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Journal of Immunological Methods
|
November 5, 1992
Superoxide production by normal and chronic granulomatous disease (CGD) patient-derived EBV-transformed B cell lines measured by chemiluminescence-based assays
C D Porter, M H Parkar, M K Collins, et al.
Blood
|
May 1, 1996
Efficient retroviral transduction of human bone marrow progenitor and long-term culture-initiating cells: partial reconstitution of cells from patients with X-linked chronic granulomatous disease by gp91-phox expression
C D Porter, M H Parkar, M K Collins, et al.
Blood
|
October 1, 1993
X-linked chronic granulomatous disease: correction of NADPH oxidase defect by retrovirus-mediated expression of gp91-phox
C D Porter, M H Parkar, R J Levinsky, et al.
Archives of Disease in Childhood
|
June 1, 1996
X linked agammaglobulinaemia with a 'leaky' phenotype
A Jones, L Bradley, L Alterman, et al.
Immunodeficiency
|
January 1, 1993
Physical and genetic mapping in the region of Xq12-21, which contains the locus for X-linked severe combined immunodeficiency
A Jones, T Morris, M de Alwis, et al.
Gene Therapy
|
June 1, 2002
T cell transduction and suicide with an enhanced mutant thymidine kinase
W Qasim, A J Thrasher, J Buddle, et al.
Genomics
|
February 1, 1993
Pulsed-field gel electrophoresis and radiation hybrid mapping analyses enable the ordering of eleven DNA loci in Xq22
M A O'Reilly, L A Alterman, J Zijlstra, et al.
Blood
|
July 27, 2001
Defective expression of the interleukin-2/interleukin-15 receptor beta subunit leads to a natural killer cell-deficient form of severe combined immunodeficiency
K C Gilmour, H Fujii, T Cranston, et al.
Journal of Medical Genetics
|
June 1, 1993
A new restriction fragment length polymorphism at the DXS101 locus allows carrier detection in a family with X linked agammaglobulinaemia
A Sweatman, R Lovering, H Middleton-Price, et al.
European Journal of Immunology
|
October 28, 1997
The X-linked immunodeficiency defect in the mouse is corrected by expression of human Bruton's tyrosine kinase from a yeast artificial chromosome transgene
A Maas, G M Dingjan, H F Savelkoul, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 100) with videos related to
Sort By:
Page
of 10
Journal of Immunological Methods
|
November 5, 1992
Superoxide production by normal and chronic granulomatous disease (CGD) patient-derived EBV-transformed B cell lines measured by chemiluminescence-based assays
C D Porter, M H Parkar, M K Collins, et al.
Blood
|
May 1, 1996
Efficient retroviral transduction of human bone marrow progenitor and long-term culture-initiating cells: partial reconstitution of cells from patients with X-linked chronic granulomatous disease by gp91-phox expression
C D Porter, M H Parkar, M K Collins, et al.
Blood
|
October 1, 1993
X-linked chronic granulomatous disease: correction of NADPH oxidase defect by retrovirus-mediated expression of gp91-phox
C D Porter, M H Parkar, R J Levinsky, et al.
Archives of Disease in Childhood
|
June 1, 1996
X linked agammaglobulinaemia with a 'leaky' phenotype
A Jones, L Bradley, L Alterman, et al.
Immunodeficiency
|
January 1, 1993
Physical and genetic mapping in the region of Xq12-21, which contains the locus for X-linked severe combined immunodeficiency
A Jones, T Morris, M de Alwis, et al.
Gene Therapy
|
June 1, 2002
T cell transduction and suicide with an enhanced mutant thymidine kinase
W Qasim, A J Thrasher, J Buddle, et al.
Genomics
|
February 1, 1993
Pulsed-field gel electrophoresis and radiation hybrid mapping analyses enable the ordering of eleven DNA loci in Xq22
M A O'Reilly, L A Alterman, J Zijlstra, et al.
Blood
|
July 27, 2001
Defective expression of the interleukin-2/interleukin-15 receptor beta subunit leads to a natural killer cell-deficient form of severe combined immunodeficiency
K C Gilmour, H Fujii, T Cranston, et al.
Journal of Medical Genetics
|
June 1, 1993
A new restriction fragment length polymorphism at the DXS101 locus allows carrier detection in a family with X linked agammaglobulinaemia
A Sweatman, R Lovering, H Middleton-Price, et al.
European Journal of Immunology
|
October 28, 1997
The X-linked immunodeficiency defect in the mouse is corrected by expression of human Bruton's tyrosine kinase from a yeast artificial chromosome transgene
A Maas, G M Dingjan, H F Savelkoul, et al.
Page
of 10