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Results of search for 'su:"Nucleic Acid Heteroduplexes"', page 107 of 143
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Authors
Bidwell, J L
Brown, T
Broyde, S
Christiano, A M
Cotton, R G
Gromova, E S
Jinks-Robertson, Sue
Jiricny, J
Kubareva, E A
Kunkel, T A
Miller, Paul S
Modrich, P
Mullins, J I
Petes, T D
Radding, C M
Radman, M
Shabarova, Z A
Sundaralingam, M
Turner, D H
Uitto, J
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Topics
Animals
Base Sequence
DNA
DNA Repair
DNA, Viral
Escherichia coli
Humans
Models, Molecular
Molecular Sequence Data
Mutation
Nucleic Acid Conformation
Nucleic Acid Heteroduplexes
Polymerase Chain Reaction
RNA
Thermodynamics
analysis
chemistry
genetics
metabolism
methods
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Results
2121.
High-throughput SNP detection by using DNA pooling and denaturing high performance liquid chromatography (DHPLC).
[electronic resource]
by
Wolford, J K
Blunt, D
Ballecer, C
Prochazka, M
Producer:
20010118
In:
Human genetics
vol. 107
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2122.
Nucleic acid duplex stability: influence of base composition on cation effects.
[electronic resource]
by
Nakano, S
Fujimoto, M
Hara, H
Sugimoto, N
Producer:
19990903
In:
Nucleic acids research
vol. 27
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2123.
MutS recognition: multiple mismatches and sequence context effects.
[electronic resource]
by
Joshi, A
Rao, B J
Producer:
20020308
In:
Journal of biosciences
vol. 26
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2124.
Nonlinear breathing modes due to a defect in a DNA chain.
[electronic resource]
by
Wattis, Jonathan A D
Producer:
20040907
In:
Philosophical transactions. Series A, Mathematical, physical, and engineering sciences
vol. 362
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2125.
Heteroduplex DNA position defines the roles of the Sgs1, Srs2, and Mph1 helicases in promoting distinct recombination outcomes.
[electronic resource]
by
Mitchel, Katrina
Lehner, Kevin
Jinks-Robertson, Sue
Producer:
20130613
In:
PLoS genetics
vol. 9
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2126.
In frame deletion (delta F311) within a short trinucleotide repeat of the first transmembrane region of the cystic fibrosis gene.
[electronic resource]
by
Meitinger, T
Golla, A
Dörner, C
Deufel, A
Aulehla-Scholz, C
Böhm, I
Reinhardt, D
Deufel, T
Producer:
19940331
In:
Human molecular genetics
vol. 2
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2127.
An alternative approach to the assessment of gamma delta T-cell clonality in celiac disease intestinal lesions through cDNA heteroduplex analysis of T-cell receptor VJ junctions.
[electronic resource]
by
Giachino, C
Rocci, M P
De Libero, G
Oderda, G
Ansaldi, N
Migone, N
Producer:
19950125
In:
Human immunology
vol. 40
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2128.
Spectrum of spontaneous HPRT- mutations in TK6 human lymphoblasts.
[electronic resource]
by
Giver, C R
Nelson, S L
Grosovsky, A J
Producer:
19931109
In:
Environmental and molecular mutagenesis
vol. 22
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2129.
Outgroup heteroduplex analysis using temperature gradient gel electrophoresis: high resolution, large scale, screening of DNA variation in the mitochondrial control region.
[electronic resource]
by
Campbell, N J
Harriss, F C
Elphinstone, M S
Baverstock, P R
Producer:
19960313
In:
Molecular ecology
vol. 4
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2130.
Molecular diagnosis of 21-hydroxylase deficiency: detection of four mutations on a single gel.
[electronic resource]
by
Siegel, S F
Hoffman, E P
Trucco, M
Producer:
19940628
In:
Biochemical medicine and metabolic biology
vol. 51
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2131.
Hereditary coproporphyria: exon screening by heteroduplex analysis detects three novel mutations in the coproporphyrinogen oxidase gene.
[electronic resource]
by
Schreiber, W E
Zhang, X
Senz, J
Jamani, A
Producer:
19971029
In:
Human mutation
vol. 10
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2132.
Migration of a Holliday junction through a nucleosome directed by the E. coli RuvAB motor protein.
[electronic resource]
by
Grigoriev, M
Hsieh, P
Producer:
19981102
In:
Molecular cell
vol. 2
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2133.
Non-inversion factor VIII mutations in 80 hemophilia A families including 24 with alloimmune responses.
[electronic resource]
by
Liu, Miao-Liang
Nakaya, Shelley
Thompson, Arthur R
Producer:
20020906
In:
Thrombosis and haemostasis
vol. 87
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2134.
Conserved regions in defective interfering viral double-stranded RNAs from a yeast virus.
[electronic resource]
by
Lee, M
Pietras, D F
Nemeroff, M E
Corstanje, B J
Field, L J
Bruenn, J A
Producer:
19860527
In:
Journal of virology
vol. 58
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2135.
An association between HIV-1 subtypes and mode of transmission in Cape Town, South Africa.
[electronic resource]
by
van Harmelen, J
Wood, R
Lambrick, M
Rybicki, E P
Williamson, A L
Williamson, C
Producer:
19970507
In:
AIDS (London, England)
vol. 11
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2136.
Novel rhodopsin mutation (M216R) in a Danish family with autosomal dominant retinitis pigmentosa.
[electronic resource]
by
Haim, M
Grundmann, K
Gal, A
Rosenberg, T
Producer:
19970328
In:
Ophthalmic genetics
vol. 17
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2137.
Diagnosis of sickle-cell disease with a universal heteroduplex generator.
[electronic resource]
by
Wood, N
Standen, G
Hows, J
Bradley, B
Bidwell, J
Producer:
19940112
In:
Lancet (London, England)
vol. 342
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2138.
Molecular diagnosis of genetic diseases.
[electronic resource]
by
Ferrari, M
Cremonesi, L
Carrera, P
Bonini, P A
Producer:
19970319
In:
Clinical biochemistry
vol. 29
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2139.
Analysis of mutational changes at the HLA locus in single human sperm.
[electronic resource]
by
Huang, M M
Erlich, H A
Goodman, M F
Arnheim, N
Producer:
19960816
In:
Human mutation
vol. 6
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2140.
Isolation and characterization of diazoate intermediate upon nitrous acid and nitric oxide treatment of 2'-deoxycytidine.
[electronic resource]
by
Suzuki, T
Nakamura, T
Yamada, M
Ide, H
Kanaori, K
Tajima, K
Morii, T
Makino, K
Producer:
19990623
In:
Biochemistry
vol. 38
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