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Acta Paediatrica Japonica : Overseas Edition
|
April 1, 1995
Persistent vacuoles in leukocytes: familial Jordans anomaly
L Ulukutlu, O N Koç, M Taşyürekli, et al.
The Journal of Experimental Medicine
|
December 1, 1994
156Pro-->Gln substitution in the light chain of cytochrome b558 of the human NADPH oxidase (p22-phox) leads to defective translocation of the cytosolic proteins p47-phox and p67-phox
J H Leusen, B G Bolscher, P M Hilarius, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 15, 1991
Point mutation in the cytoplasmic domain of the neutrophil p22-phox cytochrome b subunit is associated with a nonfunctional NADPH oxidase and chronic granulomatous disease
M C Dinauer, E A Pierce, R W Erickson, et al.
Journal of Leukocyte Biology
|
February 1, 1992
Chronic granulomatous disease with partial deficiency of cytochrome b558 and incomplete respiratory burst: variants of the X-linked, cytochrome b558-negative form of the disease
D Roos, M de Boer, N Borregard, et al.
Bone Marrow Transplantation
|
September 4, 2003
Quality control of a national bone marrow donor registry: results of a pilot study and proposal for a standardized approach
J-M Tiercy, S Stadelmann, B Chapuis, et al.
Blood
|
October 9, 1998
Successful treatment of invasive aspergillosis in chronic granulomatous disease by bone marrow transplantation, granulocyte colony-stimulating factor-mobilized granulocytes, and liposomal amphotericin-B
H Ozsahin, M von Planta, I Müller, et al.
Science (New York, N.Y.)
|
October 4, 1996
RAG mutations in human B cell-negative SCID
K Schwarz, G H Gauss, L Ludwig, et al.
Blood
|
April 15, 1997
Adenosine deaminase deficiency in adults
H Ozsahin, F X Arredondo-Vega, I Santisteban, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 68) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 68 results.
Acta Paediatrica Japonica : Overseas Edition
|
April 1, 1995
Persistent vacuoles in leukocytes: familial Jordans anomaly
L Ulukutlu, O N Koç, M Taşyürekli, et al.
The Journal of Experimental Medicine
|
December 1, 1994
156Pro-->Gln substitution in the light chain of cytochrome b558 of the human NADPH oxidase (p22-phox) leads to defective translocation of the cytosolic proteins p47-phox and p67-phox
J H Leusen, B G Bolscher, P M Hilarius, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 15, 1991
Point mutation in the cytoplasmic domain of the neutrophil p22-phox cytochrome b subunit is associated with a nonfunctional NADPH oxidase and chronic granulomatous disease
M C Dinauer, E A Pierce, R W Erickson, et al.
Journal of Leukocyte Biology
|
February 1, 1992
Chronic granulomatous disease with partial deficiency of cytochrome b558 and incomplete respiratory burst: variants of the X-linked, cytochrome b558-negative form of the disease
D Roos, M de Boer, N Borregard, et al.
Bone Marrow Transplantation
|
September 4, 2003
Quality control of a national bone marrow donor registry: results of a pilot study and proposal for a standardized approach
J-M Tiercy, S Stadelmann, B Chapuis, et al.
Blood
|
October 9, 1998
Successful treatment of invasive aspergillosis in chronic granulomatous disease by bone marrow transplantation, granulocyte colony-stimulating factor-mobilized granulocytes, and liposomal amphotericin-B
H Ozsahin, M von Planta, I Müller, et al.
Science (New York, N.Y.)
|
October 4, 1996
RAG mutations in human B cell-negative SCID
K Schwarz, G H Gauss, L Ludwig, et al.
Blood
|
April 15, 1997
Adenosine deaminase deficiency in adults
H Ozsahin, F X Arredondo-Vega, I Santisteban, et al.
Page
of 7