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Molecular Pharmaceutics|January 16, 2015
Molecular details of INH-C10 binding to wt KatG and Its S315T mutantVitor H Teixeira, Cristina Ventura, Ruben Leitão, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|July 15, 2018
Critical comparison of shake-flask, potentiometric and chromatographic methods for lipophilicity evaluation (log P<sub>o/w</sub>) of neutral, acidic, basic, amphoteric, and zwitterionic drugsAdriana Port, Magda Bordas, Raquel Enrech, et al.
Analytical Chemistry|September 19, 2002
Solute-solvent interactions in micellar electrokinetic chromatography. 6. Optimization of the selectivity of lithium dodecyl sulfate-lithium perfluorooctanesulfonate mixed micellar buffersElisabet Fuguet, Clara Ràfols, José Ramón Torres-Lapasió, et al.
Journal of Chemical Information and Computer Sciences|July 23, 2003
A QSPR study of the p solute polarity parameter to estimate retention in HPLCRamón Bosque, Joaquim Sales, Elisabeth Bosch, et al.
Journal of Chromatography. A|February 19, 2004
Hydrophobic and cation exchange mechanisms in the retention of basic compounds in a polymeric columnRebeca Ruiz, Ma José Ruiz-Angel, Ma Celia García-Alvarez-Coque, et al.
Human Genetics|July 19, 2024
The missing link: ARID1B non-truncating variants causing Coffin-Siris syndrome due to protein aggregationElisabeth Bosch, Esther Güse, Philipp Kirchner, et al.
European Journal of Medical Genetics|May 22, 2026
A multi-omics approach to characterize a deep intronic ARID1A deletion in Coffin-Siris SyndromeSarah Schuhmann, Elisabeth Bosch, Andreas Fink, et al.
The Journal of Clinical Endocrinology and Metabolism|August 12, 2021
BDV Syndrome: An Emerging Syndrome With Profound Obesity and Neurodevelopmental Delay Resembling Prader-Willi SyndromeElisabeth Bosch, Moritz Hebebrand, Bernt Popp, et al.
BMC Cancer|July 12, 2012
Prospective evaluation of quality of life effects in patients undergoing palliative radiotherapy for brain metastasesDiana Steinmann, Yvonne Paelecke-Habermann, Hans Geinitz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 12, 2026
Missense Variants in the A Isoform of FGF13 as a Novel Cause of Paroxysmal DyskinesiaCyril Mignot, Matthildi Athina Papathanasiou Terzi, Claudia Ravelli, et al.
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