Spectrum of mutations in the OCRL1 gene in the Lowe oculocerebrorenal syndrome
LIN, T, ORRISON, B. M, LEAHEY, A.-M, SUCHY, S. F, BERNARD, D. J, LEWIS, R. A, NUSSBAUM, R. L
Published in American journal of human genetics (01.06.1997)
Published in American journal of human genetics (01.06.1997)
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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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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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Journal Article
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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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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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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