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Last Updated: September 26, 2020

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Patent: 6,077,667

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Summary for Patent: 6,077,667
Title: Method for chromosomal rearrangement by consecutive gene targeting of two recombination substrates to the deletion endpoints
Abstract:The present invention involves the creation of defined chromosomal deficiencies, inversions and duplications using Cre recombinase in ES cells transmitted into the mouse germ line. These chromosomal reconstructions can extend up to 3-4 cM. Chromosomal rearrangements are the major cause of inherited human disease and fetal loss. Additionally, translocations and deletions are recognized as major genetic changes that are causally involved in neoplasia. Chromosomal variants such as deletions and inversions are exploited commonly as genetic tools in organisms such as Drosophila. Mice with defined regions of segmental haploidy are useful for genetic screening and allow accurate models of human chromosomal diseases to be generated.
Inventor(s): Bradley; Allan (Houston, TX), Ramirez-Solis; Ramiro (Missouri City, TX), Liu; Pentao (Fredrick, MD), Su; Hong (Houston, TX), Zheng; Binhai (Houston, TX)
Application Number:08/883,616
Patent Claims:see list of patent claims

Details for Patent 6,077,667

Applicant Tradename Biologic Ingredient Dosage Form BLA Number Approval Date Patent No. Assignee Estimated Patent Expiration Status Orphan Source
Schering INTRON A interferon alfa-2b VIAL 103132 001 1986-06-04   Start Trial 2016-06-26 RX search
Schering INTRON A interferon alfa-2b VIAL 103132 002 1986-06-04   Start Trial 2016-06-26 RX search
Schering INTRON A interferon alfa-2b VIAL 103132 003 1986-06-04   Start Trial 2016-06-26 RX search
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Number >Approval Date >Patent No. >Assignee >Estimated Patent Expiration >Status >Orphan >Source

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