IDH1 wt Allele

Known as: IDH, Isocitrate Dehydrogenase 1 (NADP+), Soluble wt Allele, IDP 
The IDH1 wt Allele is located in the vicinity of 2q33.3 and is approximately 19 kb in length. This allele, which encodes isocitrate dehydrogenase… (More)
National Institutes of Health

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Topic mentions per year

1969-2018
02040608019692018

Papers overview

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Highly Cited
2014
Highly Cited
2014
Calreticulin (CALR) mutations were recently described in JAK2 and MPL unmutated primary myelofibrosis (PMF) and essential… (More)
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Highly Cited
2014
Highly Cited
2014
PURPOSE Patients with 1p/19q codeleted anaplastic oligodendroglial tumors who participated in RTOG (Radiation Therapy Oncology… (More)
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Highly Cited
2012
Highly Cited
2012
Recurrent mutations in isocitrate dehydrogenase 1 (IDH1) and IDH2 have been identified in gliomas, acute myeloid leukaemias (AML… (More)
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Highly Cited
2011
Highly Cited
2011
Somatic mutations in isocitrate dehydrogenase 1 (IDH1) and IDH2 occur in gliomas and acute myeloid leukaemia (AML). Since… (More)
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Highly Cited
2010
Highly Cited
2010
OBJECTIVES Recent studies have shown that IDH1 and IDH2 mutations occur frequently in gliomas, including low-grade gliomas… (More)
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Highly Cited
2010
Highly Cited
2010
In a multi-institutional collaborative project, 1473 patients with myeloproliferative neoplasms (MPN) were screened for… (More)
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Highly Cited
2010
Highly Cited
2010
The phenotypic heterogeneity of low-grade gliomas (LGGs) is still inconsistently explained by known molecular abnormalities in… (More)
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Highly Cited
2009
Highly Cited
2009
The Author and a Colleague Reply: De Carli et al. report the IDH mutation status of pediatric gliomas. In fact, some of the… (More)
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Highly Cited
2003
Highly Cited
2003
Phagocytosis of complement-opsonized targets is a primary function of neutrophils at sites of inflammation, and the clearance of… (More)
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Highly Cited
1999
Highly Cited
1999
Human PICD was identified by homology probing the data base of expressed sequence tags with the protein sequence of Saccharomyces… (More)
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