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t(1;13)
A cytogenetic abnormality that involves a translocation between chromosomes 1 and 13.
National Institutes of Health
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Related topics
Related topics
2 relations
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 13
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2016
Review
2016
Future directions in risk stratification and therapy for advanced pediatric genitourinary rhabdomyosarcoma.
M. Harel
,
F. Ferrer
,
L. Shapiro
,
J. Makari
Urologic oncology
2016
Corpus ID: 33126707
Highly Cited
2006
Highly Cited
2006
Identification of a PAX-FKHR gene expression signature that defines molecular classes and determines the prognosis of alveolar rhabdomyosarcomas.
E. Davicioni
,
F. Finckenstein
,
V. Shahbazian
,
J. Buckley
,
T. Triche
,
M. Anderson
Cancer Research
2006
Corpus ID: 14616183
Alveolar rhabdomyosarcomas (ARMS) are aggressive soft-tissue sarcomas affecting children and young adults. Most ARMS tumors…
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Highly Cited
2004
Highly Cited
2004
Distinct patterns of genetic alterations in adenocarcinoma and squamous cell carcinoma of the lung.
S. Sy
,
N. Wong
,
+6 authors
A. Yim
European Journal of Cancer
2004
Corpus ID: 10080199
Review
2001
Review
2001
Gene fusions involving PAX and FOX family members in alveolar rhabdomyosarcoma
F. Barr
Oncogene
2001
Corpus ID: 9593620
The chromosomal translocations t(2;13)(q35;q14) and t(1;13)(p36;q14) are characteristic of alveolar rhabdomyosarcoma, a pediatric…
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2000
2000
Structural analysis of PAX7 rearrangements in alveolar rhabdomyosarcoma.
J. Fitzgerald
,
A. Scherr
,
F. Barr
Cancer Genetics and Cytogenetics
2000
Corpus ID: 41802580
Highly Cited
1999
Highly Cited
1999
PAX3 and PAX7 exhibit conserved cis-acting transcription repression domains and utilize a common gain of function mechanism in alveolar rhabdomyosarcoma
J. Bennicelli
,
S. Advani
,
B. Schäfer
,
F. Barr
Oncogene
1999
Corpus ID: 22557406
The t(2;13) and t(1;13) translocations of alveolar rhabdomyosarcoma (ARMS) result in chimeric PAX3-FKHR or PAX7-FKHR…
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Review
1998
Review
1998
Intergroup Rhabdomyosarcoma Study: Update for Pathologists
S. Qualman
,
C. Coffin
,
+4 authors
W. Crist
Pediatric and Developmental Pathology
1998
Corpus ID: 25785779
ABSTRACT Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma of childhood, and 75% of such cases in the United States…
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1997
1997
Assessment of molecular genetic detection of chromosome translocations in the differential diagnosis of pediatric sarcomas
B. Dockhorn‐Dworniczak
,
K. Schäfer
,
+6 authors
W. Böcker
Klinische Pädiatrie
1997
Corpus ID: 24929733
Background Methods Results Conclusions Hintergrund Methode Ergebnisse Schlußfolgerung
Highly Cited
1996
Highly Cited
1996
Induction of apoptosis in rhabdomyosarcoma cells through down-regulation of PAX proteins.
Michele Bernasconi
,
Andrew Remppis
,
W. Fredericks
,
Frank J. Rauscher
,
Beat W. Schäfer
Proceedings of the National Academy of Sciences…
1996
Corpus ID: 21982048
The expression of a number of human paired box-containing (PAX) genes has been correlated with various types of tumors. Novel…
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Review
1992
Review
1992
Cytogenetic studies in subgroups of rhabdomyosarcoma
J. Whang‐Peng
,
T. Knutsen
,
K. Theil
,
M. Horowitz
,
T. Triche
Genes, Chromosomes and Cancer
1992
Corpus ID: 11945389
Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma of childhood and accounts for 10% of all solid tumors in children…
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