Analysis of EIF4G1 in ethnic Chinese

EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?

(2012) Suzanne Lesage et al.   NEUROBIOLOGY OF AGING

Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson’s disease

(2012) Eva C. Schulte et al.   NEUROGENETICS

Study of the genetic variability in a Parkinson's Disease gene: EIF4G1

(2012) Arianna Tucci et al.   NEUROSCIENCE LETTERS

A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease

(2011) Alexander Zimprich et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease

(2011) Marie-Christine Chartier-Harlin et al.   AMERICAN JOURNAL OF HUMAN GENETICS

VPS35 Mutations in Parkinson Disease

(2011) Carles Vilariño-Güell et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Regulation of Translation Initiation in Eukaryotes: Mechanisms and Biological Targets

(2009) Nahum Sonenberg et al.   CELL

Essential role for eIF4GI overexpression in the pathogenesis of inflammatory breast cancer

(2009) Deborah Silvera et al.   NATURE CELL BIOLOGY

P2.206 EIF4G1 mutations in familial parkinsonism

(2009) M.-C. Chartier-Harlin et al.   PARKINSONISM & RELATED DISORDERS

Genome-wide Linkage Analysis of a Parkinsonian-Pyramidal Syndrome Pedigree by 500 K SNP Arrays

(2008) Seyedmehdi Shojaee et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Characterization of PLA2G6 as a locus for dystonia-parkinsonism

(2008) Coro Paisan-Ruiz et al.   ANNALS OF NEUROLOGY

eIF4GI links nutrient sensing by mTOR to cell proliferation and inhibition of autophagy

(2008) Francisco Ramírez-Valle et al.   JOURNAL OF CELL BIOLOGY