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Kazuhide Imai

Showing results (1-10 of 19) with videos related to

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Microbiology and Immunology|July 22, 2005
Microarray analysis of host gene-expression during intracellular nests formation of Trypanosoma cruzi amastigotesKazuhide Imai, Tatsuyuki Mimori, Makoto Kawai, et al.
Nucleic Acids Research|March 16, 2006
A new method for gene discovery in large-scale microarray dataKentaro Yano, Kazuhide Imai, Akifumi Shimizu, et al.
Molecular and Cellular Biochemistry|May 11, 2010
Knockdown of transmembrane protein 132A by RNA interference facilitates serum starvation-induced cell death in Neuro2a cellsKentaro Oh-hashi, Kazuhide Imai, Hisashi Koga, et al.
Molecular Biosystems|July 20, 2007
A novel SNP detection technique utilizing a multiple primer extension (MPEX) on a phospholipid polymer-coated surfaceKazuhide Imai, Yasukazu Ogai, Daisuke Nishizawa, et al.
Gene|September 20, 2005
Temporal change in mKIAA gene expression during the early stage of retinoic acid-induced neurite outgrowthKazuhide Imai, Makoto Kawai, Mitsuhiro Tada, et al.
Brain & Development|September 20, 2005
Congenital neuromuscular disease with uniform type-1 fibers, presenting early stage dystrophic muscle pathologySeigo Korematsu, Kazuhide Imai, Keisuke Sato, et al.
Nutrition (Burbank, Los Angeles County, Calif.)|March 25, 2023
A case of Fukuyama-type congenital muscular dystrophy with acute carnitine deficiency triggered by fever, vomiting, and gastrointestinal bleedingShin-Ichi Uchiyama, Seigo Korematsu, Rieko Wasada, et al.
Pediatric Neurosurgery|January 31, 2002
Limited dorsal myeloschisis associated with multiple vertebral segmentation disorderMitsuo Isono, Makoto Goda, Tohru Kamida, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 21, 2010
Ph+ALL in a pediatric patient with neuroblastoma in infancySo-ichi Suenobu, Yo-suke Handa, Shuji Kuga, et al.
Endocrine Journal|April 4, 2008
Clinical course of patients with nonclassical 21-hydroxylase deficiency (21-OHD) diagnosed in infancy and childhoodKen-ichi Kashimada, Makoto Ono, Toshikazu Onishi, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Microbiology and Immunology|July 22, 2005
Microarray analysis of host gene-expression during intracellular nests formation of Trypanosoma cruzi amastigotesKazuhide Imai, Tatsuyuki Mimori, Makoto Kawai, et al.
Nucleic Acids Research|March 16, 2006
A new method for gene discovery in large-scale microarray dataKentaro Yano, Kazuhide Imai, Akifumi Shimizu, et al.
Molecular and Cellular Biochemistry|May 11, 2010
Knockdown of transmembrane protein 132A by RNA interference facilitates serum starvation-induced cell death in Neuro2a cellsKentaro Oh-hashi, Kazuhide Imai, Hisashi Koga, et al.
Molecular Biosystems|July 20, 2007
A novel SNP detection technique utilizing a multiple primer extension (MPEX) on a phospholipid polymer-coated surfaceKazuhide Imai, Yasukazu Ogai, Daisuke Nishizawa, et al.
Gene|September 20, 2005
Temporal change in mKIAA gene expression during the early stage of retinoic acid-induced neurite outgrowthKazuhide Imai, Makoto Kawai, Mitsuhiro Tada, et al.
Brain & Development|September 20, 2005
Congenital neuromuscular disease with uniform type-1 fibers, presenting early stage dystrophic muscle pathologySeigo Korematsu, Kazuhide Imai, Keisuke Sato, et al.
Nutrition (Burbank, Los Angeles County, Calif.)|March 25, 2023
A case of Fukuyama-type congenital muscular dystrophy with acute carnitine deficiency triggered by fever, vomiting, and gastrointestinal bleedingShin-Ichi Uchiyama, Seigo Korematsu, Rieko Wasada, et al.
Pediatric Neurosurgery|January 31, 2002
Limited dorsal myeloschisis associated with multiple vertebral segmentation disorderMitsuo Isono, Makoto Goda, Tohru Kamida, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 21, 2010
Ph+ALL in a pediatric patient with neuroblastoma in infancySo-ichi Suenobu, Yo-suke Handa, Shuji Kuga, et al.
Endocrine Journal|April 4, 2008
Clinical course of patients with nonclassical 21-hydroxylase deficiency (21-OHD) diagnosed in infancy and childhoodKen-ichi Kashimada, Makoto Ono, Toshikazu Onishi, et al.
Pageof 2