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    Results: 1 to 50 of 368

    1.

    Mutation analysis of SOX9 and single copy number variant analysis of the upstream region in eight patients with campomelic dysplasia and acampomelic campomelic dysplasia.

    Wada Y, Nishimura G, Nagai T, Sawai H, Yoshikata M, Miyagawa S, Hanita T, Sato S, Hasegawa T, Ishikawa S, Ogata T.

    Am J Med Genet A. 2009 Nov 16. [Epub ahead of print] No abstract available. PMID: 19921652 [PubMed - as supplied by publisher]Related articles

    2.

    Prenatal diagnosis of platyspondylic skeletal dysplasia Torrance type with three-dimensional helical computed tomography.

    Tamaru S, Kikuchi A, Takagi K, Wakamatsu M, Ono K, Horikoshi T, Nishimura G.

    Prenat Diagn. 2009 Nov 12. [Epub ahead of print] No abstract available. PMID: 19911416 [PubMed - as supplied by publisher]Related articles

    3.

    Czech dysplasia occurring in a Japanese family.

    Matsui Y, Michigami T, Tachikawa K, Yamazaki M, Kawabata H, Nishimura G.

    Am J Med Genet A. 2009 Oct;149A(10):2285-9.PMID: 19764028 [PubMed - in process]Related articles

    4.

    Spinal deformity after intra-operative radiotherapy for paediatric patients.

    Kunieda E, Nishimura G, Kaneko T, Hirobe S, Masaki H, Kamagata S.

    Br J Radiol. 2009 Aug 18. [Epub ahead of print]PMID: 19690075 [PubMed - as supplied by publisher]Related articles

    5.

    Selective lymphadenectomy of para-aortic lymph nodes for advanced gastric cancer.

    Fujimura T, Nakamura K, Oyama K, Funaki H, Fujita H, Kinami S, Ninomiya I, Fushida S, Nishimura G, Kayahara M, Ohta T.

    Oncol Rep. 2009 Sep;22(3):509-14.PMID: 19639196 [PubMed - indexed for MEDLINE]Related articles

    6.

    Mutations in MMP9 and MMP13 determine the mode of inheritance and the clinical spectrum of metaphyseal anadysplasia.

    Lausch E, Keppler R, Hilbert K, Cormier-Daire V, Nikkel S, Nishimura G, Unger S, Spranger J, Superti-Furga A, Zabel B.

    Am J Hum Genet. 2009 Aug;85(2):168-78. Epub 2009 Jul 16. Erratum in: Am J Hum Genet. 2009 Sep;85(3):420. PMID: 19615667 [PubMed - indexed for MEDLINE]Related articles

    7.

    Nemaline (actin) myopathy with myofibrillar dysgenesis and abnormal ossification.

    Arai A, Mitsuhashi S, Saito Y, Komaki H, Sakuma H, Nakagawa E, Sugai K, Sasaki M, Robertson SP, Nishimura G, Yamamoto T, Nonaka I, Nishino I.

    Neuromuscul Disord. 2009 Jul;19(7):485-8. Epub 2009 Jun 23.PMID: 19553121 [PubMed - indexed for MEDLINE]Related articles

    8.

    Identification of loss-of-function mutations of SLC35D1 in patients with Schneckenbecken dysplasia, but not with other severe spondylodysplastic dysplasias group diseases.

    Furuichi T, Kayserili H, Hiraoka S, Nishimura G, Ohashi H, Alanay Y, Lerena JC, Aslanger AD, Koseki H, Cohn DH, Superti-Furga A, Unger S, Ikegawa S.

    J Med Genet. 2009 Aug;46(8):562-8. Epub 2009 Jun 8.PMID: 19508970 [PubMed - indexed for MEDLINE]Related articles

    9.

    Structure-based targeting of bioactive proteins into cypovirus polyhedra and application to immobilized cytokines for mammalian cell culture.

    Ijiri H, Coulibaly F, Nishimura G, Nakai D, Chiu E, Takenaka C, Ikeda K, Nakazawa H, Hamada N, Kotani E, Metcalf P, Kawamata S, Mori H.

    Biomaterials. 2009 Sep;30(26):4297-308. Epub 2009 May 28.PMID: 19477509 [PubMed - indexed for MEDLINE]Related articles

    10.

    Avicin D: a protein reactive plant isoprenoid dephosphorylates Stat 3 by regulating both kinase and phosphatase activities.

    Haridas V, Nishimura G, Xu ZX, Connolly F, Hanausek M, Walaszek Z, Zoltaszek R, Gutterman JU.

    PLoS One. 2009;4(5):e5578. Epub 2009 May 18.PMID: 19440292 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Replicons from genotype 1b HCV-positive sera exhibit diverse sensitivities to anti-HCV reagents.

    Nishimura G, Ikeda M, Mori K, Nakazawa T, Ariumi Y, Dansako H, Kato N.

    Antiviral Res. 2009 Apr;82(1):42-50. Epub 2009 Feb 6.PMID: 19428594 [PubMed - indexed for MEDLINE]Related articles

    12.

    Platyspondylic lethal skeletal dysplasia San Diego type (thanatophoric dysplasia type 1) associated with trisomy 21 presenting with nuchal translucency: a case report.

    Yamada T, Sawai H, Nishimura G, Numabe H, Cho K, Minakami H.

    Prenat Diagn. 2009 Jul;29(7):715-7. No abstract available. PMID: 19340824 [PubMed - indexed for MEDLINE]Related articles

    13.

    Efficacy of concurrent chemoradiotherapy for T1 and T2 laryngeal squamous cell carcinoma regarding organ preservation.

    Nishimura G, Tsukuda M, Mikami Y, Matsuda H, Horiuchi C, Taguchi T, Takahashi M, Kawakami M, Watanabe M, Niho T, Abo H, Yamomoto S.

    Anticancer Res. 2009 Feb;29(2):661-6.PMID: 19331217 [PubMed - indexed for MEDLINE]Related articles

    14.

    A ZRS duplication causes syndactyly type IV with tibial hypoplasia.

    Wu L, Liang D, Niikawa N, Ma F, Sun M, Pan Q, Long Z, Zhou Z, Yoshiura K, Wang H, Sato D, Nishimura G, Dai H, Zhang X, Xia J.

    Am J Med Genet A. 2009 Feb 15;149A(4):816-8. No abstract available. PMID: 19291772 [PubMed - indexed for MEDLINE]Related articles

    15.

    A distinct form of spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL)-leptodactylic type: radiological characteristics in seven new patients.

    Kim OH, Cho TJ, Song HR, Chung CY, Miyagawa S, Nishimura G, Superti-Furga A, Unger S.

    Skeletal Radiol. 2009 Aug;38(8):803-11. Epub 2009 Mar 11.PMID: 19277648 [PubMed - indexed for MEDLINE]Related articles

    16.

    Cytochrome P450 oxidoreductase deficiency: identification and characterization of biallelic mutations and genotype-phenotype correlations in 35 Japanese patients.

    Fukami M, Nishimura G, Homma K, Nagai T, Hanaki K, Uematsu A, Ishii T, Numakura C, Sawada H, Nakacho M, Kowase T, Motomura K, Haruna H, Nakamura M, Ohishi A, Adachi M, Tajima T, Hasegawa Y, Hasegawa T, Horikawa R, Fujieda K, Ogata T.

    J Clin Endocrinol Metab. 2009 May;94(5):1723-31. Epub 2009 Mar 3.PMID: 19258400 [PubMed - indexed for MEDLINE]Related articles

    17.

    Analysis of feasibility and toxicity of concurrent chemoradiotherapy with S-1 for locally advanced squamous cell carcinoma of the head and neck in elderly cases and/or cases with comorbidity.

    Tsukuda M, Ishitoya J, Mikami Y, Matsuda H, Horiuchi C, Taguchi T, Satake K, Kawano T, Takahashi M, Nishimura G, Kawakami M, Sakuma Y, Watanabe M, Shiono O, Komatsu M, Yamashita Y.

    Cancer Chemother Pharmacol. 2009 Oct;64(5):945-52. Epub 2009 Feb 15.PMID: 19219603 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Abnormal basiocciput development in CHARGE syndrome.

    Fujita K, Aida N, Asakura Y, Kurosawa K, Niwa T, Muroya K, Adachi M, Nishimura G, Inoue T.

    AJNR Am J Neuroradiol. 2009 Mar;30(3):629-34. Epub 2008 Dec 26.PMID: 19112063 [PubMed - indexed for MEDLINE]Related articles

    19.

    The efficacy and safety of concurrent chemoradiotherapy for maxillary sinus squamous cell carcinoma patients.

    Nishimura G, Tsukuda M, Mikami Y, Matsuda H, Horiuchi C, Satake K, Taguchi T, Takahashi M, Kawakami M, Hanamura H, Watanabe M, Utsumi A.

    Auris Nasus Larynx. 2009 Oct;36(5):547-54. Epub 2008 Dec 18.PMID: 19097833 [PubMed - in process]Related articles

    20.

    Prenatal diagnosis of thanatophoric dysplasia by 3-D helical computed tomography and genetic analysis.

    Tsutsumi S, Sawai H, Nishimura G, Hayasaka K, Kurachi H.

    Fetal Diagn Ther. 2008;24(4):420-4. Epub 2008 Nov 6.PMID: 18987480 [PubMed - indexed for MEDLINE]Related articles

    21.

    Induction of systemic bone changes by preconditioning total body irradiation for bone marrow transplantation.

    Miyazaki O, Nishimura G, Okamoto R, Masaki H, Kumagai M, Shioda Y, Nozawa K, Kitoh H.

    Pediatr Radiol. 2009 Jan;39(1):23-9. Epub 2008 Oct 25.PMID: 18953533 [PubMed - indexed for MEDLINE]Related articles

    22.

    PTD classification: proposal for a new classification of gastric cancer location based on physiological lymphatic flow.

    Kinami S, Fujimura T, Ojima E, Fushida S, Ojima T, Funaki H, Fujita H, Takamura H, Ninomiya I, Nishimura G, Kayahara M, Ohta T, Yoh Z.

    Int J Clin Oncol. 2008 Aug;13(4):320-9. Epub 2008 Aug 15.PMID: 18704632 [PubMed - indexed for MEDLINE]Related articles

    23.

    Patterns of local recurrence after intraoperative radiotherapy for advanced neuroblastoma.

    Kunieda E, Hirobe S, Kaneko T, Nagaoka T, Kamagata S, Nishimura G.

    Jpn J Clin Oncol. 2008 Aug;38(8):562-6. Epub 2008 Jul 30.PMID: 18667476 [PubMed - indexed for MEDLINE]Related articlesFree article

    24.

    Treatment results and prognostic factors for advanced squamous cell carcinoma of the head and neck treated with concurrent chemoradiotherapy.

    Taguchi T, Tsukuda M, Mikami Y, Matsuda H, Tanigaki Y, Horiuchi C, Nishimura G, Nagao J.

    Auris Nasus Larynx. 2009 Apr;36(2):199-204. Epub 2008 Jul 15.PMID: 18632233 [PubMed - indexed for MEDLINE]Related articles

    25.

    Radiological evolution in IMAGe association: a case report.

    Amano N, Naoaki H, Ishii T, Narumi S, Hachiya R, Nishimura G, Hasegawa T.

    Am J Med Genet A. 2008 Aug 15;146A(16):2130-3.PMID: 18627061 [PubMed - indexed for MEDLINE]Related articles

    26.

    Detection of sentinel and non-sentinel lymph node micrometastases by complete serial sectioning and immunohistochemical analysis for gastric cancer.

    Ishii K, Kinami S, Funaki K, Fujita H, Ninomiya I, Fushida S, Fujimura T, Nishimura G, Kayahara M.

    J Exp Clin Cancer Res. 2008 May 30;27:7.PMID: 18577253 [PubMed - indexed for MEDLINE]Related articlesFree article

    27.

    A compound heterozygote of novel and recurrent DTDST mutations results in a novel intermediate phenotype of Desbuquois dysplasia, diastrophic dysplasia, and recessive form of multiple epiphyseal dysplasia.

    Miyake A, Nishimura G, Futami T, Ohashi H, Chiba K, Toyama Y, Furuichi T, Ikegawa S.

    J Hum Genet. 2008;53(8):764-8. Epub 2008 Jun 14.PMID: 18553123 [PubMed - indexed for MEDLINE]Related articles

    28.

    Congenital joint dislocations caused by carbohydrate sulfotransferase 3 deficiency in recessive Larsen syndrome and humero-spinal dysostosis.

    Hermanns P, Unger S, Rossi A, Perez-Aytes A, Cortina H, Bonafé L, Boccone L, Setzu V, Dutoit M, Sangiorgi L, Pecora F, Reicherter K, Nishimura G, Spranger J, Zabel B, Superti-Furga A.

    Am J Hum Genet. 2008 Jun;82(6):1368-74. Erratum in: Am J Hum Genet. 2008 Aug;83(2):293. PMID: 18513679 [PubMed - indexed for MEDLINE]Related articlesFree article

    29.

    Dual anti-cancer effects of weekly intraperitoneal docetaxel in treatment of advanced gastric cancer patients with peritoneal carcinomatosis: a feasibility and pharmacokinetic study.

    Fushida S, Kinoshita J, Yagi Y, Funaki H, Kinami S, Ninomiya I, Fujimura T, Nishimura G, Kayahara M, Ohta T.

    Oncol Rep. 2008 May;19(5):1305-10.PMID: 18425392 [PubMed - indexed for MEDLINE]Related articles

    30.

    Two new cases of pure 1q terminal deletion presenting with brain malformations.

    Hiraki Y, Okamoto N, Ida T, Nakata Y, Kamada M, Kanemura Y, Yamasaki M, Fujita H, Nishimura G, Kato M, Harada N, Matsumoto N.

    Am J Med Genet A. 2008 May 15;146A(10):1241-7.PMID: 18384145 [PubMed - indexed for MEDLINE]Related articles

    31.

    Results of video-assisted thoracoscopic surgery for esophageal cancer during the induction period.

    Ninomiya I, Osugi H, Fujimura T, Kayahara M, Takamura H, Takemura M, Lee S, Nakagawara H, Nishimura G, Ohta T.

    Gen Thorac Cardiovasc Surg. 2008 Mar;56(3):119-25. Epub 2008 Mar 14.PMID: 18340511 [PubMed - indexed for MEDLINE]Related articles

    32.

    Nephrotic state as a risk factor for developing posterior reversible encephalopathy syndrome in paediatric patients with nephrotic syndrome.

    Ishikura K, Ikeda M, Hamasaki Y, Hataya H, Nishimura G, Hiramoto R, Honda M.

    Nephrol Dial Transplant. 2008 Aug;23(8):2531-6. Epub 2008 Feb 7.PMID: 18258739 [PubMed - indexed for MEDLINE]Related articles

    33.

    Clinical and radiographic delineation of odontochondrodysplasia.

    Unger S, Antoniazzi F, Brugnara M, Alanay Y, Caglayan A, Lachlan K, Ikegawa S, Nishimura G, Zabel B, Spranger J, Superti-Furga A.

    Am J Med Genet A. 2008 Mar 15;146A(6):770-8.PMID: 18241073 [PubMed - indexed for MEDLINE]Related articles

    34.

    Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes.

    Kagami M, Sekita Y, Nishimura G, Irie M, Kato F, Okada M, Yamamori S, Kishimoto H, Nakayama M, Tanaka Y, Matsuoka K, Takahashi T, Noguchi M, Tanaka Y, Masumoto K, Utsunomiya T, Kouzan H, Komatsu Y, Ohashi H, Kurosawa K, Kosaki K, Ferguson-Smith AC, Ishino F, Ogata T.

    Nat Genet. 2008 Feb;40(2):237-42. Epub 2008 Jan 6.PMID: 18176563 [PubMed - indexed for MEDLINE]Related articles

    35.

    Nucleotide-sugar transporter SLC35D1 is critical to chondroitin sulfate synthesis in cartilage and skeletal development in mouse and human.

    Hiraoka S, Furuichi T, Nishimura G, Shibata S, Yanagishita M, Rimoin DL, Superti-Furga A, Nikkels PG, Ogawa M, Katsuyama K, Toyoda H, Kinoshita-Toyoda A, Ishida N, Isono K, Sanai Y, Cohn DH, Koseki H, Ikegawa S.

    Nat Med. 2007 Nov;13(11):1363-7. Epub 2007 Oct 21.PMID: 17952091 [PubMed - indexed for MEDLINE]Related articles

    36.

    Cartilage hair hypoplasia mutations that lead to RMRP promoter inefficiency or RNA transcript instability.

    Nakashima E, Tran JR, Welting TJ, Pruijn GJ, Hirose Y, Nishimura G, Ohashi H, Schurman SH, Cheng J, Candotti F, Nagaraja R, Ikegawa S, Schlessinger D.

    Am J Med Genet A. 2007 Nov 15;143A(22):2675-81.PMID: 17937437 [PubMed - indexed for MEDLINE]Related articles

    37.

    Mandibuloacral dysplasia and a novel LMNA mutation in a woman with severe progressive skeletal changes.

    Kosho T, Takahashi J, Momose T, Nakamura A, Sakurai A, Wada T, Yoshida K, Wakui K, Suzuki T, Kasuga K, Nishimura G, Kato H, Fukushima Y.

    Am J Med Genet A. 2007 Nov 1;143A(21):2598-603.PMID: 17935239 [PubMed - indexed for MEDLINE]Related articles

    38.

    A fluorescent molecular switch driven by the input sequence of metal cations: an azamacrocyclic ligand containing bipolar anthracene fragments.

    Nishimura G, Maehara H, Shiraishi Y, Hirai T.

    Chemistry. 2008;14(1):259-71.PMID: 17886304 [PubMed]Related articles

    39.

    Early assessment of clinical response to concurrent chemoradiotherapy in head and neck carcinoma using fluoro-2-deoxy-d-glucose positron emission tomography.

    Horiuchi C, Taguchi T, Yoshida T, Nishimura G, Kawakami M, Tanigaki Y, Matsuda H, Mikami Y, Oka T, Inoue T, Tsukuda M.

    Auris Nasus Larynx. 2008 Mar;35(1):103-8. Epub 2007 Sep 6.PMID: 17825512 [PubMed - indexed for MEDLINE]Related articles

    40.

    Prenatal diagnosis of chondrodysplasia punctata tibia-metacarpal type using multidetector CT and three-dimensional reconstruction.

    Miyazaki O, Nishimura G, Sago H, Watanabe N, Ebina S.

    Pediatr Radiol. 2007 Nov;37(11):1151-4. Epub 2007 Sep 6.PMID: 17805524 [PubMed - indexed for MEDLINE]Related articles

    41.

    A family with an autosomal dominant mesomelic dysplasia resembling mesomelic dysplasia Savarirayan and Nievergelt types.

    Nakamura M, Matsuda Y, Higo M, Nishimura G.

    Am J Med Genet A. 2007 Sep 1;143A(17):2079-81. No abstract available. PMID: 17702012 [PubMed - indexed for MEDLINE]Related articles

    42.

    [Consideration of preventive free-flowing IV infusion method for vinorelbine]

    Suga Y, Hara Y, Hashimoto H, Nishigami J, Shimizu M, Akasaka H, Hayashi K, Yonejima M, Nakamura M, Inokuchi M, Kasahara K, Nishimura G, Miyamoto K.

    Gan To Kagaku Ryoho. 2007 Aug;34(8):1255-7. Japanese. PMID: 17687207 [PubMed - indexed for MEDLINE]Related articles

    43.

    A novel dominant-negative mutation in Gdf5 generated by ENU mutagenesis impairs joint formation and causes osteoarthritis in mice.

    Masuya H, Nishida K, Furuichi T, Toki H, Nishimura G, Kawabata H, Yokoyama H, Yoshida A, Tominaga S, Nagano J, Shimizu A, Wakana S, Gondo Y, Noda T, Shiroishi T, Ikegawa S.

    Hum Mol Genet. 2007 Oct 1;16(19):2366-75. Epub 2007 Jul 26.PMID: 17656374 [PubMed - indexed for MEDLINE]Related articlesFree article

    44.

    Intact kinase homology domain of natriuretic peptide receptor-B is essential for skeletal development.

    Hachiya R, Ohashi Y, Kamei Y, Suganami T, Mochizuki H, Mitsui N, Saitoh M, Sakuragi M, Nishimura G, Ohashi H, Hasegawa T, Ogawa Y.

    J Clin Endocrinol Metab. 2007 Oct;92(10):4009-14. Epub 2007 Jul 24.PMID: 17652215 [PubMed - indexed for MEDLINE]Related articlesFree article

    45.

    Concurrent chemoradiotherapy for T4 patients with hypopharyngeal and laryngeal squamous cell carcinomas.

    Nishimura G, Tsukuda M, Horiuchi C, Satake K, Yoshida T, Nagao J, Kawakami M, Kondo N, Arai Y, Taguchi T, Matsuda H, Mikami Y.

    Auris Nasus Larynx. 2007 Dec;34(4):499-504. Epub 2007 Jun 28.PMID: 17604583 [PubMed - indexed for MEDLINE]Related articles

    46.

    Effects of metal cation coordination on fluorescence properties of a diethylenetriamine bearing two end pyrene fragments.

    Shiraishi Y, Ishizumi K, Nishimura G, Hirai T.

    J Phys Chem B. 2007 Aug 2;111(30):8812-22. Epub 2007 Jun 29.PMID: 17602521 [PubMed]Related articles

    47.

    A Japanese patient with a mild Lenz-Majewski syndrome.

    Dateki S, Kondoh T, Nishimura G, Motomura K, Yoshiura K, Kinoshita A, Kuniba H, Koga Y, Moriuchi H.

    J Hum Genet. 2007;52(8):686-9. Epub 2007 Jun 26.PMID: 17593321 [PubMed - indexed for MEDLINE]Related articles

    48.

    Anti-tumor effects of bevacizumab in combination with paclitaxel on head and neck squamous cell carcinoma.

    Fujita K, Sano D, Kimura M, Yamashita Y, Kawakami M, Ishiguro Y, Nishimura G, Matsuda H, Tsukuda M.

    Oncol Rep. 2007 Jul;18(1):47-51.PMID: 17549344 [PubMed - indexed for MEDLINE]Related articles

    49.

    Expansion of intensity correlation spectroscopy for lifetime measurements--application to intracellular oxygen dynamics measurements.

    Nishimura G, Pack C, Tamura M.

    J Biomed Opt. 2007 Mar-Apr;12(2):020503.PMID: 17477702 [PubMed - indexed for MEDLINE]Related articles

    50.

    A syndactyly type IV locus maps to 7q36.

    Sato D, Liang D, Wu L, Pan Q, Xia K, Dai H, Wang H, Nishimura G, Yoshiura K, Xia J, Niikawa N.

    J Hum Genet. 2007;52(6):561-4. Epub 2007 May 3.PMID: 17476456 [PubMed - indexed for MEDLINE]Related articles

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