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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

Related topics

Related topics

33 relations
17qAleukemic Chronic Lymphocytic LeukemiaCarney ComplexChromatin
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Narrower (5)

Chromosome 17 trisomyChromosome 17, deletion 17q23 q24Chromosome 17, trisomy 17pChromosome 17q21.31 Deletion Syndrome
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Broader (1)

Chromosomes, Human, 16-18

Papers overview

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Highly Cited
2007
Highly Cited
2007
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes
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
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
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 protein isoforms, phosphorylation and role in neurodegenerative disorders
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
Tau is a candidate gene for chromosome 17 frontotemporal dementia
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
Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference
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
The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds
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
The Sry-related gene Sox9 is expressed during chondrogenesis in mouse embryos
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
Six3, a murine homologue of the sine oculis gene, demarcates the most anterior border of the developing neural plate and is expressed during eye development.
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
Differentiation therapy of acute promyelocytic leukemia with tretinoin (all-trans-retinoic acid).
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
Clonal analysis of human colorectal tumors.
The clonal composition of human colorectal tumors was studied by means of restriction fragment length polymorphisms (RFLPs… Expand
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