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Human Gene Therapy
|
September 9, 2022
Liver Gene Therapy
Amit C Nathwani, Jenny McIntosh, Rose Sheridan
Current Hematology Reports
|
July 13, 2005
An update on gene therapy for hemophilia
Amit C Nathwani, Jenny McIntosh, Andrew M Davidoff
Genetic Vaccines and Therapy
|
March 4, 2008
Performance of AAV8 vectors expressing human factor IX from a hepatic-selective promoter following intravenous injection into rats
Tracey Graham, Jenny McIntosh, Lorraine M Work, et al.
Blood
|
November 9, 2002
The spectrum of PIG-A gene mutations in aplastic anemia/paroxysmal nocturnal hemoglobinuria (AA/PNH): a high incidence of multiple mutations and evidence of a mutational hot spot
Yousef Mortazavi, Bruno Merk, Jenny McIntosh, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
December 7, 2018
Potential limits of AAV-based gene therapy with the use of new transgenes expressing factor IX fusion proteins
Sandra Le Quellec, Allison Dane, Nathalie Enjolras, et al.
Journal of Medical Primatology
|
March 24, 2022
Feasibility of combined upper and lower gastrointestinal endoscopic biopsy in the common marmoset (Callithrix jacchus) to evaluate gastrointestinal diseases
Romy M Heilmann, Jenny McIntosh, Els Acke, et al.
Blood
|
October 19, 2006
Continuous delivery of human type I interferons (alpha/beta) has significant activity against acute myeloid leukemia cells in vitro and in a xenograft model
Reuben Benjamin, Asim Khwaja, Nalini Singh, et al.
Atherosclerosis
|
October 22, 2008
Preliminary evaluation of a self-complementary AAV2/8 vector for hepatic gene transfer of human apoE3 to inhibit atherosclerotic lesion development in apoE-deficient mice
Eyman Osman, Vanessa Evans, Ian R Graham, et al.
Human Gene Therapy
|
October 6, 2010
Recombinant adeno-associated virus-mediated in utero gene transfer gives therapeutic transgene expression in the sheep
Anna L David, Jenny McIntosh, Donald M Peebles, et al.
Blood
|
November 9, 2006
Safe and efficient transduction of the liver after peripheral vein infusion of self-complementary AAV vector results in stable therapeutic expression of human FIX in nonhuman primates
Amit C Nathwani, John T Gray, Jenny McIntosh, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 30) with videos related to
Sort By:
Page
of 3
Human Gene Therapy
|
September 9, 2022
Liver Gene Therapy
Amit C Nathwani, Jenny McIntosh, Rose Sheridan
Current Hematology Reports
|
July 13, 2005
An update on gene therapy for hemophilia
Amit C Nathwani, Jenny McIntosh, Andrew M Davidoff
Genetic Vaccines and Therapy
|
March 4, 2008
Performance of AAV8 vectors expressing human factor IX from a hepatic-selective promoter following intravenous injection into rats
Tracey Graham, Jenny McIntosh, Lorraine M Work, et al.
Blood
|
November 9, 2002
The spectrum of PIG-A gene mutations in aplastic anemia/paroxysmal nocturnal hemoglobinuria (AA/PNH): a high incidence of multiple mutations and evidence of a mutational hot spot
Yousef Mortazavi, Bruno Merk, Jenny McIntosh, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
December 7, 2018
Potential limits of AAV-based gene therapy with the use of new transgenes expressing factor IX fusion proteins
Sandra Le Quellec, Allison Dane, Nathalie Enjolras, et al.
Journal of Medical Primatology
|
March 24, 2022
Feasibility of combined upper and lower gastrointestinal endoscopic biopsy in the common marmoset (Callithrix jacchus) to evaluate gastrointestinal diseases
Romy M Heilmann, Jenny McIntosh, Els Acke, et al.
Blood
|
October 19, 2006
Continuous delivery of human type I interferons (alpha/beta) has significant activity against acute myeloid leukemia cells in vitro and in a xenograft model
Reuben Benjamin, Asim Khwaja, Nalini Singh, et al.
Atherosclerosis
|
October 22, 2008
Preliminary evaluation of a self-complementary AAV2/8 vector for hepatic gene transfer of human apoE3 to inhibit atherosclerotic lesion development in apoE-deficient mice
Eyman Osman, Vanessa Evans, Ian R Graham, et al.
Human Gene Therapy
|
October 6, 2010
Recombinant adeno-associated virus-mediated in utero gene transfer gives therapeutic transgene expression in the sheep
Anna L David, Jenny McIntosh, Donald M Peebles, et al.
Blood
|
November 9, 2006
Safe and efficient transduction of the liver after peripheral vein infusion of self-complementary AAV vector results in stable therapeutic expression of human FIX in nonhuman primates
Amit C Nathwani, John T Gray, Jenny McIntosh, et al.
Page
of 3