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Loss of Heterozygosity
Known as:
LOH
, Allelic Loss
, Heterozygosity Loss
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A DNA sequence alteration process in which gain, loss, or exchange of DNA results in loss of function of one allele in a diploid cell. This term is…
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National Institutes of Health
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Related topics
Related topics
8 relations
Broader (2)
Gene Mutation
Mutation
Hemizygote
LINC00312 gene
Neoplastic Processes
Tumor Progression
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2011
Highly Cited
2011
Stress Alters Rates and Types of Loss of Heterozygosity in Candida albicans
A. Forche
,
D. Abbey
,
+5 authors
J. Berman
mBio
2011
Corpus ID: 13957060
ABSTRACT Genetic diversity is often generated during adaptation to stress, and in eukaryotes some of this diversity is thought to…
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Highly Cited
2000
Highly Cited
2000
APC mutations in sporadic colorectal tumors: A mutational "hotspot" and interdependence of the "two hits".
A. Rowan
,
H. Lamlum
,
+6 authors
I. Tomlinson
Proceedings of the National Academy of Sciences…
2000
Corpus ID: 23821406
Although APC mutations occur at a high frequency in colorectal cancers, few studies have performed a comprehensive analysis by…
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Highly Cited
2000
Highly Cited
2000
WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.3-24.1, a region frequently affected in breast cancer.
A. Bednarek
,
K. J. Laflin
,
R. Daniel
,
Q. Liao
,
K. A. Hawkins
,
Claudio Marcelo Aldaz
Cancer Research
2000
Corpus ID: 13315871
Studies were conducted with the final goal of identifying genes of interest mapping to the chromosome region 16q23.3-24.1, an…
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Highly Cited
1997
Highly Cited
1997
Cooperative effects of INK4a and ras in melanoma susceptibility in vivo.
L. Chin
,
J. Pomerantz
,
+6 authors
R. DePinho
Genes & Development
1997
Corpus ID: 38014024
The familial melanoma gene (INK4a/MTS1/CDKN2) encodes potent tumor suppressor activity. Although mice null for the ink4a homolog…
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Review
1996
Review
1996
Is human patched the gatekeeper of common skin cancers?
D. Sidransky
Nature Genetics
1996
Corpus ID: 5221628
Basal cell carcinoma (BCC) is the most common cancer in humans1. The majority of sporadic BCCs have allelic loss on chromosome…
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Highly Cited
1995
Highly Cited
1995
Allelotype of pancreatic adenocarcinoma using xenograft enrichment.
S. Hahn
,
A. Seymour
,
+9 authors
S. Kern
Cancer Research
1995
Corpus ID: 19676691
p53 and MTS1 are known to be mutationally inactivated in pancreatic adenocarcinoma. Other tumor suppressor genes are likely also…
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Highly Cited
1993
Highly Cited
1993
Prognostic significance of p53 mutations and 3p deletions in primary resected non-small cell lung cancer.
Y. Horio
,
Takashi Takahashi
,
+7 authors
R. Ueda
Cancer Research
1993
Corpus ID: 17430769
We evaluated the prognostic significance of p53 mutations and an allelic loss of chromosome 3p in 71 patients with non-small cell…
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Highly Cited
1993
Highly Cited
1993
The adenovirus E1A-associated 130-kD protein is encoded by a member of the retinoblastoma gene family and physically interacts with cyclins A and E.
Yun Li
,
Christina Graham
,
S. Lacy
,
A. Duncan
,
P. Whyte
Genes & Development
1993
Corpus ID: 13196623
The adenovirus E1A proteins form complexes with a group of cellular proteins, including a protein of 130 kD. E1A-associated p130…
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Highly Cited
1992
Highly Cited
1992
Developmental defects in gorlin syndrome related to a putative tumor suppressor gene on chromosome 9
M. Gailani
,
S. Bale
,
+10 authors
A. Bale
Cell
1992
Corpus ID: 25784843
Review
1966
Review
1966
A molecular approach to the study of genic heterozygosity in natural populations. I. The number of alleles at different loci in Drosophila pseudoobscura.
J. L. Hubby
,
R. Lewontin
Genetics
1966
Corpus ID: 9934368
cornerstone of the theory of evolution by gradual change is that the rate of A evolution is absolutely limited by the amount of…
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