Artículos de revistas sobre el tema "Transsulfuration pathway"
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Berry, Thomas, Eid Abohamza y Ahmed A. Moustafa. "Treatment-resistant schizophrenia: focus on the transsulfuration pathway". Reviews in the Neurosciences 31, n.º 2 (28 de enero de 2020): 219–32. http://dx.doi.org/10.1515/revneuro-2019-0057.
Texto completoSbodio, Juan I., Solomon H. Snyder y Bindu D. Paul. "Regulators of the transsulfuration pathway". British Journal of Pharmacology 176, n.º 4 (23 de agosto de 2018): 583–93. http://dx.doi.org/10.1111/bph.14446.
Texto completoHauck, J. Spencer, Xia Gao, William Butler, Lingfan Xu y Jiaoti Huang. "Abstract 2372: Targeting a metabolic compensatory mechanism for heat shock factor 1 inhibition in prostate cancer". Cancer Research 82, n.º 12_Supplement (15 de junio de 2022): 2372. http://dx.doi.org/10.1158/1538-7445.am2022-2372.
Texto completoBelalcázar, Andrea D., John G. Ball, Leslie M. Frost, Monica A. Valentovic y John Wilkinson. "Transsulfuration Is a Significant Source of Sulfur for Glutathione Production in Human Mammary Epithelial Cells". ISRN Biochemistry 2013 (6 de marzo de 2013): 1–7. http://dx.doi.org/10.1155/2013/637897.
Texto completoPatel, Jenil, Emine Bircan, Xinyu Tang, Mohammed Orloff, Charlotte A. Hobbs, Marilyn L. Browne, Lorenzo D. Botto et al. "Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach". PLOS Genetics 17, n.º 3 (8 de marzo de 2021): e1009413. http://dx.doi.org/10.1371/journal.pgen.1009413.
Texto completoWeber, Ross y Kıvanç Birsoy. "The Transsulfuration Pathway Makes, the Tumor Takes". Cell Metabolism 30, n.º 5 (noviembre de 2019): 845–46. http://dx.doi.org/10.1016/j.cmet.2019.10.009.
Texto completoGarcia, Joseph, Saket Jain, Erin Akins, Luis Carrete, Allison Zheng, Sabraj Gill, Sanjay Kumar y Manish Aghi. "CSIG-23. ALTERATIONS IN THE TRANSSULFURATION PATHWAY DRIVE GLIOBLASTOMA INVASION IN THE PERITUMORAL WHITE MATTER". Neuro-Oncology 24, Supplement_7 (1 de noviembre de 2022): vii43—vii44. http://dx.doi.org/10.1093/neuonc/noac209.172.
Texto completoVermeij, Paul y Michael A. Kertesz. "Pathways of Assimilative Sulfur Metabolism inPseudomonas putida". Journal of Bacteriology 181, n.º 18 (15 de septiembre de 1999): 5833–37. http://dx.doi.org/10.1128/jb.181.18.5833-5837.1999.
Texto completoVitvitsky, Victor, Sanjana Dayal, Sally Stabler, You Zhou, Hong Wang, Steven R. Lentz y Ruma Banerjee. "Perturbations in homocysteine-linked redox homeostasis in a murine model for hyperhomocysteinemia". American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 287, n.º 1 (julio de 2004): R39—R46. http://dx.doi.org/10.1152/ajpregu.00036.2004.
Texto completoRatnam, Shobhitha, Enoka P. Wijekoon, Beatrice Hall, Timothy A. Garrow, Margaret E. Brosnan y John T. Brosnan. "Effects of diabetes and insulin on betaine-homocysteine S-methyltransferase expression in rat liver". American Journal of Physiology-Endocrinology and Metabolism 290, n.º 5 (mayo de 2006): E933—E939. http://dx.doi.org/10.1152/ajpendo.00498.2005.
Texto completoBearden, Shawn E., Richard S. Beard y Jean C. Pfau. "Extracellular transsulfuration generates hydrogen sulfide from homocysteine and protects endothelium from redox stress". American Journal of Physiology-Heart and Circulatory Physiology 299, n.º 5 (noviembre de 2010): H1568—H1576. http://dx.doi.org/10.1152/ajpheart.00555.2010.
Texto completoFauste, E., S. Rodrigo, L. Rodriguez, C. Donis, J. J. Álvarez-Millan, M. I. Panadero, P. Otero y C. Bocos. "Maternal fructose affects transsulfuration pathway of female progeny". Atherosclerosis 315 (diciembre de 2020): e219. http://dx.doi.org/10.1016/j.atherosclerosis.2020.10.688.
Texto completoNguyen, Thao V., Andrea C. Alfaro, Fabrice Merien, Ronald Lulijwa y Tim Young. "Copper-induced immunomodulation in mussel (Perna canaliculus) haemocytes". Metallomics 10, n.º 7 (2018): 965–78. http://dx.doi.org/10.1039/c8mt00092a.
Texto completoCacciapuoti, Federico. "N-Acetyl-Cysteine supplementation lowers high homocysteine plasma levels and increases Glutathione synthesis in the trans-sulfuration pathway". Italian Journal of Medicine 13, n.º 4 (28 de noviembre de 2019): 234–40. http://dx.doi.org/10.4081/itjm.2019.1192.
Texto completoPanza, E., V. Vellecco, F. A. Iannotti, D. Paris, O. L. Manzo, M. Smimmo, N. Mitilini et al. "Duchenne's muscular dystrophy involves a defective transsulfuration pathway activity". Redox Biology 45 (septiembre de 2021): 102040. http://dx.doi.org/10.1016/j.redox.2021.102040.
Texto completoMota-Martorell, Natalia, Jové Mariona, Borras Consuelo, Berdún Rebeca, Obis Elia, Sol Joaquim, Cabré Rosanna et al. "Methionine transsulfuration pathway is upregulated in long-lived humans". Free Radical Biology and Medicine 162 (enero de 2021): 38–52. http://dx.doi.org/10.1016/j.freeradbiomed.2020.11.026.
Texto completoFarsi, Ali, Pratik H. Lodha, Jennifer E. Skanes, Heidi Los, Navya Kalidindi y Susan M. Aitken. "Interconversion of a pair of active-site residues in Escherichia coli cystathionine γ-synthase, E. coli cystathionine β-lyase, and Saccharomyces cerevisiae cystathionine γ-lyase and development of tools for the investigation of their mechanisms and reaction specificity". Biochemistry and Cell Biology 87, n.º 2 (abril de 2009): 445–57. http://dx.doi.org/10.1139/o08-144.
Texto completoWerge, Mikkel Parsberg, Adrian McCann, Elisabeth Douglas Galsgaard, Dorte Holst, Anne Bugge, Nicolai J. Wewer Albrechtsen y Lise Lotte Gluud. "The Role of the Transsulfuration Pathway in Non-Alcoholic Fatty Liver Disease". Journal of Clinical Medicine 10, n.º 5 (5 de marzo de 2021): 1081. http://dx.doi.org/10.3390/jcm10051081.
Texto completoMaresi, Elena, Giacomo Janson, Silvia Fruncillo, Alessandro Paiardini, Rosario Vallone, Paola Dominici y Alessandra Astegno. "Functional Characterization and Structure-Guided Mutational Analysis of the Transsulfuration Enzyme Cystathionine γ-Lyase from Toxoplasma gondii". International Journal of Molecular Sciences 19, n.º 7 (20 de julio de 2018): 2111. http://dx.doi.org/10.3390/ijms19072111.
Texto completoHwang, Byung-Joon, Hye-Jin Yeom, Younhee Kim y Heung-Shick Lee. "Corynebacterium glutamicum Utilizes both Transsulfuration and Direct Sulfhydrylation Pathways for Methionine Biosynthesis". Journal of Bacteriology 184, n.º 5 (1 de marzo de 2002): 1277–86. http://dx.doi.org/10.1128/jb.184.5.1277-1286.2002.
Texto completoNguyen, Diem-Quynh, Ho-Phuong-Thuy Ngo, Yeh-Jin Ahn, Sang Hee Lee y Lin-Woo Kang. "Expression, crystallization and preliminary X-ray crystallographic analysis of cystathionine β-lyase fromAcinetobacter baumanniiOXA-23". Acta Crystallographica Section F Structural Biology Communications 70, n.º 10 (25 de septiembre de 2014): 1368–71. http://dx.doi.org/10.1107/s2053230x14017981.
Texto completoBeard, Richard S. y Shawn E. Bearden. "Vascular complications of cystathionine β-synthase deficiency: future directions for homocysteine-to-hydrogen sulfide research". American Journal of Physiology-Heart and Circulatory Physiology 300, n.º 1 (enero de 2011): H13—H26. http://dx.doi.org/10.1152/ajpheart.00598.2010.
Texto completoRen, Haoyi, Tristan C. Liu, Yipin Lu, Kai Zhang, Ying Xu, Peng Zhou y Xue Tang. "A comparison study of the influence of milk protein versus whey protein in high-protein diets on adiposity in rats". Food & Function 12, n.º 3 (2021): 1008–19. http://dx.doi.org/10.1039/d0fo01960g.
Texto completoGarcia, Joseph H., Saket Jain, Erin A. Akins, Jordan M. Spatz, Angad S. Beniwal, Sabraj A. Gill, Kayla J. Wolfe et al. "OTME-12. Role of the transsulfuration pathway in glioblastoma invasion". Neuro-Oncology Advances 3, Supplement_2 (1 de julio de 2021): ii15—ii16. http://dx.doi.org/10.1093/noajnl/vdab070.063.
Texto completoMangoni, Arduino A., Angelo Zinellu, Ciriaco Carru, John R. Attia y Mark A. McEvoy. "437 EPIDEMIOLOGICAL IMPACT OF THE TRANSSULFURATION PATHWAY ON METHYLATED ARGININES". Journal of Hypertension 30 (septiembre de 2012): e130. http://dx.doi.org/10.1097/01.hjh.0000420293.74777.e6.
Texto completoMangoni, Arduino A., Angelo Zinellu, Ciriaco Carru, John R. Attia y Mark McEvoy. "Transsulfuration Pathway Thiols and Methylated Arginines: The Hunter Community Study". PLoS ONE 8, n.º 1 (24 de enero de 2013): e54870. http://dx.doi.org/10.1371/journal.pone.0054870.
Texto completoLyu, Zhou, Xuejie Gao, Weiyan Wang, Jinye Dang, Li Yang, Mengli Yan, Shah Arman Ali et al. "mTORC1-Sch9 regulates hydrogen sulfide production through the transsulfuration pathway". Aging 11, n.º 19 (3 de octubre de 2019): 8418–32. http://dx.doi.org/10.18632/aging.102327.
Texto completoRuiz-Rodado, Victor, Tyrone Dowdy, Jinkyu Yung, Ana Dios-Esponera, Adrian Lita, Tamalee Kramp, Kevin Camphausen, Mark Gilbert y Mioara Larion. "DDRE-16. CYSTEINE IS AN ESSENTIAL AMINO ACID IN GLIOMAS". Neuro-Oncology Advances 3, Supplement_1 (1 de marzo de 2021): i9. http://dx.doi.org/10.1093/noajnl/vdab024.038.
Texto completoStipanuk, Martha H. "Metabolism of Sulfur-Containing Amino Acids: How the Body Copes with Excess Methionine, Cysteine, and Sulfide". Journal of Nutrition 150, Supplement_1 (1 de octubre de 2020): 2494S—2505S. http://dx.doi.org/10.1093/jn/nxaa094.
Texto completoLamarre, Simon G., Anne M. Molloy, Stacey N. Reinke, Brian D. Sykes, Margaret E. Brosnan y John T. Brosnan. "Formate can differentiate between hyperhomocysteinemia due to impaired remethylation and impaired transsulfuration". American Journal of Physiology-Endocrinology and Metabolism 302, n.º 1 (1 de enero de 2012): E61—E67. http://dx.doi.org/10.1152/ajpendo.00345.2011.
Texto completoFloros, Konstantinos V., Ayesha T. Chawla, Mia O. Johnson-Berro, Rishabh Khatri, Angeliki M. Stamatouli, Sosipatros A. Boikos, Mikhail G. Dozmorov, L. Ashley Cowart y Anthony C. Faber. "MYCN upregulates the transsulfuration pathway to suppress the ferroptotic vulnerability in MYCN-amplified neuroblastoma". Cell Stress 6, n.º 2 (14 de febrero de 2022): 21–29. http://dx.doi.org/10.15698/cst2022.02.264.
Texto completoRomero, Ibeth, Jair Téllez, Lais Yamanaka, Mario Steindel, Alvaro Romanha y Edmundo Grisard. "Transsulfuration is an active pathway for cysteine biosynthesis in Trypanosoma rangeli". Parasites & Vectors 7, n.º 1 (2014): 197. http://dx.doi.org/10.1186/1756-3305-7-197.
Texto completoVitvitsky, Victor, Mark Thomas, Anuja Ghorpade, Howard E. Gendelman y Ruma Banerjee. "A Functional Transsulfuration Pathway in the Brain Links to Glutathione Homeostasis". Journal of Biological Chemistry 281, n.º 47 (27 de septiembre de 2006): 35785–93. http://dx.doi.org/10.1074/jbc.m602799200.
Texto completoWADA, Masaru, Satoru FUKIYA, Azusa SUZUKI, Nanae MATSUMOTO, Miki MATSUO y Atsushi YOKOTA. "Methionine utilization by bifidobacteria: possible existence of a reverse transsulfuration pathway". Bioscience of Microbiota, Food and Health 40, n.º 1 (2021): 80–83. http://dx.doi.org/10.12938/bmfh.2020-031.
Texto completoMcBean, Gethin J. "The transsulfuration pathway: a source of cysteine for glutathione in astrocytes". Amino Acids 42, n.º 1 (3 de marzo de 2011): 199–205. http://dx.doi.org/10.1007/s00726-011-0864-8.
Texto completoRahman, Sakhawat H., Asha R. Srinivasan y Anna Nicolaou. "Transsulfuration Pathway Defects and Increased Glutathione Degradation in Severe Acute Pancreatitis". Digestive Diseases and Sciences 54, n.º 3 (2 de julio de 2008): 675–82. http://dx.doi.org/10.1007/s10620-008-0382-z.
Texto completoLiu, Gang, Javier Casqueiro, Oscar Bañuelos, Rosa E. Cardoza, Santiago Gutiérrez y Juan F. Martı́n. "Targeted Inactivation of the mecB Gene, Encoding Cystathionine-γ-Lyase, Shows that the Reverse Transsulfuration Pathway Is Required for High-Level Cephalosporin Biosynthesis inAcremonium chrysogenum C10 but Not for Methionine Induction of the Cephalosporin Genes". Journal of Bacteriology 183, n.º 5 (1 de marzo de 2001): 1765–72. http://dx.doi.org/10.1128/jb.183.5.1765-1772.2001.
Texto completoBadiei, Alireza, William A. Beltran y Gustavo D. Aguirre. "Altered transsulfuration pathway enzymes and redox homeostasis in inherited retinal degenerative diseases". Experimental Eye Research 215 (febrero de 2022): 108902. http://dx.doi.org/10.1016/j.exer.2021.108902.
Texto completoTyagi, Richa, Solomon H. Snyder y Bindu Paul. "Inositol polyphosphate multi‐kinase is a novel regulator of reverse‐transsulfuration pathway". FASEB Journal 34, S1 (abril de 2020): 1. http://dx.doi.org/10.1096/fasebj.2020.34.s1.03015.
Texto completoKang, Eun Sil, Jaeyong Lee, Takujiro Homma, Toshihiro Kurahashi, Sho Kobayashi, Atsunori Nabeshima, Sohsuke Yamada et al. "xCT deficiency aggravates acetaminophen-induced hepatotoxicity under inhibition of the transsulfuration pathway". Free Radical Research 51, n.º 1 (2 de enero de 2017): 80–90. http://dx.doi.org/10.1080/10715762.2017.1282157.
Texto completoda Silva, Vanessa R., Maria A. Ralat, Eoin P. Quinlivan, Barbara N. DeRatt, Timothy J. Garrett, Yueh-Yun Chi, H. Frederik Nijhout, Michael C. Reed y Jesse F. Gregory. "Targeted metabolomics and mathematical modeling demonstrate that vitamin B-6 restriction alters one-carbon metabolism in cultured HepG2 cells". American Journal of Physiology-Endocrinology and Metabolism 307, n.º 1 (1 de julio de 2014): E93—E101. http://dx.doi.org/10.1152/ajpendo.00697.2013.
Texto completoBalakumaran, Manimaran, Parameshwaran Chidambaranathan, Jagannadham Prasanth Tej Kumar J. P., Anil Sirohi, Pradeep Kumar Jain, Kishore Gaikwad, Yuvaraj Iyyappan et al. "Deciphering the mechanism of anhydrobiosis in the entomopathogenic nematode Heterorhabditis indica through comparative transcriptomics". PLOS ONE 17, n.º 10 (27 de octubre de 2022): e0275342. http://dx.doi.org/10.1371/journal.pone.0275342.
Texto completoShang, Yue, Yaw L. Siow, Cara K. Isaak y Karmin O. "Downregulation of Glutathione Biosynthesis Contributes to Oxidative Stress and Liver Dysfunction in Acute Kidney Injury". Oxidative Medicine and Cellular Longevity 2016 (2016): 1–13. http://dx.doi.org/10.1155/2016/9707292.
Texto completoLiu, Nan, Xiaoli Lin y Chengying Huang. "Activation of the reverse transsulfuration pathway through NRF2/CBS confers erastin-induced ferroptosis resistance". British Journal of Cancer 122, n.º 2 (10 de diciembre de 2019): 279–92. http://dx.doi.org/10.1038/s41416-019-0660-x.
Texto completoZamora, S. A., H. J. Amin, E. M. Hyndman, D. D. McMillan, D. J. Butzner, R. B. Scott y H. G. Parsons. "Transsulfuration pathway components in premature infants duing the first month of life. 1445". Pediatric Research 41 (abril de 1997): 243. http://dx.doi.org/10.1203/00006450-199704001-01464.
Texto completoFloros, Konstantinos V., Mia O. Johnson-Berro, Richard Kurupi, Carter K. Fairchild, Krista Dalton, Bin Hu, Madhavi Puchalapalli et al. "Abstract 362: MYCN-amplified neuroblastoma is addicted to iron and vulnerable to ferroptosis". Cancer Research 82, n.º 12_Supplement (15 de junio de 2022): 362. http://dx.doi.org/10.1158/1538-7445.am2022-362.
Texto completoAbdulle, Amaal, Harry van Goor y Douwe Mulder. "Hydrogen Sulfide: A Therapeutic Option in Systemic Sclerosis". International Journal of Molecular Sciences 19, n.º 12 (19 de diciembre de 2018): 4121. http://dx.doi.org/10.3390/ijms19124121.
Texto completoVigorito, Carmela, Evgeniya Anishchenko, Luigi Mele, Giovanna Capolongo, Francesco Trepiccione, Miriam Zacchia, Patrizia Lombari, Rosanna Capasso, Diego Ingrosso y Alessandra F. Perna. "Uremic Toxin Lanthionine Interferes with the Transsulfuration Pathway, Angiogenetic Signaling and Increases Intracellular Calcium". International Journal of Molecular Sciences 20, n.º 9 (8 de mayo de 2019): 2269. http://dx.doi.org/10.3390/ijms20092269.
Texto completoChawla, R. K., C. J. Berry, M. H. Kutner y D. Rudman. "Plasma concentrations of transsulfuration pathway products during nasoenteral and intravenous hyperalimentation of malnourished patients". American Journal of Clinical Nutrition 42, n.º 4 (1 de octubre de 1985): 577–84. http://dx.doi.org/10.1093/ajcn/42.4.577.
Texto completoRavanel, Stéphane. "Methionine biosynthesis in higher plants: biochemical and molecular characterization of the transsulfuration pathway enzymes". Comptes Rendus de l'Académie des Sciences - Series III - Sciences de la Vie 320, n.º 6 (junio de 1997): 497–504. http://dx.doi.org/10.1016/s0764-4469(97)81977-4.
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