112301 ⎘
Vector systems having a special element relevant for transcription regulating transport or export of RNA, e.g. RRE, PRE, WPRE, CTE
Method for producing transgenic rats
#302Means and methods for regulating gene expression
#303Adeno-associated virus (AAV) serotype 8 sequences, vectors containing same, and uses therefor
#304Adeno-associated virus (AAV) serotype 8 sequences, vectors containing the same, and uses therefor
#305Lentiviral LTR-deleted vector
#306Lentiviral packaging constructs
#307Method for expression of small antiviral RNA molecules with reduced cytotoxicity within a cell
#308Method for expression of small antiviral RNA molecules within a cell
#309Means and methods for producing a stabilized cell of interest
#310Adenoviral expression vectors
#311Bovine immunodeficiency virus (BIV) based vectors
#312Methods and compositions relating to restricted expression lentiviral vectors and their applications
#313GM-CSF gene therapy for Crohn's disease using an improved regulated expression system
#314Adenovirus packaging cell lines
#315Hiv-dependent expression constructs and uses therefor
#316Adeno-associated virus (AAV) clades, sequences, vectors containing same, and uses therefor
#317Potent combinations of mRNA transport elements
#318Vector system
#319Lentiviral packaging constructs
#320Raav vector-based compositions and methods for the prevention and treatment of mammalian diseases
#321Treatment of disease using an improved regulated expression system
#322Adiponectin gene therapy
#323Use of apotosis inhibiting compounds in degenerative neurological disorders
#324Lentiviral vectors carrying synthetic bi-directional promoters and uses thereof
#325Lentiviral LTR-deleted vector
#326Retroviral vectors with introns
#327Optimization of transgene expression in mammalian cells
#328Adenovirus packaging cell lines
#329Retroviral vectors
#330Lentiviral vectors and uses thereof
#331Bovine immunodeficiency virus (BIV) based vectors
#332Minimal lentiviral vector system
#333Means and methods for producing a protein through chromatin openers that are capable of rendering chromatin more accessible to transcription factors
#334GFAP-based gene therapy for treatment of retinal diseases
#335Lentiviral vectors, related reagents, and methods of use thereof
#336Lentiviral LTR-deleted vector
#337Host cells containing multiple integrating vectors comprising an amplifiable marker
#338Means and methods for regulating gene expression
#339Bovine immunodeficiency virus (BIV) based vectors
#340Compositions and methods of modulating cholesterol metabolism
#341Bovine immunodeficiency virus (BIV) based vectors
#342Bovine immunodeficiency virus (BIV) based vectors
#343Reversible immortalization of human renal proximal tubular epithelial cells
#344Bispecific antibodies
#345Hepatocellular carcinoma specific promoter and uses thereof
#346Host cells containing multiple integrating vectors
#347Method of transducing ES cells
#348Expression vectors
#349Compositions and methods for enhanced expression of recombinant polypeptides from a single vector using a peptide cleavage site
#350Use of chimeric nucleases to stimulate gene targeting
#351Nucleic acid constructs capable of high effeciency delivery of polynucleotides into dna containing organelles and methods of utilizing same
#352Compositions and systems for the regulation of genes
#353Retroviral vectors comprising a functional splice donor site and a functional splice acceptor site
#354Adenovirus packaging cell lines
#355Adenoviral E1A/E1B complementing cell line
#356Compositions and methods for enhanced expression of immunoglobulins from a single vector using a peptide cleavage site
#357Vector system
#358Combination vectors and methods for treating cancer
#359Method for producing transgenic animals