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P de Castro

Showing results (191-200 of 359) with videos related to

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Nature Cell Biology|January 21, 2014
Enhancing nucleotide metabolism protects against mitochondrial dysfunction and neurodegeneration in a PINK1 model of Parkinson's diseaseRoberta Tufi, Sonia Gandhi, Inês P de Castro, et al.
Human Molecular Genetics|June 26, 2023
A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephaloceleZoe Crane-Smith, Sandra C P De Castro, Evanthia Nikolopoulou, et al.
Journal of the American Chemical Society|May 6, 2024
A Conjugated Carboranyl Main Chain Polymer with Aggregation-Induced Emission in the Near-InfraredFilip Aniés, Iain Hamilton, Catherine S P De Castro, et al.
Human Molecular Genetics|January 26, 2011
Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouseMadeleine R Brouns, Sandra C P De Castro, Els A Terwindt-Rouwenhorst, et al.
Science Advances|December 8, 2021
Scaling of mortality in 742 metropolitan areas of the AmericasUsama Bilal, Caio P de Castro, Tania Alfaro, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|January 22, 2025
Significant Efficiency Enhancements in Non-Y Series Acceptors by the Addition of Outer Side ChainsQiao He, Wisnu Tantyo Hadmojo, Xiantao Hu, et al.
Revista De Neurologia|January 29, 2009
[Coding in neuropediatrics based on the International Classification Diseases, 9th revision (ICD-9), 5th edition (2006)]A García-Pérez, M A Martínez-Granero, A Verdú-Pérez, et al.
Molecular & Cellular Proteomics : MCP|January 15, 2024
The Differential Translation Capabilities of the Human DHFR2 Gene Indicates a Developmental and Tissue-Specific Endogenous Protein of Low AbundanceNiamh Bookey, Paola Drago, Kit-Yi Leung, et al.
The Journal of Clinical Endocrinology and Metabolism|February 21, 2008
SOX2 plays a critical role in the pituitary, forebrain, and eye during human embryonic developmentDaniel Kelberman, Sandra C P de Castro, Shuwen Huang, et al.
Neurobiology of Aging|June 5, 2013
Fused in Sarcoma (FUS) gene mutations are not a frequent cause of essential tremor in EuropeansS Ortega-Cubero, O Lorenzo-Betancor, E Lorenzo, et al.
Pageof 36

Showing results (191-200 of 359) with videos related to

Sort By:
Pageof 36
Nature Cell Biology|January 21, 2014
Enhancing nucleotide metabolism protects against mitochondrial dysfunction and neurodegeneration in a PINK1 model of Parkinson's diseaseRoberta Tufi, Sonia Gandhi, Inês P de Castro, et al.
Human Molecular Genetics|June 26, 2023
A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephaloceleZoe Crane-Smith, Sandra C P De Castro, Evanthia Nikolopoulou, et al.
Journal of the American Chemical Society|May 6, 2024
A Conjugated Carboranyl Main Chain Polymer with Aggregation-Induced Emission in the Near-InfraredFilip Aniés, Iain Hamilton, Catherine S P De Castro, et al.
Human Molecular Genetics|January 26, 2011
Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouseMadeleine R Brouns, Sandra C P De Castro, Els A Terwindt-Rouwenhorst, et al.
Science Advances|December 8, 2021
Scaling of mortality in 742 metropolitan areas of the AmericasUsama Bilal, Caio P de Castro, Tania Alfaro, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|January 22, 2025
Significant Efficiency Enhancements in Non-Y Series Acceptors by the Addition of Outer Side ChainsQiao He, Wisnu Tantyo Hadmojo, Xiantao Hu, et al.
Revista De Neurologia|January 29, 2009
[Coding in neuropediatrics based on the International Classification Diseases, 9th revision (ICD-9), 5th edition (2006)]A García-Pérez, M A Martínez-Granero, A Verdú-Pérez, et al.
Molecular & Cellular Proteomics : MCP|January 15, 2024
The Differential Translation Capabilities of the Human DHFR2 Gene Indicates a Developmental and Tissue-Specific Endogenous Protein of Low AbundanceNiamh Bookey, Paola Drago, Kit-Yi Leung, et al.
The Journal of Clinical Endocrinology and Metabolism|February 21, 2008
SOX2 plays a critical role in the pituitary, forebrain, and eye during human embryonic developmentDaniel Kelberman, Sandra C P de Castro, Shuwen Huang, et al.
Neurobiology of Aging|June 5, 2013
Fused in Sarcoma (FUS) gene mutations are not a frequent cause of essential tremor in EuropeansS Ortega-Cubero, O Lorenzo-Betancor, E Lorenzo, et al.
Pageof 36