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Tomato fruit cell wall : I. Use of purified tomato polygalacturonase and pectinmethylesterase to identify developmental changes in pectins.

Plant physiology

Koch JL, Nevins DJ.
PMID: 16667142
Plant Physiol. 1989 Nov;91(3):816-22. doi: 10.1104/pp.91.3.816.

Cell wall isolation procedures were evaluated to determine their effect on the total pectin content and the degree of methylesterification of tomato (Lycopersicon esculentum L.) fruit cell walls. Water homogenates liberate substantial amounts of buffer soluble uronic acid, 5.2...

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Koch JL, Nevins DJ. Tomato fruit cell wall : I. Use of purified tomato polygalacturonase and pectinmethylesterase to identify developmental changes in pectins. Plant Physiol. 1989;91(3):816-22doi: 10.1104/pp.91.3.816.
Koch, J. L., & Nevins, D. J. (1989). Tomato fruit cell wall : I. Use of purified tomato polygalacturonase and pectinmethylesterase to identify developmental changes in pectins. Plant physiology, 91(3), 816-22. https://doi.org/10.1104/pp.91.3.816
Koch, J L, and Nevins, D J. "Tomato fruit cell wall : I. Use of purified tomato polygalacturonase and pectinmethylesterase to identify developmental changes in pectins." Plant physiology vol. 91,3 (1989): 816-22. doi: https://doi.org/10.1104/pp.91.3.816
Koch JL, Nevins DJ. Tomato fruit cell wall : I. Use of purified tomato polygalacturonase and pectinmethylesterase to identify developmental changes in pectins. Plant Physiol. 1989 Nov;91(3):816-22. doi: 10.1104/pp.91.3.816. PMID: 16667142; PMCID: PMC1062081.
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Isoenzyme frequencies in long-term selection lines of Drosophila melanogaster I. Isoenzyme frequencies of the esterases (Est) and larval alkaline phosphatases (Aph) in temperature selected lines.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik

Muhs HJ.
PMID: 24419731
Theor Appl Genet. 1975 Jan;46(2):101-8. doi: 10.1007/BF00281648.

1) Lines of Drosophila melanogaster derived from a double cross of four laboratory stocks and selected for more than 125 generations were investigated by the isoenzyme method. The reference line RE was held constantly at 25°C, the selection lines...

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Muhs HJ. Isoenzyme frequencies in long-term selection lines of Drosophila melanogaster I. Isoenzyme frequencies of the esterases (Est) and larval alkaline phosphatases (Aph) in temperature selected lines. Theor Appl Genet. 1975;46(2):101-8doi: 10.1007/BF00281648.
Muhs, H. J. (1975). Isoenzyme frequencies in long-term selection lines of Drosophila melanogaster I. Isoenzyme frequencies of the esterases (Est) and larval alkaline phosphatases (Aph) in temperature selected lines. TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 46(2), 101-8. https://doi.org/10.1007/BF00281648
Muhs, H J. "Isoenzyme frequencies in long-term selection lines of Drosophila melanogaster I. Isoenzyme frequencies of the esterases (Est) and larval alkaline phosphatases (Aph) in temperature selected lines." TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik vol. 46,2 (1975): 101-8. doi: https://doi.org/10.1007/BF00281648
Muhs HJ. Isoenzyme frequencies in long-term selection lines of Drosophila melanogaster I. Isoenzyme frequencies of the esterases (Est) and larval alkaline phosphatases (Aph) in temperature selected lines. Theor Appl Genet. 1975 Jan;46(2):101-8. doi: 10.1007/BF00281648. PMID: 24419731.
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Assessment of glycogen phosphorylase isoenzyme BB as a biomarker for pre-eclampsia and small for gestational age.

Lancet (London, England)

McCarthy F, Doyle A, Khashan A, Kenny L.
PMID: 26312889
Lancet. 2015 Feb 26;385:S67. doi: 10.1016/S0140-6736(15)60382-8.

BACKGROUND: Glycogen phosphorylase is a key enzyme in the regulation of glycogen metabolism and consists of three isoenzymes, including glycogen phosphorylase isoenzyme BB (GPBB). Pre-eclampsia, gestational hypertension, and small-for-gestational-age (SGA) infants are complications in about 15% of all nulliparous...

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McCarthy F, Doyle A, Khashan A, et al. Assessment of glycogen phosphorylase isoenzyme BB as a biomarker for pre-eclampsia and small for gestational age. Lancet. 2015;385:S67doi: 10.1016/S0140-6736(15)60382-8.
McCarthy, F., Doyle, A., Khashan, A., & Kenny, L. (2015). Assessment of glycogen phosphorylase isoenzyme BB as a biomarker for pre-eclampsia and small for gestational age. Lancet (London, England), 385S67. https://doi.org/10.1016/S0140-6736(15)60382-8
McCarthy, Fergus, et al. "Assessment of glycogen phosphorylase isoenzyme BB as a biomarker for pre-eclampsia and small for gestational age." Lancet (London, England) vol. 385 (2015): S67. doi: https://doi.org/10.1016/S0140-6736(15)60382-8
McCarthy F, Doyle A, Khashan A, Kenny L. Assessment of glycogen phosphorylase isoenzyme BB as a biomarker for pre-eclampsia and small for gestational age. Lancet. 2015 Feb 26;385:S67. doi: 10.1016/S0140-6736(15)60382-8. PMID: 26312889.
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Recent innovations in asthma therapy.

Drugs of today (Barcelona, Spain : 1998)

Vianna EO, Martin RJ.
PMID: 15010722
Drugs Today (Barc). 1998 Apr;34(4):341-51. doi: 10.1358/dot.1998.34.4.485232.

Guidelines for the diagnosis and management of asthma have been published since 1990 and already new versions are being published. The recommendations for the treatment of asthma were organized around four components of effective asthma management: i) use of...

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Vianna EO, Martin RJ. Recent innovations in asthma therapy. Drugs Today (Barc). 1998;34(4):341-51doi: 10.1358/dot.1998.34.4.485232.
Vianna, E. O., & Martin, R. J. (1998). Recent innovations in asthma therapy. Drugs of today (Barcelona, Spain : 1998), 34(4), 341-51. https://doi.org/10.1358/dot.1998.34.4.485232
Vianna, E O, and Martin, R J. "Recent innovations in asthma therapy." Drugs of today (Barcelona, Spain : 1998) vol. 34,4 (1998): 341-51. doi: https://doi.org/10.1358/dot.1998.34.4.485232
Vianna EO, Martin RJ. Recent innovations in asthma therapy. Drugs Today (Barc). 1998 Apr;34(4):341-51. doi: 10.1358/dot.1998.34.4.485232. PMID: 15010722.
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Serum adenosine deaminase and its isoenzyme activities in pregnancy.

Journal of the Turkish German Gynecological Association

Bahadır G, Döventaş YE, Turkal R, Koldaş M, Basınoğlu F, Dane B, Altunkaynak E.
PMID: 24591996
J Turk Ger Gynecol Assoc. 2011 Dec 01;12(4):209-13. doi: 10.5152/jtgga.2011.53. eCollection 2011.

OBJECTIVE: ADA is widely distributed in human tissues, which may contribute to the maturation of the immunological system, especially the proliferation and differentiation of lymphoid cells, and seems to be critical at different stages of the maturation process. The...

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Bahadır G, Döventaş YE, Turkal R, et al. Serum adenosine deaminase and its isoenzyme activities in pregnancy. J Turk Ger Gynecol Assoc. 2011;12(4):209-13doi: 10.5152/jtgga.2011.53.
Bahadır, G., Döventaş, Y. E., Turkal, R., Koldaş, M., Basınoğlu, F., Dane, B., & Altunkaynak, E. (2011). Serum adenosine deaminase and its isoenzyme activities in pregnancy. Journal of the Turkish German Gynecological Association, 12(4), 209-13. https://doi.org/10.5152/jtgga.2011.53
Bahadır, Göksel, et al. "Serum adenosine deaminase and its isoenzyme activities in pregnancy." Journal of the Turkish German Gynecological Association vol. 12,4 (2011): 209-13. doi: https://doi.org/10.5152/jtgga.2011.53
Bahadır G, Döventaş YE, Turkal R, Koldaş M, Basınoğlu F, Dane B, Altunkaynak E. Serum adenosine deaminase and its isoenzyme activities in pregnancy. J Turk Ger Gynecol Assoc. 2011 Dec 01;12(4):209-13. doi: 10.5152/jtgga.2011.53. eCollection 2011. PMID: 24591996; PMCID: PMC3939251.
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Screening for drug-induced alterations in the production and release of steroid hormones by porcine adrenocortical cells in vitro.

Toxicology in vitro : an international journal published in association with BIBRA

Jager LP, De Graaf GJ, Widjaja-Greefkes HC.
PMID: 20650241
Toxicol In Vitro. 1996 Oct;10(5):595-608. doi: 10.1016/s0887-2333(96)00047-1.

To screen drugs rapidly and at minimal expense for their potential to alter steroidogenesis, an in vitro model using porcine adrenocortical cells was developed. Pregnenolone, progesterone, deoxycorticosterone or corticosterone (all at 1 muM) were used as substrates. Drug-induced changes...

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Jager LP, De Graaf GJ, Widjaja-Greefkes HC. Screening for drug-induced alterations in the production and release of steroid hormones by porcine adrenocortical cells in vitro. Toxicol In Vitro. 1996;10(5):595-608doi: 10.1016/s0887-2333(96)00047-1.
Jager, L. P., De Graaf, G. J., & Widjaja-Greefkes, H. C. (1996). Screening for drug-induced alterations in the production and release of steroid hormones by porcine adrenocortical cells in vitro. Toxicology in vitro : an international journal published in association with BIBRA, 10(5), 595-608. https://doi.org/10.1016/s0887-2333(96)00047-1
Jager, L P, et al. "Screening for drug-induced alterations in the production and release of steroid hormones by porcine adrenocortical cells in vitro." Toxicology in vitro : an international journal published in association with BIBRA vol. 10,5 (1996): 595-608. doi: https://doi.org/10.1016/s0887-2333(96)00047-1
Jager LP, De Graaf GJ, Widjaja-Greefkes HC. Screening for drug-induced alterations in the production and release of steroid hormones by porcine adrenocortical cells in vitro. Toxicol In Vitro. 1996 Oct;10(5):595-608. doi: 10.1016/s0887-2333(96)00047-1. PMID: 20650241.
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n-Butanol production in Saccharomyces cerevisiae is limited by the availability of coenzyme A and cytosolic acetyl-CoA.

Biotechnology for biofuels

Schadeweg V, Boles E.
PMID: 26913077
Biotechnol Biofuels. 2016 Feb 24;9:44. doi: 10.1186/s13068-016-0456-7. eCollection 2016.

BACKGROUND: Butanol isomers are regarded as more suitable fuel substitutes than bioethanol. n-Butanol is naturally produced by some Clostridia species, but due to inherent problems with clostridial fermentations, industrially more relevant organisms have been genetically engineered for n-butanol production....

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Schadeweg V, Boles E. n-Butanol production in Saccharomyces cerevisiae is limited by the availability of coenzyme A and cytosolic acetyl-CoA. Biotechnol Biofuels. 2016;9:44doi: 10.1186/s13068-016-0456-7.
Schadeweg, V., & Boles, E. (2016). n-Butanol production in Saccharomyces cerevisiae is limited by the availability of coenzyme A and cytosolic acetyl-CoA. Biotechnology for biofuels, 944. https://doi.org/10.1186/s13068-016-0456-7
Schadeweg, Virginia, and Boles, Eckhard. "n-Butanol production in Saccharomyces cerevisiae is limited by the availability of coenzyme A and cytosolic acetyl-CoA." Biotechnology for biofuels vol. 9 (2016): 44. doi: https://doi.org/10.1186/s13068-016-0456-7
Schadeweg V, Boles E. n-Butanol production in Saccharomyces cerevisiae is limited by the availability of coenzyme A and cytosolic acetyl-CoA. Biotechnol Biofuels. 2016 Feb 24;9:44. doi: 10.1186/s13068-016-0456-7. eCollection 2016. PMID: 26913077; PMCID: PMC4765181.
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Sevoflurane Alleviates Myocardial Ischemia Reperfusion Injury by Inhibiting P2X7-NLRP3 Mediated Pyroptosis.

Frontiers in molecular biosciences

Wu J, Cai W, Du R, Li H, Wang B, Zhou Y, Shen D, Shen H, Lan Y, Chen L, Zheng X, Huang D, Shi G.
PMID: 34765646
Front Mol Biosci. 2021 Oct 26;8:768594. doi: 10.3389/fmolb.2021.768594. eCollection 2021.

Myocardial ischemia is common in aging population. This study investigates the protective effect of Sevoflurane on myocardial ischemia reperfusion injury (MIRI) and its underlying mechanism. A total of 87 patients with a history of myocardial ischemia who underwent abdominal...

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Wu J, Cai W, Du R, et al. Sevoflurane Alleviates Myocardial Ischemia Reperfusion Injury by Inhibiting P2X7-NLRP3 Mediated Pyroptosis. Front Mol Biosci. 2021;8:768594doi: 10.3389/fmolb.2021.768594.
Wu, J., Cai, W., Du, R., Li, H., Wang, B., Zhou, Y., Shen, D., Shen, H., Lan, Y., Chen, L., Zheng, X., Huang, D., & Shi, G. (2021). Sevoflurane Alleviates Myocardial Ischemia Reperfusion Injury by Inhibiting P2X7-NLRP3 Mediated Pyroptosis. Frontiers in molecular biosciences, 8768594. https://doi.org/10.3389/fmolb.2021.768594
Wu, Jiaxuan, et al. "Sevoflurane Alleviates Myocardial Ischemia Reperfusion Injury by Inhibiting P2X7-NLRP3 Mediated Pyroptosis." Frontiers in molecular biosciences vol. 8 (2021): 768594. doi: https://doi.org/10.3389/fmolb.2021.768594
Wu J, Cai W, Du R, Li H, Wang B, Zhou Y, Shen D, Shen H, Lan Y, Chen L, Zheng X, Huang D, Shi G. Sevoflurane Alleviates Myocardial Ischemia Reperfusion Injury by Inhibiting P2X7-NLRP3 Mediated Pyroptosis. Front Mol Biosci. 2021 Oct 26;8:768594. doi: 10.3389/fmolb.2021.768594. eCollection 2021. PMID: 34765646; PMCID: PMC8576530.
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Determination of the potency of a novel saw palmetto supercritical CO2 extract (SPSE) for 5α-reductase isoform II inhibition using a cell-free in vitro test system.

Research and reports in urology

Pais P, Villar A, Rull S.
PMID: 27186566
Res Rep Urol. 2016 Apr 21;8:41-9. doi: 10.2147/RRU.S96576. eCollection 2016.

BACKGROUND: The nicotinamide adenine dinucleotide phosphate-dependent membrane protein 5α-reductase catalyses the conversion of testosterone to the most potent androgen - 5α-dihydrotestosterone. Two 5α-reductase isoenzymes are expressed in humans: type I and type II. The latter is found primarily in...

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Pais P, Villar A, Rull S. Determination of the potency of a novel saw palmetto supercritical CO2 extract (SPSE) for 5α-reductase isoform II inhibition using a cell-free in vitro test system. Res Rep Urol. 2016;8:41-9doi: 10.2147/RRU.S96576.
Pais, P., Villar, A., & Rull, S. (2016). Determination of the potency of a novel saw palmetto supercritical CO2 extract (SPSE) for 5α-reductase isoform II inhibition using a cell-free in vitro test system. Research and reports in urology, 841-9. https://doi.org/10.2147/RRU.S96576
Pais, Pilar, et al. "Determination of the potency of a novel saw palmetto supercritical CO2 extract (SPSE) for 5α-reductase isoform II inhibition using a cell-free in vitro test system." Research and reports in urology vol. 8 (2016): 41-9. doi: https://doi.org/10.2147/RRU.S96576
Pais P, Villar A, Rull S. Determination of the potency of a novel saw palmetto supercritical CO2 extract (SPSE) for 5α-reductase isoform II inhibition using a cell-free in vitro test system. Res Rep Urol. 2016 Apr 21;8:41-9. doi: 10.2147/RRU.S96576. eCollection 2016. PMID: 27186566; PMCID: PMC4847595.
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Boeravinone B alleviates gut dysbiosis during myocardial infarction-induced cardiotoxicity in rats.

Journal of cellular and molecular medicine

Chen Y, Peng L, Shi S, Guo G, Wen H.
PMID: 34028176
J Cell Mol Med. 2021 May 24; doi: 10.1111/jcmm.16620. Epub 2021 May 24.

Myocardial infarction (MI) is the most common heart disease, and also, it is one of the leading causes of death from cardiovascular disease. It is well known that MI causes additional injury during blood flow restoration in ischaemic myocardium....

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Chen Y, Peng L, Shi S, et al. Boeravinone B alleviates gut dysbiosis during myocardial infarction-induced cardiotoxicity in rats. J Cell Mol Med. 2021;doi: 10.1111/jcmm.16620.
Chen, Y., Peng, L., Shi, S., Guo, G., & Wen, H. (2021). Boeravinone B alleviates gut dysbiosis during myocardial infarction-induced cardiotoxicity in rats. Journal of cellular and molecular medicine, . https://doi.org/10.1111/jcmm.16620
Chen, Yu, et al. "Boeravinone B alleviates gut dysbiosis during myocardial infarction-induced cardiotoxicity in rats." Journal of cellular and molecular medicine vol. (2021). doi: https://doi.org/10.1111/jcmm.16620
Chen Y, Peng L, Shi S, Guo G, Wen H. Boeravinone B alleviates gut dysbiosis during myocardial infarction-induced cardiotoxicity in rats. J Cell Mol Med. 2021 May 24; doi: 10.1111/jcmm.16620. Epub 2021 May 24. PMID: 34028176; PMCID: PMC8256339.
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Association of NQO2 With UDP-Glucuronosyltransferases Reduces Menadione Toxicity in Neuroblastoma Cells.

Frontiers in pharmacology

Chhour M, Perio P, Gayon R, Ternet-Fontebasso H, Ferry G, Nepveu F, Boutin JA, Sudor J, Reybier K.
PMID: 34040527
Front Pharmacol. 2021 May 10;12:660641. doi: 10.3389/fphar.2021.660641. eCollection 2021.

The balance between detoxification and toxicity is linked to enzymes of the drug metabolism Phase I (cytochrome P450 or oxidoreductases) and phase II conjugating enzymes (such as the UGTs). After the reduction of quinones, the product of the reaction,...

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Chhour M, Perio P, Gayon R, et al. Association of NQO2 With UDP-Glucuronosyltransferases Reduces Menadione Toxicity in Neuroblastoma Cells. Front Pharmacol. 2021;12:660641doi: 10.3389/fphar.2021.660641.
Chhour, M., Perio, P., Gayon, R., Ternet-Fontebasso, H., Ferry, G., Nepveu, F., Boutin, J. A., Sudor, J., & Reybier, K. (2021). Association of NQO2 With UDP-Glucuronosyltransferases Reduces Menadione Toxicity in Neuroblastoma Cells. Frontiers in pharmacology, 12660641. https://doi.org/10.3389/fphar.2021.660641
Chhour, Monivan, et al. "Association of NQO2 With UDP-Glucuronosyltransferases Reduces Menadione Toxicity in Neuroblastoma Cells." Frontiers in pharmacology vol. 12 (2021): 660641. doi: https://doi.org/10.3389/fphar.2021.660641
Chhour M, Perio P, Gayon R, Ternet-Fontebasso H, Ferry G, Nepveu F, Boutin JA, Sudor J, Reybier K. Association of NQO2 With UDP-Glucuronosyltransferases Reduces Menadione Toxicity in Neuroblastoma Cells. Front Pharmacol. 2021 May 10;12:660641. doi: 10.3389/fphar.2021.660641. eCollection 2021. PMID: 34040527; PMCID: PMC8142080.
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Muscle atrophy induced by overexpression of ALAS2 is related to muscle mitochondrial dysfunction.

Skeletal muscle

Peng Y, Li J, Luo D, Zhang S, Li S, Wang D, Wang X, Zhang Z, Wang X, Sun C, Gao X, Hui Y, He R.
PMID: 33785075
Skelet Muscle. 2021 Mar 30;11(1):9. doi: 10.1186/s13395-021-00263-8.

BACKGROUND: ALAS2 (delta-aminolevulinate synthase 2) is one of the two isoenzymes catalyzing the synthesis of delta-aminolevulinic acid (ALA), which is the first precursor of heme synthesis. ALAS2-overexpressing transgenic mice (Tg mice) showed syndrome of porphyria, a series of diseases...

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Peng Y, Li J, Luo D, et al. Muscle atrophy induced by overexpression of ALAS2 is related to muscle mitochondrial dysfunction. Skelet Muscle. 2021;11(1):9doi: 10.1186/s13395-021-00263-8.
Peng, Y., Li, J., Luo, D., Zhang, S., Li, S., Wang, D., Wang, X., Zhang, Z., Wang, X., Sun, C., Gao, X., Hui, Y., & He, R. (2021). Muscle atrophy induced by overexpression of ALAS2 is related to muscle mitochondrial dysfunction. Skeletal muscle, 11(1), 9. https://doi.org/10.1186/s13395-021-00263-8
Peng, Yahui, et al. "Muscle atrophy induced by overexpression of ALAS2 is related to muscle mitochondrial dysfunction." Skeletal muscle vol. 11,1 (2021): 9. doi: https://doi.org/10.1186/s13395-021-00263-8
Peng Y, Li J, Luo D, Zhang S, Li S, Wang D, Wang X, Zhang Z, Wang X, Sun C, Gao X, Hui Y, He R. Muscle atrophy induced by overexpression of ALAS2 is related to muscle mitochondrial dysfunction. Skelet Muscle. 2021 Mar 30;11(1):9. doi: 10.1186/s13395-021-00263-8. PMID: 33785075; PMCID: PMC8008657.
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Showing 1 to 12 of 740 entries