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International Journal of Molecular Sciences
|
January 2, 2019
Proteomic Studies Reveal Disrupted in Schizophrenia 1 as a Player in Both Neurodevelopment and Synaptic Function
Adriana Ramos, Carmen Rodríguez-Seoane, Isaac Rosa, et al.
Free Radical Biology & Medicine
|
August 16, 2008
Increased oxidation, glycoxidation, and lipoxidation of brain proteins in prion disease
Reinald Pamplona, Alba Naudí, Rosalina Gavín, et al.
Free Radical Biology & Medicine
|
October 9, 1999
Thyroid status modulates glycoxidative and lipoxidative modification of tissue proteins
R Pamplona, M Portero-Otín, C Ruiz, et al.
Biochemistry
|
July 9, 2009
Oligomer assembly of the C-terminal DISC1 domain (640-854) is controlled by self-association motifs and disease-associated polymorphism S704C
S Rutger Leliveld, Philipp Hendriks, Max Michel, et al.
The Journal of Biological Chemistry
|
July 11, 1997
Carboxymethylethanolamine, a biomarker of phospholipid modification during the maillard reaction in vivo
J R Requena, M U Ahmed, C W Fountain, et al.
Journal of Clinical Medicine
|
April 30, 2021
Celia's Encephalopathy (<i>BSCL2</i>-Gene-Related): Current Understanding
Sofía Sánchez-Iglesias, Antía Fernández-Pombo, Silvia Cobelo-Gómez, et al.
The Veterinary Quarterly
|
November 9, 2024
New preclinical biomarkers for prion diseases in the cerebrospinal fluid proteome revealed by mass spectrometry
Sonia Pérez-Lázaro, Tomás Barrio, Susana B Bravo, et al.
Acta Neuropathologica Communications
|
December 4, 2025
Spontaneous generation of diverse recombinant prion strains: sulfated glycan cofactors facilitate strain emergence but do not determine specific strain properties
Nuria L Lorenzo, Hasier Eraña, Enric Vidal, et al.
Scientific Reports
|
August 31, 2017
Generation of a new infectious recombinant prion: a model to understand Gerstmann-Sträussler-Scheinker syndrome
Saioa R Elezgarai, Natalia Fernández-Borges, Hasier Eraña, et al.
Molecular Neurobiology
|
March 8, 2014
Loss of prion protein leads to age-dependent behavioral abnormalities and changes in cytoskeletal protein expression
Matthias Schmitz, Catharina Greis, Philipp Ottis, et al.
Page
of 12
Search research articles
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Showing results (81-90 of 114) with videos related to
Sort By:
Page
of 12
International Journal of Molecular Sciences
|
January 2, 2019
Proteomic Studies Reveal Disrupted in Schizophrenia 1 as a Player in Both Neurodevelopment and Synaptic Function
Adriana Ramos, Carmen Rodríguez-Seoane, Isaac Rosa, et al.
Free Radical Biology & Medicine
|
August 16, 2008
Increased oxidation, glycoxidation, and lipoxidation of brain proteins in prion disease
Reinald Pamplona, Alba Naudí, Rosalina Gavín, et al.
Free Radical Biology & Medicine
|
October 9, 1999
Thyroid status modulates glycoxidative and lipoxidative modification of tissue proteins
R Pamplona, M Portero-Otín, C Ruiz, et al.
Biochemistry
|
July 9, 2009
Oligomer assembly of the C-terminal DISC1 domain (640-854) is controlled by self-association motifs and disease-associated polymorphism S704C
S Rutger Leliveld, Philipp Hendriks, Max Michel, et al.
The Journal of Biological Chemistry
|
July 11, 1997
Carboxymethylethanolamine, a biomarker of phospholipid modification during the maillard reaction in vivo
J R Requena, M U Ahmed, C W Fountain, et al.
Journal of Clinical Medicine
|
April 30, 2021
Celia's Encephalopathy (<i>BSCL2</i>-Gene-Related): Current Understanding
Sofía Sánchez-Iglesias, Antía Fernández-Pombo, Silvia Cobelo-Gómez, et al.
The Veterinary Quarterly
|
November 9, 2024
New preclinical biomarkers for prion diseases in the cerebrospinal fluid proteome revealed by mass spectrometry
Sonia Pérez-Lázaro, Tomás Barrio, Susana B Bravo, et al.
Acta Neuropathologica Communications
|
December 4, 2025
Spontaneous generation of diverse recombinant prion strains: sulfated glycan cofactors facilitate strain emergence but do not determine specific strain properties
Nuria L Lorenzo, Hasier Eraña, Enric Vidal, et al.
Scientific Reports
|
August 31, 2017
Generation of a new infectious recombinant prion: a model to understand Gerstmann-Sträussler-Scheinker syndrome
Saioa R Elezgarai, Natalia Fernández-Borges, Hasier Eraña, et al.
Molecular Neurobiology
|
March 8, 2014
Loss of prion protein leads to age-dependent behavioral abnormalities and changes in cytoskeletal protein expression
Matthias Schmitz, Catharina Greis, Philipp Ottis, et al.
Page
of 12