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The Journal of Organic Chemistry
|
July 3, 2004
Interconvertions between delta-lactam and delta-lactone derivatives initiated by unique transannular interactions of the rigid cyclohexane boat structure in pentacycloundecane
Hendrik G Kruger, Frans J C Martins, Agatha M Viljoen
Acta Medica Portuguesa
|
February 1, 1985
[Gastro-esophageal reflux. Comparison between 2 technics: scan and continuous monitoring of pH]
J C Martins, P Isaacs, N Fagg, et al.
Journal of Molecular Biology
|
November 3, 1995
Determination of the three-dimensional solution structure of scyllatoxin by 1H nuclear magnetic resonance
J C Martins, F J Van de Ven, F A Borremans
Nature Structural Biology
|
September 27, 2001
Arsenate reductase from S. aureus plasmid pI258 is a phosphatase drafted for redox duty
I Zegers, J C Martins, R Willem, et al.
Archives of Toxicology
|
September 12, 2014
Fast and sensitive LC-MS/MS method measuring human mycotoxin exposure using biomarkers in urine
B Huybrechts, J C Martins, Ph Debongnie, et al.
European Journal of Biochemistry
|
November 3, 1998
Reconsidering the energetics of ribonuclease catalysed RNA hydrolysis
S Loverix, G Laus, J C Martins, et al.
Magnetic Resonance in Chemistry : MRC
|
May 18, 2010
Assignment and conformational investigation of asymmetric phenylindenylidene ruthenium complexes bearing N,O-bidentate ligands
P M S Hendrickx, R Drozdzak, F Verpoort, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
January 5, 2002
Complexation of triorganotin derivatives of [18]crown-6- and [15]crown-5-(benzo-4-carboxylate) with alkali thiocyanates
M Kemmer, M Biesemans, M Gielen, et al.
Health Research Policy and Systems
|
September 11, 2025
Measuring impacts: a scoping review of healthcare impact evaluations
L R Correia, J C Martins, E T Rother, et al.
Magnetic Resonance in Chemistry : MRC
|
March 17, 2004
Structure elucidation of 11-amino-8-hydroxypentacyclo[5.4.0.0(2, 6).0(3, 10).0(5, 9)]undecane-8,11-lactam through selective acetylation and complete 1H and 13C NMR spectral assignment of the mono-, di- and triacetates
F J C Martins, A M Viljoen, H G Kruger, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 45) with videos related to
Sort By:
Page
of 5
The Journal of Organic Chemistry
|
July 3, 2004
Interconvertions between delta-lactam and delta-lactone derivatives initiated by unique transannular interactions of the rigid cyclohexane boat structure in pentacycloundecane
Hendrik G Kruger, Frans J C Martins, Agatha M Viljoen
Acta Medica Portuguesa
|
February 1, 1985
[Gastro-esophageal reflux. Comparison between 2 technics: scan and continuous monitoring of pH]
J C Martins, P Isaacs, N Fagg, et al.
Journal of Molecular Biology
|
November 3, 1995
Determination of the three-dimensional solution structure of scyllatoxin by 1H nuclear magnetic resonance
J C Martins, F J Van de Ven, F A Borremans
Nature Structural Biology
|
September 27, 2001
Arsenate reductase from S. aureus plasmid pI258 is a phosphatase drafted for redox duty
I Zegers, J C Martins, R Willem, et al.
Archives of Toxicology
|
September 12, 2014
Fast and sensitive LC-MS/MS method measuring human mycotoxin exposure using biomarkers in urine
B Huybrechts, J C Martins, Ph Debongnie, et al.
European Journal of Biochemistry
|
November 3, 1998
Reconsidering the energetics of ribonuclease catalysed RNA hydrolysis
S Loverix, G Laus, J C Martins, et al.
Magnetic Resonance in Chemistry : MRC
|
May 18, 2010
Assignment and conformational investigation of asymmetric phenylindenylidene ruthenium complexes bearing N,O-bidentate ligands
P M S Hendrickx, R Drozdzak, F Verpoort, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
January 5, 2002
Complexation of triorganotin derivatives of [18]crown-6- and [15]crown-5-(benzo-4-carboxylate) with alkali thiocyanates
M Kemmer, M Biesemans, M Gielen, et al.
Health Research Policy and Systems
|
September 11, 2025
Measuring impacts: a scoping review of healthcare impact evaluations
L R Correia, J C Martins, E T Rother, et al.
Magnetic Resonance in Chemistry : MRC
|
March 17, 2004
Structure elucidation of 11-amino-8-hydroxypentacyclo[5.4.0.0(2, 6).0(3, 10).0(5, 9)]undecane-8,11-lactam through selective acetylation and complete 1H and 13C NMR spectral assignment of the mono-, di- and triacetates
F J C Martins, A M Viljoen, H G Kruger, et al.
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