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Epigenetics
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November 4, 2017
Trichostatin A decreases the levels of MeCP2 expression and phosphorylation and increases its chromatin binding affinity
Katrina V Good, Alexia Martínez de Paz, Monica Tyagi, et al.
BJU International
|
July 2, 2019
Radical cystectomy pentafecta: a proposal for standardisation of outcomes reporting following robot-assisted radical cystectomy
Giovanni E Cacciamani, Matthew Winter, Luis G Medina, et al.
Vaccine
|
May 31, 2022
Robust antibody response after a third BNT162b2 vaccine compared to the second among immunocompromised and healthy individuals, a prospective longitudinal cohort study
Shirley Shapiro Ben David, Barak Mizrahi, Daniella Rahamim-Cohen, et al.
EMBO Reports
|
October 4, 2017
ASPM and CITK regulate spindle orientation by affecting the dynamics of astral microtubules
Marta Gai, Federico T Bianchi, Cristiana Vagnoni, et al.
EMBO Reports
|
August 27, 2016
ASPM and CITK regulate spindle orientation by affecting the dynamics of astral microtubules
Marta Gai, Federico T Bianchi, Cristiana Vagnoni, et al.
Nature Cell Biology
|
August 5, 2024
p16-dependent increase of PD-L1 stability regulates immunosurveillance of senescent cells
Julia Majewska, Amit Agrawal, Avi Mayo, et al.
EMBO Molecular Medicine
|
October 14, 2024
Unraveling autophagic imbalances and therapeutic insights in Mecp2-deficient models
Alessandro Esposito, Tommaso Seri, Martina Breccia, et al.
Clinical Pharmacology and Therapeutics
|
January 8, 2010
Fcgamma-receptor IIa polymorphism and the role of immunoadsorption in cardiac dysfunction in patients with dilated cardiomyopathy
A Staudt, L R Herda, C Trimpert, et al.
Molecular Neurobiology
|
November 8, 2018
A Novel Mecp2<sup>Y120D</sup> Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome
Anna Gandaglia, Elena Brivio, Sara Carli, et al.
Human Molecular Genetics
|
May 27, 2005
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome
Francesca Mari, Sara Azimonti, Ilaria Bertani, et al.
Page
of 35
Search research articles
Search
Showing results (331-340 of 346) with videos related to
Sort By:
Page
of 35
Epigenetics
|
November 4, 2017
Trichostatin A decreases the levels of MeCP2 expression and phosphorylation and increases its chromatin binding affinity
Katrina V Good, Alexia Martínez de Paz, Monica Tyagi, et al.
BJU International
|
July 2, 2019
Radical cystectomy pentafecta: a proposal for standardisation of outcomes reporting following robot-assisted radical cystectomy
Giovanni E Cacciamani, Matthew Winter, Luis G Medina, et al.
Vaccine
|
May 31, 2022
Robust antibody response after a third BNT162b2 vaccine compared to the second among immunocompromised and healthy individuals, a prospective longitudinal cohort study
Shirley Shapiro Ben David, Barak Mizrahi, Daniella Rahamim-Cohen, et al.
EMBO Reports
|
October 4, 2017
ASPM and CITK regulate spindle orientation by affecting the dynamics of astral microtubules
Marta Gai, Federico T Bianchi, Cristiana Vagnoni, et al.
EMBO Reports
|
August 27, 2016
ASPM and CITK regulate spindle orientation by affecting the dynamics of astral microtubules
Marta Gai, Federico T Bianchi, Cristiana Vagnoni, et al.
Nature Cell Biology
|
August 5, 2024
p16-dependent increase of PD-L1 stability regulates immunosurveillance of senescent cells
Julia Majewska, Amit Agrawal, Avi Mayo, et al.
EMBO Molecular Medicine
|
October 14, 2024
Unraveling autophagic imbalances and therapeutic insights in Mecp2-deficient models
Alessandro Esposito, Tommaso Seri, Martina Breccia, et al.
Clinical Pharmacology and Therapeutics
|
January 8, 2010
Fcgamma-receptor IIa polymorphism and the role of immunoadsorption in cardiac dysfunction in patients with dilated cardiomyopathy
A Staudt, L R Herda, C Trimpert, et al.
Molecular Neurobiology
|
November 8, 2018
A Novel Mecp2<sup>Y120D</sup> Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome
Anna Gandaglia, Elena Brivio, Sara Carli, et al.
Human Molecular Genetics
|
May 27, 2005
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome
Francesca Mari, Sara Azimonti, Ilaria Bertani, et al.
Page
of 35