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Gene Amplification Abnormality
Known as:
Amplification
, Gene Amplification
An increase in the copy number of a particular gene. This type of abnormality can be either inherited or somatic.
National Institutes of Health
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Related topics
Related topics
3 relations
GAS41 protein, human
Gene Amplification
Gene Amplification Technique
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Screening for Lynch syndrome in young Saudi colorectal cancer patients using microsatellite instability testing and next generation sequencing
Masood Alqahtani
,
Caitlin Edwards
,
+9 authors
B. Iacopetta
Familial Cancer
2018
Corpus ID: 4715910
Individuals with Lynch syndrome (LS) have germline variants in DNA mismatch repair (MMR) genes that confer a greatly increased…
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2017
2017
Screening for Lynch syndrome in young Saudi colorectal cancer patients using microsatellite instability testing and next generation sequencing
Masood Alqahtani
,
Caitlin Edwards
,
+9 authors
B. Iacopetta
Familial Cancer
2017
Corpus ID: 254515068
Individuals with Lynch syndrome (LS) have germline variants in DNA mismatch repair (MMR) genes that confer a greatly increased…
Expand
2014
2014
The development of an mRNA amplification positive control for the identification of body fluids
R. Fleming
,
S. Harbison
2014
Corpus ID: 71497700
Abstract With the increasing interest and use of messenger RNA (mRNA) for identifying body fluids in forensic science…
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1999
1999
Allele-Specific Amplification (AS-PCR) for Point Mutation Screening of G Protein α-Subunit (Gsα) in McCune-Albright Syndrome (MAS)
H. Domené
,
G. Sansó
,
M. Gryngarten
,
M. Escobar
Pediatric Research
1999
Corpus ID: 38472801
Allele-Specific Amplification (AS-PCR) for Point Mutation Screening of G Protein α-Subunit (Gsα) in McCune-Albright Syndrome (MAS…
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1999
1999
An AluI PCR-RFLP in the bovine survival motor neuron gene (SMN).
D. Pietrowski
,
J. Kemter
,
I. Medugorac
,
T. Goldammer
,
M. Foerster
Animal Genetics
1999
Corpus ID: 26246838
Source/description: Two 1·0 kb clones were isolated from a bovine spinal cord cDNA library using a 394-bp RT-PCR fragment from…
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1992
1992
Invariant exon skipping in the human alpha-galactosidase A pre-mRNA: Ag+1 to t substitution in a 5'-splice site causing Fabry disease.
H. Sakuraba
,
C. Eng
,
R. Desnick
,
D. Bishop
Genomics
1992
Corpus ID: 21185593
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