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Chromosomal Loss
Loss of an entire chromosome or chromosome arm.
National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
p53 and p16Ink4a/p19Arf Loss Promotes Different Pancreatic Tumor Types from PyMT-Expressing Progenitor Cells
S. Azzopardi
,
Sharon Pang
,
D. Klimstra
,
Y. Du
Neoplasia
2016
Corpus ID: 14935022
2005
2005
Pediatric pancreatoblastoma: histopathologic and cytogenetic characterization of tumor and derived cell line.
L. Barenboim-Stapleton
,
Xuezhong Yang
,
+4 authors
C. Thiele
Cancer Genetics and Cytogenetics
2005
Corpus ID: 7225337
Review
2001
Review
2001
Human hepatocellular carcinoma is characterized by a highly consistent pattern of genomic imbalances, including frequent loss of 16q23.1–24.1
B. Balsara
,
J. Pei
,
+9 authors
J. Testa
Genes, Chromosomes and Cancer
2001
Corpus ID: 22167647
Comparative genomic hybridization (CGH) analysis was used to identify chromosomal imbalances in 52 human primary hepatocellular…
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2000
2000
Loss of heterozygosity analysis of 13q and 14q in human malignant mesothelioma
A. De Rienzo
,
S. Jhanwar
,
J. Testa
Genes, Chromosomes and Cancer
2000
Corpus ID: 30346675
Cytogenetic investigations of malignant mesothelioma (MM) have revealed frequent losses in chromosomes 13 and 14, suggesting that…
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1999
1999
Papillary renal cell carcinoma with clear cell cytomorphology and chromosomal loss of 3p
L. Füzesi
,
B. Gunawan
,
F. Bergmann
,
S. Tack
,
S. Braun
,
G. Jakse
Histopathology
1999
Corpus ID: 31872306
Cytogenetic studies on renal cell carcinomas (RCCs) have disclosed a correlation between chromosome aberrations and…
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Highly Cited
1999
Highly Cited
1999
Comparative genomic hybridization and loss of heterozygosity analyses identify a common region of deletion at 15q11.1-15 in human malignant mesothelioma.
B. Balsara
,
D. Bell
,
+4 authors
J. Testa
Cancer Research
1999
Corpus ID: 19254154
Comparative genomic hybridization analysis was performed to identify chromosomal imbalances in 24 human malignant mesothelioma…
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1996
1996
FISH localization of the soluble thymidine kinase gene (TK1) to human 17q25, a region of chromosomal loss in sporadic breast tumors.
E. Petty
,
D. E. Miller
,
A. L. Grant
,
E. E. Collins
,
T. Glover
,
D. J. Law
Cytogenetics and Cell Genetics
1996
Corpus ID: 3324825
Soluble thymidine kinase (TK1) is an important 17q marker in somatic cell genetics. Its activity is increased in many…
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Review
1995
Review
1995
Molecular genetics of head and neck cancer
D. Sidransky
Current Opinion in Oncology
1995
Corpus ID: 36334685
Head and neck cancers arise and progress through specific genetic alterations. Elucidation of these genetic changes has led to…
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1995
1995
The genomic instability of yeast cdc6-1/cdc6-1 mutants involves chromosome structure and recombination
C. Bruschi
,
J. McMillan
,
M. Coglievina
,
M. Esposito
Molecular and General Genetics MGG
1995
Corpus ID: 39216005
When diploid cells of Saccharomyces cerevisiae homozygous for the temperature-sensitive cell division cycle mutation cdc6-1 are…
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Review
1991
Review
1991
Genetic alterations in human gastric cancer.
S. Hirohashi
,
T. Sugimura
Cancer cells
1991
Corpus ID: 45932387
Most types of human tumors display a consistent set of genetic alterations that are thought to play a role in tumor development…
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