Genotype & phenotype in Lowe Syndrome: specific OCRL1 patient mutations differentially impact cellular phenotypes is a research paper published in Human Molecular Genetics (2021). On theSindex it has a DataRank of 0. It has been cited 18 times.
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National Institutes of Health
Grant: 1R01DK109398-01
National Institutes of Health
Grant: R01GM123055
Clinical Translational Science Institute
Grant: 106564/8000063783
National Science Foundation
Grant: DMS1614777
National Science Foundation
Grant: CMMI1825941
National Science Foundation
Grant: MCB1925643
National Science Foundation
Grant: DBI2003635
NIDDK NIH HHS
Grant: R01 DK109398
National Science Foundation
Grant: 1825941
Nanomanufacturing of Protein Macromolecular Frameworks Through an Integrated Bioengineering and Computational Approach
National Science Foundation
Grant: 1925643
Collaborative Research: RoL: Revealing a new mechanism of action for eukaryotic transcriptional activation domains
National Institutes of Health
Grant: 5R01GM123055-02
Structural Modeling of Multifarious Protein Complexes
National Science Foundation
Grant: 2003635
IIBR Informatics: Development of Multimodal approaches for protein function prediction
National Institutes of Health
Grant: 5R01DK109398-03
Lowe Syndrome: Therapeutic Strategy by Drug Repositioning
Lowe Syndrome Association
FWCI
1.39
Citation Percentile
0.8%
Citation Trend
Fields of Study
MeSH Terms
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Sustainable Development Goals