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Current Biology : CB
|
January 9, 2007
Experience-driven axon retraction without binocular imbalance in developing visual cortex
Masayuki Haruta, Yoshio Hata
Cancer Letters
|
April 1, 2014
RASSF1A methylation may have two biological roles in neuroblastoma tumorigenesis depending on the ploidy status and age of patients
Masayuki Haruta, Takehiko Kamijo, Akira Nakagawara, et al.
Pediatric Blood & Cancer
|
September 18, 2018
Paternally inherited WT1 mutation plus uniparental disomy of 11p may be an essential mechanism for development of WT1-mutated familial Wilms tumor
Yuya Sato, Masayuki Haruta, Yasuhiko Kaneko, et al.
Genomics
|
June 5, 2003
A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids
Chiga Okita, Makiko Meguro, Hidetoshi Hoshiya, et al.
Genes, Chromosomes & Cancer
|
December 11, 2012
Meiosis error and subsequent genetic and epigenetic alterations invoke the malignant transformation of germ cell tumor
Mizuho Ichikawa, Yasuhito Arai, Masayuki Haruta, et al.
Pediatric Blood & Cancer
|
August 29, 2006
Promoter hypermethylation of the RASSF1A gene predicts the poor outcome of patients with hepatoblastoma
Waka Sugawara, Masayuki Haruta, Fumiaki Sasaki, et al.
Journal of Human Genetics
|
May 6, 2003
Predominant maternal expression of the mouse Atp10c in hippocampus and olfactory bulb
Akiko Kashiwagi, Makiko Meguro, Hidetoshi Hoshiya, et al.
Molecular Carcinogenesis
|
February 21, 2008
Combined BubR1 protein down-regulation and RASSF1A hypermethylation in Wilms tumors with diverse cytogenetic changes
Masayuki Haruta, Yoshiyuki Matsumoto, Hideki Izumi, et al.
American Journal of Neurodegenerative Disease
|
February 6, 2013
Amnestic mild cognitive impairment with low myocardial metaiodobenzylguanidine uptake
Ryuji Sakakibara, Takeshi Ogata, Masayuki Haruta, et al.
Journal of Human Genetics
|
March 4, 2005
Narrowed abrogation of the Angelman syndrome critical interval on human chromosome 15 does not interfere with epigenotype maintenance in somatic cells
Masayuki Haruta, Makiko Meguro, Yu-Ki Sakamoto, et al.
Page
of 5
Search research articles
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Showing results (1-10 of 47) with videos related to
Sort By:
Page
of 5
Current Biology : CB
|
January 9, 2007
Experience-driven axon retraction without binocular imbalance in developing visual cortex
Masayuki Haruta, Yoshio Hata
Cancer Letters
|
April 1, 2014
RASSF1A methylation may have two biological roles in neuroblastoma tumorigenesis depending on the ploidy status and age of patients
Masayuki Haruta, Takehiko Kamijo, Akira Nakagawara, et al.
Pediatric Blood & Cancer
|
September 18, 2018
Paternally inherited WT1 mutation plus uniparental disomy of 11p may be an essential mechanism for development of WT1-mutated familial Wilms tumor
Yuya Sato, Masayuki Haruta, Yasuhiko Kaneko, et al.
Genomics
|
June 5, 2003
A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids
Chiga Okita, Makiko Meguro, Hidetoshi Hoshiya, et al.
Genes, Chromosomes & Cancer
|
December 11, 2012
Meiosis error and subsequent genetic and epigenetic alterations invoke the malignant transformation of germ cell tumor
Mizuho Ichikawa, Yasuhito Arai, Masayuki Haruta, et al.
Pediatric Blood & Cancer
|
August 29, 2006
Promoter hypermethylation of the RASSF1A gene predicts the poor outcome of patients with hepatoblastoma
Waka Sugawara, Masayuki Haruta, Fumiaki Sasaki, et al.
Journal of Human Genetics
|
May 6, 2003
Predominant maternal expression of the mouse Atp10c in hippocampus and olfactory bulb
Akiko Kashiwagi, Makiko Meguro, Hidetoshi Hoshiya, et al.
Molecular Carcinogenesis
|
February 21, 2008
Combined BubR1 protein down-regulation and RASSF1A hypermethylation in Wilms tumors with diverse cytogenetic changes
Masayuki Haruta, Yoshiyuki Matsumoto, Hideki Izumi, et al.
American Journal of Neurodegenerative Disease
|
February 6, 2013
Amnestic mild cognitive impairment with low myocardial metaiodobenzylguanidine uptake
Ryuji Sakakibara, Takeshi Ogata, Masayuki Haruta, et al.
Journal of Human Genetics
|
March 4, 2005
Narrowed abrogation of the Angelman syndrome critical interval on human chromosome 15 does not interfere with epigenotype maintenance in somatic cells
Masayuki Haruta, Makiko Meguro, Yu-Ki Sakamoto, et al.
Page
of 5