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Chromosomes, Human, Pair 8

Known as: 8 chromosome, Chromosome 8 
The designation for each member of the eighth largest human autosomal chromosome pair. Chromosome 8 spans about 145 million base pairs and represents… Expand
National Institutes of Health

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Highly Cited
2006
Highly Cited
2006
The spatial organization of DNA in the cell nucleus is an emerging key contributor to genomic function. We developed 4C… Expand
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Highly Cited
2006
Highly Cited
2006
Defensins are endogenous antimicrobial peptides that protect the intestinal mucosa against bacterial invasion. It has been… Expand
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Highly Cited
1998
Highly Cited
1998
Epileptic disorders affect about 20-40 million people worldwide, and 40% of these are idiopathic generalized epilepsies (IGEs… Expand
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Highly Cited
1998
Highly Cited
1998
Schizophrenia is a common disorder characterized by psychotic symptoms; diagnostic criteria have been established. Family, twin… Expand
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Highly Cited
1996
Highly Cited
1996
The recurrent translocation t(8;16)(p11 ;p13) is a cytogenetic hallmark for the M4/M5 subtype of acute myeloid leukaemia. Here we… Expand
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Highly Cited
1994
Highly Cited
1994
Pfeiffer syndrome (PS) is one of the classic autosomal dominant craniosynostosis syndromes with craniofacial anomalies and… Expand
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Highly Cited
1993
Highly Cited
1993
The t(8;21) translocation is one of the most frequent chromosome abnormalities in acute myeloid leukemia. It has been shown that… Expand
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Highly Cited
1992
Highly Cited
1992
We have developed a restriction map of the chromosome 21 breakpoint region involved in t(8;21)(q22;q22.3) acute myelogenous… Expand
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Highly Cited
1992
Highly Cited
1992
A third member of the metallothionein (MT) gene family, designated MT-III, was cloned by virtue of its homology to a human… Expand
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Highly Cited
1982
Highly Cited
1982
Human sequences related to the transforming gene (v-myc) of avian myelocytomatosis virus (MC29) are represented by at least one… Expand
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