Lista de obras -

A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese

artículo científico publicado en 2010

A tumor of the uterine cervix with a complex histology in a Peutz-Jeghers syndrome patient with genomic deletion of the STK11 exon 1 region.

artículo científico publicado en 2014

ATM: Functions of ATM Kinase and Its Relevance to Hereditary Tumors

artículo científico publicado en 2022

Analysis of candidate target genes for mononucleotide repeat mutation in microsatellite instability-high (MSI-H) endometrial cancer.

artículo científico publicado en 2009

Carcinoma of the lower uterine segment diagnosed with Lynch syndrome based on MSH6 germline mutation: A case report.

artículo científico publicado en 2016

Clinical utility of a self-administered questionnaire for assessment of hereditary gynecologic cancer

artículo científico publicado en 2017

Clinicopathologic analysis with immunohistochemistry for DNA mismatch repair protein expression in synchronous primary endometrial and ovarian cancers

artículo científico publicado en 2015

Clinicopathological study on para-aortic lymph node metastasis without pelvic lymph node metastasis in endometrial cancer

artículo científico publicado en 2014

Development and application of fluorescent SDF-1 derivatives

artículo científico publicado en 2012

Endometrial cancer as a familial tumor: pathology and molecular carcinogenesis (review).

artículo científico publicado en 2009

Epigenetic inactivation of the CHFR gene in cervical cancer contributes to sensitivity to taxanes.

artículo científico publicado en 2007

Familial pancreatic cancer with PALB2 and NBN pathogenic variants: a case report

scientific article published on 07 January 2021

Family history and BRCA1/BRCA2 status among Japanese ovarian cancer patients and occult cancer in a BRCA1 mutant case.

artículo científico publicado en 2013

Features of ovarian cancer in Lynch syndrome (Review).

artículo científico publicado en 2014

Flexible hysteroscopy with narrow band imaging (NBI) for endoscopic diagnosis of malignant endometrial lesions.

artículo científico publicado en 2011

Hereditary gynecological tumors associated with Peutz-Jeghers syndrome (Review)

artículo científico publicado en 2013

Homologous Recombination Deficiencies and Hereditary Tumors

artículo científico publicado en 2021

Hypertriglyceridemia is frequent in endometrial cancer survivors

artículo científico publicado en 2013

Identification of a novel uterine leiomyoma GWAS locus in a Japanese population

scientific article published on 27 January 2020

Is repeated high-dose medroxyprogesterone acetate (MPA) therapy permissible for patients with early stage endometrial cancer or atypical endometrial hyperplasia who desire preserving fertility?

artículo científico publicado en 2018

Methylation Analysis of DNA Mismatch Repair Genes Using DNA Derived from the Peripheral Blood of Patients with Endometrial Cancer: Epimutation in Endometrial Carcinogenesis.

artículo científico publicado en 2016

MicroRNA and endometrial cancer: Roles of small RNAs in human tumors and clinical applications (Review).

artículo científico publicado en 2010

Molecular Features and Clinical Management of Hereditary Gynecological Cancers

artículo científico publicado en 2020

Narrow band imaging hysteroscopy: a comparative study using randomized video images

artículo científico publicado en 2011

Osteoporosis is less frequent in endometrial cancer survivors with hypertriglyceridemia

artículo científico publicado en 2014

Relationship of lower uterine segment cancer with Lynch syndrome: a novel case with an hMLH1 germline mutation

artículo científico publicado en 2012

Risk-reducing surgery in hereditary gynecological cancer: Clinical applications in Lynch syndrome and hereditary breast and ovarian cancer

artículo científico publicado en 2014

Synchronous endometrial and ovarian cancer in Lynch syndrome with a germline mutation: A case report

artículo científico publicado en 2018

Synthesis and application of fluorescein- and biotin-labeled molecular probes for the chemokine receptor CXCR4.

artículo científico publicado en 2008

Lista de obras de

A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese

A tumor of the uterine cervix with a complex histology in a Peutz-Jeghers syndrome patient with genomic deletion of the STK11 exon 1 region.

ATM: Functions of ATM Kinase and Its Relevance to Hereditary Tumors

Analysis of candidate target genes for mononucleotide repeat mutation in microsatellite instability-high (MSI-H) endometrial cancer.

Carcinoma of the lower uterine segment diagnosed with Lynch syndrome based on MSH6 germline mutation: A case report.

Clinical utility of a self-administered questionnaire for assessment of hereditary gynecologic cancer

Clinicopathologic analysis with immunohistochemistry for DNA mismatch repair protein expression in synchronous primary endometrial and ovarian cancers

Clinicopathological study on para-aortic lymph node metastasis without pelvic lymph node metastasis in endometrial cancer

Development and application of fluorescent SDF-1 derivatives

Endometrial cancer as a familial tumor: pathology and molecular carcinogenesis (review).

Epigenetic inactivation of the CHFR gene in cervical cancer contributes to sensitivity to taxanes.

Familial pancreatic cancer with PALB2 and NBN pathogenic variants: a case report

Family history and BRCA1/BRCA2 status among Japanese ovarian cancer patients and occult cancer in a BRCA1 mutant case.

Features of ovarian cancer in Lynch syndrome (Review).

Flexible hysteroscopy with narrow band imaging (NBI) for endoscopic diagnosis of malignant endometrial lesions.

Hereditary gynecological tumors associated with Peutz-Jeghers syndrome (Review)

Homologous Recombination Deficiencies and Hereditary Tumors

Hypertriglyceridemia is frequent in endometrial cancer survivors

Identification of a novel uterine leiomyoma GWAS locus in a Japanese population

Is repeated high-dose medroxyprogesterone acetate (MPA) therapy permissible for patients with early stage endometrial cancer or atypical endometrial hyperplasia who desire preserving fertility?

Methylation Analysis of DNA Mismatch Repair Genes Using DNA Derived from the Peripheral Blood of Patients with Endometrial Cancer: Epimutation in Endometrial Carcinogenesis.

MicroRNA and endometrial cancer: Roles of small RNAs in human tumors and clinical applications (Review).

Molecular Features and Clinical Management of Hereditary Gynecological Cancers

Narrow band imaging hysteroscopy: a comparative study using randomized video images

Osteoporosis is less frequent in endometrial cancer survivors with hypertriglyceridemia

Relationship of lower uterine segment cancer with Lynch syndrome: a novel case with an hMLH1 germline mutation

Risk-reducing surgery in hereditary gynecological cancer: Clinical applications in Lynch syndrome and hereditary breast and ovarian cancer

Synchronous endometrial and ovarian cancer in Lynch syndrome with a germline mutation: A case report

Synthesis and application of fluorescein- and biotin-labeled molecular probes for the chemokine receptor CXCR4.