Aminosäuren (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Aminosäuren" in German language version.

refsWebsite
Global rank German rank
2nd place
3rd place
4th place
7th place
4,455th place
3,739th place
2,106th place
139th place
75th place
133rd place
low place
low place
1st place
1st place
610th place
521st place
222nd place
272nd place
low place
low place
18th place
181st place

biologische-wertigkeit.de

doi.org

  • G. Genchi: An overview on D-amino acids. In: Amino Acids. Band 49, Nummer 9, September 2017, S. 1521–1533, doi:10.1007/s00726-017-2459-5. PMID 28681245.
  • Anton P. Novikov, Alexey V. Safonov, Konstantin E. German, Mikhail S. Grigoriev: What kind of interactions we may get moving from zwitter to “dritter” ions: C–O⋯Re(O4) and Re–O⋯Re(O4) anion⋯anion interactions make structural difference between L-histidinium perrhenate and pertechnetate. In: CrystEngComm. 1. Dezember 2023, doi:10.1039/D3CE01164J.
  • International Union of Pure and Applied Chemistry and International Union of Biochemistry: Nomenclature and Symbolism for Amino Acids and Peptides (Recommendations 1983). In: Pure & Appl. Chem. Band 56, Nr. 5, 1984, S. 595–624, doi:10.1351/pac198456050595.
  • IUPAC-IUB Commission on Biochemical Nomenclature A One-Letter Notation for Amino Acid Sequences. In: Journal of Biological Chemistry. 243. Jahrgang, Nr. 13, 10. Juli 1968, S. 3557–3559, doi:10.1016/S0021-9258(19)34176-6 (englisch, jbc.org [PDF]).
  • M. Saffran: Amino acid names and parlor games: from trivial names to a one-letter code, amino acid names have strained students' memories. Is a more rational nomenclature possible? In: Biochemical Education. 26. Jahrgang, Nr. 2, April 1998, S. 116–118, doi:10.1016/S0307-4412(97)00167-2 (englisch, elsevier.com).
  • Godwin I Adoga, Bh Nicholson: Letters to the editor. In: Biochemical Education. 16. Jahrgang, Nr. 1, Januar 1988, S. 49, doi:10.1016/0307-4412(88)90026-X (englisch, wiley.com [PDF]).
  • Katsura Asano: Why is start codon selection so precise in eukaryotes? In: Translation. Band 2, Nr. 1, März 2014, doi:10.4161/trla.28387, PMC 4705826 (freier Volltext).
  • Y. Fan, C. R. Evans, J. Ling: Rewiring protein synthesis: From natural to synthetic amino acids. In: Biochimica et Biophysica Acta. Band 1861, Nummer 11 Pt B, 2017, S. 3024–3029, doi:10.1016/j.bbagen.2017.01.014. PMID 28095316, PMC 5511583 (freier Volltext).
  • Kathrin Lang, Lloyd Davis u. a.: Genetically encoded norbornene directs site-specific cellular protein labelling via a rapid bioorthogonal reaction. In: Nature Chemistry. 2012, S. 298–304, doi:10.1038/nchem.1250.
  • W. R. Taylor: The classification of amino acid conservation. In: Journal of Theoretical Biology. Band 119, Jahrgang 1986, S. 205–218. doi:10.1016/S0022-5193(86)80075-3.
  • Jean-Pierre Mothet, Angèle T. Parent, Herman Wolosker, Roscoe O. Brady, Jr., David J. Linden, Christopher D. Ferris, Michael A. Rogawski, Solomon H. Snyder: d-Serine is an endogenous ligand for the glycine site of the N-methyl-d-aspartate receptor. In: Proc. Natl. Acad. Sci. USA. Band 97, Nr. 9, 2000, S. 4926–4931, doi:10.1073/pnas.97.9.4926, PMID 10781100, PMC 18334 (freier Volltext).
  • Karlheinz Drauz, Hans Günter Koban, Jürgen Martens, Werner Schwarze: Phosphonic and Phosphinic Acid Analogs of Penicillamine. In: Liebigs Annalen der Chemie. Band 1985, Nr. 3, 1985, S. 448–452, doi:10.1002/jlac.198519850303.
  • Y. Song, C. Xu, H. Kuroki, Y. Liao, M. Tsunoda: Recent trends in analytical methods for the determination of amino acids in biological samples. In: Journal of pharmaceutical and biomedical analysis. Band 147, Januar 2018, S. 35–49, doi:10.1016/j.jpba.2017.08.050. PMID 28927726.
  • N. Fujii, T. Takata, N. Fujii, K. Aki, H. Sakaue: D-Amino acids in protein: The mirror of life as a molecular index of aging. In: Biochimica et Biophysica Acta. [elektronische Veröffentlichung vor dem Druck] März 2018, doi:10.1016/j.bbapap.2018.03.001. PMID 29530565.
  • N. Tonouchi, H. Ito: Present Global Situation of Amino Acids in Industry. In: Advances in Biochemical Engineering/Biotechnology. Band 159, 2017, S. 3–14, doi:10.1007/10_2016_23. PMID 27832295.
  • M. D'Este, M. Alvarado-Morales, I. Angelidaki: Amino acids production focusing on fermentation technologies - A review. In: Biotechnology Advances. Band 36, Nummer 1, Jan-Feb 2018, S. 14–25, doi:10.1016/j.biotechadv.2017.09.001. PMID 28888551.
  • J. H. Lee, V. F. Wendisch: Production of amino acids - Genetic and metabolic engineering approaches. In: Bioresource Technology. Band 245, Pt B, Dezember 2017, S. 1575–1587, doi:10.1016/j.biortech.2017.05.065. PMID 28552565.
  • K. Yamamoto, A. Tsuchisaka, H. Yukawa: Branched-Chain Amino Acids. In: Advances in Biochemical Engineering/Biotechnology. Band 159, 2017, S. 103–128, doi:10.1007/10_2016_28. PMID 27872960.
  • K. V. Savelieva, S. Zhao, V. M. Pogorelov, I. Rajan, Q. Yang, E. Cullinan, T. H. Lanthorn: Genetic disruption of both tryptophan hydroxylase genes dramatically reduces serotonin and affects behavior in models sensitive to antidepressants. In: PLOS ONE. Band 3, Nr. 10, 2008, Artikel e3301, doi:10.1371/journal.pone.0003301, PMID 18923670, PMC 2565062 (freier Volltext), bibcode:2008PLoSO...3.3301S.
  • J. Tejero, A. Biswas, Z. Q. Wang, R. C. Page, M. M. Haque, C. Hemann, J. L. Zweier, S. Misra, D. J. Stuehr: Stabilization and characterization of a heme-oxy reaction intermediate in inducible nitric-oxide synthase. In: The Journal of Biological Chemistry. Band 283, Nr. 48, November 2008, S. 33498–507, doi:10.1074/jbc.M806122200, PMID 18815130, PMC 2586280 (freier Volltext).
  • C. Rodríguez-Caso, R. Montañez, M. Cascante, F. Sánchez-Jiménez, M. A. Medina: Mathematical modeling of polyamine metabolism in mammals. In: The Journal of Biological Chemistry. Band 281, Nr. 31, August 2006, S. 21799–21812, doi:10.1074/jbc.M602756200, PMID 16709566.
  • W. Ren, R. Rajendran, Y. Zhao, B. Tan, G. Wu, F. W. Bazer, G. Zhu, Y. Peng, X. Huang, J. Deng, Y. Yin: Amino Acids As Mediators of Metabolic Cross Talk between Host and Pathogen. In: Frontiers in immunology. Band 9, 2018, S. 319, doi:10.3389/fimmu.2018.00319. PMID 29535717, PMC 5835074 (freier Volltext).

elsevier.com

linkinghub.elsevier.com

  • M. Saffran: Amino acid names and parlor games: from trivial names to a one-letter code, amino acid names have strained students' memories. Is a more rational nomenclature possible? In: Biochemical Education. 26. Jahrgang, Nr. 2, April 1998, S. 116–118, doi:10.1016/S0307-4412(97)00167-2 (englisch, elsevier.com).

google.de

books.google.de

  • Katharina Munk (Hrsg.): Biochemie – Zellbiologie. Georg Thieme Verlag, Stuttgart 2008, ISBN 978-3-13-144831-6, S. 122, Google Books.
  • Wolfgang Legrum: Riechstoffe, Zwischen Gestank Und Duft: Vorkommen, Eigenschaften und Anwendung von Riechstoffen und deren Gemischen. Gabler Wissenschaftsverlage, 2011, S. 165 (eingeschränkte Vorschau in der Google-Buchsuche).

harvard.edu

ui.adsabs.harvard.edu

jbc.org

nasa.gov

stardust.jpl.nasa.gov

nih.gov

ncbi.nlm.nih.gov

  • G. Genchi: An overview on D-amino acids. In: Amino Acids. Band 49, Nummer 9, September 2017, S. 1521–1533, doi:10.1007/s00726-017-2459-5. PMID 28681245.
  • Hao Wang, David Fewer, Liisa Holm, Leo Rouhiainen, Kaarina Sivonena: Atlas of nonribosomal peptide and polyketide biosynthetic pathways reveals common occurrence of nonmodular enzymes. In: Proc Natl Acad Sci USA. Band 111, Nr. 25, Juni 2014, S. 9259–9264, PMC 4078802 (freier Volltext).
  • Katsura Asano: Why is start codon selection so precise in eukaryotes? In: Translation. Band 2, Nr. 1, März 2014, doi:10.4161/trla.28387, PMC 4705826 (freier Volltext).
  • Y. Fan, C. R. Evans, J. Ling: Rewiring protein synthesis: From natural to synthetic amino acids. In: Biochimica et Biophysica Acta. Band 1861, Nummer 11 Pt B, 2017, S. 3024–3029, doi:10.1016/j.bbagen.2017.01.014. PMID 28095316, PMC 5511583 (freier Volltext).
  • J. Kyte, R. F. Doolittle: A simple method for displaying the hydropathic character of a protein. In: Journal of Molecular Biology. Band 157, Nr. 1, 1982, S. 105–132, PMID 7108955.
  • Jean-Pierre Mothet, Angèle T. Parent, Herman Wolosker, Roscoe O. Brady, Jr., David J. Linden, Christopher D. Ferris, Michael A. Rogawski, Solomon H. Snyder: d-Serine is an endogenous ligand for the glycine site of the N-methyl-d-aspartate receptor. In: Proc. Natl. Acad. Sci. USA. Band 97, Nr. 9, 2000, S. 4926–4931, doi:10.1073/pnas.97.9.4926, PMID 10781100, PMC 18334 (freier Volltext).
  • D. A. Wellings, E. Atherton: Standard Fmoc protocols. In: Methods in enzymology. Band 289, 1997, S. 44–67. PMID 9353717
  • Y. Song, C. Xu, H. Kuroki, Y. Liao, M. Tsunoda: Recent trends in analytical methods for the determination of amino acids in biological samples. In: Journal of pharmaceutical and biomedical analysis. Band 147, Januar 2018, S. 35–49, doi:10.1016/j.jpba.2017.08.050. PMID 28927726.
  • N. Fujii, T. Takata, N. Fujii, K. Aki, H. Sakaue: D-Amino acids in protein: The mirror of life as a molecular index of aging. In: Biochimica et Biophysica Acta. [elektronische Veröffentlichung vor dem Druck] März 2018, doi:10.1016/j.bbapap.2018.03.001. PMID 29530565.
  • N. Tonouchi, H. Ito: Present Global Situation of Amino Acids in Industry. In: Advances in Biochemical Engineering/Biotechnology. Band 159, 2017, S. 3–14, doi:10.1007/10_2016_23. PMID 27832295.
  • M. D'Este, M. Alvarado-Morales, I. Angelidaki: Amino acids production focusing on fermentation technologies - A review. In: Biotechnology Advances. Band 36, Nummer 1, Jan-Feb 2018, S. 14–25, doi:10.1016/j.biotechadv.2017.09.001. PMID 28888551.
  • J. H. Lee, V. F. Wendisch: Production of amino acids - Genetic and metabolic engineering approaches. In: Bioresource Technology. Band 245, Pt B, Dezember 2017, S. 1575–1587, doi:10.1016/j.biortech.2017.05.065. PMID 28552565.
  • K. Yamamoto, A. Tsuchisaka, H. Yukawa: Branched-Chain Amino Acids. In: Advances in Biochemical Engineering/Biotechnology. Band 159, 2017, S. 103–128, doi:10.1007/10_2016_28. PMID 27872960.
  • K. V. Savelieva, S. Zhao, V. M. Pogorelov, I. Rajan, Q. Yang, E. Cullinan, T. H. Lanthorn: Genetic disruption of both tryptophan hydroxylase genes dramatically reduces serotonin and affects behavior in models sensitive to antidepressants. In: PLOS ONE. Band 3, Nr. 10, 2008, Artikel e3301, doi:10.1371/journal.pone.0003301, PMID 18923670, PMC 2565062 (freier Volltext), bibcode:2008PLoSO...3.3301S.
  • David Shemin, D. Rittenberg: The biological utilization of glycine for the synthesis of the protoporphyrin of hemoglobin. In: The Journal of Biological Chemistry. Band 166, Nr. 2, Dezember 1946, S. 621–5, PMID 20276176 (jbc.org).
  • J. Tejero, A. Biswas, Z. Q. Wang, R. C. Page, M. M. Haque, C. Hemann, J. L. Zweier, S. Misra, D. J. Stuehr: Stabilization and characterization of a heme-oxy reaction intermediate in inducible nitric-oxide synthase. In: The Journal of Biological Chemistry. Band 283, Nr. 48, November 2008, S. 33498–507, doi:10.1074/jbc.M806122200, PMID 18815130, PMC 2586280 (freier Volltext).
  • C. Rodríguez-Caso, R. Montañez, M. Cascante, F. Sánchez-Jiménez, M. A. Medina: Mathematical modeling of polyamine metabolism in mammals. In: The Journal of Biological Chemistry. Band 281, Nr. 31, August 2006, S. 21799–21812, doi:10.1074/jbc.M602756200, PMID 16709566.
  • W. Ren, R. Rajendran, Y. Zhao, B. Tan, G. Wu, F. W. Bazer, G. Zhu, Y. Peng, X. Huang, J. Deng, Y. Yin: Amino Acids As Mediators of Metabolic Cross Talk between Host and Pathogen. In: Frontiers in immunology. Band 9, 2018, S. 319, doi:10.3389/fimmu.2018.00319. PMID 29535717, PMC 5835074 (freier Volltext).

spie.org

web.archive.org

wiley.com

onlinelibrary.wiley.com