Associated Papers
Tightly-orchestrated rearrangements govern catalytic center assembly of the ribosome.
Zhou Y et al.
Nature Communications, 2019
Nmd3 is a structural mimic of eIF5A, and activates the cpGTPase Lsg1 during 60S ribosome biogenesis.
Malyutin AG et al.
The Embo Journal, 2017
A Novel Mutation in RPL10 (Ribosomal Protein L10) Causes X-Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo-Epiphyseal Dysplasia.
Zanni G et al.
Human Mutation, 2015
RPL10 mutation segregating in a family with X-linked syndromic Intellectual Disability.
Thevenon J et al.
American Journal of Medical Genetics. Part A, 2015
Monosome formation during translation initiation requires the serine/arginine-rich protein Npl3.
Baierlein C et al.
Molecular and Cellular Biology, 2013
Integrity of the P-site is probed during maturation of the 60S ribosomal subunit.
Bussiere C et al.
The Journal of Cell Biology, 2012
Mapping the functional domains of yeast NMD3, the nuclear export adapter for the 60 S ribosomal subunit.
Hedges J et al.
The Journal of Biological Chemistry, 2006
Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism.
Klauck SM et al.
Molecular Psychiatry, 2006
Release of the export adapter, Nmd3p, from the 60S ribosomal subunit requires Rpl10p and the cytoplasmic GTPase Lsg1p.
Hedges J et al.
The Embo Journal, 2005
GRC5 and NMD3 function in translational control of gene expression and interact genetically.
Karl T et al.
Current Genetics, 1999
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