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Results:
1-13
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Results: 13
Authors:
Kakkis, ED
Schuchman, E
He, X
Wan, Q
Kania, S
Wiemelt, S
Hasson, CW
O'Malley, T
Weil, MA
Aguirre, GA
Brown, DE
Haskins, ME
Citation: Ed. Kakkis et al., Enzyme replacement therapy in feline mucopolysaccharidosis I, MOL GEN MET, 72(3), 2001, pp. 199-208
Authors:
Simonaro, CM
Haskins, ME
Schuchman, EH
Citation: Cm. Simonaro et al., Articular chondrocytes from animals with a dermatan sulfate storage disease undergo a high rate of apoptosis and release nitric oxide and inflammatory cytokines: A possible mechanism underlying degenerative joint disease in the mucopolysaccharidoses, LAB INV, 81(9), 2001, pp. 1319-1328
Authors:
Vite, CH
McGowan, JC
Braund, KG
Drobatz, KJ
Glickson, JD
Wolfe, JH
Haskins, ME
Citation: Ch. Vite et al., Histopathology, electrodiagnostic testing, and magnetic resonance imaging show significant peripheral and central nervous system myelin abnormalitiesin the cat model of alpha-mannosidosis, J NE EXP NE, 60(8), 2001, pp. 817-828
Authors:
Wolfe, JH
Sands, MS
Harel, N
Weil, MA
Parente, MK
Polesky, AC
Reilly, JJ
Hasson, C
Weimelt, S
Haskins, ME
Citation: Jh. Wolfe et al., Gene transfer of low levels of beta-glucuronidase corrects hepatic lysosomal storage in a large animal model of mucopolysaccharidosis VII, MOL THER, 2(6), 2000, pp. 552-561
Authors:
Gao, CH
Sands, MS
Haskins, ME
Ponder, KP
Citation: Ch. Gao et al., Delivery of a retroviral vector expressing human beta-glucuronidase to theliver and spleen decreases lysosomal storage in mucopolysaccharidosis VII mice, MOL THER, 2(3), 2000, pp. 233-244
Authors:
Clawson, JG
Haskins, ME
Citation: Jg. Clawson et Me. Haskins, Beating the career blues, ACAD MGMT E, 14(3), 2000, pp. 91-102
Authors:
He, XX
Li, CM
Simonaro, CM
Wan, Q
Haskins, ME
Desnick, RJ
Schuchman, EH
Citation: Xx. He et al., Identification and characterization of the molecular lesion causing mucopolysaccharidosis type I in cats, MOL GEN MET, 67(2), 1999, pp. 106-112
Authors:
Sun, H
Yang, M
Haskins, ME
Patterson, DF
Wolfe, JH
Citation: H. Sun et al., Retrovirus vector-mediated correction and cross-correction of lysosomal alpha-mannosidase deficiency in human and feline fibroblasts, HUM GENE TH, 10(8), 1999, pp. 1311-1319
Authors:
Daly, TM
Okuyama, T
Vogler, C
Haskins, ME
Muzyczka, N
Sands, MS
Citation: Tm. Daly et al., Neonatal intramuscular injection with recombinant adeno-associated virus results in prolonged beta-glucuronidase expression in situ and correction ofliver pathology in mucopolysaccharidosis type VII mice, HUM GENE TH, 10(1), 1999, pp. 85-94
Authors:
Simonaro, CM
Haskins, ME
Abkowitz, JL
Brooks, DA
Hopwood, JJ
Zhang, J
Schuchman, EH
Citation: Cm. Simonaro et al., Autologous transplantation of retrovirally transduced bone marrow or neonatal blood cells into cats can lead to long-term engraftment in the absence of myeloablation, GENE THER, 6(1), 1999, pp. 107-113
Authors:
Fyfe, JC
Kurzhals, RL
Lassaline, ME
Henthorn, PS
Alur, PRK
Wang, P
Wolfe, JH
Giger, U
Haskins, ME
Patterson, DF
Sun, HC
Jain, S
Yuhki, N
Citation: Jc. Fyfe et al., Molecular basis of feline beta-glucuronidase deficiency: An animal model of mucopolysaccharidosis VII, GENOMICS, 58(2), 1999, pp. 121-128
Authors:
Daly, TM
Vogler, C
Levy, B
Haskins, ME
Sands, MS
Citation: Tm. Daly et al., Neonatal gene transfer leads to widespread correction of pathology in a murine model of lysosomal storage disease, P NAS US, 96(5), 1999, pp. 2296-2300
Authors:
Ray, J
Scarpino, V
Laing, C
Haskins, ME
Citation: J. Ray et al., Biochemical basis of the beta-glucuronidase gene defect causing canine mucopolysaccharidosis VII, J HEREDITY, 90(1), 1999, pp. 119-123
Risultati:
1-13
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