Transgenic mice that express a mini-gene version of the human gene for type I procollagen (COL1A1) develop a phenotype resembling a lethal form of osteogenesis imperfecta (Q67765285)

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scientific article published on 01 December 1991

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English	Transgenic mice that express a mini-gene version of the human gene for type I procollagen (COL1A1) develop a phenotype resembling a lethal form of osteogenesis imperfecta	scientific article published on 01 December 1991

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scholarly article

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17 September 2019

Transgenic mice that express a mini-gene version of the human gene for type I procollagen (COL1A1) develop a phenotype resembling a lethal form of osteogenesis imperfecta (English)

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17 September 2019

osteogenesis imperfecta

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based on heuristic

inferred from title

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10.1016/S0021-9258(18)54506-3

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J. S. Khillan

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A. S. Olsen

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S. Kontusaari

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B. Sokolov

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D. J. Prockop

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1 December 1991

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5 December 1991

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full work available at URL

http://intl.jbc.org/cgi/content/abstract/266/34/23373

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Journal of Biological Chemistry

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23373-23379

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17 September 2019

Reduced secretion of structurally abnormal type I procollagen in a form of osteogenesis imperfecta

1

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10.1016/S0021-9258(18)54506-3

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14 November 2022

Intron-mediated recombination may cause a deletion in an alpha 1 type I collagen chain in a lethal form of osteogenesis imperfecta

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10.1016/S0021-9258(18)54506-3

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Nucleotide sequences of complementary deoxyribonucleic acids for the pro alpha 1 chain of human type I procollagen. Statistical evaluation of structures that are conserved during evolution.

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10.1016/S0021-9258(18)54506-3

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Brittle bones--fragile molecules: disorders of collagen gene structure and expression

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10.1016/S0021-9258(18)54506-3

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Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

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10.1016/S0021-9258(18)54506-3

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Internal deletion in a collagen gene in a perinatal lethal form of osteogenesis imperfecta.

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10.1016/S0021-9258(18)54506-3

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14 November 2022

Folding of collagen IV

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10.1016/S0021-9258(18)54506-3

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The zipper-like folding of collagen triple helices and the effects of mutations that disrupt the zipper

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10.1016/S0021-9258(18)54506-3

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Characterization of 64-, 123- and 182-base-pair exons in the mouse alpha 2(IV) collagen gene.

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10.1016/S0021-9258(18)54506-3

https://api.crossref.org/works/10.1016/S0021-9258(18)54506-3

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Mutations in human procollagen genes. Consequences of the mutations in man and in transgenic mice

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10.1016/S0021-9258(18)54506-3

https://api.crossref.org/works/10.1016/S0021-9258(18)54506-3

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A rapid procedure for routine double staining of cartilage and bone in fetal and adult animals.

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10.1016/S0021-9258(18)54506-3

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14 November 2022

Introduction of the human pro alpha 1(I) collagen gene into pro alpha 1(I)-deficient Mov-13 mouse cells leads to formation of functional mouse-human hybrid type I collagen

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10.1016/S0021-9258(18)54506-3

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Detection of specific sequences among DNA fragments separated by gel electrophoresis

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10.1016/S0021-9258(18)54506-3

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Mutation in a gene for type I procollagen (COL1A2) in a woman with postmenopausal osteoporosis: evidence for phenotypic and genotypic overlap with mild osteogenesis imperfecta

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10.1016/S0021-9258(18)54506-3

https://api.crossref.org/works/10.1016/S0021-9258(18)54506-3

14 November 2022

Perinatal lethal osteogenesis imperfecta in transgenic mice bearing an engineered mutant pro-alpha 1(I) collagen gene

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10.1016/S0021-9258(18)54506-3

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Bone disease cracks genetics

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14 November 2022

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Europe PubMed Central

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17 September 2019

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