Masking selected sequence variation by incorporating mismatches into melting analysis probes (Q82255220)

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15 January 2020

title

Masking selected sequence variation by incorporating mismatches into melting analysis probes (English)

1 reference

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15 January 2020

author name string

Rebecca L Margraf

series ordinal

1

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15 January 2020

Rong Mao

series ordinal

2

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15 January 2020

Carl T Wittwer

series ordinal

3

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15 January 2020

publication date

1 March 2006

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15 January 2020

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15 January 2020

volume

27

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15 January 2020

issue

3

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15 January 2020

page(s)

269-278

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Homogeneous multiplex genotyping of hemochromatosis mutations with fluorescent hybridization probes

15 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Predicting DNA duplex stability from the base sequence

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

The minisequencing method: a simple strategy for genetic screening of MEN 2 families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

RET exon 11 (G691S) polymorphism is significantly more frequent in sporadic medullary thyroid carcinoma than in the general population

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Mutations of theRET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and Hirschsprung disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Evaluation of Electronic Microarrays for Genotyping Factor V, Factor II, and MTHFR

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Amplicon melting analysis with labeled primers: a closed-tube method for differentiating homozygotes and heterozygotes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Enhanced discrimination of single nucleotide polymorphisms by artificial mismatch hybridization

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Comparisons of substitution, insertion and deletion probes for resequencing and mutational analysis using oligonucleotide microarrays

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Pyrosequencing technology as a method for the diagnosis of multiple endocrine neoplasia type 2.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Guidelines for incorporating non-perfectly matched oligonucleotides into target-specific hybridization probes for a DNA microarray.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Genotyping of single-nucleotide polymorphisms by high-resolution melting of small amplicons

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Survey and summary: The applications of universal DNA base analogues

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Mutation detection using fluorescent hybridization probes and melting curve analysis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Sequence alterations can mask each other's presence during screening with SSCP or heteroduplex analysis: BRCA genes as examples

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Nearest-neighbor thermodynamics and NMR of DNA sequences with internal A.A, C.C, G.G, and T.T mismatches

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

A PCR-mutagenesis strategy for rapid detection of mutations in codon 634 of the ret proto-oncogene related to MEN 2A.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Germline sequence variant S836S in the RET proto-oncogene is associated with low level predisposition to sporadic medullary thyroid carcinoma in the Spanish population

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Human Gene Mutation Database (HGMD): 2003 update

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Design of molecular beacons for AmpliDet RNA assay—Characterization of binding stability and probe specificity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Detection of a novel point mutation of the prothrombin gene at position 20209.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

High-resolution genotyping by amplicon melting analysis using LCGreen

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Germline RET mutations in MEN 2A and FMTC and their detection by simple DNA diagnostic tests

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Closed-tube genotyping with unlabeled oligonucleotide probes and a saturating DNA dye.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

The effect of base sequence on the stability of RNA and DNA single base bulges.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20290

7 January 2021

Identifiers

DOI

10.1002/HUMU.20290

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16411177%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

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