Biblioteca Digital

8 resultados para mutation inhibition

em School of Medicine, Washington University, United States

A knock-in mouse model for the R120G mutation of alphaBcrystallin recapitulates human hereditary myopathy and cataracts

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A mutation in a functional Sp1 binding site of the telomerase RNA gene (hTERC) promoter in a patient with Paroxysmal Nocturnal Haemoglobinuria

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Active inhibition of plasma cell development in resting B cells by microphthalmia-associated transcription factor

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Acute gamma-secretase inhibition of nonhuman primate CNS shifts amyloid precursor protein (APP) metabolism from amyloid-beta production to alternative APP fragments without amyloid-beta rebound

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Pigment pattern in jaguar/obelix zebrafish is caused by a Kir7.1 mutation: Implications for the regulation of melanosome movement

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The mode of retinal presynaptic inhibition switches with light intensity

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αA-crystallin R49Cneo mutation influences the architecture of lens fiber cell membranes and causes posterior and nuclear cataracts in mice

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Mutation of sec63 in zebrafish causes defects in myelinated axons and liver pathology

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