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Human Genetics|February 1, 1988
The CpG dinucleotide and human genetic diseaseD N Cooper, H YoussoufianThe Journal of Clinical Investigation|May 1, 1996
Cytoplasmic localization of FAC is essential for the correction of a prerepair defect in Fanconi anemia group C cellsH YoussoufianProceedings of the National Academy of Sciences of the United States of America|August 16, 1994
Localization of Fanconi anemia C protein to the cytoplasm of mammalian cellsH YoussoufianMolecular Genetics and Metabolism|February 13, 2001
Functional analysis of the putative peroxidase domain of FANCA, the Fanconi anemia complementation group A proteinJ Ren, H YoussoufianThe Journal of Clinical Investigation|February 12, 1998
MxA overexpression reveals a common genetic link in four Fanconi anemia complementation groupsY Li, H YoussoufianMolecular Carcinogenesis|November 24, 1999
Localization of the Bloom syndrome helicase to punctate nuclear structures and the nuclear matrix and regulation during the cell cycle: comparison with the Werner's syndrome helicaseV Gharibyan, H YoussoufianBlood|September 25, 1998
The Fanconi anemia proteins FAA and FAC function in different cellular compartments to protect against cross-linking agent cytotoxicityF A Kruyt, H YoussoufianMolecular and Cellular Biology|January 1, 1993
Transcriptional inhibition of the murine erythropoietin receptor gene by an upstream repetitive elementH Youssoufian, H F LodishBlood Cells, Molecules & Diseases|April 1, 2000
Analysis of epitope-tagged forms of the dyskeratosis congenital protein (dyskerin): identification of a nuclear localization signalH Youssoufian, V Gharibyan, M QatananiPageof 22