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Biochimica Et Biophysica Acta
|
March 17, 2010
ATP hydrolysis in ATP synthases can be differently coupled to proton transport and modulated by ADP and phosphate: a structure based model of the mechanism
Manuela D'Alessandro, B Andrea Melandri
Biochimica Et Biophysica Acta
|
August 31, 2010
Quantitative evaluation of the intrinsic uncoupling modulated by ADP and P(i) in the reconstituted ATP synthase of Escherichia coli
Manuela D'Alessandro, Paola Turina, B Andrea Melandri
Biochimica Et Biophysica Acta
|
October 28, 2008
Intrinsic uncoupling in the ATP synthase of Escherichia coli
Manuela D'Alessandro, Paola Turina, B Andrea Melandri
Biochimica Et Biophysica Acta
|
June 13, 2006
Modulation of proton pumping efficiency in bacterial ATP synthases
Paola Turina, Alberto Rebecchi, Manuela D'Alessandro, et al.
Genetics
|
February 5, 2026
Two populations of heteromeric acetylcholine receptors are present at C. elegans neuromuscular junctions
Greta Maiellano, Camilla Luccardini, Oceane Romatif, et al.
Elife
|
November 9, 2018
CRELD1 is an evolutionarily-conserved maturational enhancer of ionotropic acetylcholine receptors
Manuela D'Alessandro, Magali Richard, Christian Stigloher, et al.
Developmental Cell
|
October 28, 2015
Amphiphysin 2 Orchestrates Nucleus Positioning and Shape by Linking the Nuclear Envelope to the Actin and Microtubule Cytoskeleton
Manuela D'Alessandro, Karim Hnia, Vincent Gache, et al.
Human Molecular Genetics
|
October 11, 2017
Biallelic mutation of UNC50, encoding a protein involved in AChR trafficking, is responsible for arthrogryposis
Emanuela Abiusi, Manuela D'Alessandro, Klaus Dieterich, et al.
Biomedicines
|
May 27, 2026
Dissecting GPCR Contributions to Gαo-Dependent Motor Dysfunction in <i>GNAO1</i>-Related Disorders Using <i>Caenorhabditis elegans</i>
Martina Di Rocco, Lorenzo Di Rienzo, Francesca Carmen Follo, et al.
Brain Communications
|
September 22, 2025
Biallelic <i>CRELD1</i> variants cause severe muscle weakness and infantile epilepsy
Manuela D'Alessandro, Daniel Bamborschke, Margret H Bülow, et al.
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Search research articles
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Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Biochimica Et Biophysica Acta
|
March 17, 2010
ATP hydrolysis in ATP synthases can be differently coupled to proton transport and modulated by ADP and phosphate: a structure based model of the mechanism
Manuela D'Alessandro, B Andrea Melandri
Biochimica Et Biophysica Acta
|
August 31, 2010
Quantitative evaluation of the intrinsic uncoupling modulated by ADP and P(i) in the reconstituted ATP synthase of Escherichia coli
Manuela D'Alessandro, Paola Turina, B Andrea Melandri
Biochimica Et Biophysica Acta
|
October 28, 2008
Intrinsic uncoupling in the ATP synthase of Escherichia coli
Manuela D'Alessandro, Paola Turina, B Andrea Melandri
Biochimica Et Biophysica Acta
|
June 13, 2006
Modulation of proton pumping efficiency in bacterial ATP synthases
Paola Turina, Alberto Rebecchi, Manuela D'Alessandro, et al.
Genetics
|
February 5, 2026
Two populations of heteromeric acetylcholine receptors are present at C. elegans neuromuscular junctions
Greta Maiellano, Camilla Luccardini, Oceane Romatif, et al.
Elife
|
November 9, 2018
CRELD1 is an evolutionarily-conserved maturational enhancer of ionotropic acetylcholine receptors
Manuela D'Alessandro, Magali Richard, Christian Stigloher, et al.
Developmental Cell
|
October 28, 2015
Amphiphysin 2 Orchestrates Nucleus Positioning and Shape by Linking the Nuclear Envelope to the Actin and Microtubule Cytoskeleton
Manuela D'Alessandro, Karim Hnia, Vincent Gache, et al.
Human Molecular Genetics
|
October 11, 2017
Biallelic mutation of UNC50, encoding a protein involved in AChR trafficking, is responsible for arthrogryposis
Emanuela Abiusi, Manuela D'Alessandro, Klaus Dieterich, et al.
Biomedicines
|
May 27, 2026
Dissecting GPCR Contributions to Gαo-Dependent Motor Dysfunction in <i>GNAO1</i>-Related Disorders Using <i>Caenorhabditis elegans</i>
Martina Di Rocco, Lorenzo Di Rienzo, Francesca Carmen Follo, et al.
Brain Communications
|
September 22, 2025
Biallelic <i>CRELD1</i> variants cause severe muscle weakness and infantile epilepsy
Manuela D'Alessandro, Daniel Bamborschke, Margret H Bülow, et al.
Page
of 2