Sex biases in the mutation rate (Q50856271)

24 March 2018

review article

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title

Sex biases in the mutation rate (English)

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24 March 2018

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Hurst LD

1

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24 March 2018

Ellegren H

series ordinal

2

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24 March 2018

publication date

1 November 1998

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24 March 2018

published in

Trends in Genetics

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24 March 2018

volume

14

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24 March 2018

issue

11

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24 March 2018

page(s)

446-452

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24 March 2018

The rate of spontaneous mutation of a human gene

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Evidence for a selectively favourable reduction in the mutation rate of the X chromosome

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Potential problems in estimating the male-to-female mutation rate ratio from DNA sequence data

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The Molecular Clock Runs at Different Rates Among Closely Related Members of a Gene Family

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Rates of DNA sequence evolution are not sex-biased in Drosophila melanogaster and D. simulans

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Sex ratio of the mutation frequencies in haemophilia A: estimation and meta-analysis

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Exclusive paternal origin of new mutations in Apert syndrome

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Mutations in fibroblast growth-factor receptor 3 in sporadic cases of achondroplasia occur exclusively on the paternally derived chromosome

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The high spontaneous mutation rate: Is it a health risk?

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Prevalence and parental origin of de novo RET mutations in Hirschsprung's disease

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Molecular analysis of de novo germline mutations in the von Hippel-Lindau disease gene.

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Preferential mutation of the neurofibromatosis type 1 gene in paternally derived chromosomes

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Frequency and nature of specific-locus mutations induced in female mice by radiations and chemicals: a review

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Trinucleotide repeat length instability and age of onset in Huntington's disease

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An unstable triplet repeat in a gene related to myotonic muscular dystrophy

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Studying human mutations by sperm typing: instability of CAG trinucleotide repeats in the human androgen receptor gene.

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On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis

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The factor IX gene as a model for analysis of human germline mutations: an update

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Sex difference in methylation of single-copy genes in human meiotic germ cells: Implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations

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Complex gene conversion events in germline mutation at human minisatellites

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High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions.

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7 January 2021

Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination

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7 January 2021

Sex differences in mutational rate and mutational mechanism in the NF1 gene in neurofibromatosis type 1 patients.

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7 January 2021

Parental origin of chromosome 4p deletion in Wolf-Hirschhorn syndrome

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Parental origin of chromosome 5 deletions in the cri-du-chat syndrome

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The testis: the witness of the mating system, the site of mutation and the engine of desire

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Mutation rates differ among regions of the mammalian genome

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7 January 2021

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An examination of the generation-time effect on molecular evolution

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7 January 2021

Nucleotide substitution type dependence of generation time effect of molecular evolution

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7 January 2021

Renewal of spermatogonia in man

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7 January 2021

Quantification of the paternal allele bias for new germline mutations in the retinoblastoma gene

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7 January 2021

Two maternally derived missense mutations in the tyrosine kinase domain of the RET protooncogene in a patient with de novo MEN 2B

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7 January 2021

Paternal origin of new mutations in von Recklinghausen neurofibromatosis.

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7 January 2021

Identification of RB1 germline mutations in Argentinian families with sporadic bilateral retinoblastoma

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7 January 2021

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7 January 2021

10.1016/S0168-9525(98)01577-7

Identifiers

DOI

1 reference

24 March 2018

1 reference

24 March 2018