Extensive enteric nervous system abnormalities in mice transgenic for artificial chromosomes containing Parkinson disease-associated α-synuclein gene mutations precede central nervous system changes
Kuo, Yien-Ming, Li, Zhishan, Jiao, Yun, Gaborit, Nathalie, Pani, Amar K., Orrison, Bonnie M., Bruneau, Benoit G., Giasson, Benoit I., Smeyne, Richard J., Gershon, Michael D., Nussbaum, Robert L.
Published in Human molecular genetics (01.05.2010)
Published in Human molecular genetics (01.05.2010)
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Expansion of the Parkinson disease-associated SNCA-Rep1 allele upregulates human α-synuclein in transgenic mouse brain
Cronin, Kenneth D., Ge, Dongliang, Manninger, Paul, Linnertz, Colton, Rossoshek, Anna, Orrison, Bonnie M., Bernard, David J., El-Agnaf, Omar M.A., Schlossmacher, Michael G., Nussbaum, Robert L., Chiba-Falek, Ornit
Published in Human molecular genetics (01.09.2009)
Published in Human molecular genetics (01.09.2009)
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Transgenic mice expressing S129 phosphorylation mutations in α-synuclein
Escobar, Valerie Drews, Kuo, Yien-Ming, Orrison, Bonnie M, Giasson, Benoit I, Nussbaum, Robert L
Published in Neuroscience letters (20.03.2014)
Published in Neuroscience letters (20.03.2014)
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Physical mapping and genomic structure of the Lowe syndrome gene OCRL1
NUSSBAUM, R. L, ORRISON, B. M, JÄNNE, P. A, CHARNAS, L, CHINAULT, A. C
Published in Human genetics (01.02.1997)
Published in Human genetics (01.02.1997)
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Human and mouse alpha-synuclein genes: comparative genomic sequence analysis and identification of a novel gene regulatory element
Touchman, J W, Dehejia, A, Chiba-Falek, O, Cabin, D E, Schwartz, J R, Orrison, B M, Polymeropoulos, M H, Nussbaum, R L
Published in Genome research (01.01.2001)
Published in Genome research (01.01.2001)
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Journal Article
Extensive enteric nervous system abnormalities in mice transgenic for artificial chromosomes containing Parkinson disease-associated a-synuclein gene mutations precede central nervous system changes
Kuo, Yien-Ming, Li, Zhishan, Jiao, Yun, Gaborit, Nathalie, Pani, Amar K, Orrison, Bonnie M, Bruneau, Benoit G, Giasson, Benoit I, Smeyne, Richard J, Gershon, Michael D, Nussbaum, Robert L
Published in Human molecular genetics (01.05.2010)
Published in Human molecular genetics (01.05.2010)
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Journal Article
Expansion of the Parkinson disease-associated SNCA-Rep1 allele upregulates human [alpha]-synuclein in transgenic mouse brain
Cronin, Kenneth D, Ge, Dongliang, Manninger, Paul, Colton Linnertz, Rossoshek, Anna, Orrison, Bonnie M, Bernard, David J, Omar M.a. El-agnaf, Schlossmacher, Michael G, Nussbaum, Robert L, Chiba-falek, Ornit
Published in Human molecular genetics (01.09.2009)
Published in Human molecular genetics (01.09.2009)
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Mutations are not uniformly distributed throughout the OCRL1 gene in Lowe syndrome patients
Lin, T, Orrison, B M, Suchy, S F, Lewis, R A, Nussbaum, R L
Published in Molecular genetics and metabolism (01.05.1998)
Published in Molecular genetics and metabolism (01.05.1998)
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Serine for glycine substitutions in type I collagen in two cases of type IV osteogenesis imperfecta (OI). Additional evidence for a regional model of OI pathophysiology
MARINI, J. C, LEWIS, M. B, QIN WANG, CHEN, K. J, ORRISON, B. M
Published in The Journal of biological chemistry (05.02.1993)
Published in The Journal of biological chemistry (05.02.1993)
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Induction of major histocompatibility class I antigens by interferons in undifferentiated F9 cells
Wan, Y J, Orrison, B M, Lieberman, R, Lazarovici, P, Ozato, K
Published in Journal of cellular physiology (01.02.1987)
Published in Journal of cellular physiology (01.02.1987)
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Primary cultures of rat pancreatic acinar cells in serum-free medium
Brannon, P M, Orrison, B M, Kretchmer, N
Published in In vitro cellular & developmental biology (01.01.1985)
Published in In vitro cellular & developmental biology (01.01.1985)
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New autosomal recessive syndrome of sparse hair, osteopenia, and mental retardation in Mennonite sisters
Kaler, S G, Garrity, A M, Stern, H J, Rosenbaum, K N, Orrison, B M, Marini, J C, Bernardini, I, Saal, H M
Published in American journal of medical genetics (01.08.1992)
Published in American journal of medical genetics (01.08.1992)
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