各診療班の紹介
 
業績集 欧文
 
2001
 
 
学術誌に記載された原著論文
  1. Moriuchi M, Inoue H, Moriuchi H: Reciprocal Interactions between Human T-Lymphotropic Virus Type I and Prostaglandins: Implications for Viral Transmission. J. Virol75: 192-198, 2001
  2. Moriuchi M, Moriuchi H: A milk protein lactoferrin enhances human T cell leukemia virus type I and suppresses HIV-1 infection. J. Immunol 166: 4231-4236, 2001
  3. Moriuchi M, Moriuchi H: Octamer transcription factors upregulate the expression of CCR5, a co-receptor for HIV-1 entry. J. Biol. Chem 276: 8639-8642, 2001
  4. Furukawa K, Takamiya K, Okada M, Inoue M, Fukumoto S, Furukawa K: Novel functions of complex carbohydrates elucidated by the mutant mice of glycosyltransferase genes. Biochim Biophys Acta 16: 1525(1-2): 1-12, 2001
  5. Kobayashi S, Uemura H, Kohda T, Nagai T, Chinen Y, Naritomi K, Kinoshita EI, Ohashi H, Imaizumi K, Tsukahara M, Sugio Y, Tonoki H, Kishino T, Tanaka T, Yamada M, Tsutsumi O, Niikawa N, Kaneko-Ishino T, Ishino F: No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patients. Am J Med Genet 104: 225-31, 2001
  6. Yoshiuchi K, Yamagata M, Yoshimoto Q, Zhu Q, Yang T, Nammo R, Uenaka E, Kinoshita T, Hanahusa J, Miyagawa Y, Matsuzawa: Analysis of a non-functional HNF-1α(TCF1) mutation in Japanese subjects with familial type 1 diabetes. Hum Mutat 18: 345-351, 2001
  7. Hirota T, Motomura K, Shimizu T, Kinoshita E, Moriuchi H, Kawaguchi T, Deguchi M, Yoshimoto M : Case with small testes associated with skeletal dysplasia. Clin Pediatr Endocrinol 10: 35-339, 2001
  8. Miyamoto T, Hasagawa Y, Ohnami N, Ogata K, Kinoshita E, Nishi Y,Tachibana K, Hasagawa T : Development of Growth Hormone and Adrenocorticotropic Hormone deficiencies in patients with prenatal or perinatal − onset hypothalamic hypopituitarism having invisible or thin pituitary stalk on magnetic resonance imaging. Endocrine J 48(3): 355-362, 2001
  9. Ariga T, Kondoh T, Yamaguchi K, Yamada M, Sasaki S, DL Nelson, Ikeda H, Kobayashi K, Moriuchi H, Sakiyama Y : Spontaneous in vivo reversion of an inherited mutation in the Wiskott-Aldrich Syndrome. J Immunol 166:5245-5249, 2001
  10. Kondoh T, Kamimura N, Tsuru A, Matsumoto T, Matsuzaka T, Moriuchi H : A case of Schinzel-Giedion syndrome complicated with progressive severe gingival hyperplasia and progressive brain atrophy. Pediatr Int 43: 181-184, 2001
  11. Kondoh T, Yamamoto T, Kono Y, Matsumoto T, Sugawara H, Matsumoto N, Moriuchi H : Condition of microcephaly, growth retardation, joint contractures, atopic dermatitis, and mental retardation in two Japanese sisters: A new autosomal recessive MCA/MR syndrome? Am J Med Genet 102:63-7 , 2001
  12. Kondoh T, Yoshinaga M, Matsumoto T, Takayanagi T, Uetani M, Kubota T, Nishimura G, Moriuchi H: Severe cervical kyphosis in osteopathia striata with cranial sclerosis: case report. Pediatr Radiol 31(9):659-62, 2001

学内紀要、各省庁の研究助成金及び研究委託費による研究成果
  1. Matsumoto T, Kondoh T, Niikawa N, Maeda N, Ishimaru T: A genetic counselingsystem in Nagasaki prefecture: The course and current status of the Genetic Counseling Unit in Nagasaki University Hospital. Acta Med Nagasaki 46: 7-10, 2001
 
長崎大学小児科学教室
著作権表示