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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 disease
Roberta 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 encephalocele
Zoe 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-Infrared
Filip 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 mouse
Madeleine 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 Americas
Usama 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 Chains
Qiao 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 Abundance
Niamh 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 development
Daniel 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 Europeans
S Ortega-Cubero, O Lorenzo-Betancor, E Lorenzo, et al.
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of 36
Search research articles
Search
Showing results (191-200 of 359) with videos related to
Sort By:
Page
of 36
Nature Cell Biology
|
January 21, 2014
Enhancing nucleotide metabolism protects against mitochondrial dysfunction and neurodegeneration in a PINK1 model of Parkinson's disease
Roberta 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 encephalocele
Zoe 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-Infrared
Filip 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 mouse
Madeleine 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 Americas
Usama 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 Chains
Qiao 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 Abundance
Niamh 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 development
Daniel 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 Europeans
S Ortega-Cubero, O Lorenzo-Betancor, E Lorenzo, et al.
Page
of 36