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A Imamura

Showing results (181-190 of 189) with videos related to

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Human Molecular Genetics|May 20, 1999
Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disordersN Shimozawa, Y Suzuki, Z Zhang, et al.
Internal Medicine (Tokyo, Japan)|January 11, 2000
Distribution of JC virus DNA in peripheral blood lymphocytes of hematological disease casesN Shimizu, A Imamura, O Daimaru, et al.
Gan to Kagaku Ryoho. Cancer & Chemotherapy|October 1, 1996
[Selective thermocoagulation of unresectable malignant tumors using radiofrequency]A Nakagawa, Y Kamiyama, Y Matsui, et al.
Internal Medicine (Tokyo, Japan)|June 8, 2001
Malignant lymphoma of the bone associated with systemic sarcoidosisH Kobayashi, Y Kato, M Hakamada, et al.
Artificial Organs|February 23, 1999
Ex vivo liver perfusion with arterial blood from a pig with ischemic liver failureN Nakamura, Y Kamiyama, S Takai, et al.
Biochemical and Biophysical Research Communications|March 3, 1998
Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13N Shimozawa, Y Suzuki, Z Zhang, et al.
American Journal of Human Genetics|December 5, 1998
Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghostsN Shimozawa, Y Suzuki, Z Zhang, et al.
Leukemia & Lymphoma|February 10, 2006
Disease-specific expression of VEGF and its receptors in AML cells: possible autocrine pathway of VEGF/type1 receptor of VEGF in t(15;17) AML and VEGF/type2 receptor of VEGF in t(8;21) AMLA Hiramatsu, H Miwa, M Shikami, et al.
Human Mutation|July 17, 1999
Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disordersZ Zhang, Y Suzuki, N Shimozawa, et al.
Pageof 19

Showing results (181-190 of 189) with videos related to

Sort By:
Pageof 19
You have reached the last page of results.This site can display upto 189 results.
Human Molecular Genetics|May 20, 1999
Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disordersN Shimozawa, Y Suzuki, Z Zhang, et al.
Internal Medicine (Tokyo, Japan)|January 11, 2000
Distribution of JC virus DNA in peripheral blood lymphocytes of hematological disease casesN Shimizu, A Imamura, O Daimaru, et al.
Gan to Kagaku Ryoho. Cancer & Chemotherapy|October 1, 1996
[Selective thermocoagulation of unresectable malignant tumors using radiofrequency]A Nakagawa, Y Kamiyama, Y Matsui, et al.
Internal Medicine (Tokyo, Japan)|June 8, 2001
Malignant lymphoma of the bone associated with systemic sarcoidosisH Kobayashi, Y Kato, M Hakamada, et al.
Artificial Organs|February 23, 1999
Ex vivo liver perfusion with arterial blood from a pig with ischemic liver failureN Nakamura, Y Kamiyama, S Takai, et al.
Biochemical and Biophysical Research Communications|March 3, 1998
Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13N Shimozawa, Y Suzuki, Z Zhang, et al.
American Journal of Human Genetics|December 5, 1998
Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghostsN Shimozawa, Y Suzuki, Z Zhang, et al.
Leukemia & Lymphoma|February 10, 2006
Disease-specific expression of VEGF and its receptors in AML cells: possible autocrine pathway of VEGF/type1 receptor of VEGF in t(15;17) AML and VEGF/type2 receptor of VEGF in t(8;21) AMLA Hiramatsu, H Miwa, M Shikami, et al.
Human Mutation|July 17, 1999
Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disordersZ Zhang, Y Suzuki, N Shimozawa, et al.
Pageof 19