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A Kurimasa

Showing results (1-10 of 23) with videos related to

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Human Genetics|September 1, 1993
Restoration of the cholesterol metabolism in 3T3 cell lines derived from the sphingomyelinosis mouse (spm/spm) by transfer of a human chromosome 18A Kurimasa, K Ohno, M Oshimura
Tanpakushitsu Kakusan Koso. Protein, Nucleic Acid, Enzyme|February 1, 1993
[Use of microcell-hybrid for genomic analyses]M Oshimura, A Kurimasa, M Shimizu
Pediatric Neurology|July 3, 1998
New syndrome with the Sakoda complex, bilateral anophthalmia, and cortical dysgenesisH Ehara, A Kurimasa, K Ohno, et al.
The Journal of Biological Chemistry|September 26, 2001
ATM phosphorylates histone H2AX in response to DNA double-strand breaksS Burma, B P Chen, M Murphy, et al.
The Journal of Dermatology|August 1, 1992
Proteus syndrome: report of the first Japanese case with special reference to differentiation from Klippel-Trenaunay-Weber syndromeY Hagari, M Aso, S Shimao, et al.
Human Genetics|January 1, 1994
A human gene that restores the DNA-repair defect in SCID mice is located on 8p11.1-->q11.1A Kurimasa, Y Nagata, M Shimizu, et al.
Science (New York, N.Y.)|September 29, 2001
Strand-specific postreplicative processing of mammalian telomeresS M Bailey, M N Cornforth, A Kurimasa, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 1995
Loss of the catalytic subunit of the DNA-dependent protein kinase in DNA double-strand-break-repair mutant mammalian cellsS R Peterson, A Kurimasa, M Oshimura, et al.
The Japanese Journal of Human Genetics|December 1, 1995
Cosmids and transcribed sequences from chromosome 11q23M Katoh, Y Nakagawa, T Yawata, et al.
Journal of Virology|December 19, 2000
Genetic evidence of a role for ATM in functional interaction between human T-cell leukemia virus type 1 Tax and p53P L Van, K W Yim, D Y Jin, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Human Genetics|September 1, 1993
Restoration of the cholesterol metabolism in 3T3 cell lines derived from the sphingomyelinosis mouse (spm/spm) by transfer of a human chromosome 18A Kurimasa, K Ohno, M Oshimura
Tanpakushitsu Kakusan Koso. Protein, Nucleic Acid, Enzyme|February 1, 1993
[Use of microcell-hybrid for genomic analyses]M Oshimura, A Kurimasa, M Shimizu
Pediatric Neurology|July 3, 1998
New syndrome with the Sakoda complex, bilateral anophthalmia, and cortical dysgenesisH Ehara, A Kurimasa, K Ohno, et al.
The Journal of Biological Chemistry|September 26, 2001
ATM phosphorylates histone H2AX in response to DNA double-strand breaksS Burma, B P Chen, M Murphy, et al.
The Journal of Dermatology|August 1, 1992
Proteus syndrome: report of the first Japanese case with special reference to differentiation from Klippel-Trenaunay-Weber syndromeY Hagari, M Aso, S Shimao, et al.
Human Genetics|January 1, 1994
A human gene that restores the DNA-repair defect in SCID mice is located on 8p11.1-->q11.1A Kurimasa, Y Nagata, M Shimizu, et al.
Science (New York, N.Y.)|September 29, 2001
Strand-specific postreplicative processing of mammalian telomeresS M Bailey, M N Cornforth, A Kurimasa, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 1995
Loss of the catalytic subunit of the DNA-dependent protein kinase in DNA double-strand-break-repair mutant mammalian cellsS R Peterson, A Kurimasa, M Oshimura, et al.
The Japanese Journal of Human Genetics|December 1, 1995
Cosmids and transcribed sequences from chromosome 11q23M Katoh, Y Nakagawa, T Yawata, et al.
Journal of Virology|December 19, 2000
Genetic evidence of a role for ATM in functional interaction between human T-cell leukemia virus type 1 Tax and p53P L Van, K W Yim, D Y Jin, et al.
Pageof 3