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Johji Inazawa

Showing results (31-40 of 226) with videos related to

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Cancer|April 25, 2003
Correlation between genetic alteration and long-term clinical outcome of patients with oligodendroglial tumors, with identification of a consistent region of deletion on chromosome arm 1pNaoya Hashimoto, Mamoru Murakami, Yoshinobu Takahashi, et al.
Human Pathology|July 4, 2012
Molecular alterations in AKT and its protein activation in human lung carcinomasYoh Dobashi, Maiko Kimura, Hirochika Matsubara, et al.
Cancer Genetics and Cytogenetics|March 21, 2003
A consistent region of deletion on 1p36 in meningiomas: identification and relation to malignant progressionMamoru Murakami, Naoya Hashimoto, Yoshinobu Takahashi, et al.
Cancer Science|June 26, 2003
Down-regulation of SKP2 induces apoptosis in lung-cancer cellsSana Yokoi, Kohichiroh Yasui, Toshihiko Iizasa, et al.
Cancer Science|May 8, 2021
Identification of PDHX as a metabolic target for esophageal squamous cell carcinomaJun Inoue, Masahiro Kishikawa, Hitoshi Tsuda, et al.
Biochemistry and Biophysics Reports|May 24, 2021
Augmentation of lenvatinib efficacy by topical treatment of <i>miR-634</i> ointment in anaplastic thyroid cancerMasahiro Kishikawa, Jun Inoue, Hidetoshi Hamamoto, et al.
Journal of Human Genetics|May 2, 2003
GPC5 is a possible target for the 13q31-q32 amplification detected in lymphoma cell linesWei Yu, Jun Inoue, Issei Imoto, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 29, 2003
TERC identified as a probable target within the 3q26 amplicon that is detected frequently in non-small cell lung cancersSana Yokoi, Kohichiroh Yasui, Toshihiko Iizasa, et al.
Cancer Science|December 15, 2004
Skp2 overexpression is a p27Kip1-independent predictor of poor prognosis in patients with biliary tract cancersTakahiro Sanada, Sana Yokoi, Shigeki Arii, et al.
American Journal of Medical Genetics. Part A|October 18, 2008
Heterozygous deletion at 14q22.1-q22.3 including the BMP4 gene in a patient with psychomotor retardation, congenital corneal opacity and feet polysyndactylyShin Hayashi, Nobuhiko Okamoto, Yoshio Makita, et al.
Pageof 23

Showing results (31-40 of 226) with videos related to

Sort By:
Pageof 23
Cancer|April 25, 2003
Correlation between genetic alteration and long-term clinical outcome of patients with oligodendroglial tumors, with identification of a consistent region of deletion on chromosome arm 1pNaoya Hashimoto, Mamoru Murakami, Yoshinobu Takahashi, et al.
Human Pathology|July 4, 2012
Molecular alterations in AKT and its protein activation in human lung carcinomasYoh Dobashi, Maiko Kimura, Hirochika Matsubara, et al.
Cancer Genetics and Cytogenetics|March 21, 2003
A consistent region of deletion on 1p36 in meningiomas: identification and relation to malignant progressionMamoru Murakami, Naoya Hashimoto, Yoshinobu Takahashi, et al.
Cancer Science|June 26, 2003
Down-regulation of SKP2 induces apoptosis in lung-cancer cellsSana Yokoi, Kohichiroh Yasui, Toshihiko Iizasa, et al.
Cancer Science|May 8, 2021
Identification of PDHX as a metabolic target for esophageal squamous cell carcinomaJun Inoue, Masahiro Kishikawa, Hitoshi Tsuda, et al.
Biochemistry and Biophysics Reports|May 24, 2021
Augmentation of lenvatinib efficacy by topical treatment of <i>miR-634</i> ointment in anaplastic thyroid cancerMasahiro Kishikawa, Jun Inoue, Hidetoshi Hamamoto, et al.
Journal of Human Genetics|May 2, 2003
GPC5 is a possible target for the 13q31-q32 amplification detected in lymphoma cell linesWei Yu, Jun Inoue, Issei Imoto, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 29, 2003
TERC identified as a probable target within the 3q26 amplicon that is detected frequently in non-small cell lung cancersSana Yokoi, Kohichiroh Yasui, Toshihiko Iizasa, et al.
Cancer Science|December 15, 2004
Skp2 overexpression is a p27Kip1-independent predictor of poor prognosis in patients with biliary tract cancersTakahiro Sanada, Sana Yokoi, Shigeki Arii, et al.
American Journal of Medical Genetics. Part A|October 18, 2008
Heterozygous deletion at 14q22.1-q22.3 including the BMP4 gene in a patient with psychomotor retardation, congenital corneal opacity and feet polysyndactylyShin Hayashi, Nobuhiko Okamoto, Yoshio Makita, et al.
Pageof 23