NEIL HANCHARD to Mice
This is a "connection" page, showing publications NEIL HANCHARD has written about Mice.
Connection Strength
0.075
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"Iron"ing out hemophagocytosis through PIEZO1. Cell. 2021 02 18; 184(4):856-858.
Score: 0.044
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COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay. Am J Hum Genet. 2021 09 02; 108(9):1710-1724.
Score: 0.011
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Mutations in the KIF21B kinesin gene cause neurodevelopmental disorders through imbalanced canonical motor activity. Nat Commun. 2020 05 15; 11(1):2441.
Score: 0.011
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Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans. Am J Hum Genet. 2016 Oct 06; 99(4):886-893.
Score: 0.008