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Results: 1-25/34
Authors:
Arruda, VR
Fields, PA
Milner, R
Wainwright, L
De Miguel, MP
Donovan, PJ
Herzog, RW
Nichols, TC
Biegel, JA
Razavi, M
Dake, M
Huff, D
Flake, AW
Couto, L
Kay, MA
High, KA
Citation: Vr. Arruda et al., Lack of germline transmission of vector sequences following systemic administration of recombinant AAV-2 vector in males, MOL THER, 4(6), 2001, pp. 586-592
Authors:
Park, F
Kay, MA
Citation: F. Park et Ma. Kay, Modified HIV-1 based lentiviral vectors have an effect on viral transduction efficiency and gene expression in vitro and in vivo, MOL THER, 4(3), 2001, pp. 164-173
Authors:
Stoll, SM
Sclimenti, CR
Baba, EJ
Meuse, L
Kay, MA
Calos, MP
Citation: Sm. Stoll et al., Epstein-Barr virus/human vector provides high-level, long-term expression of alpha(1)-antitrypsin in mice, MOL THER, 4(2), 2001, pp. 122-129
Authors:
Chen, ZY
Yant, SR
He, CY
Meuse, L
Shen, S
Kay, MA
Citation: Zy. Chen et al., Linear DNAs concatemerize in vivo and result in sustained transgene expression in mouse liver, MOL THER, 3(3), 2001, pp. 403-410
Authors:
Kay, MA
Glorioso, JC
Naldini, L
Citation: Ma. Kay et al., Viral vectors for gene therapy: the art of turning infectious agents into vehicles of therapeutics, NAT MED, 7(1), 2001, pp. 33-40
Authors:
Mizuguchi, H
Koizumi, N
Hosono, T
Utoguchi, N
Watanabe, Y
Kay, MA
Hayakawa, T
Citation: H. Mizuguchi et al., A simplified system for constructing recombinant adenoviral vectors containing heterologous peptides in the Hl loop of their fiber knob, GENE THER, 8(9), 2001, pp. 730-735
Authors:
Ohashi, K
Park, F
Kay, MA
Citation: K. Ohashi et al., Hepatocyte transplantation: clinical and experimental application, J MOL MED-J, 79(11), 2001, pp. 617-630
Authors:
Mizuguchi, H
Kay, MA
Hayakawa, T
Citation: H. Mizuguchi et al., In vitro ligation-based cloning of foreign DNAs into the E3 and E1 deletion regions for generation of recombinant adenovirus vectors, BIOTECHNIQU, 30(5), 2001, pp. 1112
Authors:
Kay, MA
Citation: Ma. Kay, Pregnant women violent men, MIDWIFERY, 17(3), 2001, pp. 246-246
Authors:
Kay, MA
Citation: Ma. Kay, Anthropologist of domestic care, W J NURS R, 23(8), 2001, pp. 783-794
Authors:
Alexander, I
Andres, MS
Braithwaite, CJR
Braga, JC
Cooper, MJ
Davies, PJ
Elderfield, PJ
Gilmour, H
Kay, MA
Kroon, RLF
McKenzie, D
Montaggioni, JA
Skinner, LF
Thompson, A
Vasconcelos, R
Webster, CJ
Wilson, PA
Citation: I. Alexander et al., New constraints on the origin of the Australian Great Barrier Reef: Results from an international project of deep coring, GEOLOGY, 29(6), 2001, pp. 483-486
Authors:
Ohashi, K
Meuse, L
Schwall, R
Kay, MA
Citation: K. Ohashi et al., cMet activation allows persistent engraftment of ectopically transplanted xenogenic human hepatocytes in mice, TRANSPLAN P, 33(1-2), 2001, pp. 587-588
Authors:
Vollrath, D
Feng, W
Duncan, JL
Yasumura, D
D'Cruz, PM
Chappelow, A
Matthes, MT
Kay, MA
LaVail, MM
Citation: D. Vollrath et al., Correction of the retinal dystrophy phenotype of the RCS rat by viral genetransfer of Mertk, P NAS US, 98(22), 2001, pp. 12584-12589
Authors:
Nakai, H
Yant, SR
Storm, TA
Fuess, S
Meuse, L
Kay, MA
Citation: H. Nakai et al., Extrachromosomal recombinant adeno-associated virus vector genomes are primarily responsible for stable liver transduction in vivo, J VIROLOGY, 75(15), 2001, pp. 6969-6976
Authors:
Miao, CH
Ohashi, K
Patijn, GA
Meuse, L
Ye, X
Thompson, AR
Kay, MA
Citation: Ch. Miao et al., Inclusion of the hepatic locus control region, an intron, and untranslatedregion increases and stabilizes hepatic factor IX gene expression in vivo but not in vitro, MOL THER, 1(6), 2000, pp. 522-532
Authors:
Nakai, H
Storm, TA
Kay, MA
Citation: H. Nakai et al., Increasing the size of rAAV-mediated expression cassettes in vivo by intermolecular joining of two complementary vectors, NAT BIOTECH, 18(5), 2000, pp. 527-532
Authors:
Ohashi, K
Marion, PL
Nakai, H
Meuse, L
Cullen, JM
Bordier, BB
Schwall, R
Greenberg, HB
Glenn, JS
Kay, MA
Citation: K. Ohashi et al., Sustained survival of human hepatocytes in mice: A model for in vivo infection with human hepatitis B and hepatitis delta viruses, NAT MED, 6(3), 2000, pp. 327-331
Authors:
Yant, SR
Meuse, L
Chiu, W
Ivics, Z
Izsvak, Z
Kay, MA
Citation: Sr. Yant et al., Somatic integration and long-term transgene expression in normal and haemophilic mice using a DNA transposon system, NAT GENET, 25(1), 2000, pp. 35-41
Authors:
Kay, MA
Manno, CS
Ragni, MV
Larson, PJ
Couto, LB
McClelland, A
Glader, B
Chew, AJ
Tai, SJ
Herzog, RW
Arruda, V
Johnson, F
Scallan, C
Skarsgard, E
Flake, AW
High, KA
Citation: Ma. Kay et al., Evidence for gene transfer and expression of factor IX in haemophilia B patients treated with an AAV vector, NAT GENET, 24(3), 2000, pp. 257-261
Authors:
Park, F
Ohashi, K
Chiu, W
Naldini, L
Kay, MA
Citation: F. Park et al., Efficient lentiviral transduction of liver requires cell cycling in vivo, NAT GENET, 24(1), 2000, pp. 49-52
Authors:
Miao, CH
Nakai, H
Thompson, AR
Storm, TA
Chiu, W
Snyder, RO
Kay, MA
Citation: Ch. Miao et al., Nonrandom transduction of recombinant adeno-associated virus vectors in mouse hepatocytes in vivo: Cell cycling does not influence hepatocyte transduction, J VIROLOGY, 74(8), 2000, pp. 3793-3803
Authors:
Nakai, H
Storm, TA
Kay, MA
Citation: H. Nakai et al., Recruitment of single-stranded recombinant adeno-associated virus vector genomes and intermolecular recombination are responsible for stable transduction of liver in vivo, J VIROLOGY, 74(20), 2000, pp. 9451-9463
Authors:
Lieber, A
Kay, MA
Li, ZY
Citation: A. Lieber et al., Nuclear import of moloney murine leukemia virus DNA mediated by adenoviruspreterminal protein is not sufficient for efficient retroviral transduction in nondividing cells, J VIROLOGY, 74(2), 2000, pp. 721-734
Authors:
Park, F
Ohashi, K
Kay, MA
Citation: F. Park et al., Therapeutic levels of human factor VIII and IX using HIV-1-based lentiviral vectors in mouse liver, BLOOD, 96(3), 2000, pp. 1173-1176
Authors:
Snyder, RO
Miao, C
Meuse, L
Tubb, J
Donahue, BA
Lin, HF
Stafford, DW
Patel, S
Thompson, AR
Nichols, T
Read, MS
Bellinger, DA
Brinkhous, KM
Kay, MA
Citation: Ro. Snyder et al., Correction of hemophilia B in canine and murine models using recombinant adeno-associated viral vectors, NAT MED, 5(1), 1999, pp. 64-70