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Correction to Supporting Information for Woerman et al., Familial Parkinson's point mutation abolishes multiple system atrophy prion replication. [PDF]
Proc Natl Acad Sci U S Aeuropepmc +1 more source
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Pathological role of a point mutation (T315I) in BCR‐ABL1 protein—A computational insight
Journal of Cellular Biochemistry, 2018V. Rajendran +2 more
semanticscholar +1 more source
Inverse PCR for Point Mutation Introduction.
Methods in molecular biology, 2017Diogo Silva +3 more
semanticscholar +1 more source
Impact of point mutation P29S in RAC1 on tumorigenesis
Tumor Biology, 2016V. Rajendran +2 more
semanticscholar +1 more source
The Y-chromosome point mutation rate in humans
Nature Genetics, 2015A. Helgason +8 more
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Generalized lymphoproliferative disease in mice, caused by a point mutation in the fas ligand
Cell, 1994Tomohiro Takahashi +6 more
semanticscholar +1 more source
Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A.
Science, 1993H. Brunner +4 more
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Repeat-Induced Point Mutation: A Fungal-Specific, Endogenous Mutagenesis Process
, 2015James K. Hane +4 more
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A quantum dot-based microRNA nanosensor for point mutation assays.
Chemical Communications, 2014Ya-ping Zeng +5 more
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