Chromosomes, Human, Pair 14

Known as: 14 chromosome, Chromosome 14 
The designation for each member of the fourteenth largest human autosomal chromosome pair. Chromosome 14 spans about 105 million base pairs and… (More)
National Institutes of Health

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Highly Cited
2011
Highly Cited
2011
MOTIVATION Next-generation sequencing technologies generate very large numbers of short reads. Even with very deep genome… (More)
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Highly Cited
2008
Highly Cited
2008
Human chromosome 14q32.2 carries a cluster of imprinted genes including paternally expressed genes (PEGs) such as DLK1 and RTL1… (More)
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Highly Cited
2002
Highly Cited
2002
Preadipocyte factor 1 (Pref-1/Dlk1) inhibits in vitro adipocyte differentiation and has been recently reported to be a paternally… (More)
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Highly Cited
2001
Highly Cited
2001
At least two distinct recurrent chromosomal translocations have been implicated in the pathogenesis of MALT lymphoma. The first… (More)
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Highly Cited
2001
Highly Cited
2001
FISH identified a cryptic t(5;14)(q35;q32) in T acute lymphoblastic leukemia (ALL), whereas it was not observed in B ALL samples… (More)
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Highly Cited
2000
Highly Cited
2000
The evolution of genomic imprinting in mammals occurred more than 100 million years ago, and resulted in the formation of genes… (More)
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Highly Cited
1999
Highly Cited
1999
Missense mutations in the human presenilin-1 (PS1) gene, which is found on chromosome 14, cause early-onset familial Alzheimer’s… (More)
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Review
1999
Review
1999
The major constituent of senile plaques in Alzheimer's disease is a 42-aa peptide, referred to as beta-amyloid (Abeta). Abeta is… (More)
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Highly Cited
1997
Highly Cited
1997
A novel member of the tumor necrosis factor (TNF) cytokine family, designated TRANCE, was cloned during a search for apoptosis… (More)
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Highly Cited
1985
Highly Cited
1985
Specific chromosomal translocations found in distinct neoplasms suggest that genes that flank such breakpoints play a critical… (More)
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