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C Kaplan

Showing results (521-530 of 1,185) with videos related to

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Nature|January 19, 1989
Absence of significant RNA-dependent DNA polymerase activity in lymphocytes from patients with Kawasaki syndromeM E Melish, N J Marchette, J C Kaplan, et al.
Transfusion|April 22, 2008
New mutations on platelet GPIIb in Sub-Saharan African populations revealed by genotyping discrepanciesL Hallé, V Jallu, G Mulen-Imandy, et al.
Acta Haematologica|January 1, 1978
Congenital methemoglobin-reductase (cytochrome b5 reductase) deficiency associated with mental retardation in a Spanish girlJ L Vives-Corrons, A Pujades, E Vela, et al.
Biochemical and Biophysical Research Communications|April 15, 1993
Expression of the dystrophin gene in cultured fibroblastsJ P Hugnot, H Gilgenkrantz, P Chafey, et al.
JAMA Surgery|March 29, 2023
Association of Obesity With Diverticulitis in the Hispanic Community Health Study/Study of LatinosWenjie Ma, Simin Hua, Edward L Giovannucci, et al.
Thrombosis and Haemostasis|January 5, 2002
A naturally occurring point mutation in the beta3 integrin MIDAS-like domain affects differently alphavbeta3 and alphaIIIbbeta3 receptor functionM C Morel-Kopp, C Melchior, P Chen, et al.
Human Mutation|January 1, 1992
A novel mutation (Arg-->Leu in exon 18) in factor VIII gene responsible for moderate hemophilia AK Nafa, M Baudis, N Deburgrave, et al.
British Journal of Haematology|February 1, 1977
International Committee for Standardization in Haematology: recommended methods for red-cell enzyme analysisE Beutler, K G Blume, J C Kaplan, et al.
Human Immunology|October 1, 1994
Susceptibility to alloimmunization to platelet HPA-1a antigen involves TAP1 polymorphismV Braud, D Chevrier, A Cesbron, et al.
Human Genetics|January 19, 1978
Heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Algeria. Study in Northern Algeria with description of five new variantsM Benabadji, F Merad, M Benmoussa, et al.
Pageof 119

Showing results (521-530 of 1,185) with videos related to

Sort By:
Pageof 119
Nature|January 19, 1989
Absence of significant RNA-dependent DNA polymerase activity in lymphocytes from patients with Kawasaki syndromeM E Melish, N J Marchette, J C Kaplan, et al.
Transfusion|April 22, 2008
New mutations on platelet GPIIb in Sub-Saharan African populations revealed by genotyping discrepanciesL Hallé, V Jallu, G Mulen-Imandy, et al.
Acta Haematologica|January 1, 1978
Congenital methemoglobin-reductase (cytochrome b5 reductase) deficiency associated with mental retardation in a Spanish girlJ L Vives-Corrons, A Pujades, E Vela, et al.
Biochemical and Biophysical Research Communications|April 15, 1993
Expression of the dystrophin gene in cultured fibroblastsJ P Hugnot, H Gilgenkrantz, P Chafey, et al.
JAMA Surgery|March 29, 2023
Association of Obesity With Diverticulitis in the Hispanic Community Health Study/Study of LatinosWenjie Ma, Simin Hua, Edward L Giovannucci, et al.
Thrombosis and Haemostasis|January 5, 2002
A naturally occurring point mutation in the beta3 integrin MIDAS-like domain affects differently alphavbeta3 and alphaIIIbbeta3 receptor functionM C Morel-Kopp, C Melchior, P Chen, et al.
Human Mutation|January 1, 1992
A novel mutation (Arg-->Leu in exon 18) in factor VIII gene responsible for moderate hemophilia AK Nafa, M Baudis, N Deburgrave, et al.
British Journal of Haematology|February 1, 1977
International Committee for Standardization in Haematology: recommended methods for red-cell enzyme analysisE Beutler, K G Blume, J C Kaplan, et al.
Human Immunology|October 1, 1994
Susceptibility to alloimmunization to platelet HPA-1a antigen involves TAP1 polymorphismV Braud, D Chevrier, A Cesbron, et al.
Human Genetics|January 19, 1978
Heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Algeria. Study in Northern Algeria with description of five new variantsM Benabadji, F Merad, M Benmoussa, et al.
Pageof 119