Chromosomal domains and escape from X inactivation: comparative X inactivation analysis in mouse and human

[1]  H. Willard,et al.  A first-generation X-inactivation profile of the human X chromosome. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[2]  C. Disteche,et al.  Escapees on the X chromosome. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[3]  P. Sharp,et al.  Promoter-specific hypoacetylation of X-inactivated genes. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[4]  A. Agulnik,et al.  Mouse H-Y encoding Smcy gene and its X Chromosomal homolog Smcx , 1999, Mammalian Genome.

[5]  H. Willard,et al.  Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[6]  L. Carrel,et al.  Germ cell development in the XXY mouse: evidence that X chromosome reactivation is independent of sexual differentiation. , 1999, Developmental biology.

[7]  H. Willard,et al.  Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[8]  Song-Yu Yang,et al.  A Human Brain l-3-Hydroxyacyl-coenzyme A Dehydrogenase Is Identical to an Amyloid β-Peptide-binding Protein Involved in Alzheimer’s Disease* , 1998, The Journal of Biological Chemistry.

[9]  V. Chapman,et al.  Escape from X inactivation of Smcx is preceded by silencing during mouse development , 1998, Nature Genetics.

[10]  Brian D. Hendrich,et al.  Identification and characterization of the human XIST gene promoter: implications for models of X chromosome inactivation , 1997, Nucleic Acids Res..

[11]  H. Willard,et al.  Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene. , 1996, Human molecular genetics.

[12]  J. Lawrence,et al.  X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse. , 1996, Human molecular genetics.

[13]  D. Page,et al.  CpG islands in human ZFX and ZFY and mouse Zfx genes: sequence similarities and methylation differences. , 1995, Genomics.

[14]  D. Adler,et al.  The mouse Sb1.8 gene located at the distal end of the X chromosome is subject to X inactivation. , 1995, Human molecular genetics.

[15]  A. Bird,et al.  Sp1 sites in the mouse aprt gene promoter are required to prevent methylation of the CpG island. , 1994, Genes & development.

[16]  Z. Siegfried,et al.  Spl elements protect a CpG island from de novo methylation , 1994, Nature.

[17]  Jingshi Wu,et al.  The murine Xe169 gene escapes X–inactivation like its human homologue , 1994, Nature Genetics.

[18]  R. Dubner,et al.  Cloning of a DNA binding protein that is a tyrosine kinase substrate and recognizes an upstream initiator-like sequence in the promoter of the preprodynorphin gene. , 1994, Brain research. Molecular brain research.

[19]  A. Agulnik,et al.  A novel X gene with a widely transcribed Y-linked homologue escapes X-inactivation in mouse and human. , 1994, Human molecular genetics.

[20]  D. Page,et al.  Functional equivalence of human X– and Y–encoded isoforms of ribosomal protein S4 consistent with a role in Turner syndrome , 1993, Nature Genetics.

[21]  James M. Sikela,et al.  Single pass sequencing and physical and genetic mapping of human brain cDNAs , 1992, Nature Genetics.

[22]  V. Chapman,et al.  Inactivation of the Rps4 gene on the mouse X chromosome. , 1991, Genomics.

[23]  V. Chapman,et al.  Inactivation of the Zfx gene on the mouse X chromosome. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[24]  A. Ashworth,et al.  X-chromosome inactivation may explain the difference in viability of XO humans and mice , 1991, Nature.

[25]  P. Beer-Romero,et al.  Homologous ribosomal protein genes on the human X and Y chromosomes: Escape from X inactivation and possible implications for turner syndrome , 1990, Cell.

[26]  H. Lehrach,et al.  Yeast artificial chromosomes: an alternative approach to the molecular analysis of mouse developmental mutations. , 1990, Genetical research.

[27]  E. Southern,et al.  A model for the separation of large DNA molecules by crossed field gel electrophoresis. , 1987, Nucleic acids research.

[28]  P. Avner,et al.  X-chromosome inactivation in mammals. , 1997, Annual review of genetics.

[29]  C. Disteche,et al.  Escape from X inactivation in human and mouse. , 1995, Trends in genetics : TIG.

[30]  E. Salido,et al.  Isolation and characterization of XE169, a novel human gene that escapes X-inactivation. , 1994, Human molecular genetics.

[31]  A. Bird CpG islands as gene markers in the vertebrate nucleus , 1987 .