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Plant Cell Reports
|
June 10, 2009
Expression of the PsMTA1 gene in white poplar engineered with the MAT system is associated with heavy metal tolerance and protection against 8-hydroxy-2'-deoxyguanosine mediated-DNA damage
Alma Balestrazzi, Silvia Botti, Samantha Zelasco, et al.
The Journal of Physical Chemistry. B
|
April 20, 2017
Integrated Computational Approach to the Electron Paramagnetic Resonance Characterization of Rigid 3<sub>10</sub>-Helical Peptides with TOAC Nitroxide Spin Labels
Marco Gerolin, Mirco Zerbetto, Alessandro Moretto, et al.
Chemical Science
|
May 14, 2023
Isoamphipathic antibacterial molecules regulating activity and toxicity through positional isomerism
Swagatam Barman, Sudip Mukherjee, Logia Jolly, et al.
Biochemical Pharmacology
|
September 21, 2020
Role of proteolytic enzymes in the COVID-19 infection and promising therapeutic approaches
Magda Gioia, Chiara Ciaccio, Paolo Calligari, et al.
The Journal of Physical Chemistry Letters
|
October 3, 2024
Fluorescent Labeling Can Significantly Perturb Measured Binding Affinity and Selectivity of Peptide-Protein Interactions
Sara Bobone, Claudia Storti, Chiara Fulci, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 30, 2024
Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome
Serena Galosi, Cecilia Mancini, Anna Commone, et al.
Scientific Reports
|
January 20, 2018
Macrophage sensing of single-walled carbon nanotubes via Toll-like receptors
Sourav P Mukherjee, Olesja Bondarenko, Pekka Kohonen, et al.
Human Mutation
|
March 1, 2020
Pathogenic PTPN11 variants involving the poly-glutamine Gln<sup>255</sup> -Gln<sup>256</sup> -Gln<sup>257</sup> stretch highlight the relevance of helix B in SHP2's functional regulation
Simone Martinelli, Luca Pannone, Christina Lissewski, et al.
American Journal of Human Genetics
|
November 20, 2020
A Recurrent Gain-of-Function Mutation in CLCN6, Encoding the ClC-6 Cl<sup>-</sup>/H<sup>+</sup>-Exchanger, Causes Early-Onset Neurodegeneration
Maya M Polovitskaya, Carlo Barbini, Diego Martinelli, et al.
American Journal of Human Genetics
|
October 6, 2018
Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome
Christiane K Bauer, Paolo Calligari, Francesca Clementina Radio, et al.
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Search research articles
Search
Showing results (21-30 of 32) with videos related to
Sort By:
Page
of 4
Plant Cell Reports
|
June 10, 2009
Expression of the PsMTA1 gene in white poplar engineered with the MAT system is associated with heavy metal tolerance and protection against 8-hydroxy-2'-deoxyguanosine mediated-DNA damage
Alma Balestrazzi, Silvia Botti, Samantha Zelasco, et al.
The Journal of Physical Chemistry. B
|
April 20, 2017
Integrated Computational Approach to the Electron Paramagnetic Resonance Characterization of Rigid 3<sub>10</sub>-Helical Peptides with TOAC Nitroxide Spin Labels
Marco Gerolin, Mirco Zerbetto, Alessandro Moretto, et al.
Chemical Science
|
May 14, 2023
Isoamphipathic antibacterial molecules regulating activity and toxicity through positional isomerism
Swagatam Barman, Sudip Mukherjee, Logia Jolly, et al.
Biochemical Pharmacology
|
September 21, 2020
Role of proteolytic enzymes in the COVID-19 infection and promising therapeutic approaches
Magda Gioia, Chiara Ciaccio, Paolo Calligari, et al.
The Journal of Physical Chemistry Letters
|
October 3, 2024
Fluorescent Labeling Can Significantly Perturb Measured Binding Affinity and Selectivity of Peptide-Protein Interactions
Sara Bobone, Claudia Storti, Chiara Fulci, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 30, 2024
Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome
Serena Galosi, Cecilia Mancini, Anna Commone, et al.
Scientific Reports
|
January 20, 2018
Macrophage sensing of single-walled carbon nanotubes via Toll-like receptors
Sourav P Mukherjee, Olesja Bondarenko, Pekka Kohonen, et al.
Human Mutation
|
March 1, 2020
Pathogenic PTPN11 variants involving the poly-glutamine Gln<sup>255</sup> -Gln<sup>256</sup> -Gln<sup>257</sup> stretch highlight the relevance of helix B in SHP2's functional regulation
Simone Martinelli, Luca Pannone, Christina Lissewski, et al.
American Journal of Human Genetics
|
November 20, 2020
A Recurrent Gain-of-Function Mutation in CLCN6, Encoding the ClC-6 Cl<sup>-</sup>/H<sup>+</sup>-Exchanger, Causes Early-Onset Neurodegeneration
Maya M Polovitskaya, Carlo Barbini, Diego Martinelli, et al.
American Journal of Human Genetics
|
October 6, 2018
Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome
Christiane K Bauer, Paolo Calligari, Francesca Clementina Radio, et al.
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of 4