業績集 欧文
  1. Qualitative and quantitative characterization of Fas (CD95) expression and its role in primary human acute leukemia cells.
    Li, Q., Tsuruda, K., Sugahara, K., Dateki, N., Ohishi, E., Yamada, Y., Tomonaga, M., Moriuchi,H., Tsuji, Y., and Kamihira, S
    Leuk. Res. 24:437-444 (2000)
  2. Inefficient formation of a complex among CXCR4, CD4 and gp120 in U937 clones resistant to X4 gp120-gp41-mediated fusion.
    Xiao, X., Norwood, D., Feng, Y.R., Moriuchi, M., Jones-Trower, A., Stantchev, T.S., Moriuchi, H., Broder, C.C., Dimitrov, D.S:
    Exp. Mol. Pathol. 68:139-146 (2000)
  3. In Vitro Reactivation of HIV-1 from Latently Infected, Resting CD4+ T Cells upon Bacterial Stimulation.
    Moriuchi, H., Moriuchi, M., Mizell, S.B., Ehler, L.A., and Fauci, A.S:
    J. Infect. Dis 181:2041-2044 (2000)
  4. Class I-Unrestricted Non-Cytotoxic Anti-HTLV-I Activity of CD8+ T Cells.
    Moriuchi, M., and Moriuchi, H
    Blood 96:1994-1995 (2000)
  5. Cathepsin G, a neutrophil-derived serine protease, increases susceptibility of macrophages to acute human immunodeficiency virus type 1 infection.
    Moriuchi, H., Moriuchi, M., and Fauci, A.S
    J. Virol. 74:6849-6855 (2000)
  6. Role of varicella-zoster virus in stroke syndromes.
    Moriuchi, H., and W. Rodriguez
    Pediatr. Infect. Dis. J. 19:653-658 (2000)
  7. Herpes Simplex Virus Infection Induces Replication of Human Immunodeficiency Virus Type 1.
    Moriuchi, M., Moriuchi, H., Williams, R, and Straus, S.E:
    Virology (in press; Dec 2000)
  8. In Vitro Induction of HIV-1 Replication in Resting CD4+ T Cells Derived from Individuals with Undetectable Plasma Viremia upon Stimulation with Human T-Cell Leukemia Virus Type I.
    Moriuchi, H., and Moriuchi, M
    Virology (in press; Dec 2000)
  9. Novel mutation of the ACTH receptor gene in a female adult patient with adrenal unresponsiveness to ACTH.
    T. Ishii, T. Ogata, G. Sasaki, S. Sato, E. Kinoshita, N. Matsuo
    Clin Endocrinol 53: 389-392, (2000)
  10. MR imaging of the pituitary gland in children and young adults with congenital combined pituitary hormone deficiency associated with PROP1 mutations.
    Fofanova,O, Takamura,N, Kinoshita,E, Vorontsov,A, Dedov,I, Peterkova,V, Yamashita,S
    Am J Roentgenol 174: 555-559 (2000)
  11. Young-Simpson syndrome comprising transient hypothyroidiam, normal growth, macular degeneration and torticolis.
    Kondoh,T, Kinoshita,E, Moriuchi,H, Niikawa,N, Matsumoto,T, Masuno,M:
    Am J Med Genet 90, 85-86 (2000).
  12. Improvement of C-reactive protein levels and body temperature of an elderly patient infected with Pseudomonas aeruginosa on treatment with Mao-Bushi-Saishin-To.
    Kamei,T , Kondoh,T, Nagura,S, Toriumi,Y, Kumano,H, Tomioka,H:
    The J Alternative and Complementary Medicine 6, 235-239 (2000).
  13. Determination of carreir status for the Wiskott-Aldrich syndrome by flow cytometric analysis of Wiskott-Aldrich syndrome protein expression in peripheral blood mononuclear cells.
    Yamada,M, Ariga,T, Kawamura,N, Yamaguchi,K, Ohtsu,M, Nelson,DL, Kondoh,T, Kobayashi,I,Okano,M, Kobayashi,K, Sakiyama,Y:
    J Immunol. 165: 1119-1122 (2000).
  14. A case of achondroplasia with severe respiratory failure, profound developmantal delay and hyperceatine phosphokinasemia.
    Y.Imamura, T.Kondoh, T.Kamei, A.Tsuru, Y.Shimasaki, E.Kinoshita, T.Matsumoto, H.Moriuchi:
    Pediatric International, 42, 564-567 (2000).
  15. Alteration of tumor phenotypes of B16 melanoma after genetic remodeling of the ganglioside profile.
    Tsurifune T, Ito T, Li XJ, Yamashiro S, Okada M, Kanematsu T, Shiku H, Furukawa K
    Int J Oncol. 17:159-65 (2000).
  16. GD3 synthase gene expression in PC12 cells results in the continuous activation of TrkA and ERK1/2 and enhanced proliferation.
    Fukumoto S, Mutoh T, Hasegawa T, Miyazaki H, Okada M, Goto G, Furukawa K, Urano T
    J Biol Chem. 25;275(8):5832-8 (2000).
  17. Walker-Warburg syndrome is genetically distinct from Fukuyama type congenital muscular dystrophy.
    Chadani Y, Kondoh T, Kaminura N, Matsumoto T, Kobayashi O, Kondo-Iida E, Kobayashi K, Nonaka I, Toda T:
    J Neurol Sci 177: 150-153 (2000).
  18. Effect of half the standard dose of Ma0-bushi-to in two MRSA patients and one decubitus ulcer patient.
    Kamei T, Nagura S, Toriumi Y, Kumano H, Kondoh T, Tomioka H
    Am J Chin Med 28: 301-3-4 (2000).
  19. The vasocontractibe action of norepinephrine and serotonin in deep arterioles in rat cerebral gray matter.
    Takahashi R, Sakai T, Furuyama Y, Inoue CN, Kondo Y, Onuma S, Iinuma K:
    Tohoku J Exp Med 190: 129-142 (2000).
  20. Peculiar respiratory response observed during sleep-onset REM sleep of an infant with Ondine's curse.
    Takahashi R, Kakizawa H, Ito T, Yamada M, Nakae S:
    Neuropediatrics 31: 269-272 (2000).
  21. Neonatal submandibular suppurative sialadenitis.
    Takahashi R, Chikaoka S, Ito T, Yamada M, Matsutane S, Nakae S:
    Eur J Pediatr 159: 868 (2000).
  22. New radiologic finding by magnetic resonance imaging examination of the brain in Coffin-Lowry syndrome.
    Kondoh T, Matsumoto T, Ochi M, Sukegawa K, Tsuji Y
    J Hum Genet 43:59-61, 1998
  23. A severe case of Moebius syndrome with calcification on the fourth ventricular floor.
    Matsunaaga Y, Amamoto N, Kondoh T, Ohtsuka Y, Miyazoe H, Kamimura N, Matsumoto T, Tsuji Y
    J Hum Genet 43:62-64, 1998<
  24. A case of complete type DiGeorge syndrome treated by bone marrow transplantation.
    Matsumoto T, Amamoto N, Kondoh T, Nakayama M, Tsuji Y
    Bone Marrow Transplant 1988 (in press)
  25. The Gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32.
    Fujimoto M, Kantaputra PN, Ikegawa S, Fukushima Y, Sonta S, Matsuo M, Ishida T, Matsumoto T,Kondo S, Tomita H, Deng HX, Ventruto V, Takagi T, Nakamura Y, Niikawa N
    J Hum Genet 43:32-36, 1998
  26. Origin and mechanism of formation of 45,X/47,XX,+21 mosaicism in a fetus.
    Harada N, Abe K, Nishimura T, Sasaki K, Ishikawa M, Fujimoto M, Matsumoto T, Niikawa N
    Am J Med Genet 75:432-427, 1998
  27. Clinical study on accentuated antagonism in the regulation of heart rate in children.
    Miyazoe H, Harada Y, Yamasaki S, Tsuji Y
    Jpn Heart J 39:481-487, 1998
  28. A mutational hot spot in the Prop-1 gene in Russian children with combined pituitary hormone deficiency.
    Fofanova OV, Kinoshita E, et al
    Pituitary 1:45-48, 1998
  29. Rarity of Pit-1 gene involvement in children from Russia with combined pituitary hormone deficiency.
    Fofanova OV, Kinoshita E, Yoshimoto M, Tsuji Y, et al.
    Am J Med Genet 77:360-365, 1998
  30. Compoud heterozygous deletion of the Prop-1 gene in children with combined pituitary hormone deficiency.
    Fofanova OV, Kinoshita E, et al
    J Clin Endoclinol Metab 1998 (in press)
  31. A common mutation in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasia.
    Fofanova OV, Kinoshita E, et al
    Endocrine J 1988 (in press)
  32. The fates of the collosal neurons in neocortex after bisection of corpus callosum, using the technique of retrograde neuronal labeling with to fluorescent dyes.
    Orihara YI, Kishikawa M, Ono K
    Brain Res 778:393-396, 1997
  33. Genetic remodeling of gangliosides resulted in the enhanced reactions to the foreign substance in skin.
    Fukumoto S, Yamamoto A, Hasegawa T, Abe K, Okada M, Min ZJ, Miyazaki H, Tsuji Y, Goto G, Suzuki M, Shiku H, Furukawa K
    Glycobiology 7:1111-1120, 1997
  34. Expression cloning of rat cDNA encoding UDP-galactose:GD2 beta 1,3-galactosyltransferase that determines the expression of GD1b/GM1/GA1.
    Miyazaki H, Fukumoto S, Okada M, Hasegawa T, Furukawa K
    J Biol Chem 272:24794-24799, 1997
  35. Wiskott-Aldrich syndrome in two sisters.
    Kondoh T, Matsumoto T, Tsuji Y
    Am J Med Genet 74:218-219, 1997
  36. Children with chronic granulomatous disease: Their contributions toward understanding of phagocytic cells.
    Tsuji Y, Kondoh T, Quie PG
    Acta Med Nagasaki 42:1-4, 1997
  37. A Nager acrofacial dysostosis syndrome patient with severe respiratory distress syndrome (RDS).
    Kondoh T, Ito M, Ariyama A, Shitijoh T, Matsumoto T, Tsuji Y
    Jpn J Hum Genet 42:445-449, 1997
  38. Childhood leukemia: Epidemiologocal investigation and effectiveness of tratment in Nagasaki over the past 12 years.
    Kusuyama M, Matsumoto K, Matsumoto T, Tsuji Y
    Acta Pediatr Jpn 39:181-187, 1997
  39. Insulin-like growth faactor 2 gene imprinting in cleaar cell carcinooma of the kidney.
    Sohda T, Soejima H, Matsumoto T, Yun K
    Human Pathology 28:1315-1318, 1997
  40. Influence of forhead exposure to red photodiode light on NK activity.
    Kamei T, Kumano H, Matsumoto T, Yasuhi M, Jimbo S
    Photomedicine and Photobiology 19:145-148, 1997
  41. NF-kB potently upregulates expression of RANTES, an anti-HIV chemokine.
    Moriuchi H, Moriuchi M, Fauci AS
    J Immunol 158:3483-91, 1997
  42. Disseminated zoster and aseptic meningitis in a previously healthy patient.
    Moriuchi H, Moriuchi M, Sun CCJ, Trucksis M
    J Infect 35:183-5, 1997
  43. Cloning and analysis of the promoter region of CXCR4, a coreceptor for HIV-1 entry.
    Moriuchi H, Moriuchi M, Turner W, Fauci AS
    J Immunol 159:4322-9, 1997
  44. Cloning and analysis of the promoter region of CCR5, a coreceptor for HIV-1 entry.
    Moriuchi H, Moriuchi M, Fauci AS
    J Immunol 159:5441-9, 1997
  45. Promonocytic U397 cell cones expressing CD4 and CXCR4 are resistant to infection with and cell-to-cell fusion by T-tropic HIV-1.
    Moriuchi H, Moriuchi M, Arthor J, Hoxie J, Fauci AS
    J Virol 71:9664-71, 1997
  46. Differentiation of promonocytic U937 subclones into macrophagelike phenotypes regulates a cellular factor (s) which modulates fusion / entry of macrophagetropic human immunodeficiency virus type 1.
    Moriuchi H, Moriuchi M, Fauci AS
    J Virol 72:3394-3400, 1997
  47. CXCR4 and CCR5 genetic polymorphisms in long-termnonprogressive human immunodeficiency virus infection : lack of association with mutations other than CCR5-Delta32.
    Cohen OJ, Moriuchi H, et al.
    J Virol 72:6215-6217, 1997
  48. Cancer incidence in Nagasaki prefecture 1988-1992.
    Soda M, Ikeda T, Saeki S, Ishikawa H, Shibata Y
    Cancer Incidence in Five Countries Vol.VII, Ed by Parkin DM, p390-393, 1997
  49. Salivary grand tumors among Atomic bomb survivors, 1950-1987.
    Suku T, Hayashi Y, Takahara O, Matsuura H, Tokunaga M, Tokuoka S, Soda M, Mabuchi K, Land CE
    Cancer 79:1465-75, 1997
  50. DAX-1 gene mutations and deletions in Japanese patients with adrenal hypoplasia congenita and hypogonadotropic hypogonadism.
    Kinoshita E, Yoshimoto M, Motomura K, Kawaguchi T, Mori R, Baba T, et al
    Horm Res 48:29-34, 1997
  51. Pubertal changes in testicular 3beta-hydroxysteroid dehydrogenase activity in a male with classical 3beta-hydroxysteroid dehydrogenase deficiency showing spontaneous secondary sexual maturation.
    Yoshimoto M, Kawaguchi T, Mori R, Kinoshita E, Baba T, et al
    Horm Res 48:83-87, 1997
  52. Primary prevention of HTLV-1 in Japan.
    Hino S, Tsuji Y, et al.
    Leukemia, 11(Suppl): 57-59, 1997
  53. Morphological subtyping of acute myeloid leukemia with maturation (AML-M2) : homogeneous pink-colored cytoplasm of mature neutrophils is most characteristic of AML-M2 with t(8 ; 21).
    Nakamura H, Matsumoto K, Tsuji Y, et al.
    Leukemia 11:651-655, 1997
  54. Treatment outcome and prognostic factors in childhood acute myeloblastic leukemia: a report from the Japanese Children's Cancer and Leukemia Study Group (CCLSG).
    Katano N, Yanai M, Tsuji Y, et al.
    Int J Hematol 66:103-110, 1997