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Cancer Science
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April 3, 2008
Identification of SMURF1 as a possible target for 7q21.3-22.1 amplification detected in a pancreatic cancer cell line by in-house array-based comparative genomic hybridization
Ayako Suzuki, Tatsuhiro Shibata, Yutaka Shimada, et al.
Lung Cancer (Amsterdam, Netherlands)
|
March 27, 2010
Overexpression of NF-κB inducing kinase underlies constitutive NF-κB activation in lung cancer cells
Yasunori Saitoh, Vicente Javier Martínez Bruyn, Shin Uota, et al.
Histopathology
|
February 22, 2012
ACTN4 gene amplification and actinin-4 protein overexpression drive tumour development and histological progression in a high-grade subset of ovarian clear-cell adenocarcinomas
Sohei Yamamoto, Hitoshi Tsuda, Kazufumi Honda, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms
|
July 30, 2013
Junctional Rab13-binding protein (JRAB) regulates cell spreading via filamins
Ayuko Sakane, Ahmed Alamir Mahmoud Abdallah, Kiyoshi Nakano, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
June 11, 2003
Association of 17q21-q24 gain in ovarian clear cell adenocarcinomas with poor prognosis and identification of PPM1D and APPBP2 as likely amplification targets
Akira Hirasawa, Fumiko Saito-Ohara, Jun Inoue, et al.
Nucleic Acids Research
|
May 30, 2002
An alternatively spliced isoform of transcriptional repressor ATF3 and its induction by stress stimuli
Yoshinori Hashimoto, Chun Zhang, Junya Kawauchi, et al.
Cancer Research
|
July 3, 2008
Frequent inactivation of a putative tumor suppressor, angiopoietin-like protein 2, in ovarian cancer
Ryoko Kikuchi, Hitoshi Tsuda, Ken-ichi Kozaki, et al.
Journal of Human Genetics
|
August 31, 2002
MYEOV, a gene at 11q13, is coamplified with CCND1, but epigenetically inactivated in a subset of esophageal squamous cell carcinomas
Johannes W G Janssen, Issei Imoto, Jun Inoue, et al.
American Journal of Medical Genetics. Part A
|
December 22, 2017
Manifestation of recessive combined D-2-, L-2-hydroxyglutaric aciduria in combination with 22q11.2 deletion syndrome
Mariko Eguchi, Erina Ozaki, Toshifumi Yamauchi, et al.
Human Genome Variation
|
September 23, 2016
A novel missense mutation of COL5A2 in a patient with Ehlers-Danlos syndrome
Miki Watanabe, Ryuji Nakagawa, Takuya Naruto, et al.
Page
of 25
Search research articles
Search
Showing results (101-110 of 241) with videos related to
Sort By:
Page
of 25
Cancer Science
|
April 3, 2008
Identification of SMURF1 as a possible target for 7q21.3-22.1 amplification detected in a pancreatic cancer cell line by in-house array-based comparative genomic hybridization
Ayako Suzuki, Tatsuhiro Shibata, Yutaka Shimada, et al.
Lung Cancer (Amsterdam, Netherlands)
|
March 27, 2010
Overexpression of NF-κB inducing kinase underlies constitutive NF-κB activation in lung cancer cells
Yasunori Saitoh, Vicente Javier Martínez Bruyn, Shin Uota, et al.
Histopathology
|
February 22, 2012
ACTN4 gene amplification and actinin-4 protein overexpression drive tumour development and histological progression in a high-grade subset of ovarian clear-cell adenocarcinomas
Sohei Yamamoto, Hitoshi Tsuda, Kazufumi Honda, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms
|
July 30, 2013
Junctional Rab13-binding protein (JRAB) regulates cell spreading via filamins
Ayuko Sakane, Ahmed Alamir Mahmoud Abdallah, Kiyoshi Nakano, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
June 11, 2003
Association of 17q21-q24 gain in ovarian clear cell adenocarcinomas with poor prognosis and identification of PPM1D and APPBP2 as likely amplification targets
Akira Hirasawa, Fumiko Saito-Ohara, Jun Inoue, et al.
Nucleic Acids Research
|
May 30, 2002
An alternatively spliced isoform of transcriptional repressor ATF3 and its induction by stress stimuli
Yoshinori Hashimoto, Chun Zhang, Junya Kawauchi, et al.
Cancer Research
|
July 3, 2008
Frequent inactivation of a putative tumor suppressor, angiopoietin-like protein 2, in ovarian cancer
Ryoko Kikuchi, Hitoshi Tsuda, Ken-ichi Kozaki, et al.
Journal of Human Genetics
|
August 31, 2002
MYEOV, a gene at 11q13, is coamplified with CCND1, but epigenetically inactivated in a subset of esophageal squamous cell carcinomas
Johannes W G Janssen, Issei Imoto, Jun Inoue, et al.
American Journal of Medical Genetics. Part A
|
December 22, 2017
Manifestation of recessive combined D-2-, L-2-hydroxyglutaric aciduria in combination with 22q11.2 deletion syndrome
Mariko Eguchi, Erina Ozaki, Toshifumi Yamauchi, et al.
Human Genome Variation
|
September 23, 2016
A novel missense mutation of COL5A2 in a patient with Ehlers-Danlos syndrome
Miki Watanabe, Ryuji Nakagawa, Takuya Naruto, et al.
Page
of 25