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Microbiology and Immunology
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July 22, 2005
Microarray analysis of host gene-expression during intracellular nests formation of Trypanosoma cruzi amastigotes
Kazuhide Imai, Tatsuyuki Mimori, Makoto Kawai, et al.
Nucleic Acids Research
|
March 16, 2006
A new method for gene discovery in large-scale microarray data
Kentaro 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 cells
Kentaro 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 surface
Kazuhide 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 outgrowth
Kazuhide 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 pathology
Seigo 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 bleeding
Shin-Ichi Uchiyama, Seigo Korematsu, Rieko Wasada, et al.
Pediatric Neurosurgery
|
January 31, 2002
Limited dorsal myeloschisis associated with multiple vertebral segmentation disorder
Mitsuo 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 infancy
So-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 childhood
Ken-ichi Kashimada, Makoto Ono, Toshikazu Onishi, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 19) with videos related to
Sort By:
Page
of 2
Microbiology and Immunology
|
July 22, 2005
Microarray analysis of host gene-expression during intracellular nests formation of Trypanosoma cruzi amastigotes
Kazuhide Imai, Tatsuyuki Mimori, Makoto Kawai, et al.
Nucleic Acids Research
|
March 16, 2006
A new method for gene discovery in large-scale microarray data
Kentaro 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 cells
Kentaro 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 surface
Kazuhide 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 outgrowth
Kazuhide 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 pathology
Seigo 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 bleeding
Shin-Ichi Uchiyama, Seigo Korematsu, Rieko Wasada, et al.
Pediatric Neurosurgery
|
January 31, 2002
Limited dorsal myeloschisis associated with multiple vertebral segmentation disorder
Mitsuo 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 infancy
So-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 childhood
Ken-ichi Kashimada, Makoto Ono, Toshikazu Onishi, et al.
Page
of 2