Search research articles
Contact Us
Filters
Showing results (171-180 of 196) with videos related to
Page
of 20
Sort By:
Tissue Antigens
|
October 22, 2004
High frequency of QPY allele and linkage disequilibrium of granzyme-B in Epstein-Barr-virus-associated hemophagocytic lymphohistiocytosis
M Zaitsu, K Yamamoto, E Ishii, et al.
Medical and Pediatric Oncology
|
March 4, 1999
Clonal dissemination of T-lymphocytes in scid mice from familial hemophagocytic lymphohistiocytosis
E Ishii, N Yoshida, N Kimura, et al.
Journal of the American Medical Informatics Association : JAMIA
|
May 20, 1999
Great earthquakes and medical information systems, with special reference to telecommunications
M Miyamoto, M Sako, M Kimura, et al.
Journal of Medical Genetics
|
October 7, 2004
Identification of novel MUNC13-4 mutations in familial haemophagocytic lymphohistiocytosis and functional analysis of MUNC13-4-deficient cytotoxic T lymphocytes
K Yamamoto, E Ishii, M Sako, et al.
Blood
|
July 11, 2000
Genetic defect in human X-linked agammaglobulinemia impedes a maturational evolution of pro-B cells into a later stage of pre-B cells in the B-cell differentiation pathway
K Nomura, H Kanegane, H Karasuyama, et al.
British Journal of Haematology
|
December 3, 1999
WASP is involved in proliferation and differentiation of human haemopoietic progenitors in vitro
M Kajiwara, S Nonoyama, M Eguchi, et al.
Journal of Immunological Methods
|
January 17, 2002
Flow cytometric determination of intracytoplasmic Wiskott-Aldrich syndrome protein in peripheral blood lymphocyte subpopulations
S Kawai, M Minegishi, Y Ohashi, et al.
Leukemia
|
May 10, 2000
An effective chemotherapeutic regimen for acute myeloid leukemia and myelodysplastic syndrome in children with Down's syndrome
S Kojima, M Sako, K Kato, et al.
Journal of Medical Genetics
|
July 10, 2008
Neurodevelopmental abnormalities associated with severe congenital neutropenia due to the R86X mutation in the HAX1 gene
N Ishikawa, S Okada, M Miki, et al.
Le Mali Medical
|
November 25, 2024
[Venous Thromboembolic Disease In Women In The Cardiology Department Of The Kati University Hospital]
B Sonfo, C A Thiam, A Kéita, et al.
Page
of 20
Search research articles
Search
Showing results (171-180 of 196) with videos related to
Sort By:
Page
of 20
Tissue Antigens
|
October 22, 2004
High frequency of QPY allele and linkage disequilibrium of granzyme-B in Epstein-Barr-virus-associated hemophagocytic lymphohistiocytosis
M Zaitsu, K Yamamoto, E Ishii, et al.
Medical and Pediatric Oncology
|
March 4, 1999
Clonal dissemination of T-lymphocytes in scid mice from familial hemophagocytic lymphohistiocytosis
E Ishii, N Yoshida, N Kimura, et al.
Journal of the American Medical Informatics Association : JAMIA
|
May 20, 1999
Great earthquakes and medical information systems, with special reference to telecommunications
M Miyamoto, M Sako, M Kimura, et al.
Journal of Medical Genetics
|
October 7, 2004
Identification of novel MUNC13-4 mutations in familial haemophagocytic lymphohistiocytosis and functional analysis of MUNC13-4-deficient cytotoxic T lymphocytes
K Yamamoto, E Ishii, M Sako, et al.
Blood
|
July 11, 2000
Genetic defect in human X-linked agammaglobulinemia impedes a maturational evolution of pro-B cells into a later stage of pre-B cells in the B-cell differentiation pathway
K Nomura, H Kanegane, H Karasuyama, et al.
British Journal of Haematology
|
December 3, 1999
WASP is involved in proliferation and differentiation of human haemopoietic progenitors in vitro
M Kajiwara, S Nonoyama, M Eguchi, et al.
Journal of Immunological Methods
|
January 17, 2002
Flow cytometric determination of intracytoplasmic Wiskott-Aldrich syndrome protein in peripheral blood lymphocyte subpopulations
S Kawai, M Minegishi, Y Ohashi, et al.
Leukemia
|
May 10, 2000
An effective chemotherapeutic regimen for acute myeloid leukemia and myelodysplastic syndrome in children with Down's syndrome
S Kojima, M Sako, K Kato, et al.
Journal of Medical Genetics
|
July 10, 2008
Neurodevelopmental abnormalities associated with severe congenital neutropenia due to the R86X mutation in the HAX1 gene
N Ishikawa, S Okada, M Miki, et al.
Le Mali Medical
|
November 25, 2024
[Venous Thromboembolic Disease In Women In The Cardiology Department Of The Kati University Hospital]
B Sonfo, C A Thiam, A Kéita, et al.
Page
of 20