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Department of Otolaryngology, Tokyo Medical and Dental University | 論文
- 新規自然発症ミオシン6-nullマウスの表現型および発現解析
- A familial case of mitochondrial disease resembling Alport syndrome
- Detection of mRNA of Kinesin Superfamily 3A in the Cerebrum and Cerebellum : Biotin-Tyramine-Catalyzed Signal Amplification for In Situ Hybridization
- Time Course of Changes in μ-Opioid Receptor mRNA Levels in the Periaqueductal Gray of Rat Brain by a Single or Repeated Injections of Antisense Oligodeoxynucleotides
- A Case of Generalized Morphea with a High Titer of Anti-Borrelia burgdorferi Antibodies
- Effects of Peptidase Inhibitors on the Enkephalin-Induced Anti-nociception in Rats
- Role of Follicular Dendritic Cells in the Early HIV-1 Infection : In vitro Model without Specific Antibody
- A Case of Descending Necrotizing Mediastinitis Penetrating to the Esophagus
- Hereditary Hearing Loss and Deafness Genes in Japan
- 新規自然発症ミオシン6-nullマウスの表現型および発現解析
- Secondary Hyperbaric Oxygen Therapy for Idiopathic Sudden Sensorineural Hearing Loss in the Subacute and Chronic Phases
- Immunohistochemical Localization of PhospholipaseA in the Guinea Pig Nasal Mucosa
- Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss
- Extended screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss