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14q32.33

A chromosome band present on 14q
National Institutes of Health

Related topics

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9 relations
BAG5 wt AlleleCEP170B wt AlleleChromosomesHSP90AA1 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Somatic copy number alterations predict response to platinum therapy in epithelial ovarian cancer.
Highly Cited
2014
Highly Cited
2014
Novel somatic and germline mutations in intracranial germ cell tumours
Intracranial germ cell tumours (IGCTs) are a group of rare heterogeneous brain tumours that are clinically and histologically… 
Highly Cited
2009
Highly Cited
2009
Biallelic inactivation of TRAF3 in a subset of B-cell lymphomas with interstitial del(14)(q24.1q32.33)
Biallelic inactivation of TRAF3 in a subset of B-cell lymphomas with interstitial del(14)(q24.1q32.33) 
2009
2009
Imatinib mesylate causes growth plate closure in vivo
K. Vandyke, A.L. Dewar, S. Fitter, D. Menicanin, L.B. To, T.P. Hughes and A.C.W. Zannettino 
Highly Cited
2007
Highly Cited
2007
Comparative genomic hybridization array analysis and real time PCR reveals genomic alterations in squamous cell carcinomas of the lung.
Review
2007
Review
2007
Genomics and premalignant breast lesions: clues to the development and progression of lobular breast cancer
Advances in genomic technology have improved our understanding of the genetic events that parallel breast cancer development… 
Highly Cited
2006
Highly Cited
2006
Identification of DNA copy-number aberrations by array-comparative genomic hybridization in patients with schizophrenia.
Highly Cited
2005
Highly Cited
2005
Array comparative genomic hybridization analysis of uterine leiomyosarcoma.
Highly Cited
1997
Highly Cited
1997
The Ig heavy chain gene is frequently involved in chromosomal translocations in multiple myeloma and plasma cell leukemia as detected by in situ hybridization.
Chromosome rearrangement of 14q32.33 has recurrently occurred with variable partner sites, including 11q13.3, 8q24.1, 18q21.3… 
Highly Cited
1992
Highly Cited
1992
Frequent loss of heterozygosity on chromosome 18 in ovarian adenocarcinoma which does not always include the DCC locus.
Inactivation of the DCC gene on chromosome 18 owing to loss of heterozygosity is a common finding in colorectal cancer. Because… 
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