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Public Health Genomics
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September 10, 2015
Stability of Attitudes to the Ethical Issues Raised by the Return of Incidental Genomic Research Findings in Children: A Follow-Up Study
Conrad V Fernandez, Colleen OʼConnell, Meghan Ferguson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 30, 2005
Membrane metabolism mediated by Sec14 family members influences Arf GTPase activating protein activity for transport from the trans-Golgi
Tania A Wong, Gregory D Fairn, Pak P Poon, et al.
The Journal of Biological Chemistry
|
December 25, 2025
Sphingosine-1-phosphate receptor 2 inhibition ameliorates familial exudative vitreoretinopathy models
Hirad A Feridooni, Rachel Fody, Mahtab Tavasoli, et al.
Pediatric Blood & Cancer
|
April 3, 2016
Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia
Marissa A LeBlanc, Amanda Bettle, Jason N Berman, et al.
Molecular Genetics and Metabolism Reports
|
November 30, 2016
Mitochondrial damage and cholesterol storage in human hepatocellular carcinoma cells with silencing of <i>UBIAD1</i> gene expression
Carlos R Morales, Lubov S Grigoryeva, Xuefang Pan, et al.
American Journal of Ophthalmology Case Reports
|
April 17, 2024
Multimodal imaging of white preretinal lesions in atypical familial exudative vitreoretinopathy: Case report and literature review
Liam D Redden, Douglas S M Iaboni, Sarah van der Ende, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
December 5, 2025
Polymyalgia rheumatica patients presenting with atypical clinical features still exhibit characteristic <sup>18</sup>F-FDG PET/CT findings
Emily Martin, Christopher R McMaster, Aurora Mt Poon, et al.
Nucleic Acids Research
|
June 16, 2018
Optimized knock-in of point mutations in zebrafish using CRISPR/Cas9
Sergey V Prykhozhij, Charlotte Fuller, Shelby L Steele, et al.
The Journal of Biological Chemistry
|
November 27, 2025
Neurodevelopmental disease-causing variants in choline kinase CHKA gene couple phosphatidylcholine synthesis to oxidative stress damage and disease etiology
Mahtab Tavasoli, Mariam Alkandari, Gabriel Dorighello, et al.
Orphanet Journal of Rare Diseases
|
June 19, 2012
A generalizable pre-clinical research approach for orphan disease therapy
Chandree L Beaulieu, Mark E Samuels, Sean Ekins, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 79) with videos related to
Sort By:
Page
of 8
Public Health Genomics
|
September 10, 2015
Stability of Attitudes to the Ethical Issues Raised by the Return of Incidental Genomic Research Findings in Children: A Follow-Up Study
Conrad V Fernandez, Colleen OʼConnell, Meghan Ferguson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 30, 2005
Membrane metabolism mediated by Sec14 family members influences Arf GTPase activating protein activity for transport from the trans-Golgi
Tania A Wong, Gregory D Fairn, Pak P Poon, et al.
The Journal of Biological Chemistry
|
December 25, 2025
Sphingosine-1-phosphate receptor 2 inhibition ameliorates familial exudative vitreoretinopathy models
Hirad A Feridooni, Rachel Fody, Mahtab Tavasoli, et al.
Pediatric Blood & Cancer
|
April 3, 2016
Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia
Marissa A LeBlanc, Amanda Bettle, Jason N Berman, et al.
Molecular Genetics and Metabolism Reports
|
November 30, 2016
Mitochondrial damage and cholesterol storage in human hepatocellular carcinoma cells with silencing of <i>UBIAD1</i> gene expression
Carlos R Morales, Lubov S Grigoryeva, Xuefang Pan, et al.
American Journal of Ophthalmology Case Reports
|
April 17, 2024
Multimodal imaging of white preretinal lesions in atypical familial exudative vitreoretinopathy: Case report and literature review
Liam D Redden, Douglas S M Iaboni, Sarah van der Ende, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
December 5, 2025
Polymyalgia rheumatica patients presenting with atypical clinical features still exhibit characteristic <sup>18</sup>F-FDG PET/CT findings
Emily Martin, Christopher R McMaster, Aurora Mt Poon, et al.
Nucleic Acids Research
|
June 16, 2018
Optimized knock-in of point mutations in zebrafish using CRISPR/Cas9
Sergey V Prykhozhij, Charlotte Fuller, Shelby L Steele, et al.
The Journal of Biological Chemistry
|
November 27, 2025
Neurodevelopmental disease-causing variants in choline kinase CHKA gene couple phosphatidylcholine synthesis to oxidative stress damage and disease etiology
Mahtab Tavasoli, Mariam Alkandari, Gabriel Dorighello, et al.
Orphanet Journal of Rare Diseases
|
June 19, 2012
A generalizable pre-clinical research approach for orphan disease therapy
Chandree L Beaulieu, Mark E Samuels, Sean Ekins, et al.
Page
of 8