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Rie Yoshida

Showing results (1-10 of 65) with videos related to

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BMJ Case Reports|November 1, 2016
Diagnosis of cystic fibrosis in a patient of Egyptian backgroundRie Yoshida, Bobby Ruge
Pediatric Endocrinology Reviews : PER|October 7, 2005
PTPN11 mutations and genotype-phenotype correlations in Noonan and LEOPARD syndromesTsutomu Ogata, Rie Yoshida
Biotechnology and Bioengineering|December 17, 2013
A novel platform for antibody library selection in mammalian cells based on a growth signalobodyRie Yoshida, Masahiro Kawahara, Teruyuki Nagamune
The Journal of Toxicological Sciences|February 3, 2009
Mutagenicity of water-soluble ZnO nanoparticles in Ames testRie Yoshida, Daisuke Kitamura, Shinya Maenosono
Journal of Biochemistry|January 25, 2015
Domain structure of growth signalobodies critically affects the outcome of antibody library selectionRie Yoshida, Masahiro Kawahara, Teruyuki Nagamune
The Journal of Toxicological Sciences|June 2, 2009
Evaluation of genotoxicity of amine-terminated water-dispersible FePt nanoparticles in the Ames test and in vitro chromosomal aberration testShinya Maenosono, Rie Yoshida, Soichiro Saita
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 12, 2002
Urinary 8-oxo-7,8-dihydro-2'-deoxyguanosine values measured by an ELISA correlated well with measurements by high-performance liquid chromatography with electrochemical detectionRie Yoshida, Yasutaka Ogawa, Hiroshi Kasai
Scientific Reports|December 11, 2025
Brain network and activity in frontal regions change in the process of visuomotor adaptationSaki Niiyama, Rie Yoshida, Megumi Miyashita, et al.
Journal of Paediatrics and Child Health|June 22, 2022
It is not Black and White: A spotlight on racial diversity in paediatricsKaylita Chantiluke, Rie Yoshida, Ngaree Blow, et al.
Pediatric Blood & Cancer|February 7, 2008
Hepatoblastoma in a Noonan syndrome patient with a PTPN11 mutationRie Yoshida, Tsutomu Ogata, Nobuhide Masawa, et al.
Pageof 7

Showing results (1-10 of 65) with videos related to

Sort By:
Pageof 7
BMJ Case Reports|November 1, 2016
Diagnosis of cystic fibrosis in a patient of Egyptian backgroundRie Yoshida, Bobby Ruge
Pediatric Endocrinology Reviews : PER|October 7, 2005
PTPN11 mutations and genotype-phenotype correlations in Noonan and LEOPARD syndromesTsutomu Ogata, Rie Yoshida
Biotechnology and Bioengineering|December 17, 2013
A novel platform for antibody library selection in mammalian cells based on a growth signalobodyRie Yoshida, Masahiro Kawahara, Teruyuki Nagamune
The Journal of Toxicological Sciences|February 3, 2009
Mutagenicity of water-soluble ZnO nanoparticles in Ames testRie Yoshida, Daisuke Kitamura, Shinya Maenosono
Journal of Biochemistry|January 25, 2015
Domain structure of growth signalobodies critically affects the outcome of antibody library selectionRie Yoshida, Masahiro Kawahara, Teruyuki Nagamune
The Journal of Toxicological Sciences|June 2, 2009
Evaluation of genotoxicity of amine-terminated water-dispersible FePt nanoparticles in the Ames test and in vitro chromosomal aberration testShinya Maenosono, Rie Yoshida, Soichiro Saita
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 12, 2002
Urinary 8-oxo-7,8-dihydro-2'-deoxyguanosine values measured by an ELISA correlated well with measurements by high-performance liquid chromatography with electrochemical detectionRie Yoshida, Yasutaka Ogawa, Hiroshi Kasai
Scientific Reports|December 11, 2025
Brain network and activity in frontal regions change in the process of visuomotor adaptationSaki Niiyama, Rie Yoshida, Megumi Miyashita, et al.
Journal of Paediatrics and Child Health|June 22, 2022
It is not Black and White: A spotlight on racial diversity in paediatricsKaylita Chantiluke, Rie Yoshida, Ngaree Blow, et al.
Pediatric Blood & Cancer|February 7, 2008
Hepatoblastoma in a Noonan syndrome patient with a PTPN11 mutationRie Yoshida, Tsutomu Ogata, Nobuhide Masawa, et al.
Pageof 7