Search research articles
Contact Us
Filters
Showing results (1-10 of 266) with videos related to
Page
of 27
Sort By:
Nihon Eiseigaku Zasshi. Japanese Journal of Hygiene
|
October 12, 2016
Reproductive/Developmental Abnormalities Induced by Epigenetic Aberrations and Possible Environmental Causes
Tomoko Kawai, Kenichiro Hata
Clinical Calcium
|
March 19, 2005
[Injectable bone]
Yoichi Yamada, Kenichiro Hata, Minoru Ueda
Advances in Experimental Medicine and Biology
|
June 30, 2018
Placental Development and Nutritional Environment
Kosuke Taniguchi, Tomoko Kawai, Kenichiro Hata
Methods in Molecular Biology (Clifton, N.J.)
|
September 29, 2022
Reduced Representation Bisulfite Sequencing (RRBS)
Kazuhiko Nakabayashi, Michihiro Yamamura, Keita Haseagawa, et al.
Development (Cambridge, England)
|
April 6, 2002
Dnmt3L cooperates with the Dnmt3 family of de novo DNA methyltransferases to establish maternal imprints in mice
Kenichiro Hata, Masaki Okano, Hong Lei, et al.
Brain & Development
|
September 30, 2018
Reading disability due to an ocular motor disorder: A case of an adolescent girl with a previous diagnosis of dyslexia
Tsunehiko Kurokami, Tatsuya Koeda, Ohsuke Migita, et al.
Regenerative Therapy
|
October 2, 2018
Human resource development contributes to the creation of outstanding regenerative medicine products
Fusako Nishigaki, Sachikon Ezoe, Hideki Kitajima, et al.
Genomics Data
|
March 17, 2016
Lists of HumanMethylation450 BeadChip probes with nucleotide-variant information obtained from the Phase 3 data of the 1000 Genomes Project
Kohji Okamura, Tomoko Kawai, Kenichiro Hata, et al.
Human Genome Variation
|
May 20, 2022
A novel TP63 variant in a patient with ankyloblepharon-ectodermal defect-cleft lip/palate syndrome and Rapp-Hodgkin syndrome-like ectodermal dysplasia
Asuka Hori, Ohsuke Migita, Nobutaka Isogawa, et al.
American Journal of Medical Genetics. Part A
|
September 20, 2015
Macrothrombocytopenia and developmental delay with a de novo CDC42 mutation: Yet another locus for thrombocytopenia and developmental delay
Toshiki Takenouchi, Rika Kosaki, Takahiro Niizuma, et al.
Page
of 27
Search research articles
Search
Showing results (1-10 of 266) with videos related to
Sort By:
Page
of 27
Nihon Eiseigaku Zasshi. Japanese Journal of Hygiene
|
October 12, 2016
Reproductive/Developmental Abnormalities Induced by Epigenetic Aberrations and Possible Environmental Causes
Tomoko Kawai, Kenichiro Hata
Clinical Calcium
|
March 19, 2005
[Injectable bone]
Yoichi Yamada, Kenichiro Hata, Minoru Ueda
Advances in Experimental Medicine and Biology
|
June 30, 2018
Placental Development and Nutritional Environment
Kosuke Taniguchi, Tomoko Kawai, Kenichiro Hata
Methods in Molecular Biology (Clifton, N.J.)
|
September 29, 2022
Reduced Representation Bisulfite Sequencing (RRBS)
Kazuhiko Nakabayashi, Michihiro Yamamura, Keita Haseagawa, et al.
Development (Cambridge, England)
|
April 6, 2002
Dnmt3L cooperates with the Dnmt3 family of de novo DNA methyltransferases to establish maternal imprints in mice
Kenichiro Hata, Masaki Okano, Hong Lei, et al.
Brain & Development
|
September 30, 2018
Reading disability due to an ocular motor disorder: A case of an adolescent girl with a previous diagnosis of dyslexia
Tsunehiko Kurokami, Tatsuya Koeda, Ohsuke Migita, et al.
Regenerative Therapy
|
October 2, 2018
Human resource development contributes to the creation of outstanding regenerative medicine products
Fusako Nishigaki, Sachikon Ezoe, Hideki Kitajima, et al.
Genomics Data
|
March 17, 2016
Lists of HumanMethylation450 BeadChip probes with nucleotide-variant information obtained from the Phase 3 data of the 1000 Genomes Project
Kohji Okamura, Tomoko Kawai, Kenichiro Hata, et al.
Human Genome Variation
|
May 20, 2022
A novel TP63 variant in a patient with ankyloblepharon-ectodermal defect-cleft lip/palate syndrome and Rapp-Hodgkin syndrome-like ectodermal dysplasia
Asuka Hori, Ohsuke Migita, Nobutaka Isogawa, et al.
American Journal of Medical Genetics. Part A
|
September 20, 2015
Macrothrombocytopenia and developmental delay with a de novo CDC42 mutation: Yet another locus for thrombocytopenia and developmental delay
Toshiki Takenouchi, Rika Kosaki, Takahiro Niizuma, et al.
Page
of 27