スポンサーリンク
Riken Tokyo Jpn | 論文
- Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease
- Correlation of genetic etiology with response to β-adrenergic blockade among symptomatic patients with familial long-QT syndrome
- Radioimmunotherapy of human synovial sarcoma using a monoclonal antibody against FZD10
- Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population
- Expression profiles of two types of human knee-joint cartilage
- Activation of an estrogen/estrogen receptor signaling by BIG3 through its inhibitory effect on nuclear transport of PHB2/REA in breast cancer
- SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population
- Induction of remission following a single dose of rituximab alone in a patient with minimal change nephrotic syndrome
- Long-term beneficial effects of angiotensin-converting enzyme inhibitor and angiotensin receptor blocker therapy for patients with advanced immunoglobulin A nephropathy and impaired renal function
- A case of acute renal failure after exercise with renal hypouricemia demonstrated compound heterozygous mutations of uric acid transporter 1
- Comparison of inhibitors of renin-angiotensin-aldosterone system (RAS) and combination therapy of steroids plus RAS inhibitors for patients with advanced immunoglobulin A nephropathy and impaired renal function