M. Sakayori

发表

Impact of palliative chemotherapy and best supportive care on overall survival and length of hospitalization in patients with incurable Cancer: a 4-year single institution experience in Japan

Kazunori Otsuka, Y. Murakawa, M. Sakayori, 2019, BMC Palliative Care.

Collaboration of breast cancer clinic and genetic counseling division for BRCA1 and BRCA2 mutation family in Japan

C. Ishioka, M. Takeda, N. Ohuchi, 2004, Breast cancer.

A novel germline mutation of the LKB1 gene in a patient with Peutz-Jeghers syndrome with early-onset gastric cancer

S. Kato, H. Shibata, C. Ishioka, 2004, Journal of Gastroenterology.

Identification and evaluation of 55 genetic variations in the BRCA1 and the BRCA2 genes of patients from 50 Japanese breast cancer families

C. Ishioka, M. Takeda, N. Ohuchi, 2004, Journal of Human Genetics.

Trajectories of hospitalization in three groups of patients with incurable gastric cancer identified by hierarchical clustering: A retrospecitve analysis

Kazunori Otsuka, Y. Murakawa, M. Sakayori, 2020, Journal of Cancer Science and Clinical Therapeutics.

AFP-producing hepatoid adenocarcinoma in association with Barrett's esophagus with multiple liver metastasis responding to paclitaxel/CDDP: a case report.

Kazunori Otsuka, H. Shibata, C. Ishioka, 2005, Anticancer research.

Evaluation of the diagnostic accuracy of the stop codon (SC) assay for identifying protein-truncating mutations in the BRCA1 and BRCA2 genes in familial breast cancer

R. Kanamaru, C. Ishioka, N. Ohuchi, 2003, Journal of Human Genetics.

Loss of protein phosphatase 6 in mouse keratinocytes increases susceptibility to ultraviolet-B-induced carcinogenesis.

H. Kato, R. Katakura, N. Tanuma, 2015, Cancer Letters.

Abrogation of protein phosphatase 6 promotes skin carcinogenesis induced by DMBA

H. Kiyonari, H. Kato, Y. Sakamoto, 2014, Oncogene.

Analysis of the human APC mutation spectrum in a saccharomyces cerevisiae strain with a mismatch repair defect

Kazunori Otsuka, H. Shibata, R. Kanamaru, 2003, International journal of cancer.

Aberrant splicing caused by a MLH1 splice donor site mutation found in a young Japanese patient with Lynch syndrome

Yusuke Nakamura, Y. Furukawa, C. Ishioka, 2012, Familial Cancer.

Isolation of Temperature-sensitive p53 Mutations from a Comprehensive Missense Mutation Library*

S. Kato, Shuang-yin Han, Wen Liu, 2004, Journal of Biological Chemistry.

Dose escalation study of docetaxel and nedaplatin in patients with relapsed or refractory squamous cell carcinoma of the esophagus pretreated using cisplatin, 5-fluorouracil, and radiation

S. Kato, H. Shibata, C. Ishioka, 2006, International Journal of Clinical Oncology.