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Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1993
Gene targeting of X chromosome-linked chronic granulomatous disease locus in a human myeloid leukemia cell line and rescue by expression of recombinant gp91phox
L Zhen, A A King, Y Xiao, et al.
Journal of Clinical Microbiology
|
June 10, 1998
Rapid extraction of genomic DNA from medically important yeasts and filamentous fungi by high-speed cell disruption
F M Müller, K E Werner, M Kasai, et al.
Blood
|
March 9, 2000
Recombination events between the p47-phox gene and its highly homologous pseudogenes are the main cause of autosomal recessive chronic granulomatous disease
J Roesler, J T Curnutte, J Rae, et al.
AIDS (London, England)
|
March 15, 1997
Early foscarnet failure in herpes simplex virus infection in a patient with AIDS
B H Segal, H D Engler, R Little, et al.
Biochemistry
|
March 15, 1994
Isolation of a complex of respiratory burst oxidase components from resting neutrophil cytosol
J W Park, J E Benna, K E Scott, et al.
Blood
|
December 10, 1999
Variant genotypes of the low-affinity Fcgamma receptors in two control populations and a review of low-affinity Fcgamma receptor polymorphisms in control and disease populations
T Lehrnbecher, C B Foster, S Zhu, et al.
Genes and Immunity
|
August 31, 2001
Genetic polymorphisms in molecules of innate immunity and susceptibility to infection with Wuchereria bancrofti in South India
E H Choi, P A Zimmerman, C B Foster, et al.
Journal of Clinical Microbiology
|
September 17, 1999
Transmission of an azole-resistant isogenic strain of Candida albicans among human immunodeficiency virus-infected family members with oropharyngeal candidiasis
F M Müller, M Kasai, A Francesconi, et al.
The Journal of Clinical Investigation
|
October 23, 1997
A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease
A Görlach, P L Lee, J Roesler, et al.
Leukemia
|
August 19, 2005
Common genetic variants in the interleukin-6 and chitotriosidase genes are associated with the risk for serious infection in children undergoing therapy for acute myeloid leukemia
T Lehrnbecher, T Bernig, M Hanisch, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 90) with videos related to
Sort By:
Page
of 9
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1993
Gene targeting of X chromosome-linked chronic granulomatous disease locus in a human myeloid leukemia cell line and rescue by expression of recombinant gp91phox
L Zhen, A A King, Y Xiao, et al.
Journal of Clinical Microbiology
|
June 10, 1998
Rapid extraction of genomic DNA from medically important yeasts and filamentous fungi by high-speed cell disruption
F M Müller, K E Werner, M Kasai, et al.
Blood
|
March 9, 2000
Recombination events between the p47-phox gene and its highly homologous pseudogenes are the main cause of autosomal recessive chronic granulomatous disease
J Roesler, J T Curnutte, J Rae, et al.
AIDS (London, England)
|
March 15, 1997
Early foscarnet failure in herpes simplex virus infection in a patient with AIDS
B H Segal, H D Engler, R Little, et al.
Biochemistry
|
March 15, 1994
Isolation of a complex of respiratory burst oxidase components from resting neutrophil cytosol
J W Park, J E Benna, K E Scott, et al.
Blood
|
December 10, 1999
Variant genotypes of the low-affinity Fcgamma receptors in two control populations and a review of low-affinity Fcgamma receptor polymorphisms in control and disease populations
T Lehrnbecher, C B Foster, S Zhu, et al.
Genes and Immunity
|
August 31, 2001
Genetic polymorphisms in molecules of innate immunity and susceptibility to infection with Wuchereria bancrofti in South India
E H Choi, P A Zimmerman, C B Foster, et al.
Journal of Clinical Microbiology
|
September 17, 1999
Transmission of an azole-resistant isogenic strain of Candida albicans among human immunodeficiency virus-infected family members with oropharyngeal candidiasis
F M Müller, M Kasai, A Francesconi, et al.
The Journal of Clinical Investigation
|
October 23, 1997
A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease
A Görlach, P L Lee, J Roesler, et al.
Leukemia
|
August 19, 2005
Common genetic variants in the interleukin-6 and chitotriosidase genes are associated with the risk for serious infection in children undergoing therapy for acute myeloid leukemia
T Lehrnbecher, T Bernig, M Hanisch, et al.
Page
of 9