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Masking selected sequence variation by incorporating mismatches into melting analysis probes
scientific article published on 01 March 2006
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16411177
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16411177%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 January 2020
title
Masking selected sequence variation by incorporating mismatches into melting analysis probes
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16411177
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16411177%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 January 2020
author name string
Rebecca L Margraf
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16411177
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16411177%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 January 2020
Rong Mao
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16411177
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16411177%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 January 2020
Carl T Wittwer
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16411177
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16411177%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 January 2020
publication date
1 March 2006
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16411177
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16411177%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 January 2020
published in
Human Mutation
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16411177
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16411177%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 January 2020
volume
27
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16411177
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16411177%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 January 2020
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16411177
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16411177%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 January 2020
page(s)
269-278
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16411177
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16411177%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 January 2020
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A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1
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RET exon 11 (G691S) polymorphism is significantly more frequent in sporadic medullary thyroid carcinoma than in the general population
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7 January 2021
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Mutations of theRET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and Hirschsprung disease
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Evaluation of Electronic Microarrays for Genotyping Factor V, Factor II, and MTHFR
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Amplicon melting analysis with labeled primers: a closed-tube method for differentiating homozygotes and heterozygotes
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Enhanced discrimination of single nucleotide polymorphisms by artificial mismatch hybridization
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Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis
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Comparisons of substitution, insertion and deletion probes for resequencing and mutational analysis using oligonucleotide microarrays
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Pyrosequencing technology as a method for the diagnosis of multiple endocrine neoplasia type 2.
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Guidelines for incorporating non-perfectly matched oligonucleotides into target-specific hybridization probes for a DNA microarray.
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Genotyping of single-nucleotide polymorphisms by high-resolution melting of small amplicons
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Mutation detection using fluorescent hybridization probes and melting curve analysis
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Sequence alterations can mask each other's presence during screening with SSCP or heteroduplex analysis: BRCA genes as examples
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Nearest-neighbor thermodynamics and NMR of DNA sequences with internal A.A, C.C, G.G, and T.T mismatches
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A PCR-mutagenesis strategy for rapid detection of mutations in codon 634 of the ret proto-oncogene related to MEN 2A.
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Germline sequence variant S836S in the RET proto-oncogene is associated with low level predisposition to sporadic medullary thyroid carcinoma in the Spanish population
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Germline RET mutations in MEN 2A and FMTC and their detection by simple DNA diagnostic tests
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Closed-tube genotyping with unlabeled oligonucleotide probes and a saturating DNA dye.
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Identifiers
DOI
10.1002/HUMU.20290
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16411177
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16411177%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 January 2020
PubMed publication ID
16411177
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16411177
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16411177%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 January 2020
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