Jian Ming Xu - Plano TX Patrick N. Sollee - Richardson TX Adam E. T. Bryant - Oxfordshire, GB
Assignee:
Nortel Networks Corporation - Montreal
International Classification:
H04Q 720
US Classification:
455435
Abstract:
A system and method for increasing capacity of a cellular system by reducing call overhead processing and transmission congestion previously required in updating a subscriber's mobile station data position as the subscriber moves among locations within a geographic area served by a network service provider is presented. A predetermined N number of copies of mobile station subscriber data is distributed among multiple Visiting Location Registers (VLRs) within the area served by a cellular system. Unlike previous systems, when mobile stations traverse location boundaries, the current VLR corresponding to the current location does not need to update the subscriber data if that data has not changed since the subscriber was last in that location.
Distributed Subscriber Data Management In Wireless Networks From A Central Perspective
Jian Ming Xu - Plano TX Patrick N. Sollee - Richardson TX Adam E. T. Bryant - Benson, GB
Assignee:
Nortel Networks Corporation - Montreal
International Classification:
H04Q 720
US Classification:
455433
Abstract:
A system and method for increasing capacity of a cellular system by reducing call overhead processing and transmission congestion previously required in updating a subscriber's mobile station data position as the subscriber moves among locations within a geographic area served by a network service provider is presented. A predetermined N number of copies of mobile station subscriber data is distributed among multiple Visiting Location Registers (VLRs) within the area served by a cellular system. Unlike previous systems, when mobile stations traverse location boundaries, the current VLR corresponding to the current location does not need to update the subscriber data if that data has not changed since the subscriber was last in that location.
Targeting Bcl11A Distal Regulatory Elements For Fetal Hemoglobin Reinduction
Provided herein are methods and compositions for increasing fetal hemoglobin levels in a cell by disrupting BCL11A expression at the genomic level. Also provided herein are methods and compositions relating to the treatment of hemoglobinopathies by reinduction of fetal hemoglobin levels.
In Situ And In Vivo Analysis Of Chromatin Interactions By Biotinylated Dcas9 Protein
The present invention includes a method for detecting or isolating one or more specific genomic target regions and molecules interacting therewith comprising: contacting a recombinant nuclease-deficient Cas9 fusion protein (dCas9) modified to comprise a biotinylation sequence and one or more sequence-specific guide RNAs, with one or more specific genomic DNA targets in cells to form a CRISPR complex; and detecting or isolating the CRISPR complex with a streptavidin or an avidin to detect or isolate the one or more specific genomic target regions and molecules in the CRISPR complex.
Targeting Bcl11A Distal Regulatory Elements For Fetal Hemoglobin Reinduction
Provided herein are methods and compositions for increasing fetal hemoglobin levels in a cell by disrupting BCL11A expression at the genomic level. Also provided herein are methods and compositions relating to the treatment of hemoglobinopathies by reinduction of fetal hemoglobin levels.
Targeting Bcl11A Distal Regulatory Elements For Fetal Hemoglobin Reinduction
- Boston MA, US Daniel E. BAUER - Cambridge MA, US Jian XU - Plano TX, US
Assignee:
CHILDREN'S MEDICAL CENTER CORPORATION - Boston MA
International Classification:
C12N 15/01 A61K 38/46 A61K 35/12 C12N 9/22
Abstract:
Provided herein are methods and compositions for increasing fetal hemoglobin levels in a cell by disrupting BCL11A expression at the genomic level. Also provided herein are methods and compositions relating to the treatment of hemoglobinopathies by reinduction of fetal hemoglobin levels.