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Chromosomes, Human, Pair 17

Known as: Chromosome 17 
The designation for each member of the seventeenth largest human autosomal chromosome pair. Chromosome 17 spans more than 81 million base pairs and… Expand
National Institutes of Health

Papers overview

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Highly Cited
2007
Highly Cited
2007
We performed a genome-wide association scan to search for sequence variants conferring risk of prostate cancer using 1,501… Expand
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Highly Cited
2006
Highly Cited
2006
Frontotemporal dementia (FTD) is the second most common cause of dementia in people under the age of 65 years. A large proportion… Expand
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Review
2000
Review
2000
Tau proteins belong to the family of microtubule-associated proteins. They are mainly expressed in neurons where they play an… Expand
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Highly Cited
1998
Highly Cited
1998
Frontotemporal dementia with parkinsonism, chromosome 17 type (FTDP‐17), a recently defined disease entity, is clinically… Expand
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Review
1997
Review
1997
We held an international consensus conference on frontotemporal dementia, behavioral disturbances, and parkinsonism linked to… Expand
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Highly Cited
1996
Highly Cited
1996
Breast carcinoma is the most common malignancy among women in developed countries. Because family history remains the strongest… Expand
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Highly Cited
1995
Highly Cited
1995
Mutations in the human SRY–related gene, SOX9, located on chromosome 17, have recently been associated with the sex reversal and… Expand
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Highly Cited
1995
Highly Cited
1995
The Drosophila sine oculis homeobox-containing gene is known to play an essential role in controlling the initial events of… Expand
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Highly Cited
1991
Highly Cited
1991
BACKGROUND AND METHODS Patients with acute promyelocytic leukemia have a characteristic (15;17) translocation, with a breakpoint… Expand
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Highly Cited
1987
Highly Cited
1987
The clonal composition of human colorectal tumors was studied by means of restriction fragment length polymorphisms (RFLPs… Expand
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