Literature DB >> 1668821

Rapid, nonradioactive screening for activating ras oncogene mutations using PCR-primer introduced restriction analysis (PCR-PIRA)

D R Jacobson1, T Moskovits.   

Abstract

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Year:  1991        PMID： 1668821     DOI： 10.1101/gr.1.2.146

Source DB:  PubMed          Journal:  PCR Methods Appl        ISSN： 1054-9803


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  11 in total

1.  A specific test for transthyretin 122 (Val----Ile), based on PCR-primer-introduced restriction analysis (PCR-PIRA): confirmation of the gene frequency in blacks.

Authors:  D R Jacobson
Journal:  Am J Hum Genet       Date:  1992-01       Impact factor: 11.025

2.  A new detection method for the K variant of butyrylcholinesterase based on PCR primer introduced restriction analysis (PCR-PIRA).

Authors:  K Shibuta; M Abe; T Suzuki
Journal:  J Med Genet       Date:  1994-07       Impact factor: 6.318

3.  Mutations affecting the Rossman fold of isoleucyl-tRNA synthetase are correlated with low-level mupirocin resistance in Staphylococcus aureus.

Authors:  Martin Antonio; Neil McFerran; Mark J Pallen
Journal:  Antimicrob Agents Chemother       Date:  2002-02       Impact factor: 5.191

4.  Alpha-tubulin missense mutations correlate with antimicrotubule drug resistance in Eleusine indica.

Authors:  E Yamamoto; L Zeng; W V Baird
Journal:  Plant Cell       Date:  1998-02       Impact factor: 11.277

5.  Temperature-sensitive splicing in the floral homeotic mutant apetala3-1.

Authors:  R W Sablowski; E M Meyerowitz
Journal:  Plant Cell       Date:  1998-09       Impact factor: 11.277

6.  MADS-box protein complexes control carpel and ovule development in Arabidopsis.

Authors:  Rebecca Favaro; Anusak Pinyopich; Raffaella Battaglia; Maarten Kooiker; Lorenzo Borghi; Gary Ditta; Martin F Yanofsky; Martin M Kater; Lucia Colombo
Journal:  Plant Cell       Date:  2003-10-10       Impact factor: 11.277

7.  Transthyretin Pro55, a variant associated with early-onset, aggressive, diffuse amyloidosis with cardiac and neurologic involvement.

Authors:  D R Jacobson; D E McFarlin; I Kane; J N Buxbaum
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

8.  Identification of allele-specific p22-phox mutations in a compound heterozygous patient with chronic granulomatous disease by mismatch PCR and restriction enzyme analysis.

Authors:  J P Hossle; M de Boer; R A Seger; D Roos
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

9.  High prevalence of a point mutation in the porphobilinogen deaminase gene in Dutch patients with acute intermittent porphyria.

Authors:  X F Gu; F de Rooij; J S Lee; K Te Velde; J C Deybach; Y Nordmann; B Grandchamp
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

10.  Molecular characterization of minor gene rearrangements in Finnish patients with heterozygous familial hypercholesterolemia: identification of two common missense mutations (Gly823-->Asp and Leu380-->His) and eight rare mutations of the LDL receptor gene.

Authors:  U M Koivisto; J S Viikari; K Kontula
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025
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