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17p13

A chromosome band present on 17p
National Institutes of Health

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11 relations
ARRB2 wt AlleleCD68 wt AlleleCTDNEP1 wt AlleleCXCL16 wt Allele

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del(17p13)

Papers overview

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2010
2010
Expression and prognostic relevance of MAGE-C1/CT7 and MAGE-C2/CT10 in osteolytic lesions of patients with multiple myeloma.
2008
2008
Loss of Heterozygosity of 17p13, With Possible Involvement of ACADVL and ALOX15B, in the Pathogenesis of Adrenocortical Tumors
Objective:To determine the minimal common region of loss on 17p13 in a cohort of adrenocortical carcinomas (ACCs) (defined by a… 
2004
2004
Cytogenetics and fluorescence in situ hybridization studies of diffuse large B-cell lymphoma in children and young adults.
2004
2004
New chromosomal syndrome: Miller-Dieker syndrome and monosomy 17p13
SummaryThe Miller-Dieker Syndrome (MDS) consists of lissencephaly, characteristic facies, pre- and postnatal growth retardation… 
2002
2002
P53 autoantibodies in sera from Danish ovarian cancer patients and their correlation with clinical data and prognosis
The p53 gene, a tumour suppressor gene located on the short arm of chromosome 17 (17pl3), is frequently mutated in various human… 
Highly Cited
2001
Highly Cited
2001
Frequent inactivation of the TP53 gene in esophageal squamous cell carcinoma from a high-risk population in China.
Esophageal squamous cell carcinoma (ESCC) is one of the most common fatal cancers worldwide, and north central China has some of… 
2000
2000
Can molecular assessment improve classification of head and neck premalignancy?
The carcinogenic process is multistep and requires the accumulation of multiple genetic alterations in epithelial cells in the… 
Highly Cited
1995
Highly Cited
1995
p53 mutations and prognosis in bladder tumors.
1992
1992
Loss of heterozygosity on chromosome 17p13 in breast carcinomas identifies tumors with high proliferation index.
The capacity of breast tumor cells to proliferate is considered a potential prognostic factor together with other histopathologic… 
Highly Cited
1992
Highly Cited
1992
Chromosome alterations in human small cell lung cancer: frequent involvement of 5q.
Deletions of the 3p chromosome region and molecular alterations of the tumor suppressor genes RB1 and TP53, located, respectively… 
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