Oncoretroviral gene transfer to NOD/SCID repopulating cells using three different viral envelopes.

about

Hematopoietic stem cell gene therapy:assessing the relevance of preclinical models Genetic modification of human hematopoietic cells: preclinical optimization of oncoretroviral-mediated gene transfer for clinical trials Hematopoietic stem cell gene therapy with drug resistance genes: an update.

P2860

Q26859147-380C8387-4C4E-410A-A909-30033DF4B7AD Q35180417-9C921CED-050F-4E72-82D0-88C77AECC021 Q36204222-E62CD501-A9FA-4954-9968-7DE573084DD5

P2860

Oncoretroviral gene transfer to NOD/SCID repopulating cells using three different viral envelopes.

Item

http://www.wikidata.org/entity/Q45884756

description

2002 nî lūn-bûn

@nan

2002年の論文

@ja

2002年学术文章

@wuu

2002年学术文章

@zh-cn

2002年学术文章

@zh-hans

2002年学术文章

@zh-my

2002年学术文章

@zh-sg

2002年學術文章

@yue

2002年學術文章

@zh

2002年學術文章

@zh-hant

name

Oncoretroviral gene transfer t ...... ree different viral envelopes.

@en

Oncoretroviral gene transfer t ...... ree different viral envelopes.

@nl

type

Item

label

Oncoretroviral gene transfer t ...... ree different viral envelopes.

@en

Oncoretroviral gene transfer t ...... ree different viral envelopes.

@nl

prefLabel

Oncoretroviral gene transfer t ...... ree different viral envelopes.

@en

Oncoretroviral gene transfer t ...... ree different viral envelopes.

@nl

P1476

Oncoretroviral gene transfer t ...... ree different viral envelopes.

@en

P2093

Johan Richter

http://www.w3.org/2001/XMLSchema#string

Stefan Karlsson

http://www.w3.org/2001/XMLSchema#string

Thomas Relander

http://www.w3.org/2001/XMLSchema#string

P2860

Cell-surface receptors for gibbon ape leukemia virus and amphotropic murine retrovirus are inducible sodium-dependent phosphate symporters

Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease

Identification of primitive human hematopoietic cells capable of repopulating NOD/SCID mouse bone marrow: implications for gene therapy

Bone morphogenetic proteins regulate the developmental program of human hematopoietic stem cells.

Quantitative analysis reveals expansion of human hematopoietic repopulating cells after short-term ex vivo culture.

Vesicular stomatitis virus G glycoprotein pseudotyped retroviral vectors: concentration to very high titer and efficient gene transfer into mammalian and nonmammalian cells.

Expansion in vitro of transplantable human cord blood stem cells demonstrated using a quantitative assay of their lympho-myeloid repopulating activity in nonobese diabetic-scid/scid mice.

Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection

Purification of primitive human hematopoietic cells capable of repopulating immune-deficient mice.

Lentivirus gene transfer in murine hematopoietic progenitor cells is compromised by a delay in proviral integration and results in transduction mosaicism and heterogeneous gene expression in progeny cells.

P304

122-132

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/JGM.246

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2002-03-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

11933213

http://www.w3.org/2001/XMLSchema#string

Oncoretroviral gene transfer to NOD/SCID repopulating cells using three different viral envelopes.

about

P2860

P2860

Oncoretroviral gene transfer to NOD/SCID repopulating cells using three different viral envelopes.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698