「Screening for Lynch syndrome using risk assessment criteria in patients with ovarian cancer (本文)」の関連論文
-
The association of thyroglobulin single nucleotide polymorphism with miniature dachshunds-specific inflammatory colorectal polyps and its involvement in interleukin-6 amplifier induced chronic inflammation
-
Immunohistochemical assessment of sex-determining region Y (SRY)-related high mobility group (HMG)-box 2 (Sox2) and Krüppel-like factor 4 (Klf4) in ameloblastomas
-
Studies on Cytotoxic Effects of Tumor Necrosis Factor-Related Apoptosis Inducing Ligand (TRAIL) to Canine Cell Lines Derived from Hemangiosarcoma and Mammary Epithelial Tumor
-
Combined Hypophysitis and Type 1 Diabetes Mellitus Related to Immune Checkpoint Inhibitors
-
Disease modeling of pulmonary fibrosis using human pluripotent stem cell-derived alveolar organoids
-
Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes
-
Etiology, diagnosis, treatment, and prevention of human papilloma virus-associated oropharyngeal squamous cell carcinoma
-
Changes in the sexual function of male patients with rectal cancer over a 2‐year period from diagnosis to 24‐month follow‐up: A prospective, multicenter, cohort study
-
Cryptotanshinone is a candidate therapeutic agent for interstitial lung disease associated with a BRICHOS-domain mutation of SFTPC
-
Clinicopathological significance of EGFR pathway gene mutations and CRTC1/3–MAML2 fusions in salivary gland mucoepidermoid carcinoma
-
Genotype-specific cortisol production associated with Cushing's syndrome adenoma with PRKACA mutations
-
Genotype-specific cortisol production associated with Cushing's syndrome adenoma with PRKACA mutations
-
Effect of body-mass index on the risk of gastric cancer among a Japanese population
-
ミスマッチ修復機能欠損のtype2子宮体癌における免疫チェックポイント阻害剤の有用性の検討
-
Functional and genomic characterization of patient-derived xenograft model to study adaptation to mTORC1 inhibitor in clear cell renal cell carcinoma
-
Different factors are associated with conventional adenoma and serrated colorectal neoplasia
-
Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis
-
Novel genes and variants associated with congenital pituitary hormone deficiency in the era of next-generation sequencing
-
The loss of endothelin-2 exhibits an anticancer effect in A549 human lung adenocarcinoma cell line
-
PD1 gene polymorphism is associated with a poor prognosis in hepatocellular carcinoma following liver resection, cohort study
-
PD1 gene polymorphism is associated with a poor prognosis in hepatocellular carcinoma following liver resection, cohort study
-
Anti-diabetic drug metformin inhibits cell proliferation and tumor growth in gallbladder cancer via G0/G1 cell cycle arrest
-
Pancreatic RECK inactivation promotes cancer formation, epithelial-mesenchymal transition, and metastasis
-
The impact of contour maps on estimating the risk of gastrointestinal stromal tumor recurrence: indications for adjuvant therapy: an analysis of the Kinki GIST registry
-
BRCA1 haploinsufficiency promotes chromosomal amplification under Fenton reaction-based carcinogenesis through ferroptosis-resistance
-
Paraproteinemia and neuropathy
-
Risk estimation model for nonalcoholic fatty liver disease in the Japanese using multiple genetic markers
-
Failure of internal fixation for ankle joint Charcot neuroarthropathy with beta(2)-microglobulin amyloidosis: a case report
-
A case of eosinophilic polyangiitis with granulomatosis that evolved to cardiac arrest due to advanced atrioventricular block
-
Ancient evolutionary history of human papillomavirus type 16, 18 and 58 variants prevalent exclusively in Japan (本文)
-
Investigation of the current situation regarding diagnosis and treatment of Alport syndrome in Asian countries: results of survey of the Asian Paediatric Nephrology association (AsPNA) tubular and inherited working group
-
A genome-wide association study identifying single nucleotide polymorphisms in the PPFIBP2 gene was predictive for interstitial lung disease in rheumatoid arthritis patients
-
Structure-based screening combined with computational and biochemical analyses identified the inhibitor targeting the binding of DNA Ligase 1 to UHRF1
-
The ocular involvement did not accompany with the genital ulcer or the gastrointestinal symptoms at the early stage Behcet’s disease
-
Upregulation of cyclase-associated actin cytoskeleton regulatory protein 2 in epithelial ovarian cancer correlates with aggressive histologic types and worse outcomes (本文)
-
Congenital Dysfibrinogenemia Presented with Massive Hematomas Formed after Hysterectomy
-
Downregulation of 5-hydroxymethylcytosine is associated with the progression of cervical intraepithelial neoplasia
-
Tooth brushing, tooth loss, and risk of upper aerodigestive tract cancer: a cohort study of Japanese dentisits
-
Targeting AURKA in treatment of peritoneal tumor dissemination in gastrointestinal cancer (本文)
-
Sessile serrated lesions with dysplasia: is it possible to nip them in the bud?
-
A case of Cockayne syndrome with unusually mild clinical manifestations
-
Activation of BAX and BAK is an attractive combination therapy in melanoma
-
Chronic Active Epstein–Barr Virus Infection Indistinguishable from Autoimmune Hepatitis: A Case Report
-
Beneficial screening of Fabry disease in patients with hypohidrosis
-
Hereditary Congenital Methemoglobinemia Diagnosed at the Age of 79 Years: A Case Report
-
PTEN is a predictive biomarker of trastuzumab resistance and prognostic factor in HER2-overexpressing gastroesophageal adenocarcinoma
-
Gut bacteria identified in colorectal cancer patients promote tumourigenesis via butyrate secretion
-
SOX6 is a Novel Immunohistochemical Marker for Differential Diagnosis of Epithelioid Mesothelioma From Lung Adenocarcinoma
-
SOX6 is a Novel Immunohistochemical Marker for Differential Diagnosis of Epithelioid Mesothelioma From Lung Adenocarcinoma
-
Cell migration is impaired in XPA-deficient cells