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Showing 1 to 12 of 45 entries
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Estimation of Protein-Proteoses in Crude Liver Extracts for Parenteral Use.

The Indian medical gazette

Iyengar NK, Chakravarti MD, Biswas HK.
PMID: 29014426
Ind Med Gaz. 1955 Jan;90(1):3-4.

No abstract available.

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Iyengar NK, Chakravarti MD, Biswas HK. Estimation of Protein-Proteoses in Crude Liver Extracts for Parenteral Use. Ind Med Gaz. 1955;90(1):3-4
Iyengar, N. K., Chakravarti, M. D., & Biswas, H. K. (1955). Estimation of Protein-Proteoses in Crude Liver Extracts for Parenteral Use. The Indian medical gazette, 90(1), 3-4.
Iyengar, N K, et al. "Estimation of Protein-Proteoses in Crude Liver Extracts for Parenteral Use." The Indian medical gazette vol. 90,1 (1955): 3-4.
Iyengar NK, Chakravarti MD, Biswas HK. Estimation of Protein-Proteoses in Crude Liver Extracts for Parenteral Use. Ind Med Gaz. 1955 Jan;90(1):3-4. PMID: 29014426; PMCID: PMC5182539.
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Studies of single-walled carbon nanotubes-induced hepatotoxicity by NMR-based metabonomics of rat blood plasma and liver extracts.

Nanoscale research letters

Lin B, Zhang H, Lin Z, Fang Y, Tian L, Yang H, Yan J, Liu H, Zhang W, Xi Z.
PMID: 23680025
Nanoscale Res Lett. 2013 May 16;8(1):236. doi: 10.1186/1556-276X-8-236.

The toxicological effects of single-walled carbon nanotubes (SWCNTs) were investigated after intratracheal instillation in male Wistar rats over a 15-day period using metabonomic analysis of 1H (nuclear magnetic resonance) NMR spectra of blood plasma and liver tissue extracts. Concurrent...

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Lin B, Zhang H, Lin Z, et al. Studies of single-walled carbon nanotubes-induced hepatotoxicity by NMR-based metabonomics of rat blood plasma and liver extracts. Nanoscale Res Lett. 2013;8(1):236doi: 10.1186/1556-276X-8-236.
Lin, B., Zhang, H., Lin, Z., Fang, Y., Tian, L., Yang, H., Yan, J., Liu, H., Zhang, W., & Xi, Z. (2013). Studies of single-walled carbon nanotubes-induced hepatotoxicity by NMR-based metabonomics of rat blood plasma and liver extracts. Nanoscale research letters, 8(1), 236. https://doi.org/10.1186/1556-276X-8-236
Lin, Bencheng, et al. "Studies of single-walled carbon nanotubes-induced hepatotoxicity by NMR-based metabonomics of rat blood plasma and liver extracts." Nanoscale research letters vol. 8,1 (2013): 236. doi: https://doi.org/10.1186/1556-276X-8-236
Lin B, Zhang H, Lin Z, Fang Y, Tian L, Yang H, Yan J, Liu H, Zhang W, Xi Z. Studies of single-walled carbon nanotubes-induced hepatotoxicity by NMR-based metabonomics of rat blood plasma and liver extracts. Nanoscale Res Lett. 2013 May 16;8(1):236. doi: 10.1186/1556-276X-8-236. PMID: 23680025; PMCID: PMC3664573.
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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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Metabolism of steroids: The isolation of cholestane-3:5:6-triol and other substances from ox liver extracts.

The Biochemical journal

Haslewood GA.
PMID: 16747438
Biochem J. 1941 Jun;35(5):708-11. doi: 10.1042/bj0350708.

No abstract available.

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Haslewood GA. Metabolism of steroids: The isolation of cholestane-3:5:6-triol and other substances from ox liver extracts. Biochem J. 1941;35(5):708-11doi: 10.1042/bj0350708.
Haslewood, G. A. (1941). Metabolism of steroids: The isolation of cholestane-3:5:6-triol and other substances from ox liver extracts. The Biochemical journal, 35(5), 708-11. https://doi.org/10.1042/bj0350708
Haslewood, G A. "Metabolism of steroids: The isolation of cholestane-3:5:6-triol and other substances from ox liver extracts." The Biochemical journal vol. 35,5 (1941): 708-11. doi: https://doi.org/10.1042/bj0350708
Haslewood GA. Metabolism of steroids: The isolation of cholestane-3:5:6-triol and other substances from ox liver extracts. Biochem J. 1941 Jun;35(5):708-11. doi: 10.1042/bj0350708. PMID: 16747438; PMCID: PMC1265547.
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Ultrasensitive determination of trans-beta-carotene in rat and beef livers by means of high-performance liquid chromatography coupled with thermal lens detection.

Talanta

Luterotti S, Sikovec M, Bicanic D.
PMID: 18968093
Talanta. 2000 Oct 02;53(1):103-13. doi: 10.1016/s0039-9140(00)00388-x.

Hyphenated high-performance liquid chromatography (HPLC)-thermal lens spectrometry (TLS) was demonstrated as a method capable of selectively profiling carotenoids in animal livers and suitable for ultrasensitive determination of trans-beta-carotene in the same tissues. The new approach, HPLC-TLS, a first choice...

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Luterotti S, Sikovec M, Bicanic D. Ultrasensitive determination of trans-beta-carotene in rat and beef livers by means of high-performance liquid chromatography coupled with thermal lens detection. Talanta. 2000;53(1):103-13doi: 10.1016/s0039-9140(00)00388-x.
Luterotti, S., Sikovec, M., & Bicanic, D. (2000). Ultrasensitive determination of trans-beta-carotene in rat and beef livers by means of high-performance liquid chromatography coupled with thermal lens detection. Talanta, 53(1), 103-13. https://doi.org/10.1016/s0039-9140(00)00388-x
Luterotti, S, et al. "Ultrasensitive determination of trans-beta-carotene in rat and beef livers by means of high-performance liquid chromatography coupled with thermal lens detection." Talanta vol. 53,1 (2000): 103-13. doi: https://doi.org/10.1016/s0039-9140(00)00388-x
Luterotti S, Sikovec M, Bicanic D. Ultrasensitive determination of trans-beta-carotene in rat and beef livers by means of high-performance liquid chromatography coupled with thermal lens detection. Talanta. 2000 Oct 02;53(1):103-13. doi: 10.1016/s0039-9140(00)00388-x. PMID: 18968093.
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Analysis of size characterized manganese species from liver extracts using capillary zone electrophoresis coupled to inductively coupled plasma mass spectrometry (CZE-ICP-MS).

Analytica chimica acta

Quintana M, Klouda AD, Gondikas A, Ochsenkühn-Petropoulou M, Michalke B.
PMID: 17723521
Anal Chim Acta. 2006 Jul 28;573:172-80. doi: 10.1016/j.aca.2006.02.045. Epub 2006 Apr 04.

Mn is of toxicological concern because overexposure can lead to progressive, permanent neurodegenerative damage. Monomethyl-Mn-pentadienyl-tricarbonyl (MMT) is used as an anti-knock agent in fuel. Exhausted Mn compounds are absorbed in the lung and transported to the liver. Extended exposure...

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Quintana M, Klouda AD, Gondikas A, et al. Analysis of size characterized manganese species from liver extracts using capillary zone electrophoresis coupled to inductively coupled plasma mass spectrometry (CZE-ICP-MS). Anal Chim Acta. 2006;573:172-80doi: 10.1016/j.aca.2006.02.045.
Quintana, M., Klouda, A. D., Gondikas, A., Ochsenkühn-Petropoulou, M., & Michalke, B. (2006). Analysis of size characterized manganese species from liver extracts using capillary zone electrophoresis coupled to inductively coupled plasma mass spectrometry (CZE-ICP-MS). Analytica chimica acta, 573172-80. https://doi.org/10.1016/j.aca.2006.02.045
Quintana, Mercedes, et al. "Analysis of size characterized manganese species from liver extracts using capillary zone electrophoresis coupled to inductively coupled plasma mass spectrometry (CZE-ICP-MS)." Analytica chimica acta vol. 573 (2006): 172-80. doi: https://doi.org/10.1016/j.aca.2006.02.045
Quintana M, Klouda AD, Gondikas A, Ochsenkühn-Petropoulou M, Michalke B. Analysis of size characterized manganese species from liver extracts using capillary zone electrophoresis coupled to inductively coupled plasma mass spectrometry (CZE-ICP-MS). Anal Chim Acta. 2006 Jul 28;573:172-80. doi: 10.1016/j.aca.2006.02.045. Epub 2006 Apr 04. PMID: 17723521.
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A SPECIFIC POISON IN THE LIVER EXTRACTS OF RABBITS INOCULATED WITH TYPHOID AND PRODIGIOSUS BACILLI INTRAVENOUSLY.

The Journal of experimental medicine

Parker JT.
PMID: 19868279
J Exp Med. 1918 Oct 31;28(5):571-83. doi: 10.1084/jem.28.5.571.

1. The livers of rabbits inoculated with cultures of Bacillus typhosus or Bacillus prodigiosus under certain conditions contain a toxic substance extractable with salt solution. When the toxic extracts are injected intravenously into normal rabbits the latter animals develop...

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Parker JT. A SPECIFIC POISON IN THE LIVER EXTRACTS OF RABBITS INOCULATED WITH TYPHOID AND PRODIGIOSUS BACILLI INTRAVENOUSLY. J Exp Med. 1918;28(5):571-83doi: 10.1084/jem.28.5.571.
Parker, J. T. (1918). A SPECIFIC POISON IN THE LIVER EXTRACTS OF RABBITS INOCULATED WITH TYPHOID AND PRODIGIOSUS BACILLI INTRAVENOUSLY. The Journal of experimental medicine, 28(5), 571-83. https://doi.org/10.1084/jem.28.5.571
Parker, J T. "A SPECIFIC POISON IN THE LIVER EXTRACTS OF RABBITS INOCULATED WITH TYPHOID AND PRODIGIOSUS BACILLI INTRAVENOUSLY." The Journal of experimental medicine vol. 28,5 (1918): 571-83. doi: https://doi.org/10.1084/jem.28.5.571
Parker JT. A SPECIFIC POISON IN THE LIVER EXTRACTS OF RABBITS INOCULATED WITH TYPHOID AND PRODIGIOSUS BACILLI INTRAVENOUSLY. J Exp Med. 1918 Oct 31;28(5):571-83. doi: 10.1084/jem.28.5.571. PMID: 19868279; PMCID: PMC2126299.
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Nontargeted quantitation of lipid classes using hydrophilic interaction liquid chromatography-electrospray ionization mass spectrometry with single internal standard and response factor approach.

Analytical chemistry

Cífková E, Holčapek M, Lísa M, Ovčačíková M, Lyčka A, Lynen F, Sandra P.
PMID: 23072569
Anal Chem. 2012 Nov 20;84(22):10064-70. doi: 10.1021/ac3024476. Epub 2012 Nov 01.

The identification and quantitation of a wide range of lipids in complex biological samples is an essential requirement for the lipidomic studies. High-performance liquid chromatography-mass spectrometry (HPLC/MS) has the highest potential to obtain detailed information on the whole lipidome,...

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Cífková E, Holčapek M, Lísa M, et al. Nontargeted quantitation of lipid classes using hydrophilic interaction liquid chromatography-electrospray ionization mass spectrometry with single internal standard and response factor approach. Anal Chem. 2012;84(22):10064-70doi: 10.1021/ac3024476.
Cífková, E., Holčapek, M., Lísa, M., Ovčačíková, M., Lyčka, A., Lynen, F., & Sandra, P. (2012). Nontargeted quantitation of lipid classes using hydrophilic interaction liquid chromatography-electrospray ionization mass spectrometry with single internal standard and response factor approach. Analytical chemistry, 84(22), 10064-70. https://doi.org/10.1021/ac3024476
Cífková, Eva, et al. "Nontargeted quantitation of lipid classes using hydrophilic interaction liquid chromatography-electrospray ionization mass spectrometry with single internal standard and response factor approach." Analytical chemistry vol. 84,22 (2012): 10064-70. doi: https://doi.org/10.1021/ac3024476
Cífková E, Holčapek M, Lísa M, Ovčačíková M, Lyčka A, Lynen F, Sandra P. Nontargeted quantitation of lipid classes using hydrophilic interaction liquid chromatography-electrospray ionization mass spectrometry with single internal standard and response factor approach. Anal Chem. 2012 Nov 20;84(22):10064-70. doi: 10.1021/ac3024476. Epub 2012 Nov 01. PMID: 23072569.
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Traditional Chinese medicine Lingguizhugan decoction ameliorate HFD-induced hepatic-lipid deposition in mice by inhibiting STING-mediated inflammation in macrophages.

Chinese medicine

Cao L, Xu E, Zheng R, Zhangchen Z, Zhong R, Huang F, Ye J, Sun H, Fan Y, Xie S, Chen Y, Xu Y, Cao J, Cao W, Liu C.
PMID: 34983596
Chin Med. 2022 Jan 05;17(1):7. doi: 10.1186/s13020-021-00559-3.

BACKGROUND: Stimulator of IFN genes (STING) is highly expressed in the livers of non-alcoholic fatty liver disease (NAFLD) patients and high fat diet (HFD) induced NAFLD mice model. The STING signaling-mediated inflammation has been shown to play a critical...

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Cao L, Xu E, Zheng R, et al. Traditional Chinese medicine Lingguizhugan decoction ameliorate HFD-induced hepatic-lipid deposition in mice by inhibiting STING-mediated inflammation in macrophages. Chin Med. 2022;17(1):7doi: 10.1186/s13020-021-00559-3.
Cao, L., Xu, E., Zheng, R., Zhangchen, Z., Zhong, R., Huang, F., Ye, J., Sun, H., Fan, Y., Xie, S., Chen, Y., Xu, Y., Cao, J., Cao, W., & Liu, C. (2022). Traditional Chinese medicine Lingguizhugan decoction ameliorate HFD-induced hepatic-lipid deposition in mice by inhibiting STING-mediated inflammation in macrophages. Chinese medicine, 17(1), 7. https://doi.org/10.1186/s13020-021-00559-3
Cao, Lin, et al. "Traditional Chinese medicine Lingguizhugan decoction ameliorate HFD-induced hepatic-lipid deposition in mice by inhibiting STING-mediated inflammation in macrophages." Chinese medicine vol. 17,1 (2022): 7. doi: https://doi.org/10.1186/s13020-021-00559-3
Cao L, Xu E, Zheng R, Zhangchen Z, Zhong R, Huang F, Ye J, Sun H, Fan Y, Xie S, Chen Y, Xu Y, Cao J, Cao W, Liu C. Traditional Chinese medicine Lingguizhugan decoction ameliorate HFD-induced hepatic-lipid deposition in mice by inhibiting STING-mediated inflammation in macrophages. Chin Med. 2022 Jan 05;17(1):7. doi: 10.1186/s13020-021-00559-3. PMID: 34983596.
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Salmon Eggshell Protein Expression: A Marker for Environmental Estrogens.

Marine biotechnology (New York, N.Y.)

Oppen-Berntsen DO, Arukwe A, Yadetie F, Lorens JB, Male R.
PMID: 10383999
Mar Biotechnol (NY). 1999 May;1(3):252-260. doi: 10.1007/pl00011774.

: A liver complementary DNA expression library from Atlantic salmon (Salmo salar) pretreated with estradiol-17beta (E2) was constructed and screened with antibodies raised against salmon eggshell (zona radiata) proteins. Two clones, SalZr2_19 and SalZr2_23 were sequenced and shown to...

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Oppen-Berntsen DO, Arukwe A, Yadetie F, et al. Salmon Eggshell Protein Expression: A Marker for Environmental Estrogens. Mar Biotechnol (NY). 1999;1(3):252-260doi: 10.1007/pl00011774.
Oppen-Berntsen, D. O., Arukwe, A., Yadetie, F., Lorens, J. B., & Male, R. (1999). Salmon Eggshell Protein Expression: A Marker for Environmental Estrogens. Marine biotechnology (New York, N.Y.), 1(3), 252-260. https://doi.org/10.1007/pl00011774
Oppen-Berntsen, et al. "Salmon Eggshell Protein Expression: A Marker for Environmental Estrogens." Marine biotechnology (New York, N.Y.) vol. 1,3 (1999): 252-260. doi: https://doi.org/10.1007/pl00011774
Oppen-Berntsen DO, Arukwe A, Yadetie F, Lorens JB, Male R. Salmon Eggshell Protein Expression: A Marker for Environmental Estrogens. Mar Biotechnol (NY). 1999 May;1(3):252-260. doi: 10.1007/pl00011774. PMID: 10383999.
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Statins Do Not Directly Inhibit the Activity of Major Epigenetic Modifying Enzymes.

Cancers

Bridgeman S, Northrop W, Ellison G, Sabapathy T, Melton PE, Newsholme P, Mamotte CDS.
PMID: 30974899
Cancers (Basel). 2019 Apr 10;11(4). doi: 10.3390/cancers11040516.

The potential anticancer effects of statins-a widely used class of cholesterol lowering drugs-has generated significant interest, as has the use of epigenetic modifying drugs such as HDAC and DNMT inhibitors. We set out to investigate the effect of statin...

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Bridgeman S, Northrop W, Ellison G, et al. Statins Do Not Directly Inhibit the Activity of Major Epigenetic Modifying Enzymes. Cancers (Basel). 2019;11(4)doi: 10.3390/cancers11040516.
Bridgeman, S., Northrop, W., Ellison, G., Sabapathy, T., Melton, P. E., Newsholme, P., & Mamotte, C. D. S. (2019). Statins Do Not Directly Inhibit the Activity of Major Epigenetic Modifying Enzymes. Cancers, 11(4), . https://doi.org/10.3390/cancers11040516
Bridgeman, Stephanie, et al. "Statins Do Not Directly Inhibit the Activity of Major Epigenetic Modifying Enzymes." Cancers vol. 11,4 (2019). doi: https://doi.org/10.3390/cancers11040516
Bridgeman S, Northrop W, Ellison G, Sabapathy T, Melton PE, Newsholme P, Mamotte CDS. Statins Do Not Directly Inhibit the Activity of Major Epigenetic Modifying Enzymes. Cancers (Basel). 2019 Apr 10;11(4). doi: 10.3390/cancers11040516. PMID: 30974899; PMCID: PMC6521159.
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Chymase inhibitor ameliorates hepatic steatosis and fibrosis on established non-alcoholic steatohepatitis in hamsters fed a methionine- and choline-deficient diet.

Hepatology research : the official journal of the Japan Society of Hepatology

Masubuchi S, Takai S, Jin D, Tashiro K, Komeda K, Li ZL, Otsuki Y, Okamura H, Hayashi M, Uchiyama K.
PMID: 23301878
Hepatol Res. 2013 Sep;43(9):970-8. doi: 10.1111/hepr.12042. Epub 2013 Jan 10.

AIM: Chymase plays a role in the augmentation of angiotensin II formation, which is involved in liver fibrosis. The therapeutic effects of a chymase inhibitor, TY-51469, on established hepatic steatosis and fibrosis were investigated in a model of developed...

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Masubuchi S, Takai S, Jin D, et al. Chymase inhibitor ameliorates hepatic steatosis and fibrosis on established non-alcoholic steatohepatitis in hamsters fed a methionine- and choline-deficient diet. Hepatol Res. 2013;43(9):970-8doi: 10.1111/hepr.12042.
Masubuchi, S., Takai, S., Jin, D., Tashiro, K., Komeda, K., Li, Z. L., Otsuki, Y., Okamura, H., Hayashi, M., & Uchiyama, K. (2013). Chymase inhibitor ameliorates hepatic steatosis and fibrosis on established non-alcoholic steatohepatitis in hamsters fed a methionine- and choline-deficient diet. Hepatology research : the official journal of the Japan Society of Hepatology, 43(9), 970-8. https://doi.org/10.1111/hepr.12042
Masubuchi, Shinsuke, et al. "Chymase inhibitor ameliorates hepatic steatosis and fibrosis on established non-alcoholic steatohepatitis in hamsters fed a methionine- and choline-deficient diet." Hepatology research : the official journal of the Japan Society of Hepatology vol. 43,9 (2013): 970-8. doi: https://doi.org/10.1111/hepr.12042
Masubuchi S, Takai S, Jin D, Tashiro K, Komeda K, Li ZL, Otsuki Y, Okamura H, Hayashi M, Uchiyama K. Chymase inhibitor ameliorates hepatic steatosis and fibrosis on established non-alcoholic steatohepatitis in hamsters fed a methionine- and choline-deficient diet. Hepatol Res. 2013 Sep;43(9):970-8. doi: 10.1111/hepr.12042. Epub 2013 Jan 10. PMID: 23301878.
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Showing 1 to 12 of 45 entries