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Chromosome Breakpoints
Known as:
Breakpoint, Chromosome
, Breakpoints, Chromosome
, Chromosome Breakpoint
The locations in specific DNA sequences where CHROMOSOME BREAKS have occurred.
National Institutes of Health
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Related topics
1 relation
aspects of radiation effects
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2009
Highly Cited
2009
Distinct retroelement classes define evolutionary breakpoints demarcating sites of evolutionary novelty
Mark Longo
,
Dawn M. Carone
,
E. Green
,
M. O’Neill
,
R. O’Neill
BMC Genomics
2009
Corpus ID: 6029498
BackgroundLarge-scale genome rearrangements brought about by chromosome breaks underlie numerous inherited diseases, initiate or…
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Highly Cited
2005
Highly Cited
2005
Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia.
G. Velagaleti
,
G. Bien-Willner
,
+6 authors
P. Stankiewicz
American Journal of Human Genetics
2005
Corpus ID: 7505635
Campomelic dysplasia (CD) is a semilethal skeletal malformation syndrome with or without XY sex reversal. In addition to the…
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Highly Cited
2003
Highly Cited
2003
Combined 24-color karyotyping and comparative genomic hybridization analysis indicates predominant rearrangements of early replicating chromosome regions in neuroblastoma.
G. Schleiermacher
,
I. Janoueix-Lerosey
,
+4 authors
O. Delattre
Cancer Genetics and Cytogenetics
2003
Corpus ID: 32701266
Highly Cited
2001
Highly Cited
2001
Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation
J. E. Willett-Brozick
,
S. Savul
,
L. Richey
,
B. Baysal
Human Genetics
2001
Corpus ID: 19558202
Abstract. Constitutional chromosomal translocations are relatively common causes of human morbidity, yet the DNA double-strand…
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Highly Cited
2000
Highly Cited
2000
Intronic U50 small‐nucleolar‐RNA (snoRNA) host gene of no protein‐coding potential is mapped at the chromosome breakpoint t(3;6)(q27;q15) of human B‐cell lymphoma
Ritsuko Tanaka
,
H. Satoh
,
+6 authors
S. Mori
Genes to Cells
2000
Corpus ID: 37200110
In eukaryotic cells, nucleolar processing of preribosomal RNAs (prerRNAs) is assisted by a large number of small nucleolar RNAs…
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Highly Cited
1999
Highly Cited
1999
Chromosome abnormalities in ovarian adenocarcinoma: I. nonrandom chromosome abnormalities from 244 cases
R. Taetle
,
M. Aickin
,
+10 authors
D. Alberts
Genes, Chromosomes and Cancer
1999
Corpus ID: 9377562
Cytogenetics provides important insights into the molecular pathogenesis of human cancers. Although extensive data exist on…
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Highly Cited
1995
Highly Cited
1995
Mapping the X chromosome breakpoint in two papillary renal cell carcinoma cell lines with a t(X;1)(p11.2;q21.2) and the first report of a female case.
J. Shipley
,
S. Birdsall
,
+7 authors
C. Cooper
Cytogenetics and Cell Genetics
1995
Corpus ID: 46795761
A t(X;1)(p11.2;q21.2) has been reported in cases of papillary renal cell tumors arising in males. In this study two cell lines…
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Highly Cited
1992
Highly Cited
1992
Cloning and characterization of chromosome breakpoints of Plasmodium falciparum: breakage and new telomere formation occurs frequently and randomly in subtelomeric genes.
Artur Scherf
,
Denise Mattei
Nucleic Acids Research
1992
Corpus ID: 15366135
We analysed the genetic stability of two subtelomeric genes of the human malaria parasite Plasmodium falciparum. A PCR based…
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Highly Cited
1988
Highly Cited
1988
Thermostable DNA polymerase chain amplification of t(14;18) chromosome breakpoints and detection of minimal residual disease.
Macro Crescenzi
,
M. Seto
,
G. Herzig
,
Peter D. Weiss
,
R. Griffith
,
S. Korsmeyer
Proceedings of the National Academy of Sciences…
1988
Corpus ID: 1973855
Achieving the capacity to detect minimal numbers of neoplastic cells is a major cancer diagnostic challenge. Chromosomal…
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Highly Cited
1986
Highly Cited
1986
Heterogeneity of chromosome 22 breakpoint in Philadelphia-positive (Ph+) acute lymphocytic leukemia.
J. Erikson
,
Constance A. GRIFFINt
,
+7 authors
C. Croce
Proceedings of the National Academy of Sciences…
1986
Corpus ID: 45095305
In chronic myelogenous leukemias (CML) with the t(9;22)(q34;q11) chromosome translocation the breakpoints on chromosome 22 occur…
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