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Gene Therapy (36)
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Showing 1–50 of 67 results

Advanced filters: Author: M Perricaudet Clear advanced filters

Adenovirus–mediated in vivo gene transfer and expression in normal rat liver

H. A. Jaffe
C. Danel
R. G. Crystal
Research01 Aug 1992
Nature Genetics

Volume: 1, P: 372-378
Augmentation of blood platelet levels by intratracheal administration of an adenovirus vector encoding human thrombopoietin cDNA

Salvatore J. Cannizzo
Beat M. Frey
Ronald G. Crystal
Research01 Jun 1997
Nature Biotechnology

Volume: 15, P: 570-573
Adenovirus mediated expression of therapeutic plasma levels of human factor IX in mice

Theodore A. G. Smith
Michele G. Mehaffey
Michael Kaleko
Research01 Dec 1993
Nature Genetics

Volume: 5, P: 397-402
Immune responses to transgene–encoded proteins limit the stability of gene expression after injection of replication–defective adenovirus vectors

Sandeep K. Tripathy
Hugh B. Black
Jeffrey M. Leiden
Research01 May 1996
Nature Medicine

Volume: 2, P: 545-550
Expression of class I major histocompatibility antigens switched off by highly oncogenic adenovirus 12 in transformed rat cells

P. I. Schrier
R. Bernards
A. J. van der Eb
Research27 Oct 1983
Nature

Volume: 305, P: 771-775
Direct gene transfer of human CFTR into human bronchial epithelia of xenografts with E1–deleted adenoviruses

John F. Engelhardt
Yiping Yang
James M. Wilson
Research01 May 1993
Nature Genetics

Volume: 4, P: 27-34
Intracoronary gene transfer of fibroblast growth factor–5 increases blood flow and contractile function in an ischemic region of the heart

Frank J. Giordano
Peipei Ping
H. Kirk Hammond
Research01 May 1996
Nature Medicine

Volume: 2, P: 534-539
Nucleotide sequence homology at 12 intron–exon junctions in the chick ovalbumin gene

J. F. Catterall
B. W. O'Malley
G. G. Brownlee
Research12 Oct 1978
Nature

Volume: 275, P: 510-513
Recombinant IL–12 prevents formation of blocking IgA antibodies to recombinant adenovirus and allows repeated gene therapy to mouse lung

Yiping Yang
Giorgio Trinchieri
James M. Wilson
Research01 Sept 1995
Nature Medicine

Volume: 1, P: 890-893
Tumorigenicity of cells transformed by adenovirus type 12 by evasion of T-cell immunity

R. Bernards
P. I. Schrier
C. J. M. Melief
Research27 Oct 1983
Nature

Volume: 305, P: 776-779
A model system for in vivo gene transfer into the central nervous system using an adenoviral vector

Beverly L. Davidson
Edward D. Allen
Blake J. Roessler
Research01 Mar 1993
Nature Genetics

Volume: 3, P: 219-223
Adenovirus-mediated gene transfer in dog prostate: a preclinical study of a relevant model system for gene therapy of human prostatic cancer

M Andrawiss
P Opolon
O Cussenot
Research22 Feb 1999
Prostate Cancer and Prostatic Diseases

Volume: 2, P: 25-35
Adenovirus vectors for gene transduction into mobilized blood CD34⁺ cells

M Bregni
S Shammah
AM Gianni
Research30 Apr 1998
Gene Therapy

Volume: 5, P: 465-472
A method to codetect introduced genes and their products in gene therapy protocols

Emanuela Gussoni
Yaming Wang
Louis M. Kunkel
Research01 Aug 1996
Nature Biotechnology

Volume: 14, P: 1012-1016
Efficient adenovirus-mediated gene transduction of normal and leukemic hematopoietic cells

MR Huang
M Olsson
TH Tötterman
Research01 Oct 1997
Gene Therapy

Volume: 4, P: 1093-1099
DNA sequence and expression of the B95-8 Epstein—Barr virus genome

R. Baer
A. T. Bankier
B. G. Barrell
Research19 Jul 1984
Nature

Volume: 310, P: 207-211
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

W. K. Cavenee
T. P. Dryja
R. L. White
Research27 Oct 1983
Nature

Volume: 305, P: 779-784
Inter- and intraspecific variation in restriction maps of Drosophila mitochondrial DNAs

D. M. Shah
C. H. Langley
Research25 Oct 1979
Nature

Volume: 281, P: 696-699
Inactivation of E2a in recombinant adenoviruses improves the prospect for gene therapy in cystic fibrosis

Yiping Yang
Frederick A. Nunes
James M. Wilson
Research01 Jul 1994
Nature Genetics

Volume: 7, P: 362-369
Structural insights into influenza A virus ribonucleoproteins reveal a processive helical track as transcription mechanism

In this Article, the authors identify the mechanism of influenza virus transcription in viral ribonucleoproteins (vRNPs). This processive helical track mechanism is enabled by the extreme flexibility of the helical part of the vRNP, which allows the polymerase to move over the genome while bound to both RNA ends.

Rocío Coloma
Rocío Arranz
Jaime Martín-Benito
Research09 Mar 2020
Nature Microbiology

Volume: 5, P: 727-734
Improved efficiency of arterial gene transfer by use of poloxamer 407 as a vehicle for adenoviral vectors

LJ Feldman
CJ Pastore
JM Isner
Research01 Mar 1997
Gene Therapy

Volume: 4, P: 189-198
In vivo adenovirus-mediated delivery of a uPA/uPAR antagonist reduces retinal neovascularization in a mouse model of retinopathy

L Le Gat
K Gogat
M Abitbol
Research03 Nov 2003
Gene Therapy

Volume: 10, P: 2098-2103
Pre-treatment with elastase improves the efficiency of percutaneous adenovirus-mediated gene transfer to the arterial media

L Maillard
M Ziol
PhG Steg
Research17 Aug 1998
Gene Therapy

Volume: 5, P: 1023-1030
Adenovirus-mediated delivery of a uPA/uPAR antagonist suppresses angiogenesis-dependent tumor growth and dissemination in mice

H Li
H Lu
P Yeh
Research17 Aug 1998
Gene Therapy

Volume: 5, P: 1105-1113
Adenovirus-mediated gene transfer of a human IL-6 antagonist

I Saggio
L Ciapponi
M Perricaudet
Research01 Aug 1997
Gene Therapy

Volume: 4, P: 839-845
Are U4 small nuclear ribonucleoproteins involved in polyadenylation?

Susan M. Berget
Research10 May 1984
Nature

Volume: 309, P: 179-182
Differences in A and B forms of monoamine oxidase revealed by limited proteolysis and peptide mapping

Richard M. Cawthon
Xandra O. Breakefield
Research25 Oct 1979
Nature

Volume: 281, P: 692-694
Specific integration of REV proviruses in avian bursal lymphomas

M. Reza Noori-Daloii
Robert A. Swift
Richard L. Witter
Research10 Dec 1981
Nature

Volume: 294, P: 574-576
Differential toxicity of ganciclovir for rat neurons and astrocytes in primary culture following adenovirus-mediated transfer of the HSVtk gene

A Maron
N Havaux
J-N Octave
Research01 Jan 1997
Gene Therapy

Volume: 4, P: 25-31
Tumor cell-specific transgene expression prevents liver toxicity of the adeno-HSVtk/GCV approach

K Brand
P Löser
M Strauss
Research14 Oct 1998
Gene Therapy

Volume: 5, P: 1363-1371
Foetal gene delivery in mice by intra-amniotic administration of retroviral producer cells and adenovirus

A-M Douar
S Adebakin
C Coutelle
Research01 Sept 1997
Gene Therapy

Volume: 4, P: 883-890
Photodynamic treatment of adenoviral vectors with visible light: an easy and convenient method for viral inactivation

F H E Schagen
A C E Moor
R C Hoeben
Research14 May 1999
Gene Therapy

Volume: 6, P: 873-881
Phase I clinical trial with IL-2-transfected xenogeneic cells administered in subcutaneous metastatic tumours: clinical and immunological findings

E Tartour
M Mehtali
T Dorval
ResearchOpen Access14 Nov 2000
British Journal of Cancer

Volume: 83, P: 1454-1461
In vitro and in vivo asessment of adenovirus 41 as a vector for gene delivery to the intestine

MA Croyle
M Stone
BJ Roessler
Research21 May 1998
Gene Therapy

Volume: 5, P: 645-654
Adenovirus-mediated gene transfer: influence of transgene, mouse strain and type of immune response on persistence of transgene expression

AI Michou
L Santoro
M Mehtali
Research01 May 1997
Gene Therapy

Volume: 4, P: 473-482
Adenovirus-mediated gene transfer results in decreased lysosomal storage in brain and total correction in liver of aspartylglucosaminuria (AGU) mouse

M Peltola
A Kyttälä
A Jalanko
Research14 Oct 1998
Gene Therapy

Volume: 5, P: 1314-1321
Gene therapy for long-term restoration of circulating thymulin in thymectomized mice and rats

P C Reggiani
C B Hereñú
R G Goya
Research13 Apr 2006
Gene Therapy

Volume: 13, P: 1214-1221
Efficient gene transfer and long-term expression in neurons using a recombinant adenovirus with a neuron-specific promoter

V Navarro
S Millecamps
G Le Gal La Salle
Research16 Nov 1999
Gene Therapy

Volume: 6, P: 1884-1892
Chemosensitization of HER-2/neu-overexpressing human breast cancer cells to paclitaxel (Taxol) by adenovirus type 5 E1A

Naoto T Ueno
Dihua Yu
Mien-Chie Hung
Research21 Aug 1997
Oncogene

Volume: 15, P: 953-960
Myosin regulatory elements as vectors for gene transfer by intramuscular injection

M Skarli
A Kiri
G Goldspink
Research30 Apr 1998
Gene Therapy

Volume: 5, P: 514-520
Evaluation of cellular immune responses in rhesus monkeys subjected to adenovirus-mediated gene transfer into the cervix

Asis K Sarkar
Michele Follen Mitchell
K Jagannadha Sastry
Research01 Jun 1999
Cancer Gene Therapy

Volume: 6, P: 220-227
Induction of apoptosis and G2/M arrest by infection with replication-deficient adenovirus at high multiplicity of infection

K Brand
R Klocke
M Strauss
Research25 Jun 1999
Gene Therapy

Volume: 6, P: 1054-1063
Immune rejection of human dystrophin following intramuscular injections of naked DNA in mdx mice

S Braun
C Thioudellet
A Pavirani
Research20 Sept 2000
Gene Therapy

Volume: 7, P: 1447-1457
The ratio of single- to double-strand DNA breaks and their absolute values determine cell death pathway

O Tounekti
A Kenani
L M Mir
ResearchOpen Access01 May 2001
British Journal of Cancer

Volume: 84, P: 1272-1279
The cellular oncogene EWS/activating transcription factor 1 is unable to activate adenovirus-borne promoters: Implications for cytotoxic prodrug therapy of malignant melanoma of soft parts

Raymond W M Lung
Kevin A W Lee
Research24 May 2000
Cancer Gene Therapy

Volume: 7, P: 396-406
Demonstration of mixed properties of RU486 in progesterone receptor (PR)-transfected MDA-MB-231 cells: a model for studying the functions of progesterone analogues

V C-L Lin
S E Aw
M G-K Tan
ResearchOpen Access11 Dec 2001
British Journal of Cancer

Volume: 85, P: 1978-1986
Severe hepatic dysfunction after adenovirus-mediated transfer of the herpes simplex virus thymidine kinase gene and ganciclovir administration

MM van der Eb
SJ Cramer
RC Hoeben
Research30 Apr 1998
Gene Therapy

Volume: 5, P: 451-458
Ex vivo gene transfer using adenovirus-mediated full-length dystrophin delivery to dystrophic muscles

SS Floyd Jr
PR Clemens
J Huard
Research04 Mar 1998
Gene Therapy

Volume: 5, P: 19-30
Heterologous expression of adenovirus E3-gp19K in an E1a-deleted adenovirus vector inhibits MHC I expression in vitro, but does not prolong transgene expression in vivo

DB Schowalter
JC Tubb
MA Kay
Research01 Apr 1997
Gene Therapy

Volume: 4, P: 351-360
Major effects of TPO delivered by a single injection of a recombinant adenovirus on prevention of septicemia and anemia associated with myelosuppression in mice: risk of sustained expression inducing myelofibrosis due to immunosuppression

MA Abina
M Tulliez
H Haddada
Research30 Apr 1998
Gene Therapy

Volume: 5, P: 497-506

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