Citation: J. Ren et H. Youssoufian, Functional analysis of the putative peroxidase domain of FANCA, the Fanconi anemia complementation group A protein, MOL GEN MET, 72(1), 2001, pp. 54-60
Authors:
Cumming, RC
Lightfoot, J
Beard, K
Youssoufian, H
O'Brien, PJ
Buchwald, M
Citation: Rc. Cumming et al., Fanconi anemia group C protein prevents apoptosis in hematopoietic cells through redox regulation of GSTP1, NAT MED, 7(7), 2001, pp. 816-822
Authors:
Holmes, RK
Harutyunyan, K
Shah, M
Joenje, H
Youssoufian, H
Citation: Rk. Holmes et al., Correction of cross-linker sensitivity of Fanconi anemia group F cells by CD33-mediated protein transfer, BLOOD, 98(13), 2001, pp. 3817-3822
Citation: Fae. Kruyt et H. Youssoufian, Do Fanconi anemia genes control cell response to cross-linking agents by modulating cytochrome P-450 reductase activity?, DRUG RESIST, 3(4), 2000, pp. 211-215
Authors:
Wong, JCY
Alon, N
Norga, K
Kruyt, FAE
Youssoufian, H
Buchwald, M
Citation: Jcy. Wong et al., Cloning and analysis of the mouse Fanconi anemia group a cDNA and an overlapping penta zinc finger cDNA, GENOMICS, 67(3), 2000, pp. 273-283
Authors:
Wang, L
Ogburn, CE
Ware, CB
Ladiges, WC
Youssoufian, H
Martin, GM
Oshima, J
Citation: L. Wang et al., Cellular Werner phenotypes in mice expressing a putative dominant-negativehuman WRN gene, GENETICS, 154(1), 2000, pp. 357-362
Citation: H. Youssoufian et al., Analysis of epitope-tagged forms of the dyskeratosis congenita protein (dyskerin): Identification of a nuclear localization signal, BL CELL M D, 25(20), 1999, pp. 305-309
Citation: V. Gharibyan et H. Youssoufian, Localization of the Bloom syndrome helicase to punctate nuclear structuresand the nuclear matrix and regulation during the cell cycle: Comparison with the Werner's syndrome helicase, MOL CARCINO, 26(4), 1999, pp. 261-273
Authors:
Abou-Zahr, F
Bejjani, B
Kruyt, FAE
Kurg, R
Bacino, C
Shapira, SK
Youssoufian, H
Citation: F. Abou-zahr et al., Normal expression of the Fanconi anemia proteins FAA and FAC and sensitivity to mitomycin C in two patients with Seckel syndrome, AM J MED G, 83(5), 1999, pp. 388-391
Authors:
Waisfisz, Q
de Winter, JP
Kruyt, FAE
de Groot, J
van der Weel, L
Dijkmans, LM
Zhi, Y
Arwert, F
Scheper, RJ
Youssoufian, H
Hoatlin, ME
Joenje, H
Citation: Q. Waisfisz et al., A physical complex of the Fanconi anemia proteins FANCG/XRCC9 and FANCA, P NAS US, 96(18), 1999, pp. 10320-10325
Authors:
Kruyt, FAE
Abou-Zahr, F
Mok, H
Youssoufian, H
Citation: Fae. Kruyt et al., Resistance to mitomycin C requires direct interaction between the fanconi anemia proteins FANCA and FANCG in the nucleus through an arginine-rich domain, J BIOL CHEM, 274(48), 1999, pp. 34212-34218
Authors:
Datta, YH
Youssoufian, H
Marks, PW
Ewenstein, BM
Citation: Yh. Datta et al., Targeting of a heterologous protein to a regulated secretion pathway in cultured endothelial cells, BLOOD, 94(8), 1999, pp. 2696-2703
Citation: Fae. Kruyt et H. Youssoufian, Regulated binding of the Fanconi anemia proteins, FANCA and FANCC - Response, BLOOD, 93(4), 1999, pp. 1431-1432
Citation: H. Youssoufian et al., Protein replacement by receptor-mediated endocytosis corrects the sensitivity of Fanconi anemia group C cells to mitomycin C, BLOOD, 93(1), 1999, pp. 363-369