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Items: 1 to 20 of 29

2.

Detection of single base substitutions by ribonuclease cleavage at mismatches in RNA:DNA duplexes.

Myers RM, Larin Z, Maniatis T.

Science. 1985 Dec 13;230(4731):1242-6.

PMID:
4071043
3.

Detection of single base substitutions in total genomic DNA.

Myers RM, Lumelsky N, Lerman LS, Maniatis T.

Nature. 1985 Feb 7-13;313(6002):495-8.

PMID:
3969155
4.

Full-length cDNA for rabbit tryptophan hydroxylase: functional domains and evolution of aromatic amino acid hydroxylases.

Grenett HE, Ledley FD, Reed LL, Woo SL.

Proc Natl Acad Sci U S A. 1987 Aug;84(16):5530-4.

5.

Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction.

Mullis KB, Faloona FA.

Methods Enzymol. 1987;155:335-50. No abstract available.

PMID:
3431465
6.
7.

Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria.

DiLella AG, Marvit J, Lidsky AS, Güttler F, Woo SL.

Nature. 1986 Aug 28-Sep 3;322(6082):799-803.

PMID:
3018584
9.

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia.

Saiki RK, Scharf S, Faloona F, Mullis KB, Horn GT, Erlich HA, Arnheim N.

Science. 1985 Dec 20;230(4732):1350-4.

PMID:
2999980
10.

Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase.

Kwok SC, Ledley FD, DiLella AG, Robson KJ, Woo SL.

Biochemistry. 1985 Jan 29;24(3):556-61.

PMID:
2986678
11.

An amino-acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haplotype 2.

DiLella AG, Marvit J, Brayton K, Woo SL.

Nature. 1987 May 28-Jun 3;327(6120):333-6.

PMID:
2884570
13.

Direct detection of point mutations by mismatch analysis: application to haemophilia B.

Montandon AJ, Green PM, Giannelli F, Bentley DR.

Nucleic Acids Res. 1989 May 11;17(9):3347-58.

14.

Detection of single base changes in nucleic acids.

Cotton RG.

Biochem J. 1989 Oct 1;263(1):1-10. Review. No abstract available.

16.

CpG dinucleotides are mutation hot spots in phenylketonuria.

Abadie V, Lyonnet S, Maurin N, Berthelon M, Caillaud C, Giraud F, Mattei JF, Rey J, Rey F, Munnich A.

Genomics. 1989 Nov;5(4):936-9.

PMID:
2574153
17.

Detection and localization of base changes in RNA using a chemical cleavage method.

Dahl HH, Lamande SR, Cotton RG, Bateman JF.

Anal Biochem. 1989 Dec;183(2):263-8.

PMID:
2483035
18.

Scanning detection of mutations in human ornithine transcarbamoylase by chemical mismatch cleavage.

Grompe M, Muzny DM, Caskey CT.

Proc Natl Acad Sci U S A. 1989 Aug;86(15):5888-92.

19.

Pyruvate dehydrogenase deficiency caused by deletion of a 7-bp repeat sequence in the E1 alpha gene.

Dahl HH, Maragos C, Brown RM, Hansen LL, Brown GK.

Am J Hum Genet. 1990 Aug;47(2):286-93.

20.

Improvement of PCR amplified DNA sequencing with the aid of detergents.

Bachmann B, Lüke W, Hunsmann G.

Nucleic Acids Res. 1990 Mar 11;18(5):1309. No abstract available.

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