"Crystallography, X-Ray" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The study of crystal structure using X-RAY DIFFRACTION techniques. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
| Descriptor ID |
D018360
|
| MeSH Number(s) |
E05.196.309.742.225
|
| Concept/Terms |
Crystallography, X-Ray- Crystallography, X-Ray
- Crystallography, Xray
- X Ray Crystallography
- X-Ray Crystallography
- Xray Crystallography
- Crystallography, X Ray
- Crystallographies, X Ray
- X Ray Crystallographies
|
Below are MeSH descriptors whose meaning is more general than "Crystallography, X-Ray".
Below are MeSH descriptors whose meaning is more specific than "Crystallography, X-Ray".
This graph shows the total number of publications written about "Crystallography, X-Ray" by people in this website by year, and whether "Crystallography, X-Ray" was a major or minor topic of these publications.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 0 | 1 | 1 |
| 2004 | 0 | 4 | 4 |
| 2005 | 0 | 2 | 2 |
| 2007 | 0 | 1 | 1 |
| 2008 | 0 | 1 | 1 |
| 2009 | 1 | 3 | 4 |
| 2011 | 0 | 1 | 1 |
| 2012 | 0 | 4 | 4 |
| 2013 | 0 | 1 | 1 |
| 2014 | 0 | 2 | 2 |
| 2015 | 0 | 2 | 2 |
| 2016 | 0 | 2 | 2 |
| 2017 | 0 | 2 | 2 |
| 2018 | 0 | 1 | 1 |
| 2019 | 0 | 2 | 2 |
| 2020 | 0 | 2 | 2 |
| 2021 | 0 | 1 | 1 |
| 2025 | 0 | 2 | 2 |
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click here.
Below are the most recent publications written about "Crystallography, X-Ray" by people in Profiles.
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Role of the Mobile Active Site Flap in IMP Dehydrogenase Inhibitor Binding. ACS Infect Dis. 2025 Feb 14; 11(2):442-452.
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Genetic Algorithm-Enhanced Direct Method in Protein Crystallography. Molecules. 2025 Jan 13; 30(2).
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Targeted Degradation of the Oncogenic Phosphatase SHP2. Biochemistry. 2021 08 31; 60(34):2593-2609.
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Receptor-interacting protein kinase 2 (RIPK2) and nucleotide-binding oligomerization domain (NOD) cell signaling inhibitors based on a 3,5-diphenyl-2-aminopyridine scaffold. Eur J Med Chem. 2020 Aug 15; 200:112417.
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Periodic Tendril Perversion and Helices in the AMoO2F3 (A = K, Rb, NH4, Tl) Family. J Am Chem Soc. 2020 04 01; 142(13):6375-6380.
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Insight into tartrate inhibition patterns in vitro and in vivo based on cocrystal structure with UDP-glucuronosyltransferase 2B15. Biochem Pharmacol. 2020 Feb; 172:113753.
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1-Aminopyridinium Ylides as Monodentate Directing Groups for sp3 C-H Bond Functionalization. J Am Chem Soc. 2019 09 18; 141(37):14728-14735.
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Activation loop targeting strategy for design of receptor-interacting protein kinase 2 (RIPK2) inhibitors. Bioorg Med Chem Lett. 2018 02 15; 28(4):577-583.
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IgG Fc domains that bind C1q but not effector Fc? receptors delineate the importance of complement-mediated effector functions. Nat Immunol. 2017 Aug; 18(8):889-898.
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Antimalarials inhibit hematin crystallization by unique drug-surface site interactions. Proc Natl Acad Sci U S A. 2017 07 18; 114(29):7531-7536.