Literature DB >> 864721

Higher frequencies of transitions among point mutations.

F Vogel, M Kopun.   

Abstract

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Year:  1977        PMID: 864721     DOI: 10.1007/bf01732746

Source DB:  PubMed          Journal:  J Mol Evol        ISSN: 0022-2844            Impact factor:   2.395


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  20 in total

Review 1.  Darwinian evolution in the genealogy of haemoglobin.

Authors:  M Goodman; G W Moore; G Matsuda
Journal:  Nature       Date:  1975-02-20       Impact factor: 49.962

Review 2.  Mutational pressure as the main cause of molecular evolution and polymorphism.

Authors:  T Ota
Journal:  Nature       Date:  1974-11-29       Impact factor: 49.962

3.  Relations between chemical structure and biological activity in peptides.

Authors:  P H Sneath
Journal:  J Theor Biol       Date:  1966-11       Impact factor: 2.691

Review 4.  [Amino acids sequence. Nucleotide sequence and evolution].

Authors:  J Derancourt; A S Lebor; E Zuckerkandl
Journal:  Bull Soc Chim Biol (Paris)       Date:  1967

5.  Point mutations and human hemoglobin variants.

Authors:  F Vogel
Journal:  Humangenetik       Date:  1969

6.  Selective constraints on amino-acid substitutions during the evolution of proteins.

Authors:  B Clarke
Journal:  Nature       Date:  1970-10-10       Impact factor: 49.962

Review 7.  Spontaneous mutation in man.

Authors:  F Vogel; R Rathenberg
Journal:  Adv Hum Genet       Date:  1975

8.  Role of the amino-acid "code" and of selection for conformation in the evolution of proteins.

Authors:  C J Epstein
Journal:  Nature       Date:  1966-04-02       Impact factor: 49.962

9.  [Mutation processes in the formation of hemoglobin variants].

Authors:  F Vogel; G Röhrborn
Journal:  Humangenetik       Date:  1965

10.  Amino-acid substitutions in haemoglobins and the mutation process.

Authors:  F Vogel; G Röhrborn
Journal:  Nature       Date:  1966-04-02       Impact factor: 49.962

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  32 in total

1.  A SNP resource for human chromosome 22: extracting dense clusters of SNPs from the genomic sequence.

Authors:  E Dawson; Y Chen; S Hunt; L J Smink; A Hunt; K Rice; S Livingston; S Bumpstead; R Bruskiewich; P Sham; R Ganske; M Adams; K Kawasaki; N Shimizu; S Minoshima; B Roe; D Bentley; I Dunham
Journal:  Genome Res       Date:  2001-01       Impact factor: 9.043

2.  Single nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population.

Authors:  Yun Freudenberg-Hua; Jan Freudenberg; Nadine Kluck; Sven Cichon; Peter Propping; Markus M Nöthen
Journal:  Genome Res       Date:  2003-10       Impact factor: 9.043

Review 3.  The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions.

Authors:  D N Cooper; M Krawczak
Journal:  Hum Genet       Date:  1990-06       Impact factor: 4.132

4.  The CpG dinucleotide and human genetic disease.

Authors:  D N Cooper; H Youssoufian
Journal:  Hum Genet       Date:  1988-02       Impact factor: 4.132

5.  An estimate of unique DNA sequence heterozygosity in the human genome.

Authors:  D N Cooper; B A Smith; H J Cooke; S Niemann; J Schmidtke
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

6.  Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human gene.

Authors:  D D Koeberl; C D Bottema; R P Ketterling; P J Bridge; D P Lillicrap; S S Sommer
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

7.  Two types of amino acid substitutions in protein evolution.

Authors:  T Miyata; S Miyazawa; T Yasunaga
Journal:  J Mol Evol       Date:  1979-03-15       Impact factor: 2.395

Review 8.  DNA restriction fragment length polymorphisms and heterozygosity in the human genome.

Authors:  D N Cooper; J Schmidtke
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  Nonrandomness of point mutation as reflected in nucleotide substitutions in pseudogenes and its evolutionary implications.

Authors:  W H Li; C I Wu; C C Luo
Journal:  J Mol Evol       Date:  1984       Impact factor: 2.395

Review 10.  Estimating the total number of nucleotide substitutions since the common ancestor of a pair of homologous genes: comparison of several methods and three beta hemoglobin messenger RNA's.

Authors:  W M Fitch
Journal:  J Mol Evol       Date:  1980-12       Impact factor: 2.395

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