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CCND1 wt Allele

Known as: PRAD1, Cyclin D1 wt Allele, U21B31 
Human CCND1 wild-type allele is located within 11q13 and is approximately 13 kb in length. This allele, which encodes G1/S-specific cyclin-D1 protein… Expand
National Institutes of Health

Papers overview

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2008
2008
Haemophilia A is the most common inherited X-linked recessive bleeding disorder. The aim was to investigate the usefulness of two… Expand
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Review
2002
Review
2002
  • Yasuo Imanishi
  • Journal of Bone and Mineral Metabolism
  • 2002
  • Corpus ID: 30175381
the PTH gene’s 5 flanking region from PTH coding exons, and the DNA recombined with chromosome 11q13 [2] (Fig. 1). A candidate… Expand
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Review
1996
Review
1996
Abstract The role of the PRAD1 gene in human tumorigenesis was demonstrated by its initial cloning from the breakpoint region on… Expand
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Review
1993
Review
1993
The D-type cyclins are among the candidate 'G1 cyclins' in higher eukaryotes that may regulate G1-S-phase progression. The human… Expand
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1993
1993
PRAD1 (cyclin D1) is a recently identified member of the family of cyclin genes, believed to play roles in regulating transitions… Expand
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1993
1993
Originally identified as a 'mitotic cyclin', cyclin A exhibits properties of growth factor sensitivity, susceptibility to viral… Expand
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1992
1992
Cyclins regulate cell cycle progression by complexing with and activating cdc2 or related kinases. PRAD1/cyclin D1 is a recently… Expand
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Highly Cited
1991
Highly Cited
1991
Rearrangement of the BCL1 (B-cell lymphoma 1) region on chromosome 11q13 appears to be highly characteristic of centrocytic… Expand
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Highly Cited
1991
Highly Cited
1991
We report the detailed molecular characterization of a human parathyroid adenoma with a clonal parathyroid hormone gene… Expand
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Review
1991
Review
1991
WE have previously identified a candidate oncogene (PRAD1 or D11S287E) on chromosome Ilql3 which is clonally rearranged with the… Expand
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