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Peroxisome Biogenesis Disorder, Complementation Group G

Known as: CGG 
National Institutes of Health

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Peroxisomal Disorders

Papers overview

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Highly Cited
2007
Highly Cited
2007
Cancer‐germline gene expression in pediatric solid tumors using quantitative real‐time PCR
Cancer‐germline genes (CGGs) code for immunogenic antigens that are present on various human tumors but not on normal tissues… 
Highly Cited
1999
Highly Cited
1999
Expansion and Deletion of Triplet Repeat Sequences inEscherichia coli Occur on the Leading Strand of DNA Replication*
Expansions and deletions of triplet repeat sequences that cause human hereditary neurological diseases were previously suggested… 
Highly Cited
1998
Highly Cited
1998
Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.
In at least 98% of fragile X syndrome cases, the disease results from expansion of the CGG repeat in the 5' end of FMR1. The use… 
Highly Cited
1997
Highly Cited
1997
An efficient and economic site-specific deuteration strategy for NMR studies of homologous oligonucleotide repeat sequences.
We describe herein the use of a 2H-labeling strategy to achieve specific assignments of considerably overlapped cross peaks in… 
Highly Cited
1996
Highly Cited
1996
FMR1 in global populations.
Fragile X syndrome, a frequent form of inherited mental retardation, results from the unstable expansion of a cryptic CGG repeat… 
Highly Cited
1996
Highly Cited
1996
Fragile X founder chromosomes in Italy: a few initial events and possible explanation for their heterogeneity.
A total of 137 fragile X and 235 control chromosomes from various regions of Italy were haplotyped by analyzing two neighbouring… 
Highly Cited
1994
Highly Cited
1994
Emotional and neurocognitive deficits in fragile X.
We have studied the neurocognitive deficit in premutation and full mutation women as compared to control women and to explore the… 
Highly Cited
1994
Highly Cited
1994
Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes.
The mutation observed in the fragile X syndrome, an X-linked inherited disorder causing mental retardation, is almost exclusively… 
Highly Cited
1993
Highly Cited
1993
A study of the physical, behavioral, and medical phenotype, including anthropometric measures, of females with fragile X syndrome.
The physical features of fragile X, including a long face, prominent ears, and hyperextensible joints, are present in affected… 
Highly Cited
1993
Highly Cited
1993
Mental Status and Fragile X Expression in Relation to FMR-1 Gene Mutation
The fragile X mental retardation syndrome is caused by unstable expansion of a CGG repeat in the FMR-1 gene. Clinical expression… 
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