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H Tonoki

Showing results (41-50 of 65) with videos related to

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The Japanese Journal of Human Genetics|December 1, 1995
Predominance of the mutation at 1138 of the cDNA for the fibroblast growth factor receptor 3 in Japanese patients with achondroplasiaH Tonoki, J Nakae, T Tajima, et al.
Clinical Genetics|January 1, 1991
Pigmentary dysplasias in long survivors with mosaic trisomy 18: report of two casesI Murano, H Ohashi, M Tsukahara, et al.
European Journal of Pediatrics|January 1, 1992
A symptomatic female patient with Duchenne muscular dystrophy diagnosed by dystrophin-staining: a case reportK Shigihara-Yasuda, H Tonoki, Y Goto, et al.
The Journal of Investigative Dermatology|October 26, 2001
Induction of apoptosis in melanoma cell lines by p53 and its related proteinsT Yamashita, T Tokino, H Tonoki, et al.
Japanese Heart Journal|July 27, 1999
A novel A-kinase anchoring protein in the heart interacts with G alpha 13M Suzuki, K Furuuchi, H Tonoki, et al.
American Journal of Medical Genetics|June 24, 1998
4q33-qter deletion and absorptive hypercalciuria: report of two unrelated girlsK Imamura, H Tonoki, K Wakui, et al.
Oncogene|December 24, 1997
High frequency of p53 mutations in human oral epithelial dysplasia and primary squamous cell carcinoma detected by yeast functional assayH Kashiwazaki, H Tonoki, M Tada, et al.
Pediatric Research|March 1, 1994
Endotoxin induces glutathione reductase activity in lungs of miceD C Hamburg, H Tonoki, S E Welty, et al.
Human Genetics|March 10, 1999
A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCRT Kubota, S Nonoyama, H Tonoki, et al.
American Journal of Medical Genetics|May 1, 1986
The Wiedemann-Beckwith syndrome: pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivityN Niikawa, S Ishikiriyama, S Takahashi, et al.
Pageof 7

Showing results (41-50 of 65) with videos related to

Sort By:
Pageof 7
The Japanese Journal of Human Genetics|December 1, 1995
Predominance of the mutation at 1138 of the cDNA for the fibroblast growth factor receptor 3 in Japanese patients with achondroplasiaH Tonoki, J Nakae, T Tajima, et al.
Clinical Genetics|January 1, 1991
Pigmentary dysplasias in long survivors with mosaic trisomy 18: report of two casesI Murano, H Ohashi, M Tsukahara, et al.
European Journal of Pediatrics|January 1, 1992
A symptomatic female patient with Duchenne muscular dystrophy diagnosed by dystrophin-staining: a case reportK Shigihara-Yasuda, H Tonoki, Y Goto, et al.
The Journal of Investigative Dermatology|October 26, 2001
Induction of apoptosis in melanoma cell lines by p53 and its related proteinsT Yamashita, T Tokino, H Tonoki, et al.
Japanese Heart Journal|July 27, 1999
A novel A-kinase anchoring protein in the heart interacts with G alpha 13M Suzuki, K Furuuchi, H Tonoki, et al.
American Journal of Medical Genetics|June 24, 1998
4q33-qter deletion and absorptive hypercalciuria: report of two unrelated girlsK Imamura, H Tonoki, K Wakui, et al.
Oncogene|December 24, 1997
High frequency of p53 mutations in human oral epithelial dysplasia and primary squamous cell carcinoma detected by yeast functional assayH Kashiwazaki, H Tonoki, M Tada, et al.
Pediatric Research|March 1, 1994
Endotoxin induces glutathione reductase activity in lungs of miceD C Hamburg, H Tonoki, S E Welty, et al.
Human Genetics|March 10, 1999
A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCRT Kubota, S Nonoyama, H Tonoki, et al.
American Journal of Medical Genetics|May 1, 1986
The Wiedemann-Beckwith syndrome: pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivityN Niikawa, S Ishikiriyama, S Takahashi, et al.
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