Literature DB >> 4647441

Spontaneous frequencies of point mutations in mice.

A G Searle.   

Abstract

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Year:  1972        PMID： 4647441     DOI： 10.1007/bf00393982

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  7 in total

1.  Genetic analysis of induced deletions and of spontaneous nondisjunction involving chromosome 2 of the mouse.

Authors:  L B RUSSELL; W L RUSSELL
Journal:  J Cell Comp Physiol       Date:  1960-11

2.  Genetic hazard of ionizing radiations.

Authors:  T C CARTER; M F LYON; R J PHILLIPS
Journal:  Nature       Date:  1958-08-09       Impact factor: 49.962

3.  Spontaneous mutations and mutation rates in the house mouse.

Authors:  G Schlager; M M Dickie
Journal:  Genetics       Date:  1967-10       Impact factor: 4.562

4.  Natural mutation rates in the house mouse. Estimates for five specific loci and dominant mutations.

Authors:  G Schlager; M M Dickie
Journal:  Mutat Res       Date:  1971-01       Impact factor: 2.433

5.  The ineffectiveness of chronic irradiation with neutrons and gamma rays in inducing mutations in female mice.

Authors:  A L Batchelor; R J Phillips; A G Searle
Journal:  Br J Radiol       Date:  1969-06       Impact factor: 3.039

6.  Gene and chromosome mutation after large fractionated or unfractionated radiation doses to mouse spermatogonia.

Authors:  M F Lyon; T Morris
Journal:  Mutat Res       Date:  1969 Jul-Aug       Impact factor: 2.433

7.  Estimates of the genetic risks from ionizing irradiation.

Authors:  K G Lüning; A G Searle
Journal:  Mutat Res       Date:  1971-07       Impact factor: 2.433
  7 in total
  3 in total

1.  A probable sex difference in some mutation rates.

Authors:  F Vogel
Journal:  Am J Hum Genet       Date:  1977-05       Impact factor: 11.025

2.  Protein mapping by combined isoelectric focusing and electrophoresis of mouse tissues. A novel approach to testing for induced point mutations in mammals.

Authors:  J Klose
Journal:  Humangenetik       Date:  1975

3.  Estimation of male to female ratio of mutation rates from carrier-detection tests in X-linked disorders.

Authors:  R M Winter
Journal:  Am J Hum Genet       Date:  1980-07       Impact factor: 11.025
  3 in total

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