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17q21
A chromosome band present on 17q
National Institutes of Health
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Related topics
Related topics
16 relations
17q
ACACA wt Allele
BECN1 wt Allele
BRCA1 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2006
Highly Cited
2006
A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD.
J. van der Zee
,
R. Rademakers
,
+14 authors
B. Dermaut
Brain : a journal of neurology
2006
Corpus ID: 27430852
Among patients with frontotemporal lobar degeneration (FTLD), the respective frequencies of dominant 17q21-linked tau-negative…
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Review
2006
Review
2006
Progranulin mutations in ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.
M. Cruts
,
S. Kumar-Singh
,
C. van Broeckhoven
Current Alzheimer Research
2006
Corpus ID: 10586291
Two genetically distinct types of frontotemporal dementia (FTD) are linked to chromosome 17q21. FTD with parkinsonism (FTDP-17…
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Highly Cited
2002
Highly Cited
2002
Absence of HER2/neu gene expression in osteosarcoma and skeletal Ewing's sarcoma.
Dafydd G. Thomas
,
T. Giordano
,
Donita L Sanders
,
J. S. Biermann
,
L. Baker
,
O. Surgery
Clinical Cancer Research
2002
Corpus ID: 7323021
PURPOSE Osteosarcoma (OS) and skeletal Ewing's sarcoma (EWS), the most common pediatric primary bone tumors, are aggressive…
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Highly Cited
1999
Highly Cited
1999
Allelic imbalance in the clonal evolution of prostate carcinoma
Liang Cheng
,
D. Bostwick
,
+4 authors
Z. Zhuang
Cancer
1999
Corpus ID: 2280544
To understand better the genetic basis of the clonal evolution of prostate carcinoma, the authors analyzed the pattern of allelic…
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Highly Cited
1997
Highly Cited
1997
Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21–22
M. Baker
,
J. Kwok
,
+17 authors
M. Hutton
Annals of Neurology
1997
Corpus ID: 25736097
An Australian family with autosomal dominant presenile nonspecific dementia was recently described. The disease results in…
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Highly Cited
1995
Highly Cited
1995
Suppression of malignant phenotype in a human prostate cancer cell line by fragments of normal chromosomal region 17q.
Yoshinori S. Murakami
,
A. Brothman
,
R. Leach
,
Raymond White
Cancer Research
1995
Corpus ID: 8132096
Recent evidence obtained by in situ hybridization indicates that chromosomal region 17q is often lost in prostate tumors. To…
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Highly Cited
1994
Highly Cited
1994
Genetic studies of 457 breast cancers. Clinicopathologic parameters compared with genetic alterations
Y. Harada
,
T. Katagiri
,
+5 authors
F. Kasumi
Cancer
1994
Corpus ID: 7797346
Background. Human breast cancers frequently show loss of heterozygosity (LOH) and/or amplification at specific chromosomal…
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Highly Cited
1993
Highly Cited
1993
Cytogenetic studies of epithelial ovarian carcinoma.
Robert B. Jenkins
,
D. Bartelt
,
+5 authors
Lynn C. Hartmann
Cancer Genetics and Cytogenetics
1993
Corpus ID: 43627426
Highly Cited
1993
Highly Cited
1993
THRA1 and D17S183 flank an interval of < 4 cM for the breast-ovarian cancer gene (BRCA1) on chromosome 17q21.
A. Bowcock
,
L. Anderson
,
+6 authors
Mary Claire King
American Journal of Human Genetics
1993
Corpus ID: 20351204
In order to pinpoint the locale of the gene for early-onset familial breast and ovarian cancer (BRCA1), polymorphisms were…
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Highly Cited
1987
Highly Cited
1987
Localization of the gene for the erythroid anion exchange protein, band 3 (EMPB3), to human chromosome 17.
L. Showe
,
M. Ballantine
,
K. Huebner
Genomics
1987
Corpus ID: 10329903
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