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The EMBO Journal
|
June 14, 2022
Cooperative amyloid fibre binding and disassembly by the Hsp70 disaggregase
Joseph George Beton, Jim Monistrol, Anne Wentink, et al.
Toxicology
|
December 9, 2008
Acute and chronic effects of intravitreally injected beta-amyloid on the neurotransmitter system in the retina
Okezie I Aruoma, Sheila S M Jen, Helena R Watts, et al.
Frontiers in Nutrition
|
March 10, 2022
Exercise-Induced Hyponatremia: An Assessment of the International Hydration Recommendations Followed During the Gran Trail De Peñalara and Vitoria-Gasteiz Ironman Competitions
Diego López de Lara, Jorge Gabriel Ruiz-Sánchez, Martín Cuesta, et al.
Plos One
|
March 30, 2021
Selective killing of homologous recombination-deficient cancer cell lines by inhibitors of the RPA:RAD52 protein-protein interaction
Mona Al-Mugotir, Jeffrey J Lovelace, Joseph George, et al.
Genes & Development
|
June 4, 2014
MuLV-related endogenous retroviral elements and Flt3 participate in aberrant end-joining events that promote B-cell leukemogenesis
Radia M Johnson, Eniko Papp, Ildiko Grandal, et al.
Journal of Lipid Research
|
March 18, 2005
Complete functional rescue of the ABCA1-/- mouse by human BAC transgenesis
Jonathan M Coutinho, Roshni R Singaraja, Martin Kang, et al.
Journal of Medical Genetics
|
March 25, 2011
Euchromatic 9q13-q21 duplication variants are tandem segmental amplifications of sequence reciprocal to 9q13-q21 deletions
Ann M Joseph-George, Yongshu He, Christian R Marshall, et al.
Journal of the American Geriatrics Society
|
June 16, 2026
A Scoping Review on Strategies for Navigating Conflicting Rights Between Safety and Autonomy in Residential Long-Term Care in the United States
Angela K Perone, Leyi Zhou, Ann Glusker, et al.
Clinical Genetics
|
December 1, 2010
Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorder
M T Carter, S M Nikkel, B A Fernandez, et al.
Journal of Medical Genetics
|
September 17, 2009
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder
Bridget A Fernandez, Wendy Roberts, Brian Chung, et al.
Page
of 13
Search research articles
Search
Showing results (111-120 of 124) with videos related to
Sort By:
Page
of 13
The EMBO Journal
|
June 14, 2022
Cooperative amyloid fibre binding and disassembly by the Hsp70 disaggregase
Joseph George Beton, Jim Monistrol, Anne Wentink, et al.
Toxicology
|
December 9, 2008
Acute and chronic effects of intravitreally injected beta-amyloid on the neurotransmitter system in the retina
Okezie I Aruoma, Sheila S M Jen, Helena R Watts, et al.
Frontiers in Nutrition
|
March 10, 2022
Exercise-Induced Hyponatremia: An Assessment of the International Hydration Recommendations Followed During the Gran Trail De Peñalara and Vitoria-Gasteiz Ironman Competitions
Diego López de Lara, Jorge Gabriel Ruiz-Sánchez, Martín Cuesta, et al.
Plos One
|
March 30, 2021
Selective killing of homologous recombination-deficient cancer cell lines by inhibitors of the RPA:RAD52 protein-protein interaction
Mona Al-Mugotir, Jeffrey J Lovelace, Joseph George, et al.
Genes & Development
|
June 4, 2014
MuLV-related endogenous retroviral elements and Flt3 participate in aberrant end-joining events that promote B-cell leukemogenesis
Radia M Johnson, Eniko Papp, Ildiko Grandal, et al.
Journal of Lipid Research
|
March 18, 2005
Complete functional rescue of the ABCA1-/- mouse by human BAC transgenesis
Jonathan M Coutinho, Roshni R Singaraja, Martin Kang, et al.
Journal of Medical Genetics
|
March 25, 2011
Euchromatic 9q13-q21 duplication variants are tandem segmental amplifications of sequence reciprocal to 9q13-q21 deletions
Ann M Joseph-George, Yongshu He, Christian R Marshall, et al.
Journal of the American Geriatrics Society
|
June 16, 2026
A Scoping Review on Strategies for Navigating Conflicting Rights Between Safety and Autonomy in Residential Long-Term Care in the United States
Angela K Perone, Leyi Zhou, Ann Glusker, et al.
Clinical Genetics
|
December 1, 2010
Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorder
M T Carter, S M Nikkel, B A Fernandez, et al.
Journal of Medical Genetics
|
September 17, 2009
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder
Bridget A Fernandez, Wendy Roberts, Brian Chung, et al.
Page
of 13