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Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

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J Inazawa

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Genes, Chromosomes & Cancer|January 1, 1994

Mapping of the 8q23 translocation breakpoint of t(8;13) observed in a patient with multiple exostosesK Yoshiura, J Inazawa, K Koyama, et al.

Gene|June 19, 1998

The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader-Willi syndrome deletion regionY Nakada, H Taniura, T Uetsuki, et al.

American Journal of Hematology|April 1, 1994

Myelomonocytic crisis with t(5;17) and a p53 mutation in a patient with chronic myelogenous leukemiaH Nakagawa, H Fujii, H Nakai, et al.

Genomics|July 1, 1993

High-resolution cytogenetic mapping of 342 new cosmid markers including 43 RFLP markers on human chromosome 17 by fluorescence in situ hybridizationJ Inazawa, H Saito, T Ariyama, et al.

DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|December 31, 1996

Breakpoint junction of interstitial homozygous deletion at chromosome 2q33 in a small cell lung carcinomaT Kohno, T Otsuka, J Inazawa, et al.

Cytogenetics and Cell Genetics|January 1, 1996

Molecular cloning and mapping of a human cDNA (SC5DL) encoding a protein homologous to fungal sterol-C5-desaturaseM Matsushima, J Inazawa, E Takahashi, et al.

The Journal of Biological Chemistry|January 10, 1997

cDNA cloning and chromosomal localization of the human telencephalin and its distinctive interaction with lymphocyte function-associated antigen-1T Mizuno, Y Yoshihara, J Inazawa, et al.

Blood|August 1, 1995

Microsatellite instability is an early genetic event in myelodysplastic syndromeH Kaneko, S Horiike, J Inazawa, et al.

Genomics|May 23, 1998

Detection and isolation of a novel human gene located on Xp11.2-p11.4 that escapes X-inactivation using a two-dimensional DNA mapping methodH Yoshikawa, A Fujiyama, K Nakai, et al.

Cytogenetics and Cell Genetics|January 1, 1996

FISH localization of human cytoplasmic actin genes ACTB to 7p22 and ACTG1 to 17q25 and characterization of related pseudogenesH Ueyama, J Inazawa, H Nishino, et al.

Pageof 27

Search research articles

Showing results (31-40 of 263) with videos related to

Sort By:

Pageof 27

Genes, Chromosomes & Cancer|January 1, 1994

Mapping of the 8q23 translocation breakpoint of t(8;13) observed in a patient with multiple exostosesK Yoshiura, J Inazawa, K Koyama, et al.

Gene|June 19, 1998

The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader-Willi syndrome deletion regionY Nakada, H Taniura, T Uetsuki, et al.

American Journal of Hematology|April 1, 1994

Myelomonocytic crisis with t(5;17) and a p53 mutation in a patient with chronic myelogenous leukemiaH Nakagawa, H Fujii, H Nakai, et al.

Genomics|July 1, 1993

High-resolution cytogenetic mapping of 342 new cosmid markers including 43 RFLP markers on human chromosome 17 by fluorescence in situ hybridizationJ Inazawa, H Saito, T Ariyama, et al.

DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|December 31, 1996

Breakpoint junction of interstitial homozygous deletion at chromosome 2q33 in a small cell lung carcinomaT Kohno, T Otsuka, J Inazawa, et al.

Cytogenetics and Cell Genetics|January 1, 1996

Molecular cloning and mapping of a human cDNA (SC5DL) encoding a protein homologous to fungal sterol-C5-desaturaseM Matsushima, J Inazawa, E Takahashi, et al.

The Journal of Biological Chemistry|January 10, 1997

cDNA cloning and chromosomal localization of the human telencephalin and its distinctive interaction with lymphocyte function-associated antigen-1T Mizuno, Y Yoshihara, J Inazawa, et al.

Blood|August 1, 1995

Microsatellite instability is an early genetic event in myelodysplastic syndromeH Kaneko, S Horiike, J Inazawa, et al.

Genomics|May 23, 1998

Detection and isolation of a novel human gene located on Xp11.2-p11.4 that escapes X-inactivation using a two-dimensional DNA mapping methodH Yoshikawa, A Fujiyama, K Nakai, et al.

Cytogenetics and Cell Genetics|January 1, 1996

FISH localization of human cytoplasmic actin genes ACTB to 7p22 and ACTG1 to 17q25 and characterization of related pseudogenesH Ueyama, J Inazawa, H Nishino, et al.

Pageof 27