochem J. 1966 Sep;100(3):664-70. doi: 10.1042/bj1000664. PMID: 16742414; PMCID: PMC1265199.
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Changes of purine and pyrimidine nucleotide biosynthesis during shoot initiation from epicotyl explants of white spruce (Picea glauca).

Plant science : an international journal of experimental plant biology

Stasolla C, Loukanina N, Ashihara H, Yeung EC, Thorpe TA.
PMID: 22980203
Plant Sci. 2006 Sep;171(3):345-54. doi: 10.1016/j.plantsci.2006.04.004. Epub 2006 May 15.

Nucleotide metabolism was investigated during white spruce organogenesis by following the metabolic fate of (14)C-labeled adenine, adenosine and inosine, as purine precursors, and orotic acid, uridine, and uracil, as pyrimidine intermediates. Key enzymes of purine and pyrimidine metabolism were...

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Stasolla C, Loukanina N, Ashihara H, et al. Changes of purine and pyrimidine nucleotide biosynthesis during shoot initiation from epicotyl explants of white spruce (Picea glauca). Plant Sci. 2006;171(3):345-54doi: 10.1016/j.plantsci.2006.04.004.
Stasolla, C., Loukanina, N., Ashihara, H., Yeung, E. C., & Thorpe, T. A. (2006). Changes of purine and pyrimidine nucleotide biosynthesis during shoot initiation from epicotyl explants of white spruce (Picea glauca). Plant science : an international journal of experimental plant biology, 171(3), 345-54. https://doi.org/10.1016/j.plantsci.2006.04.004
Stasolla, Claudio, et al. "Changes of purine and pyrimidine nucleotide biosynthesis during shoot initiation from epicotyl explants of white spruce (Picea glauca)." Plant science : an international journal of experimental plant biology vol. 171,3 (2006): 345-54. doi: https://doi.org/10.1016/j.plantsci.2006.04.004
Stasolla C, Loukanina N, Ashihara H, Yeung EC, Thorpe TA. Changes of purine and pyrimidine nucleotide biosynthesis during shoot initiation from epicotyl explants of white spruce (Picea glauca). Plant Sci. 2006 Sep;171(3):345-54. doi: 10.1016/j.plantsci.2006.04.004. Epub 2006 May 15. PMID: 22980203.
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Adenine Phosphoribosyltransferase Deficiency: A Potentially Reversible Cause of CKD.

Kidney international reports

Li J, Shingde M, Nankivell BJ, Tchan MC, Bose B, Chapman JR, Kable K, Kim SK, Vucak-Dzumhur M, Wong G, Rangan GK.
PMID: 31440706
Kidney Int Rep. 2019 May 07;4(8):1161-1170. doi: 10.1016/j.ekir.2019.04.021. eCollection 2019 Aug.

No abstract available.

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Li J, Shingde M, Nankivell BJ, et al. Adenine Phosphoribosyltransferase Deficiency: A Potentially Reversible Cause of CKD. Kidney Int Rep. 2019;4(8):1161-1170doi: 10.1016/j.ekir.2019.04.021.
Li, J., Shingde, M., Nankivell, B. J., Tchan, M. C., Bose, B., Chapman, J. R., Kable, K., Kim, S. K., Vucak-Dzumhur, M., Wong, G., & Rangan, G. K. (2019). Adenine Phosphoribosyltransferase Deficiency: A Potentially Reversible Cause of CKD. Kidney international reports, 4(8), 1161-1170. https://doi.org/10.1016/j.ekir.2019.04.021
Li, Jennifer, et al. "Adenine Phosphoribosyltransferase Deficiency: A Potentially Reversible Cause of CKD." Kidney international reports vol. 4,8 (2019): 1161-1170. doi: https://doi.org/10.1016/j.ekir.2019.04.021
Li J, Shingde M, Nankivell BJ, Tchan MC, Bose B, Chapman JR, Kable K, Kim SK, Vucak-Dzumhur M, Wong G, Rangan GK. Adenine Phosphoribosyltransferase Deficiency: A Potentially Reversible Cause of CKD. Kidney Int Rep. 2019 May 07;4(8):1161-1170. doi: 10.1016/j.ekir.2019.04.021. eCollection 2019 Aug. PMID: 31440706; PMCID: PMC6698309.
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Dihydroxyadenine crystal-induced nephropathy presenting with rapidly progressive renal failure.

Kidney research and clinical practice

Verma R, Niraimathi M, Prasad P, Agrawal V.
PMID: 30254853
Kidney Res Clin Pract. 2018 Sep;37(3):287-291. doi: 10.23876/j.krcp.2018.37.3.287. Epub 2018 Sep 30.

Adenine phosphoribosyltransferase enzyme deficiency is a rare, autosomal recessive disorder. It is a disease limited to the renal system and usually presents with urolithiasis. Herein, we report a young female with dihydroxyadenine (DHA) crystal-induced nephropathy presenting with rapidly progressive...

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Verma R, Niraimathi M, Prasad P, et al. Dihydroxyadenine crystal-induced nephropathy presenting with rapidly progressive renal failure. Kidney Res Clin Pract. 2018;37(3):287-291doi: 10.23876/j.krcp.2018.37.3.287.
Verma, R., Niraimathi, M., Prasad, P., & Agrawal, V. (2018). Dihydroxyadenine crystal-induced nephropathy presenting with rapidly progressive renal failure. Kidney research and clinical practice, 37(3), 287-291. https://doi.org/10.23876/j.krcp.2018.37.3.287
Verma, Ritu, et al. "Dihydroxyadenine crystal-induced nephropathy presenting with rapidly progressive renal failure." Kidney research and clinical practice vol. 37,3 (2018): 287-291. doi: https://doi.org/10.23876/j.krcp.2018.37.3.287
Verma R, Niraimathi M, Prasad P, Agrawal V. Dihydroxyadenine crystal-induced nephropathy presenting with rapidly progressive renal failure. Kidney Res Clin Pract. 2018 Sep;37(3):287-291. doi: 10.23876/j.krcp.2018.37.3.287. Epub 2018 Sep 30. PMID: 30254853; PMCID: PMC6147197.
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Adenine Phosphoribosyltransferase Deficiency: A Rare Cause of Recurrent Urolithiasis.

Journal of endourology case reports

Jaffer A, Joyce A, Koenig P, Biyani CS.
PMID: 28466077
J Endourol Case Rep. 2017 Apr 01;3(1):49-51. doi: 10.1089/cren.2017.0015. eCollection 2017.

No abstract available.

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Jaffer A, Joyce A, Koenig P, et al. Adenine Phosphoribosyltransferase Deficiency: A Rare Cause of Recurrent Urolithiasis. J Endourol Case Rep. 2017;3(1):49-51doi: 10.1089/cren.2017.0015.
Jaffer, A., Joyce, A., Koenig, P., & Biyani, C. S. (2017). Adenine Phosphoribosyltransferase Deficiency: A Rare Cause of Recurrent Urolithiasis. Journal of endourology case reports, 3(1), 49-51. https://doi.org/10.1089/cren.2017.0015
Jaffer, Ata, et al. "Adenine Phosphoribosyltransferase Deficiency: A Rare Cause of Recurrent Urolithiasis." Journal of endourology case reports vol. 3,1 (2017): 49-51. doi: https://doi.org/10.1089/cren.2017.0015
Jaffer A, Joyce A, Koenig P, Biyani CS. Adenine Phosphoribosyltransferase Deficiency: A Rare Cause of Recurrent Urolithiasis. J Endourol Case Rep. 2017 Apr 01;3(1):49-51. doi: 10.1089/cren.2017.0015. eCollection 2017. PMID: 28466077; PMCID: PMC5399732.
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Phosphorylation of cytokinin by adenosine kinase from wheat germ.

Plant physiology

Chen CM, Eckert RL.
PMID: 16659870
Plant Physiol. 1977 Mar;59(3):443-7. doi: 10.1104/pp.59.3.443.

Adenosine kinase was partially purified from wheat germ. This enzyme preparation, which was devoid of adenine phosphoribosyltransferase and nearly free of adenosine deaminase but contained adenylate kinase, rapidly phosphorylated adenosine and a cytokinin, N(6)-(delta(2)-isopentenyl)adenosine. Electrophoretic analysis indicated that only...

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Chen CM, Eckert RL. Phosphorylation of cytokinin by adenosine kinase from wheat germ. Plant Physiol. 1977;59(3):443-7doi: 10.1104/pp.59.3.443.
Chen, C. M., & Eckert, R. L. (1977). Phosphorylation of cytokinin by adenosine kinase from wheat germ. Plant physiology, 59(3), 443-7. https://doi.org/10.1104/pp.59.3.443
Chen, C M, and Eckert, R L. "Phosphorylation of cytokinin by adenosine kinase from wheat germ." Plant physiology vol. 59,3 (1977): 443-7. doi: https://doi.org/10.1104/pp.59.3.443
Chen CM, Eckert RL. Phosphorylation of cytokinin by adenosine kinase from wheat germ. Plant Physiol. 1977 Mar;59(3):443-7. doi: 10.1104/pp.59.3.443. PMID: 16659870; PMCID: PMC542421.
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Adenine phosphoribosyltransferase (APRT) deficiency: a new genetic mutation with early recurrent renal stone disease in kidney transplantation.

NDT plus

Micheli V, Massarino F, Jacomelli G, Bertelli M, Corradi MR, Guerrini A, Cucchiara A, Ravetti JL, Negretti L, Cannella G.
PMID: 25984046
NDT Plus. 2010 Oct;3(5):436-8. doi: 10.1093/ndtplus/sfq096. Epub 2010 Jun 02.

Adenine phosphoribosyltransferase (APRT) deficiency, a rare inborn error inherited as an autosomic recessive trait, presents with 2,8-dihydroxyadenine (2,8-DHA) crystal nephropathy. We describe clinical, biochemical and molecular findings in a renal transplant recipient with renal failure, 2,8-DHA stones and no...

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Micheli V, Massarino F, Jacomelli G, et al. Adenine phosphoribosyltransferase (APRT) deficiency: a new genetic mutation with early recurrent renal stone disease in kidney transplantation. NDT Plus. 2010;3(5):436-8doi: 10.1093/ndtplus/sfq096.
Micheli, V., Massarino, F., Jacomelli, G., Bertelli, M., Corradi, M. R., Guerrini, A., Cucchiara, A., Ravetti, J. L., Negretti, L., & Cannella, G. (2010). Adenine phosphoribosyltransferase (APRT) deficiency: a new genetic mutation with early recurrent renal stone disease in kidney transplantation. NDT plus, 3(5), 436-8. https://doi.org/10.1093/ndtplus/sfq096
Micheli, Vanna, et al. "Adenine phosphoribosyltransferase (APRT) deficiency: a new genetic mutation with early recurrent renal stone disease in kidney transplantation." NDT plus vol. 3,5 (2010): 436-8. doi: https://doi.org/10.1093/ndtplus/sfq096
Micheli V, Massarino F, Jacomelli G, Bertelli M, Corradi MR, Guerrini A, Cucchiara A, Ravetti JL, Negretti L, Cannella G. Adenine phosphoribosyltransferase (APRT) deficiency: a new genetic mutation with early recurrent renal stone disease in kidney transplantation. NDT Plus. 2010 Oct;3(5):436-8. doi: 10.1093/ndtplus/sfq096. Epub 2010 Jun 02. PMID: 25984046; PMCID: PMC4421695.
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Lack of cross-resistance to FF-10501, an inhibitor of inosine-5'-monophosphate dehydrogenase, in azacitidine-resistant cell lines selected from SKM-1 and MOLM-13 leukemia cell lines.

Pharmacology research & perspectives

Murase M, Iwamura H, Komatsu K, Saito M, Maekawa T, Nakamura T, Yokokawa T, Shimada Y.
PMID: 26977297
Pharmacol Res Perspect. 2016 Jan 28;4(1):e00206. doi: 10.1002/prp2.206. eCollection 2016 Feb.

Resistance to azacitidine is a major issue in the treatments of myelodysplastic syndrome and acute myeloid leukemia, and previous studies suggest that changes in drug metabolism are involved in the resistance. Therefore, drugs with mechanisms resistant or alternative to...

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Murase M, Iwamura H, Komatsu K, et al. Lack of cross-resistance to FF-10501, an inhibitor of inosine-5'-monophosphate dehydrogenase, in azacitidine-resistant cell lines selected from SKM-1 and MOLM-13 leukemia cell lines. Pharmacol Res Perspect. 2016;4(1):e00206doi: 10.1002/prp2.206.
Murase, M., Iwamura, H., Komatsu, K., Saito, M., Maekawa, T., Nakamura, T., Yokokawa, T., & Shimada, Y. (2016). Lack of cross-resistance to FF-10501, an inhibitor of inosine-5'-monophosphate dehydrogenase, in azacitidine-resistant cell lines selected from SKM-1 and MOLM-13 leukemia cell lines. Pharmacology research & perspectives, 4(1), e00206. https://doi.org/10.1002/prp2.206
Murase, Motohiko, et al. "Lack of cross-resistance to FF-10501, an inhibitor of inosine-5'-monophosphate dehydrogenase, in azacitidine-resistant cell lines selected from SKM-1 and MOLM-13 leukemia cell lines." Pharmacology research & perspectives vol. 4,1 (2016): e00206. doi: https://doi.org/10.1002/prp2.206
Murase M, Iwamura H, Komatsu K, Saito M, Maekawa T, Nakamura T, Yokokawa T, Shimada Y. Lack of cross-resistance to FF-10501, an inhibitor of inosine-5'-monophosphate dehydrogenase, in azacitidine-resistant cell lines selected from SKM-1 and MOLM-13 leukemia cell lines. Pharmacol Res Perspect. 2016 Jan 28;4(1):e00206. doi: 10.1002/prp2.206. eCollection 2016 Feb. PMID: 26977297; PMCID: PMC4777262.
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Use of LightCycler mutation analysis to detect type II adenine phosphoribosyltransferase deficiency in two patients with 2,8-dihydroxyadeninuria.

CEN case reports

Ikeda H, Watanabe T, Toyama D, Isoyama K.
PMID: 28509161
CEN Case Rep. 2016 May;5(1):34-39. doi: 10.1007/s13730-015-0186-x. Epub 2015 May 26.

Recently, a number of methods have been devised for detection of mutations in the field of molecular genetics. The LightCycler system has been used for rapid PCR, while simultaneously quantifying and analyzing the amplification results. We tried to apply...

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Ikeda H, Watanabe T, Toyama D, et al. Use of LightCycler mutation analysis to detect type II adenine phosphoribosyltransferase deficiency in two patients with 2,8-dihydroxyadeninuria. CEN Case Rep. 2015;5(1):34-39doi: 10.1007/s13730-015-0186-x.
Ikeda, H., Watanabe, T., Toyama, D., & Isoyama, K. (2016). Use of LightCycler mutation analysis to detect type II adenine phosphoribosyltransferase deficiency in two patients with 2,8-dihydroxyadeninuria. CEN case reports, 5(1), 34-39. https://doi.org/10.1007/s13730-015-0186-x
Ikeda, Hirokazu, et al. "Use of LightCycler mutation analysis to detect type II adenine phosphoribosyltransferase deficiency in two patients with 2,8-dihydroxyadeninuria." CEN case reports vol. 5,1 (2016): 34-39. doi: https://doi.org/10.1007/s13730-015-0186-x
Ikeda H, Watanabe T, Toyama D, Isoyama K. Use of LightCycler mutation analysis to detect type II adenine phosphoribosyltransferase deficiency in two patients with 2,8-dihydroxyadeninuria. CEN Case Rep. 2016 May;5(1):34-39. doi: 10.1007/s13730-015-0186-x. Epub 2015 May 26. PMID: 28509161; PMCID: PMC5411657.
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An Unusual Course of a 2,8-Dihydroxyadeninuria Crystalline Nephropathy Secondary to Adenine Phosphoribosyltransferase Deficiency.

Nephron

Nourié N, Nassereddine H, Azar H.
PMID: 34044400
Nephron. 2021;145(5):503-507. doi: 10.1159/000516281. Epub 2021 May 27.

Adenine phosphoribosyltransferase (APRT) deficiency is a rare disorder caused by an autosomal recessive genetic disease leading to the deposition of 2,8-dihydroxyadenine (2,8-DHA) in the kidney. The disease remains under-recognized, oftentimes diagnosed in late stages of renal insufficiency or a...

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Nourié N, Nassereddine H, Azar H. An Unusual Course of a 2,8-Dihydroxyadeninuria Crystalline Nephropathy Secondary to Adenine Phosphoribosyltransferase Deficiency. Nephron. 2021;145(5):503-507doi: 10.1159/000516281.
Nourié, N., Nassereddine, H., & Azar, H. (2021). An Unusual Course of a 2,8-Dihydroxyadeninuria Crystalline Nephropathy Secondary to Adenine Phosphoribosyltransferase Deficiency. Nephron, 145(5), 503-507. https://doi.org/10.1159/000516281
Nourié, Nicole, et al. "An Unusual Course of a 2,8-Dihydroxyadeninuria Crystalline Nephropathy Secondary to Adenine Phosphoribosyltransferase Deficiency." Nephron vol. 145,5 (2021): 503-507. doi: https://doi.org/10.1159/000516281
Nourié N, Nassereddine H, Azar H. An Unusual Course of a 2,8-Dihydroxyadeninuria Crystalline Nephropathy Secondary to Adenine Phosphoribosyltransferase Deficiency. Nephron. 2021;145(5):503-507. doi: 10.1159/000516281. Epub 2021 May 27. PMID: 34044400.
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Integrated analysis of transcriptomic and proteomic analyses reveals different metabolic patterns in the livers of Tibetan and Yorkshire pigs.

Animal bioscience

Duan M, Wang Z, Guo X, Wang K, Liu S, Zhang B, Shang P.
PMID: 33152227
Anim Biosci. 2021 May;34(5):922-930. doi: 10.5713/ajas.20.0342. Epub 2020 Oct 13.

OBJECTIVE: Tibetan pigs, predominantly originating from the Tibetan Plateau, have been subjected to long-term natural selection in an extreme environment. To characterize the metabolic adaptations to hypoxic conditions, transcriptomic and proteomic expression patterns in the livers of Tibetan and...

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Duan M, Wang Z, Guo X, et al. Integrated analysis of transcriptomic and proteomic analyses reveals different metabolic patterns in the livers of Tibetan and Yorkshire pigs. Anim Biosci. 2020;34(5):922-930doi: 10.5713/ajas.20.0342.
Duan, M., Wang, Z., Guo, X., Wang, K., Liu, S., Zhang, B., & Shang, P. (2021). Integrated analysis of transcriptomic and proteomic analyses reveals different metabolic patterns in the livers of Tibetan and Yorkshire pigs. Animal bioscience, 34(5), 922-930. https://doi.org/10.5713/ajas.20.0342
Duan, Mengqi, et al. "Integrated analysis of transcriptomic and proteomic analyses reveals different metabolic patterns in the livers of Tibetan and Yorkshire pigs." Animal bioscience vol. 34,5 (2021): 922-930. doi: https://doi.org/10.5713/ajas.20.0342
Duan M, Wang Z, Guo X, Wang K, Liu S, Zhang B, Shang P. Integrated analysis of transcriptomic and proteomic analyses reveals different metabolic patterns in the livers of Tibetan and Yorkshire pigs. Anim Biosci. 2021 May;34(5):922-930. doi: 10.5713/ajas.20.0342. Epub 2020 Oct 13. PMID: 33152227; PMCID: PMC8100475.
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Showing 1 to 12 of 37 entries