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NDRG1 wt Allele

Known as: TDD5, PROXY1, HMSNL 
Human NDRG1 wild-type allele is located in the vicinity of 8q24.3 and is approximately 60 kb in length. This allele, which encodes protein NDRG1, is… Expand
National Institutes of Health

Papers overview

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Highly Cited
2006
Highly Cited
2006
Cap43 has been identified as a nickel- and calcium-induced gene, and is also known as N-myc downstream-regulated gene 1 (NDRG1… Expand
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Highly Cited
2003
Highly Cited
2003
Drg-1 was previously identified (N. van Belzen et al., Lab. Investig., 77: 85-92, 1997) as a gene that was up-regulated by the… Expand
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Highly Cited
2000
Highly Cited
2000
Hereditary motor and sensory neuropathies, to which Charcot-Marie-Tooth (CMT) disease belongs, are a common cause of disability… Expand
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Highly Cited
2000
Highly Cited
2000
Carcinogenic nickel compounds alter the program of gene expression in normal cells and induce a pattern of gene expression… Expand
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Highly Cited
1999
Highly Cited
1999
To identify genes regulated by N-myc, subtraction of whole embryo cDNA was carried out between wild type and N-myc-deficient… Expand
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Highly Cited
1998
Highly Cited
1998
Through a differential screening technique, we have identified a cDNA clone with differential expression in normal versus tumor… Expand
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Highly Cited
1998
Highly Cited
1998
Nodal-related 1 (ndr1) and nodal-related 2 (ndr2) genes in zebrafish encode members of the nodal subgroup of the transforming… Expand
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Highly Cited
1998
Highly Cited
1998
To better understand the molecular mechanism(s) involved in the essentiality, toxicity, and/or carcinogenicity of nickel… Expand
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Highly Cited
1998
Highly Cited
1998
A previously unrecognized neuropathy was identified in Bulgarian gypsies, and was designated hereditary motor and sensory… Expand
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Highly Cited
1996
Highly Cited
1996
BACKGROUND & AIMS Cadherins and their associated molecules, such as alpha-catenin, have been shown recently to play a pivotal… Expand