Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Genetic Analysis of Variation in Human Meiotic Recombination
by
Sherman, Stephanie L.
, Cheung, Vivian G.
, Feingold, Eleanor
, Bois, Philippe R. J.
, Chowdhury, Reshmi
in
Autistic Disorder - genetics
/ Deoxyribonucleic acid
/ DNA
/ Female
/ Gene Expression Regulation
/ Gene loci
/ Genetic Markers
/ Genetic recombination
/ Genetic Variation
/ Genetics and Genomics
/ Genetics and Genomics/Chromosome Biology
/ Genetics and Genomics/Complex Traits
/ Genome, Human - genetics
/ Genome-Wide Association Study
/ Genomics
/ Humans
/ Male
/ Meiosis
/ Meiosis - genetics
/ Myocardium - metabolism
/ Phenotype
/ Physiological aspects
/ Quantitative Trait Loci - genetics
/ Recombination, Genetic
/ Reproducibility of Results
/ Single nucleotide polymorphisms
2009
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Genetic Analysis of Variation in Human Meiotic Recombination
by
Sherman, Stephanie L.
, Cheung, Vivian G.
, Feingold, Eleanor
, Bois, Philippe R. J.
, Chowdhury, Reshmi
in
Autistic Disorder - genetics
/ Deoxyribonucleic acid
/ DNA
/ Female
/ Gene Expression Regulation
/ Gene loci
/ Genetic Markers
/ Genetic recombination
/ Genetic Variation
/ Genetics and Genomics
/ Genetics and Genomics/Chromosome Biology
/ Genetics and Genomics/Complex Traits
/ Genome, Human - genetics
/ Genome-Wide Association Study
/ Genomics
/ Humans
/ Male
/ Meiosis
/ Meiosis - genetics
/ Myocardium - metabolism
/ Phenotype
/ Physiological aspects
/ Quantitative Trait Loci - genetics
/ Recombination, Genetic
/ Reproducibility of Results
/ Single nucleotide polymorphisms
2009
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Genetic Analysis of Variation in Human Meiotic Recombination
by
Sherman, Stephanie L.
, Cheung, Vivian G.
, Feingold, Eleanor
, Bois, Philippe R. J.
, Chowdhury, Reshmi
in
Autistic Disorder - genetics
/ Deoxyribonucleic acid
/ DNA
/ Female
/ Gene Expression Regulation
/ Gene loci
/ Genetic Markers
/ Genetic recombination
/ Genetic Variation
/ Genetics and Genomics
/ Genetics and Genomics/Chromosome Biology
/ Genetics and Genomics/Complex Traits
/ Genome, Human - genetics
/ Genome-Wide Association Study
/ Genomics
/ Humans
/ Male
/ Meiosis
/ Meiosis - genetics
/ Myocardium - metabolism
/ Phenotype
/ Physiological aspects
/ Quantitative Trait Loci - genetics
/ Recombination, Genetic
/ Reproducibility of Results
/ Single nucleotide polymorphisms
2009
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Genetic Analysis of Variation in Human Meiotic Recombination
Journal Article
Genetic Analysis of Variation in Human Meiotic Recombination
2009
Request Book From Autostore
and Choose the Collection Method
Overview
The number of recombination events per meiosis varies extensively among individuals. This recombination phenotype differs between female and male, and also among individuals of each gender. In this study, we used high-density SNP genotypes of over 2,300 individuals and their offspring in two datasets to characterize recombination landscape and to map the genetic variants that contribute to variation in recombination phenotypes. We found six genetic loci that are associated with recombination phenotypes. Two of these (RNF212 and an inversion on chromosome 17q21.31) were previously reported in the Icelandic population, and this is the first replication in any other population. Of the four newly identified loci (KIAA1462, PDZK1, UGCG, NUB1), results from expression studies provide support for their roles in meiosis. Each of the variants that we identified explains only a small fraction of the individual variation in recombination. Notably, we found different sequence variants associated with female and male recombination phenotypes, suggesting that they are regulated by different genes. Characterization of genetic variants that influence natural variation in meiotic recombination will lead to a better understanding of normal meiotic events as well as of non-disjunction, the primary cause of pregnancy loss.
Publisher
Public Library of Science,Public Library of Science (PLoS)
This website uses cookies to ensure you get the best experience on our website.