Polymorphic X-Chromosome Inactivation of the Human TIMP1 Gene
- 1 September 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 65 (3) , 699-708
- https://doi.org/10.1086/302556
Abstract
No abstract availableKeywords
Funding Information
- Medical Research Council (MT-13690)
This publication has 54 references indexed in Scilit:
- UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1–p11.2European Journal of Human Genetics, 1998
- Escape from X Inactivation of Two New Genes Associated with DXS6974E and DXS7020EGenomics, 1997
- The mouse Smcx gene exhibits developmental and tissue specific variation in degree of escape from X inactivationHuman Molecular Genetics, 1996
- Polymorphic Functional Imprinting of the Human IGF2 Gene among Individuals, in Blood Cells, Is Associated with H19 ExpressionBiochemical and Biophysical Research Communications, 1996
- Cloning and Characterization of a Novel Zinc Finger Gene in Xp11.2Genomics, 1995
- Characterization of a small supernumerary ring X chromosome by fluorescence in situ hybridizationAmerican Journal of Medical Genetics, 1993
- Physical linkage of the A-raf-1, properdin, synapsin I, and TIMP genes on the human and mouse X chromosomesGenomics, 1992
- Age-related reactivation of an X-linked gene close to the inactivation centre in the mouseGenetics Research, 1988
- Position effect variegation in the mouseGenetics Research, 1974
- Stability of X Chromosomal Inactivation in Human Somatic CellsNature, 1972