MARY DICKINSON to Mice, Knockout
This is a "connection" page, showing publications MARY DICKINSON has written about Mice, Knockout.
Connection Strength
0.750
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Impact of essential genes on the success of genome editing experiments generating 3313 new genetically engineered mouse lines. Sci Rep. 2024 09 30; 14(1):22626.
Score: 0.127
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Comparative analysis of single-stranded DNA donors to generate conditional null mouse alleles. BMC Biol. 2018 Jun 21; 16(1):69.
Score: 0.082
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High-throughput discovery of novel developmental phenotypes. Nature. 2016 09 22; 537(7621):508-514.
Score: 0.072
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Ocular Phenotyping of Knockout Mice Identifies Genes Associated With Late Adult Retinal Phenotypes. Invest Ophthalmol Vis Sci. 2025 06 02; 66(6):64.
Score: 0.033
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Systematic ocular phenotyping of 8,707 knockout mouse lines identifies genes associated with abnormal corneal phenotypes. BMC Genomics. 2025 Jan 20; 26(1):48.
Score: 0.032
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Alzheimer's disease risk gene CD2AP is a dose-sensitive determinant of synaptic structure and plasticity. Hum Mol Genet. 2024 10 07; 33(20):1815-1832.
Score: 0.032
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Genome-wide screening reveals the genetic basis of mammalian embryonic eye development. BMC Biol. 2023 02 03; 21(1):22.
Score: 0.028
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Three-dimensional microCT imaging of mouse heart development from early post-implantation to late fetal stages. Mamm Genome. 2023 06; 34(2):156-165.
Score: 0.028
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Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genes. Sci Rep. 2022 12 01; 12(1):20791.
Score: 0.028
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Mendelian gene identification through mouse embryo viability screening. Genome Med. 2022 10 13; 14(1):119.
Score: 0.028
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Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen. Pain. 2022 06 01; 163(6):1139-1157.
Score: 0.026
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A resource of targeted mutant mouse lines for 5,061 genes. Nat Genet. 2021 04; 53(4):416-419.
Score: 0.025
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A global Slc7a7 knockout mouse model demonstrates characteristic phenotypes of human lysinuric protein intolerance. Hum Mol Genet. 2020 08 03; 29(13):2171-2184.
Score: 0.024
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Human and mouse essentiality screens as a resource for disease gene discovery. Nat Commun. 2020 01 31; 11(1):655.
Score: 0.023
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Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes. Am J Hum Genet. 2019 03 07; 104(3):422-438.
Score: 0.021
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The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia. Hum Mol Genet. 2018 06 15; 27(12):2064-2075.
Score: 0.020
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A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction. Nat Commun. 2017 10 12; 8(1):886.
Score: 0.020
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Loss of Apela Peptide in Mice Causes Low Penetrance Embryonic Lethality and Defects in Early Mesodermal Derivatives. Cell Rep. 2017 Aug 29; 20(9):2116-2130.
Score: 0.019
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Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium. Nat Genet. 2017 Aug; 49(8):1231-1238.
Score: 0.019
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Yap and Taz play a crucial role in neural crest-derived craniofacial development. Development. 2016 Feb 01; 143(3):504-15.
Score: 0.017
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Cardiovascular Patterning as Determined by Hemodynamic Forces and Blood Vessel Genetics. PLoS One. 2015; 10(9):e0137175.
Score: 0.017
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Macrophages engulf endothelial cell membrane particles preceding pupillary membrane capillary regression. Dev Biol. 2015 Jul 01; 403(1):30-42.
Score: 0.016
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Transcription factor FoxO1 is essential for enamel biomineralization. PLoS One. 2012; 7(1):e30357.
Score: 0.013