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X.O Breakefield

Veröffentlichungen von X.O Breakefield zu Breakefield, X. O. ->
weitere Veröffentlichungen von X.O Breakefield:
Molecular Genetic Insights into Neurologic Diseases (1987)
Dexamethasone selectively increases monoamine oxidase type a in human skin fibroblasts (1981)
Highly polymorphic (GT)"n repeat sequence in intron II of the human MAOB gene (1992)
Isolation of the mRNA encoding ratliver catechol-O-methyltransferase (1989)
Differences in monoamine oxidase activity between cultured noradrenergic and cholinergic sympathetic neurons (1987)
Physical fine-mapping of a deletion spanning the Norrie gene (1989)
Characterization and mapping of the mouse NDP (Norrie disease) locus (Ndp) (1996)
Genetik der Dystonien (2000)
Monoamine oxidase and catechol-o-methyltransferase activities in cultured fibroblasts and blood cells from children with autism and the Gilles de la Tourette syndrome (1980)
Isolation and characterization of a candidate gene for Norrie disease (1992)
A mutation in the Norrie disease gene (NDP) associated with X–linked familial exudative vitreoretinopathy (1993)
Plasma amine oxidase activities in Norrie disease patients with an X-chromosomal deletion affecting monoamine oxidase (1991)
A genetic linkage map of human chromosome 9q (1992)
Organization of the human monoamine oxidase genes and long-range physical mapping around them (1992)
Organization of the human monoamine oxidase genes and long-range physical mapping around them (1992)
Veröffentlichungen zu Breakefield, X. O.
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1
Breakefield, X O., Cambi, F. Molecular Genetic Insights into Neurologic Diseases
in: Annual Review of Neuroscience, in: Annual Review of Neuroscience. - Palo Alto, Calif., ISSN 0147-006X Vol. 10 (1987), p. 535-594
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1987
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2
Edelstein, S.B., Breakefield, X.O. Dexamethasone selectively increases monoamine oxidase type a in human skin fibroblasts
in: Biochemical and Biophysical Research Communications, in: Biochemical and Biophysical Research Communications . - Amsterdam : Elsevier, ISSN 0006-291X, ZDB-ID 1461396-7 Vol. 98, No. 3 (1981), p. 836-843
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1981
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3
Konradi, C., Ozelius, L., ... Highly polymorphic (GT)"n repeat sequence in intron II of the human MAOB gene
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 12, No. 1 (1992), p. 176-177
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1992
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4
Grossman, M.H., Creveling, C.R., ... Isolation of the mRNA encoding ratliver catechol-O-methyltransferase
in: Biochemical and Biophysical Research Communications, in: Biochemical and Biophysical Research Communications . - Amsterdam : Elsevier, ISSN 0006-291X, ZDB-ID 1461396-7 Vol. 158, No. 3 (1989), p. 776-782
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1989
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5
Pintar, J.E., Breakefield, X.O., ... Differences in monoamine oxidase activity between cultured noradrenergic and cholinergic sympathetic neurons
in: Developmental Biology, in: Developmental Biology . - Amsterdam : Elsevier, ISSN 0012-1606, ZDB-ID 1463203-2 Vol. 120, No. 1 (1987), p. 305-308
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1987
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6
Diergaarde, P. J., Wieringa, B., ... Physical fine-mapping of a deletion spanning the Norrie gene
in: Human genetics , ISSN 1432-1203, Vol. 84 (1. 1989), p. 22-26
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1989
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7
Battinelli, E.M., Boyd, Y., ... Characterization and mapping of the mouse NDP (Norrie disease) locus (Ndp)
in: Mammalian genome , ISSN 1432-1777, Vol. 7 (2. 1996), p. 93-97
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1996
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8
Klein, Ch., Kann, M., ... Genetik der Dystonien
in: Der Nervenarzt , ISSN 1433-0407, Vol. 71 (6. 2000), p. 431-441
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2000
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9
Giller, E.L., Young, J.G., ... Monoamine oxidase and catechol-o-methyltransferase activities in cultured fibroblasts and blood cells from children with autism and the Gilles de la Tourette syndrome
in: Psychiatry Research, in: Psychiatry Research . - Amsterdam : Elsevier, ISSN 0165-1781, ZDB-ID 1500675-X Vol. 2, No. 2 (1980), p. 187-197
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1980
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10
Chen, Z-Y., Hendriks, R.W., ... Isolation and characterization of a candidate gene for Norrie disease
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 1, No. 3 (1992), p. 204-208
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1992
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11
Chen, Z-Y., Battinelli, E.M., ... A mutation in the Norrie disease gene (NDP) associated with X–linked familial exudative vitreoretinopathy
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 5, No. 2 (1993), p. 180-183
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1993
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12
Murphy, D. L., Sims, K. B., ... Plasma amine oxidase activities in Norrie disease patients with an X-chromosomal deletion affecting monoamine oxidase
in: Journal of neural transmission , ISSN 1435-1463, Vol. 83 (1/2. 1991), p. 1-12
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1991
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13
Ozelius, L.J., Kwiatkowski, D.J., ... A genetic linkage map of human chromosome 9q
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 14, No. 3 (1992), p. 715-720
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1992
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14
Chen, Z.Y., Powell, J.F., ... Organization of the human monoamine oxidase genes and long-range physical mapping around them
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 14, No. 1 (1992), p. 75-82
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1992
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15
Chen, Z.Y., Powell, J.F., ... Organization of the human monoamine oxidase genes and long-range physical mapping around them
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 14, No. 1 (1992), p. 75-82
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1992
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16
Ozelius, L.J., Kwiatkowski, D.J., ... A genetic linkage map of human chromosome 9q
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 14, No. 3 (1992), p. 715-720
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1992
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17
Levy, E.R., Powell, J.F., ... Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization: Implications for norrie disease
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 5, No. 2 (1989), p. 368-370
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1989
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18
Breakefield, X.O., Giller, E.L., ... Monoamine oxidase type a in fibroblasts from patients with bipolar depressive illness
in: Psychiatry Research, in: Psychiatry Research . - Amsterdam : Elsevier, ISSN 0165-1781, ZDB-ID 1500675-X Vol. 2, No. 3 (1980), p. 307-314
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1980
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19
Ozelius, L., Hsu, Y.-P.P., ... Human monoamine oxidase gene (MAOA): Chromosome position (Xp21-p11) and DNA polymorphism
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 3, No. 1 (1988), p. 53-58
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1988
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20
Chen, Z.-Y., Battinelli, E.M., ... Norrie Disease Gene: Characterization of Deletions and Possible Function
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 16, No. 2 (1993), p. 533-535
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1993