about
Identification of functional domains in the RAD51L2 (RAD51C) protein and its requirement for gene conversionImpaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficitsGeneration of mice with a conditional Foxp2 null alleleHumanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performanceAn aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learningFoxp1/2/4 regulate endochondral ossification as a suppresser complexThe FOXP1, FOXP2 and FOXP4 transcription factors are required for islet alpha cell proliferation and function in mice.What can mice tell us about Foxp2 function?Role of mammalian RAD51L2 (RAD51C) in recombination and genetic stability.Foxp transcription factors suppress a non-pulmonary gene expression program to permit proper lung development
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P50
description
hulumtuese
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researcher
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wetenschapper
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հետազոտող
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name
Catherine A French
@nl
Catherine A French
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Catherine A. French
@en
Catherine A. French
@es
Catherine French
@fr
type
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Catherine A French
@nl
Catherine A French
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Catherine A. French
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Catherine A. French
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Catherine French
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prefLabel
Catherine A French
@nl
Catherine A French
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Catherine A. French
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Catherine A. French
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Catherine French
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