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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1953 1
1963 10
1964 9
1965 10
1966 6
1967 18
1968 27
1969 41
1970 47
1971 63
1972 99
1973 85
1974 88
1975 60
1976 81
1977 51
1978 42
1979 55
1980 49
1981 52
1982 37
1983 55
1984 80
1985 86
1986 77
1987 61
1988 84
1989 93
1990 147
1991 174
1992 233
1993 277
1994 311
1995 353
1996 380
1997 362
1998 461
1999 485
2000 551
2001 592
2002 720
2003 674
2004 747
2005 721
2006 767
2007 787
2008 772
2009 800
2010 866
2011 925
2012 1037
2013 1064
2014 1062
2015 948
2016 903
2017 967
2018 928
2019 853
2020 930
2021 863
2022 667
2023 628
2024 980
2025 1372
2026 749

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25,294 results

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Page 1
Tensin.
Lo SH. Lo SH. Int J Biochem Cell Biol. 2004 Jan;36(1):31-4. doi: 10.1016/s1357-2725(03)00171-7. Int J Biochem Cell Biol. 2004. PMID: 14592531 Review.
In addition, tensin has an Src Homology 2 (SH2) domain capable of interacting with tyrosine-phosphorylated proteins. Furthermore, several factors induce tyrosine phosphorylation of tensin. Thus, tensin functions as a platform for dis/assembly of signaling complexes …
In addition, tensin has an Src Homology 2 (SH2) domain capable of interacting with tyrosine-phosphorylated proteins. Furthermore, sev …
The shikimate pathway and aromatic amino Acid biosynthesis in plants.
Maeda H, Dudareva N. Maeda H, et al. Annu Rev Plant Biol. 2012;63:73-105. doi: 10.1146/annurev-arplant-042811-105439. Annu Rev Plant Biol. 2012. PMID: 22554242 Review.
L-tryptophan, L-phenylalanine, and L-tyrosine are aromatic amino acids (AAAs) that are used for the synthesis of proteins and that in plants also serve as precursors of numerous natural products, such as pigments, alkaloids, hormones, and cell wall components. ...It also i …
L-tryptophan, L-phenylalanine, and L-tyrosine are aromatic amino acids (AAAs) that are used for the synthesis of proteins and that in …
Tyrosine, phenylalanine, and catecholamine synthesis and function in the brain.
Fernstrom JD, Fernstrom MH. Fernstrom JD, et al. J Nutr. 2007 Jun;137(6 Suppl 1):1539S-1547S; discussion 1548S. doi: 10.1093/jn/137.6.1539S. J Nutr. 2007. PMID: 17513421 Free article. Review.
Aromatic amino acids in the brain function as precursors for the monoamine neurotransmitters serotonin (substrate tryptophan) and the catecholamines [dopamine, norepinephrine, epinephrine; substrate tyrosine (Tyr)]. Unlike almost all other neurotransmitter biosynthetic pat …
Aromatic amino acids in the brain function as precursors for the monoamine neurotransmitters serotonin (substrate tryptophan) and the catech …
Role of tyrosine phosphorylation in modulating cancer cell metabolism.
Taddei ML, Pardella E, Pranzini E, Raugei G, Paoli P. Taddei ML, et al. Biochim Biophys Acta Rev Cancer. 2020 Dec;1874(2):188442. doi: 10.1016/j.bbcan.2020.188442. Epub 2020 Oct 2. Biochim Biophys Acta Rev Cancer. 2020. PMID: 33017632 Review.
Moreover, recent studies demonstrated that tyrosine phosphorylation influences the activity of some metabolic enzymes, even if it remains to be clarified whether tyrosine phosphorylation can be considered a general mechanism involving most of the metabolic …
Moreover, recent studies demonstrated that tyrosine phosphorylation influences the activity of some metabolic enzymes, even if …
Protein-tyrosine kinases.
Hunter T, Cooper JA. Hunter T, et al. Annu Rev Biochem. 1985;54:897-930. doi: 10.1146/annurev.bi.54.070185.004341. Annu Rev Biochem. 1985. PMID: 2992362 Review. No abstract available.
Acetaminophen-induced hepatotoxicity.
James LP, Mayeux PR, Hinson JA. James LP, et al. Drug Metab Dispos. 2003 Dec;31(12):1499-506. doi: 10.1124/dmd.31.12.1499. Drug Metab Dispos. 2003. PMID: 14625346 Review.
These findings indicated that acetaminophen was metabolically activated by cytochrome P450 enzymes to a reactive metabolite that depleted glutathione (GSH) and covalently bound to protein. ...In inducible nitric oxide synthase (iNOS) knockout mice, acetaminophen did not in …
These findings indicated that acetaminophen was metabolically activated by cytochrome P450 enzymes to a reactive metabolite that depl …
Calcitonin.
Potts JT Jr, Niall HD, Deftos LJ. Potts JT Jr, et al. Curr Top Exp Endocrinol. 1971;1:151-73. doi: 10.1016/b978-0-12-153201-7.50011-9. Curr Top Exp Endocrinol. 1971. PMID: 4949942 Review. No abstract available.
[Application of tyrosine phosphoproteomics in biomedical research: a review].
Li K, Xu F, Xu P. Li K, et al. Sheng Wu Gong Cheng Xue Bao. 2021 Jan 25;37(1):100-111. doi: 10.13345/j.cjb.200246. Sheng Wu Gong Cheng Xue Bao. 2021. PMID: 33501793 Free article. Review. Chinese.
The application of tyrosine phosphoproteomics technology can identify tyrosine kinases related to cancer and other major diseases, so as to help finding tyrosine kinase inhibitors. In short, tyrosine phosphoproteomics technology can be applied in biome …
The application of tyrosine phosphoproteomics technology can identify tyrosine kinases related to cancer and other major disea …
Role of Tyrosine Kinases and their Inhibitors in Cancer Therapy: A Comprehensive Review.
Kumar V, Kaur N, Sahu S, Sharma V, Kumar D, Sharma A, Wadhwa P. Kumar V, et al. Curr Med Chem. 2023;30(13):1464-1481. doi: 10.2174/0929867329666220727122952. Curr Med Chem. 2023. PMID: 35894454 Review.
OBJECTIVE: The current review focused on structural aspects of different chemical agents for inhibition of tyrosine kinases as anticancer agents. ...The review also highlighted the structural aspects of the interaction between inhibitors and amino acid residu …
OBJECTIVE: The current review focused on structural aspects of different chemical agents for inhibition of tyrosine kinases as …
Pharmacokinetics of levodopa.
Nutt JG, Fellman JH. Nutt JG, et al. Clin Neuropharmacol. 1984;7(1):35-49. doi: 10.1097/00002826-198403000-00002. Clin Neuropharmacol. 1984. PMID: 6367973 Review. No abstract available.
25,294 results
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