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t(16;16)
A cytogenetic abnormality that involves a translocation occurring within chromosome 16.
National Institutes of Health
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Related topics
Related topics
1 relation
Chromosomes, Human, Pair 16
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Slow relapse in acute myeloid leukemia with inv(16) or t(16;16)
T. Clozel
,
Aline Renneville
,
+7 authors
L. Adès
Haematologica
2009
Corpus ID: 140699
Acute myeloid leukemia (AML) with inv(16)(p13q22) or t(16;16)(p13;q22), resulting in CBFβ-MYH11 fusion transcript detectable by…
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2009
2009
Type and Number of Secondary Molecular Lesions Improve Outcome Prediction in Acute Myeloid Leukemia (AML) with inv(16) or t(16;16): A Study of the German-Austrian AML Study Group (AMLSG).
P. Paschka
,
Juan Du
,
+13 authors
K. Döhner
2009
Corpus ID: 78408806
Abstract 824 [][1] Background: Although acute myeloid leukemia (AML) with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) [hereafter…
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2007
2007
Semiquantitative RT-PCR evaluation of the MDR1 gene expression in patients with acute myeloid leukemia.
Z. Trnkova
,
R. Bedrlíková
,
J. Marková
,
K. Michalová
,
P. Stöckbauer
,
J. Schwarz
Neoplasma (Bratislava)
2007
Corpus ID: 44764430
Resistance to chemotherapy is one of the major obstacles to effective treatment in acute myeloid leukemia (AML). The most…
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2005
2005
Clinical and biological features of favorable-risk acute myelogenous leukemia – is favorable-risk AML really favorable?
Gary J. Schiller
Leukemia
2005
Corpus ID: 31359506
Clinical and biological features of favorable-risk acute myelogenous leukemia – is favorable-risk AML really favorable?
Highly Cited
2000
Highly Cited
2000
Cytogenetically cryptic AML1–ETO and CBFβ–MYH11 gene rearrangements: incidence in 412 cases of acute myeloid leukaemia
David W. Rowe
,
Simon Cotterill
,
+10 authors
Nick Bown
British Journal of Haematology
2000
Corpus ID: 29644295
The rearrangements t(8;21)(q22;22) and inv(16)(p13q22) are two of the most frequently seen in acute myeloid leukaemia (AML…
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Review
2000
Review
2000
Monosomy 16 as the sole abnormality in myeloid malignancies.
E. McGhee
,
N. R. Cohen
,
J. Wolf
,
C. Ledesma
,
P. Cotter
Cancer Genetics and Cytogenetics
2000
Corpus ID: 34410221
Review
1999
Review
1999
Variant three-way translocation of inversion 16 in AML-M4Eo confirmed by fluorescence in situ hybridization analysis.
J. Martínez-Climent
,
A. Comes
,
+12 authors
J. Garcia-conde
Cancer Genetics and Cytogenetics
1999
Corpus ID: 32166479
1998
1998
Characterization and Use of an Antibody Detecting the CBFβ-SMMHC Fusion Protein in inv(16)/t(16;16)-Associated Acute Myeloid Leukemias
D. Viswanatha
,
I. Chen
,
+4 authors
C. Willman
1998
Corpus ID: 196581077
The inv(16)(p13q22) and t(16;16)(p13;q22) cytogenetic abnormalities occur commonly in acute myeloid leukemia (AML), typically…
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1998
1998
Characterization and use of an antibody detecting the CBFbeta-SMMHC fusion protein in inv(16)/t(16;16)-associated acute myeloid leukemias.
D. Viswanatha
,
I. Chen
,
+4 authors
C. Willman
Blood
1998
Corpus ID: 30195755
The inv(16)(p13q22) and t(16;16)(p13;q22) cytogenetic abnormalities occur commonly in acute myeloid leukemia (AML), typically…
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1994
1994
Karyotypically defined risk groups in acute myeloid leukaemia.
A. Burnett
Leukemia research : a Forum for Studies on…
1994
Corpus ID: 22966564
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