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Results of search for 'au:"Orrison, B M"'
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Authors
Bernard, D J
Bernardini, I
Brannon, P M
Cabin, D E
Charnas, L
Chen, K J
Chiba-Falek, O
Chinault, A C
Dehejia, A
Filie, J D
Lewis, M B
Lewis, R A
Lin, T
Marini, J C
Nussbaum, R L
Orrison, B M
Ozato, K
Suchy, S F
Wan, Y J
Wang, Q
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Topics
Amino Acid Sequence
Animals
Base Sequence
Cell Line
Child, Preschool
Collagen
DNA
Exons
Female
Fibroblasts
Humans
Male
Mice
Molecular Sequence Data
Mutation
Oculocerebrorenal Syndrome
Osteogenesis Imperfecta
Point Mutation
RNA, Messenger
genetics
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English
Your search returned 11 results.
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1.
Primary cultures of rat pancreatic acinar cells in serum-free medium.
[electronic resource]
by
Brannon, P M
Orrison, B M
Kretchmer, N
Producer:
19860326
In:
In vitro cellular & developmental biology : journal of the Tissue Culture Association
vol. 21
Online resources:
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2.
Mouse major histocompatibility class I gene expression begins at midsomite stage and is inducible in earlier-stage embryos by interferon.
[electronic resource]
by
Ozato, K
Wan, Y J
Orrison, B M
Producer:
19850603
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 82
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3.
Two additional cases of osteogenesis imperfecta with substitutions for glycine in the alpha 2(I) collagen chain. A regional model relating mutation location with phenotype.
[electronic resource]
by
Wang, Q
Orrison, B M
Marini, J C
Producer:
19931220
In:
The Journal of biological chemistry
vol. 268
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4.
Induction of major histocompatibility class I antigens by interferons in undifferentiated F9 cells.
[electronic resource]
by
Wan, Y J
Orrison, B M
Lieberman, R
Lazarovici, P
Ozato, K
Producer:
19870420
In:
Journal of cellular physiology
vol. 130
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5.
Mutations are not uniformly distributed throughout the OCRL1 gene in Lowe syndrome patients.
[electronic resource]
by
Lin, T
Orrison, B M
Suchy, S F
Lewis, R A
Nussbaum, R L
Producer:
19981006
In:
Molecular genetics and metabolism
vol. 64
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6.
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.
[electronic resource]
by
Marini, J C
Lewis, M B
Wang, Q
Chen, K J
Orrison, B M
Producer:
19930308
In:
The Journal of biological chemistry
vol. 268
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7.
A de novo G+1-->A mutation at the alpha 2(I) exon 16 splice donor site causes skipping of exon 16 in the cDNA of one allele of an OI type IV proband.
[electronic resource]
by
Filie, J D
Orrison, B M
Wang, Q
Lewis, M B
Marini, J C
Producer:
19940119
In:
Human mutation
vol. 2
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8.
Physical mapping and genomic structure of the Lowe syndrome gene OCRL1.
[electronic resource]
by
Nussbaum, R L
Orrison, B M
Jänne, P A
Charnas, L
Chinault, A C
Producer:
19970326
In:
Human genetics
vol. 99
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9.
Spectrum of mutations in the OCRL1 gene in the Lowe oculocerebrorenal syndrome.
[electronic resource]
by
Lin, T
Orrison, B M
Leahey, A M
Suchy, S F
Bernard, D J
Lewis, R A
Nussbaum, R L
Producer:
19970710
In:
American journal of human genetics
vol. 60
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10.
Human and mouse alpha-synuclein genes: comparative genomic sequence analysis and identification of a novel gene regulatory element.
[electronic resource]
by
Touchman, J W
Dehejia, A
Chiba-Falek, O
Cabin, D E
Schwartz, J R
Orrison, B M
Polymeropoulos, M H
Nussbaum, R L
Producer:
20010301
In:
Genome research
vol. 11
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11.
New autosomal recessive syndrome of sparse hair, osteopenia, and mental retardation in Mennonite sisters.
[electronic resource]
by
Kaler, S G
Garrity, A M
Stern, H J
Rosenbaum, K N
Orrison, B M
Marini, J C
Bernardini, I
Saal, H M
Producer:
19921113
In:
American journal of medical genetics
vol. 43
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