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Departmemt of Cardiology, Surugadai Nihon University Hospital | 論文
- -100-EFFECTS OF VASOPRESSIN AND THE SYMPATHETIC NERVOUS SYSTEM IN THE CARDIOVASCULAR RESPONSE TO CAROTID SINUS REFLEX
- COMPARISON OF LIPOXYGENASE PATHWAY AND ANGIOTENSIN CONVERTING ENZYME INHIBITION ON BLOOD PRESSURE IN THE SPONTANEOUSLY HYPERTENSIVE RAT
- Inhibitory Effects of 1'-Acetoxychavicol Acetate on N-Nitrosobis(2-oxopropyl)-amine-induced Initiation of Cholangiocarcinogenesis in Syrian Hamsters
- Possible Mechanism of Acute Coronary Events Caused by Focal Vasospasm : Evaluation by Plaque Appearance and High-Sensitive C-reactive Protein(Acute Coronary Syndrome, Basic/Clinical 6 (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation S
- Simultaneous Determination of _L-Phenylalanine and Branched-chain _L-Amino Acids in Plasma by Liquid Chromatographic System with a Coimmobilized Enzyme Reactor and Fluorescence Detection
- PJ-432 Angiotensin 2 as a Maker of Prognosis in Hyper Acute Phase of Acute Coronary Syndromes (ACS)(Acute coronary syndrome, basic/clinical-7 (IHD) PJ73,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation S
- OJ-292 Outcome and Medical Cost of Facilitated Percutaneous Coronary Intervention (PCI) (Thrombolysis Alone vs Rescue POBA vs Rescue STENT)(Acute coronary syndrome, basic/clinical-3 (IHD) OJ49,Oral Presentation (Japanese),The 70th Anniversary Annual Scien
- Experimantal Study of Inclusive Reaction ^C(γ,π^-) at 44.2°
- OJ-046 Impact of Increased Hign-density Lipoprotein Cholesterol Level by Combination Therapy with Pravastatin and Lifestyle Modification on Coronary Atherosclerosis Regression(Atherosclerosis, clinical(03)(IHD),Oral Presentation(Japanese),The 72nd Annual
- Possible Anti-tumor Promoting Properties of Edible Plants from Thailand, and Identification of an Active Constituent, Cardamonin, of Boesenbergia pandurata
- A Novel Mutation in the Cornea-Specific Keratin 12 Gene in Meesmann Corneal Dystrophy
- Novel Mutation (V505D) of the TGFBI Gene Found in A Chinese Family with Lattice Corneal Dystrophy, Type I
- Mutations in the Membrane Component, Chromosome 1, Surface Marker 1 (M1S1) Gene in Gelatinous Drop-like Corneal Dystrophy
- Analysis of COL8A2 Gene Mutation in Japanese Patients with Fuchs' Endothelial Dystrophy and Posterior Polymorphous Dystrophy
- Mutation Analysis of the TGFBI Gene in Vietnamese with Granular and Avellino Corneal Dystrophy
- OPA1 Gene Mutations in Japanese Patients with Bilateral Optic Atrophy Unassociated with Mitochondrial DNA Mutations at nt 11778, 3460, and 14484
- Multiplex Polymerase Chain Reaction for Detection of Herpes Simplex Virus Type 1, Type 2, Cytomegalovirus, and Varicella-Zoster Virus in Ocular Viral Infections
- A Novel Mutation of the TGFBI Gene Found in a Vietnamese Family with Atypical Granular Corneal Dystrophy
- Transferrin-Polyethylenimine Conjugate, FuGENE6 and TransIT-LT as Nonviral Vectors for Gene Transfer to the Corneal Endothelium
- MISSENSE MUTATION OF RHODOPSIN GENE CODON 15 FOUND IN JAPANESE AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA
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