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Biophysical Journal
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November 5, 2015
Functional and Modeling Studies of the Transmembrane Region of the TRPM8 Channel
Gabriel Bidaux, Miriam Sgobba, Loic Lemonnier, et al.
JACS Au
|
March 27, 2026
Cryptic Binding Pockets in PDC‑3 β‑Lactamase Modulate Resistance Profiles
Shuang Chen, Fedaa Attana, Andrea M Hujer, et al.
Nucleic Acids Research
|
May 27, 2020
Native de novo structural determinations of non-canonical nucleic acid motifs by X-ray crystallography at long wavelengths
Yashu Zhang, Kamel El Omari, Ramona Duman, et al.
Biochimica Et Biophysica Acta. General Subjects
|
December 17, 2016
Folding of guanine quadruplex molecules-funnel-like mechanism or kinetic partitioning? An overview from MD simulation studies
Jiří Šponer, Giovanni Bussi, Petr Stadlbauer, et al.
Physiologia Plantarum
|
September 5, 2025
Cysteine Alleviates the Toxicity of Cadmium Telluride Quantum Dots (CdTe QDs) by Modulating the Antioxidant System and Root Metabolic Pathways in Rice
Qiu-Yun Shi, Teng Li, Hao Xiang, et al.
EMBO Reports
|
April 28, 2006
Structural and functional analysis of the putative pH sensor in the Kir1.1 (ROMK) potassium channel
Markus Rapedius, Shozeb Haider, Katharine F Browne, et al.
The Biochemical Journal
|
July 14, 2020
Structure-based enzyme engineering improves donor-substrate recognition of Arabidopsis thaliana glycosyltransferases
Aishat Akere, Serena H Chen, Xiaohan Liu, et al.
Pharmaceutics
|
April 23, 2022
In Vivo Investigation of (2-Hydroxypropyl)-β-cyclodextrin-Based Formulation of Spironolactone in Aqueous Solution for Paediatric Use
Antonio Lopalco, Annachiara Manni, Alexander Keeley, et al.
EMBO Reports
|
May 3, 2005
A gating mutation at the internal mouth of the Kir6.2 pore is associated with DEND syndrome
Peter Proks, Christophe Girard, Shozeb Haider, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 30, 2013
Structure-phenotype correlations of human CYP21A2 mutations in congenital adrenal hyperplasia
Shozeb Haider, Barira Islam, Valentina D'Atri, et al.
Page
of 17
Search research articles
Search
Showing results (71-80 of 161) with videos related to
Sort By:
Page
of 17
Biophysical Journal
|
November 5, 2015
Functional and Modeling Studies of the Transmembrane Region of the TRPM8 Channel
Gabriel Bidaux, Miriam Sgobba, Loic Lemonnier, et al.
JACS Au
|
March 27, 2026
Cryptic Binding Pockets in PDC‑3 β‑Lactamase Modulate Resistance Profiles
Shuang Chen, Fedaa Attana, Andrea M Hujer, et al.
Nucleic Acids Research
|
May 27, 2020
Native de novo structural determinations of non-canonical nucleic acid motifs by X-ray crystallography at long wavelengths
Yashu Zhang, Kamel El Omari, Ramona Duman, et al.
Biochimica Et Biophysica Acta. General Subjects
|
December 17, 2016
Folding of guanine quadruplex molecules-funnel-like mechanism or kinetic partitioning? An overview from MD simulation studies
Jiří Šponer, Giovanni Bussi, Petr Stadlbauer, et al.
Physiologia Plantarum
|
September 5, 2025
Cysteine Alleviates the Toxicity of Cadmium Telluride Quantum Dots (CdTe QDs) by Modulating the Antioxidant System and Root Metabolic Pathways in Rice
Qiu-Yun Shi, Teng Li, Hao Xiang, et al.
EMBO Reports
|
April 28, 2006
Structural and functional analysis of the putative pH sensor in the Kir1.1 (ROMK) potassium channel
Markus Rapedius, Shozeb Haider, Katharine F Browne, et al.
The Biochemical Journal
|
July 14, 2020
Structure-based enzyme engineering improves donor-substrate recognition of Arabidopsis thaliana glycosyltransferases
Aishat Akere, Serena H Chen, Xiaohan Liu, et al.
Pharmaceutics
|
April 23, 2022
In Vivo Investigation of (2-Hydroxypropyl)-β-cyclodextrin-Based Formulation of Spironolactone in Aqueous Solution for Paediatric Use
Antonio Lopalco, Annachiara Manni, Alexander Keeley, et al.
EMBO Reports
|
May 3, 2005
A gating mutation at the internal mouth of the Kir6.2 pore is associated with DEND syndrome
Peter Proks, Christophe Girard, Shozeb Haider, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 30, 2013
Structure-phenotype correlations of human CYP21A2 mutations in congenital adrenal hyperplasia
Shozeb Haider, Barira Islam, Valentina D'Atri, et al.
Page
of 17