Male-driven evolution

WH Li, S Yi, K Makova - Current opinion in genetics & development, 2002 - Elsevier
The strength of male-driven evolution–that is, the magnitude of the sex ratio of mutation rate–
has been a controversial issue, particularly in primates. While earlier studies estimated the …

Sex biases in the mutation rate

LD Hurst, H Ellegren - Trends in Genetics, 1998 - cell.com
Men have more germ-line cell divisions than women. Does this lead to a higher mutation
rate in males? Most estimates of the proportion of mutations originating in men come either …

Sex: differences in mutation, recombination, selection, gene flow, and genetic drift

PW Hedrick - Evolution, 2007 - academic.oup.com
In many instances, there are large sex differences in mutation rates, recombination rates,
selection, rates of gene flow, and genetic drift. Mutation rates are often higher in males, a …

Characterization of the factor VIII defect in 147 patients with sporadic hemophilia A: family studies indicate a mutation type-dependent sex ratio of mutation frequencies …

J Becker, R Schwaab, A Möller-Taube… - American journal of …, 1996 - ncbi.nlm.nih.gov
The clinical manifestation of hemophilia A is caused by a wide range of different mutations.
In this study the factor VIII genes of 147 severe hemophilia A patients--all exclusively from …

Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene

EGD Tuddenham, R Schwaab, J Seehafer… - Nucleic acids …, 1994 - academic.oup.com
A large number of different mutations in the factor VIII (F8) gene have been identified as a
cause of haemophilia A. This compilation lists known single base-pair substitutions …

Do variations in substitution rates and male mutation bias correlate with life‐history traits? A study of 32 mammalian genomes

MAW Sayres, C Venditti, M Pagel, KD Makova - Evolution, 2011 - academic.oup.com
Life‐history traits vary substantially across species, and have been demonstrated to affect
substitution rates. We compute genome‐wide, branch‐specific estimates of male mutation …

[HTML][HTML] Deep intronic 'mutations' cause hemophilia A: application of next generation sequencing in patients without detectable mutation in F8 cDNA

B Pezeshkpoor, N Zimmer, N Marquardt… - Journal of Thrombosis …, 2013 - Elsevier
Background In a small group of typical hemophilia A (HA) patients no mutations in the F8
coding sequence (cDNA) could be found. In the current study, we performed a systematic …

Mucopolysaccharidosis type II (Hunter syndrome): mutation" hot spots" in the iduronate-2-sulfatase gene.

M Rathmann, S Bunge, M Beck, H Kresse… - American journal of …, 1996 - ncbi.nlm.nih.gov
Abstract Mucopolysaccharidosis type II (MPS II, Hunter syndrome) is an X-chromosomal
storage disorder due to deficiency of the lysosomal enzyme iduronate-2-sulfatase (IDS). We …

Molecular Evolution of the Avian CHD1 Genes on the Z and W Sex Chromosomes

AK Fridolfsson, H Ellegren - Genetics, 2000 - academic.oup.com
Genes shared between the nonrecombining parts of the two types of sex chromosomes offer
a potential means to study the molecular evolution of the same gene exposed to different …

Age and sex effects on human mutation rates: an old problem with new complexities

JF Crow - Journal of radiation research, 2006 - jstage.jst.go.jp
Base substitution mutations are far more common in human males than in females, and the
frequency increases with paternal age. Both can be accounted for by the greater number of …