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H Tonoki

Showing results (31-40 of 65) with videos related to

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Clinical Genetics|September 1, 1991
Identification of a marker chromosome as inv dup(15) by molecular analysisY Shibuya, H Tonoki, N Kajii, et al.
Journal of Medical Genetics|April 1, 1997
A 4 Mb cryptic deletion associated with inv(8)(q13.1q24.11) in a patient with trichorhinophalangeal syndrome type IT Sasaki, H Tonoki, H Soejima, et al.
Clinical Genetics|September 14, 2007
Mosaic paternally derived inv dup(15) may partially rescue the Prader-Willi syndrome phenotype with uniparental disomyS Saitoh, K Hosoki, K Takano, et al.
Human Genetics|August 1, 1988
Origin of the extra chromosome in trisomy 18. A study on five patients using a restriction fragment length polymorphismT Kondoh, H Tonoki, T Matsumoto, et al.
Biochemical Medicine and Metabolic Biology|February 1, 1993
Expression of recombinant human glutathione reductase in eukaryotic cells after DNA-mediated gene transferS Cholin, H Tonoki, T N Hansen, et al.
American Journal of Medical Genetics|April 6, 1999
Mutchinick syndrome in a Japanese girlH Tonoki, T Hattori, H Kamoshida, et al.
The Journal of Pediatrics|August 1, 1990
Negative dystrophin staining in muscles of patients with complex glycerol kinase deficiencyH Tonoki, K Fujieda, N Kajii, et al.
Microbiology and Immunology|December 28, 1999
Adenovirus type 5 E1A immortalizes primary rat cells expressing wild-type p53T Yamashita, H Tonoki, D Nakata, et al.
Mutation Research|February 7, 2001
Transcriptional slippage of p53 gene enhanced by cellular damage in rat liver: monitoring the slippage by a yeast functional assayY Ba, H Tonoki, M Tada, et al.
American Journal of Medical Genetics|August 1, 1989
Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3)S Ishikiriyama, H Tonoki, Y Shibuya, et al.
Pageof 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
Clinical Genetics|September 1, 1991
Identification of a marker chromosome as inv dup(15) by molecular analysisY Shibuya, H Tonoki, N Kajii, et al.
Journal of Medical Genetics|April 1, 1997
A 4 Mb cryptic deletion associated with inv(8)(q13.1q24.11) in a patient with trichorhinophalangeal syndrome type IT Sasaki, H Tonoki, H Soejima, et al.
Clinical Genetics|September 14, 2007
Mosaic paternally derived inv dup(15) may partially rescue the Prader-Willi syndrome phenotype with uniparental disomyS Saitoh, K Hosoki, K Takano, et al.
Human Genetics|August 1, 1988
Origin of the extra chromosome in trisomy 18. A study on five patients using a restriction fragment length polymorphismT Kondoh, H Tonoki, T Matsumoto, et al.
Biochemical Medicine and Metabolic Biology|February 1, 1993
Expression of recombinant human glutathione reductase in eukaryotic cells after DNA-mediated gene transferS Cholin, H Tonoki, T N Hansen, et al.
American Journal of Medical Genetics|April 6, 1999
Mutchinick syndrome in a Japanese girlH Tonoki, T Hattori, H Kamoshida, et al.
The Journal of Pediatrics|August 1, 1990
Negative dystrophin staining in muscles of patients with complex glycerol kinase deficiencyH Tonoki, K Fujieda, N Kajii, et al.
Microbiology and Immunology|December 28, 1999
Adenovirus type 5 E1A immortalizes primary rat cells expressing wild-type p53T Yamashita, H Tonoki, D Nakata, et al.
Mutation Research|February 7, 2001
Transcriptional slippage of p53 gene enhanced by cellular damage in rat liver: monitoring the slippage by a yeast functional assayY Ba, H Tonoki, M Tada, et al.
American Journal of Medical Genetics|August 1, 1989
Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3)S Ishikiriyama, H Tonoki, Y Shibuya, et al.
Pageof 7