Hierholzer A, Chureau C, Liverziani A, Ruiz N, Cattanach B, Young A
Proc Natl Acad Sci U S A. 2022; 119(28):e2118182119.
PMID: 35787055
PMC: 9282422.
DOI: 10.1073/pnas.2118182119.
Pacini G, Dunkel I, Mages N, Mutzel V, Timmermann B, Marsico A
Nat Commun. 2021; 12(1):3638.
PMID: 34131144
PMC: 8206119.
DOI: 10.1038/s41467-021-23643-6.
Sun K, Oreper D, Schoenrock S, McMullan R, Giusti-Rodriguez P, Zhabotynsky V
Genetics. 2021; 218(1).
PMID: 33693696
PMC: 8128399.
DOI: 10.1093/genetics/iyab034.
Lakhotia S
J Genet. 2015; 94(4):575-84.
PMID: 26690511
DOI: 10.1007/s12041-015-0566-1.
Horst Schroder J
Theor Appl Genet. 2014; 46(3):135-42.
PMID: 24419866
DOI: 10.1007/BF00264868.
Genetic architecture of skewed X inactivation in the laboratory mouse.
Calaway J, Lenarcic A, Didion J, Wang J, Searle J, McMillan L
PLoS Genet. 2013; 9(10):e1003853.
PMID: 24098153
PMC: 3789830.
DOI: 10.1371/journal.pgen.1003853.
Genetic control of X chromosome inactivation in mice: definition of the Xce candidate interval.
Helbling Chadwick L, Pertz L, Broman K, Bartolomei M, Willard H
Genetics. 2006; 173(4):2103-10.
PMID: 16582439
PMC: 1569705.
DOI: 10.1534/genetics.105.054882.
Genetic and parent-of-origin influences on X chromosome choice in Xce heterozygous mice.
Helbling Chadwick L, Willard H
Mamm Genome. 2005; 16(9):691-9.
PMID: 16245026
DOI: 10.1007/s00335-005-0059-2.
X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndrome.
Young J, Zoghbi H
Am J Hum Genet. 2004; 74(3):511-20.
PMID: 14973779
PMC: 1182264.
DOI: 10.1086/382228.
Skewing X chromosome choice by modulating sense transcription across the Xist locus.
Nesterova T, Johnston C, Appanah R, Newall A, Godwin J, Alexiou M
Genes Dev. 2003; 17(17):2177-90.
PMID: 12952890
PMC: 196458.
DOI: 10.1101/gad.271203.
An N-ethyl-N-nitrosourea mutagenesis screen for epigenetic mutations in the mouse.
Percec I, Thorvaldsen J, Plenge R, Krapp C, Nadeau J, Willard H
Genetics. 2003; 164(4):1481-94.
PMID: 12930754
PMC: 1462673.
DOI: 10.1093/genetics/164.4.1481.
Characterization of the genomic Xist locus in rodents reveals conservation of overall gene structure and tandem repeats but rapid evolution of unique sequence.
Nesterova T, Slobodyanyuk S, Elisaphenko E, Shevchenko A, Johnston C, Pavlova M
Genome Res. 2001; 11(5):833-49.
PMID: 11337478
PMC: 311126.
DOI: 10.1101/gr.174901.
Regulation of X-chromosome inactivation in development in mice and humans.
Goto T, Monk M
Microbiol Mol Biol Rev. 1998; 62(2):362-78.
PMID: 9618446
PMC: 98919.
DOI: 10.1128/MMBR.62.2.362-378.1998.
Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28.
Pegoraro E, Whitaker J, Surti U, Lanasa M, Hoffman E
Am J Hum Genet. 1997; 61(1):160-70.
PMID: 9245997
PMC: 1715880.
DOI: 10.1086/513901.
Identification and characterization of the human XIST gene promoter: implications for models of X chromosome inactivation.
Hendrich B, Plenge R, Willard H
Nucleic Acids Res. 1997; 25(13):2661-71.
PMID: 9185579
PMC: 146792.
DOI: 10.1093/nar/25.13.2661.
Creation of a deletion series of mouse YACs covering a 500 kb region around Xist.
Heard E, Avner P, Rothstein R
Nucleic Acids Res. 1994; 22(10):1830-7.
PMID: 8208607
PMC: 308081.
DOI: 10.1093/nar/22.10.1830.
The role of X-chromosome inactivation during spermatogenesis (Drosophila-allocycly-chromosome evolution-male sterility-dosage compensation).
Lifschytz E, LINDSLEY D
Proc Natl Acad Sci U S A. 1972; 69(1):182-6.
PMID: 4621547
PMC: 427571.
DOI: 10.1073/pnas.69.1.182.
Aromatic amino acid metabolism in brindled (Mobr) and viable-brindled (Movbr), two alleles at the mottled locus in the mouse.
Hunt D, Johnson D
Biochem Genet. 1972; 6(1):31-40.
PMID: 4147174
DOI: 10.1007/BF00485963.
Localized Derepression on the Human Inactive X Chromosone in Mouse-Human Cell Hybrids.
Kahan B, Demars R
Proc Natl Acad Sci U S A. 1975; 72(4):1510-4.
PMID: 1055421
PMC: 432566.
DOI: 10.1073/pnas.72.4.1510.
