Literature DB >> 3657583

Hybridization of genomic DNA to oligonucleotide probes in the presence of tetramethylammonium chloride.

A G DiLella, S L Woo.   

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Year:  1987        PMID： 3657583     DOI： 10.1016/0076-6879(87)52052-3

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN： 0076-6879            Impact factor:   1.600


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  27 in total

1.  The third subunit of protein phosphatase 2A (PP2A), a 55-kilodalton protein which is apparently substituted for by T antigens in complexes with the 36- and 63-kilodalton PP2A subunits, bears little resemblance to T antigens.

Authors:  D C Pallas; W Weller; S Jaspers; T B Miller; W S Lane; T M Roberts
Journal:  J Virol       Date:  1992-02       Impact factor: 5.103

2.  Detection of enteroviruses in cell cultures by using in situ transcription.

Authors:  J M Carstens; S Tracy; N M Chapman; C J Gauntt
Journal:  J Clin Microbiol       Date:  1992-01       Impact factor: 5.948

3.  Comparative sequence analysis of the Clostridium difficile toxins A and B.

Authors:  C von Eichel-Streiber; R Laufenberg-Feldmann; S Sartingen; J Schulze; M Sauerborn
Journal:  Mol Gen Genet       Date:  1992-05

4.  Intracisternal A-particle-specific oligonucleotides provide multilocus probes for genetic linkage studies in the mouse.

Authors:  J A Mietz; E L Kuff
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

5.  Molecular detection and identification of enteroviruses using enzymatic amplification and nucleic acid hybridization.

Authors:  N M Chapman; S Tracy; C J Gauntt; U Fortmueller
Journal:  J Clin Microbiol       Date:  1990-05       Impact factor: 5.948

6.  Segregation of the N301T mutation in the family of the index patient with mevalonate kinase deficiency.

Authors:  B Goebel-Schreiner; R Schreiner; G F Hoffmann; K M Gibson
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

7.  Characterization of frequent deletions causing steroid 21-hydroxylase deficiency.

Authors:  P C White; A Vitek; B Dupont; M I New
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

8.  GT to AT transition at a splice donor site causes skipping of the preceding exon in phenylketonuria.

Authors:  J Marvit; A G DiLella; K Brayton; F D Ledley; K J Robson; S L Woo
Journal:  Nucleic Acids Res       Date:  1987-07-24       Impact factor: 16.971

9.  Identification of a missense phenylketonuria mutation at codon 408 in Chinese.

Authors:  C H Lin; K J Hsiao; T F Tsai; H K Chao; T S Su
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

10.  Characterization of point mutations in the same arginine codon in three unrelated patients with ornithine transcarbamylase deficiency.

Authors:  A Maddalena; J E Spence; W E O'Brien; R L Nussbaum
Journal:  J Clin Invest       Date:  1988-10       Impact factor: 14.808
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