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—é–؍N”VC‹´–{@—²CÜ‹’‰•vF”]ŠÌtÇŒóŒQiZellweger ÇŒóŒQjCˆä‘º—T•vC”öŒ`‰x˜YC‚‹vŽj–›C‚ˆä´ˆê˜Yi•ÒjCÅV“à‰ÈŠw‘åŒn11Cƒ~ƒgƒRƒ“ƒhƒŠƒA•aCƒŠƒ\ƒ\[ƒ€•aD ’†ŽR‘“XC1996D 340-343
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‹ß“¡’¼ŽÀFAtaxia telangiectasia ‚É‚¨‚¯‚鈫«ƒŠƒ“ƒpŽî‚Æ”’ŒŒ•a‚Ì”­ÇCAnnual Review ŒŒ‰t 1997C‚‹vŽj–E‹{èŸ—Y‚ç•ÒC“Œ‹žC’†ŠOˆãŠwŽÐC1997D 177-184
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‹ß“¡’¼ŽÀFAtaxia telangiectasia‚ÆATMˆâ“`ŽqCAnnual Review _Œo1997CŒã“¡•¶’jE‚‘qŒö•ü‚ç•ÒC“Œ‹žC’†ŠOˆãŠwŽÐC1997D 282-287
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‹ß“¡’¼ŽÀFƒAƒgƒs[«”畆‰ŠC¬Ž™‰ÈŠwC”’–ؘa•vE‘OìŠì•½‚ç•ÒC“Œ‹žCˆãŠw‘‰@C1997D 767-773
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—é–؍N”VFZellweger ÇŒóŒQC¬Ž™‰ÈŠwC”’–ؘa•vE‘OìŠì•½•ÒC“Œ‹žCˆãŠw‘‰@C1997D 291-294
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—é–؍N”VFƒÀŽ_‰»y‘fŒ‡‘¹ÇC¬Ž™‰ÈŠwC”’–ؘa•vE‘OìŠì•½•ÒC“Œ‹žCˆãŠw‘‰@ C1997D 296-297
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‹ß“¡’¼ŽÀFIgER‘ÌŽY¶CƒAƒŒƒ‹ƒM|Ž¾Š³ƒCƒ‰ƒXƒgƒŒƒCƒeƒbƒhCX“c@Š°E‰i‘qr˜a•ÒC“Œ‹žCƒƒfƒBƒJƒ‹ƒŒƒrƒ…|ŽÐC1998D 120-124@
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Kondo NFCorticosteroids present and future useDInFCurrent Advances in Pediatric Allergy and Clinical ImmunolrgyDShinomiya K edCChurchill LivingstoneCNew YorkC1996D119-120
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Agata HCNaiki YCShinoda SCFukao TCKaneko HCShinbara MCFukutomi OCKondo NFGlucocorticoid effects in asthma at a molecular levelD InFCurrent Advances in Pediatric Allergy and Clinical ImmunologyDShinomiya K edCChurchill LivingstoneCNew YorkC1996D87-93
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Fukutomi OCKato ZCYamazaki MCShinoda SCAgata HCInoue RCKondo NFAdministration protocol for theophyllineDInFCurrent Advances in Pediatric Allergy and Clinical ImmunologyD Shinomiya K edCChurchill LivingstoneCNew YorkC1996D197-203

Kondo NFThe role of helper T lymphocytes in food allergyDInFProgress in Allergy and Clinical Immunology 4DOehling A KCHuerta Lopez J G edCHogrefe & Huber Publishers SeattleCCancuLnC1997D61-64
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Suzuki YCOrii TFPeroxisomal DisordersDZellweger syndrome and adrenoleukodystrophyDInFClinical Studies in Medical BiochemistryDGlew R HCNinomiya Y edCOxford University PressCNew YorkC1997D247-259
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‹ß“¡’¼ŽÀFH•¨ƒAƒŒƒ‹ƒM[‚̐f’fDMedico 27i2jC6-12i1996j
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‹ß“¡’¼ŽÀFƒAƒ~ƒmƒtƒBƒŠƒ“»Ü’†‚ÉŠÜ‚Ü‚ê‚éƒGƒ`ƒŒƒ“ƒWƒAƒ~ƒ“‚É‚æ‚è—U“±‚³‚ꂽ‚ƍl‚¦‚ç‚ê‚é‹CŠÇŽxšb‘§”­ì‚Ì‘žˆ«‚Ì‚P—áC•›ì—pÇ—áƒf[ƒ^ƒx[ƒXDf’f‚ÆŽ¡—à 84 ‘Š§†C335i1996j
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‹ß“¡’¼ŽÀFIgE ŽY¶ˆâ“`ŽqDšb‘§ 9i3jC45-52i1996j
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‚‹´K—˜F”A’†ƒIƒŠƒS“œC¬Ž™‰Èf—ÁC59C‘Š§†C168-171i1996j
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•Ÿ“c½ŽiCŒË¼rŽ¡C—Sì˜aŽqCŽRŠÝ“ÄŽŠCGolam MdDMaruf RezviC‰Á“¡‘Pˆê˜YCŽR“c’¼lCˆéŠLŒõŽ¡C‹ß“¡’¼ŽÀCÜ‹’‰•vFƒ€ƒR‘½ “œÇ‚̈â“`ŽqƒŒƒxƒ‹‚Å‚Ì•aˆö‰ðÍD“ú–{æ“V‘ãŽÓˆÙíŠw‰ïŽ 12i1jC35-41i1996j
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‹ß“¡’¼ŽÀFAtaxia telangiectasia‚̐ӔCˆâ“`ŽqATMDˆãŠw‚Ì‚ ‚ä‚Ý 180C226-227i1997j
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ˆÉã—Ç•ãC‹àŽq‰p—YC‹ß“¡’¼ŽÀFChediak-Higashi ÇŒóŒQD¬Ž™“à‰È 29‘Š§†C1050-1054i1997j
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—Sì˜aŽqCŒË¼rŽ¡CÜ‹’‰•vC‹ß“¡’¼ŽÀFƒ€ƒR‘½“œÇIVŒ^iMorquioÇŒóŒQCƒÀ-galactosidase Œ‡‘¹ÇjD“ú–{—Տ°•ÊûCæ“V‘ãŽÓˆÙíÇŒóŒQ 19C442-445i1998j
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‰ºàVLsFRhizomelic chondrodysplasia punctataiRCDPjD“ú–{—Տ°•ÊûCæ“V‘ãŽÓˆÙíÇC19C310-312i1998j
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‹ß“¡’¼ŽÀFŽ„‚ÍŽv‚¤DExperiments of NatureCƒAƒŒƒ‹ƒM[‚̗Տ° 18C34-35i1998j
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Suzuki YCShimozawa NCTakahashi YCImamura ACKondo NCOrii TFPeroxisomal disordersCclinical aspectsCAnn NY Acad SciC804C442-449i1996j
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ŽR“c’¼lC•Ÿ•x@’îCŒË¼rŽ¡C—é–؍N”VC‰ª–{”Ž”VCŽ›àV‘‰îCˆÉ²ˆä Š]C“c’†@_C¬ì’B–çC’†“ˆ‹`‹LC––ΗTCꠁ@–¾ŽqC‘é”ö@–¾C‘å‹{Žj˜NC’Ø“àm“ñC‹ß“¡’¼ŽÀF¬Ž™‹CŠÇŽxšb‘§‚ɑ΂·‚éƒyƒ~ƒƒ‰ƒXƒgƒJƒŠƒEƒ€iƒAƒŒƒMƒT[ƒ‹ùCƒhƒ‰ƒCƒVƒƒbƒvj‚̗Տ°“I—L—p«‚ÉŠÖ‚·‚錟“¢D¬Ž™‰È—Տ° 50C153-164i1997j
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Ž­–씎–¾C‰Á“¡‹`OC‰Á“¡‘Pˆê˜YCˆÉã—Ç•ãCŠâ“c‰ëŽqCŽR“cKŽ¡C´“‡^—ŽqC–k“‡N—YC‹ß“¡’¼ŽÀF”畆Œ^Œ‹ß«‘½”­“®–¬‰Š‚Ì‚P—áD¬Ž™‰È—Տ° 50C2419-2423i1997j
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—é–؍N”VC‰ºàVLsC––ΗTCó–쏃ˆêC•Ÿ“c½ŽiC¡‘º@~Cˆäã‹±ŽqC“àŽR@‰·C’£@’‰‹`C‹ß“¡’¼ŽÀCÜ‹’‰•vC¡–ìŒõ—YC•–ؗǘaC’Ë–{—˜˜NC‘å‹÷@—²C“¡–؍K•vFƒyƒ‹ƒIƒLƒVƒ\[ƒ€•a‚̐¬ˆö‚ÆŽ¡—ÂɊւ·‚錤‹†D“ú–{æ“V‘ãŽÓˆÙíŠw‰ïŽ 13C209-214i1997j
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‹ß“¡’¼ŽÀF“ú–{l‚É‚¨‚¯‚éƒAƒgƒs[«Ž¾Š³‚ÆFcƒÃRIƒÀˆâ“`Žq‚ÌŠÖ˜A«‚ɂ‚¢‚āDŒÄ‹z 16i2jC318-319i1997j
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“c’†‚½‚¦ŽqCˆéŠLŒõŽ¡CŽR“cKŽ¡C‰ºàVLsC—é–؍N”VCŽ›àV‘‰îC‹ß“¡’¼ŽÀFŒŒ¬”ÂŒ¸­‚ðŒ_‹@‚É”­Ç‚µ‚½‹}«‚`Œ^ŠÌ‰Š‚Ì1’jŽ™—áDi‘æ99‰ñŠò•ŒŠ´õÇ’k˜b‰ïjCŠò•Œ‘åŠw‹I—v 45C299i1997j
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ŽR“c’¼lC‚‹´K—˜C‰ºàVLsCˆéŠLŒõŽ¡CŽR“cKŽ¡C‰Á“¡‹`OC‹ß“¡’¼ŽÀF–³‹Û«‘–Œ‰Šiƒ€ƒ“ƒvƒXj‚ÉŽ‹_Œo‰Š‚𔺂Á‚½1Ç—áDi‘æ37‰ñŠò•Œ—Տ°_ŒoW’k‰ïjCŠò•Œ‘åŠwˆãŠw•”‹I—v 45C437-438i1997j
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‚‹´K—˜F“û—cŽ™Šú‚É‚Ä‚ñ‚©‚ñ”­ì‚Æ‚Ü‚¿‚ª‚í‚ꂽs“®‚ð’悵‚½Ç—áDŠò•ŒŒ§¬Ž™‰Èˆã‰ï•ñ 22C3-9i1997j
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Ž­–씎–¾C‰Á“¡‹`OCŽ›“c’mVCŒã“¡_ŽqC‹ß“¡’¼ŽÀF”x“®–¬•ÙˆÊ‚É‹‘åánæ҂ð”F‚ß‚½Š´õ«S“à–Œ‰Š‚Ì‚P—áD¬Ž™‰È—Տ° 51C975-978i1998j
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Ž­–씎–¾C“c’†‚½‚¦ŽqCX–{qC‘ì¯˜NCŽR“c’¼lC”ª–Ø‹`ŒvC––ΗTF–³ŒÄ‹zƒ‚ƒjƒ^[‚ª—LŒø‚Å‚ ‚Á‚½“û—cŽ™“Ë”­«Šë‹}Ž–‘ԁiALTEj‚Ì1—áDNeonatal Care 10C1067-1072i1998j
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ˆÉ“¡Ž‡C‘åˆä’·˜aC‰–‰®ŒhˆêC—Sì˜aŽqC¼‘q–΁F’·Šú¶‘¶‚ÌSanfilippoÇŒóŒQAŒ^ŒZ’í—á‚̗Տ°“I‚¨‚æ‚ѐ_Œo•úŽËüŠw“IŒŸ“¢D”]_Œo 50C165-169i1998j
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…–ìW“ñC“ì—§—R‰ÌC‰–’J^—R”üC^“ç’mŽqCŒã“¡—T•vC¯@”ŽºC‚‹´K—˜C‰Á“¡‘Pˆê˜Y@‹ß“¡’¼ŽÀ F99mTc-ECD SPECT‚ð—p‚¢‚½”]ŒŒ—¬—ʂ̉Á—î•Ï‰»‚Ì•]‰¿DRADIOISOTOPES 47C8-13i1998j
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…–ìW“ñCŒã“¡—T•vC¯@”ŽºCŽR“c’¼lC‰Á“¡‘Pˆê˜YC‚‹´K—˜C‰º‘òLsC‹ß“¡’¼ŽÀFáz¹dÏ‚É”º‚¤’áŽ_‘f”]Ç‚Ì2—cŽ™—áDŠjˆãŠw 35C141-145i1998j
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“n•Ó‚݂ÂفC‚‹´K—˜C•½–ì–¾ŽqC‰Á“¡‹`OCˆéŠLŒõŽ¡CŽO—Ö—RC‹ß“¡’¼ŽÀF‚Ä‚ñ‚©‚ñ”­ìdÏŒã‚ÉWestÇŒóŒQ‚𔭏ǂµ‚½1—áDŠò•Œ‘åŠwˆãŠw•”‹I—v 46C55i1998j
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Šâ“c‰ëŽqC‚‹´K—˜CŽR“c’¼lC’†“‡–F”ŽC’†‘º@mC‰º‘òLsC—é–؍N”VC‹ß“¡’¼ŽÀF”]‰ŠŒã‚Ɉê‰ß«‚ÌŽ¸ŒêÇ‚ð”F‚ß‚½1—áDŠò•Œ‘åŠwˆãŠw•”‹I—v 46C55i1998j

Œ´’˜i‰¢•¶E‘“à j
Suzuki YCShimozawa NCYajima SCInoue KCOrii TCKondo NFIncidence of peroxisomal disorders in JapanDJpn J Hum an Genet 41C167-175i1996j
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Suzuki YCShimozawa NCImamura ACFukuda YCIchihashi HCOrii TCKondo NFTrial of docosahexaenoic acid supplementation on a Japanese patient with a peroxisome biogenesis defectDActa Paediatrica Japonica 38C520-523i1996j
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Kato ZCKato TCKondo NCOrii TFInterstitial deletion of the short arm of chromosome 10CReport of a case and review of the literatureDJpn J Hum Genet 41C111-116i1996j
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Œ´’˜i‰¢•¶E ‘ŠOj
Kondo NCKaneko HCFukao TCInoue RCTeramoto TCTashita HCYokoyama YDFHigh sensitivity and specificity of proliferative responses of lymphocytes to food antigens for detection of the offending food patients with food-sensitive atopic dermatitisDPediatric AsthmaCAllergy & Immunology 10C175-180i1996j
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Kondo NCAgata HCFukutomi OFEfeitos do farmaco antialergico hidrocloreto de azelastina nas respostas proliferativas de linfocitos para antigenos alimentares em pacientes com dermatite atopica alimento-sensitivaDDigest Alergia 2C17i1996j
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Mayumi MCOhshima YCKatamura KCIto SCHirao TCAkutagawa HCKondo NCMorikawa AFAllergic march in childrenCAtopic dermatitis in Japanese children with bronchial asthmaDAllergology International 45C145-149i1996j
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Rabbani HCPan QCKondo NCSmith CIECHammarstrom LFDuplications and deletions of the human IGHC locusCevolutionary implicationsDImmunogenetics 45C136-141i1996j
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Cole D E CCFukuda SCGordon B ACRip J WCLecouteur A NCRupar C ACTomatsu SCOgawa TCSukegawa K and Orii TFHeteroallelic missense mutations of the galactosamine-‚U-sulfate sulfataseiGALNSjgene in a mild form of Morquio diseaseiMPSIVAjDAm J Med Genet 63C558-565i1996j
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Hommma ACIkeda HCIshii RCSukegawa KCHayasaka KFMultiple sulphatase deficiency and carotenaemiaDJ Inher Metab Dis 19C88-89i1996j
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Shimozawa NCSuzuki YCTomatsu SCTsukamoto TCOsumi TCFujiki YCKamijo KCHashimoto TCKondo NCOrii TFCorrection by gene expression of biochemical abnormalities in fibroblasts from Zellweger patientsDPediatric Research 39i5jC812-815i1996j
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Inoue KCSuzuki YCYajima SCShimozawa NCTomatsu SCOrii TCKondo NFCarrier identification of X-linked adrenoleukodystrophy by measurement of very long chain fatty acids and lignoceric acid oxidationDClin Genet 50C348-352i1996j
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Tomatsu SCFukuda SCYamagishi ACCooper ACWraith J ECHori TCKato ZCYamada NCIsogai KCSukegawa KCKondo NCSuzuki YCShimozawa NCOrii TFMucopolysaccharidosis IVACFour new exonic mutations in patients with N-acetylgalactosamine-‚U-sulfate sulfatase deficiencyDAm J Hum Genet 58i5jC950-962i1996j
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Fukao TCSong X-QCYamaguchi SCHashimoto TCOrii TCKondo NFImmunotitration analysis of cytosolic acetoacetyl-CoA thiolase activity in human fibroblastsDPediatr Res 39C1055-1058i1996j
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Fukao TCSong X-QCWatanabe HCHirayama KCSakazaki HCShintaku HCImanaka MCOrii TCKondo NFPrenatal diagnosis of succinyl-coenzyme AC3 - ketoacid coenzyme A transferase deficiencyDPrenatal Diagnosis 16C471-474i1996j
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Fukao TCSakai SCShimozawa NCKuwahara TCKano MCGoto ECNakashima YCKatagiri-Kawade MCIchihashi HCMasuno MCOrii TCKondo NFLife threatening cardiac involvement throughout life in a case of Costello syndromeDClinical Genetics 50C244-247i1996j
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Fukao TCKodama ACAoyanagi NCTsukino RCUemura SCSong X-QCWatanabe HCKuhara TCOrii TCKondo NFMild form of beta-ketothiolase deficiencyimitochondrial acetoacetyl-CoA thiolase deficiencyjin two Japanese siblingsCidentification of detectable residual activity and cross-reactive material in EB-transformed lymphocytesDClinical Genetics 50C263-266i1996j
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Masuno MCFukao TCSong X-QCYamaguchi SCOrii TCKondo NCImaizumi KCKuroki YFAssignment of the human cytosolic acetoacetyl-coenzyme A thiolaseiACAT 2jgene to chromosome 6q25D3-q26DGenomics 36C217-218i1996j
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Kassovska-Bratinoba SCFukao TCSong X-QCM V Duncan ACChen H SCRobert M-FCPerez-Cerda CCUgarte MCChartrand PCVobecky SCKondo NCMitchell G-AFSuccinyl-CoAF3 -Oxoacid CoA transferaseiSCOTjChuman cDNA cloningChuman chromosomal maing to 5p 13Cand mutation detection in a SCOT-deficient patientDAm J Hum Genet 59C519-528i1996j
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Fukao TCKaneko HCTeramoto TCTashita HCKondo NFAssociation between FcƒÃRIƒÀ and atopic disorder in Japanese populationH Lancet 348C407i1996j
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Xia Y-RCWelch C LCWarden C HCLange ECFukao TCLusis A JCGatti G AFAssignment of the mouse ataxia-telangiectasia geneiatmjto mouse chromosome ‚XDMammalian Genome 7C554-555i1996j
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Matsuda YCTakashi ICShiomi TCSaito TCYamauchi MCFukao TCAkao YCSeki NCIto HCHori TFComparative genome maing of the ataxia-telangiectasia region in mouseCratCand syrian hamsterDGenomics 34C347-352i1996j
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Pecker ICAvraham K BCGilbert D JCSavitsky KCRotman GCHarnik RCFukao TCSchrock ECHirotsune SCTagle DCCollins F SCWynshaw-Boris ACRied TCCopeland N GCJenkins N ACShiloh YCZiv YFIdentification and chromosome localization of ATMCthe murine homologue of the ataxia-telangiectasia geneDGenomics 35i1jC39-45i1996j
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Yamada TCKaneko HCIizuka KCMatsubayashi YCKokai Y and Fujimoto JFElevation of lymphocytes and hematopoietic stem cell numbers in mice transgenic for human granulocyte colony-stimulating factorDLaboratory Investigation 74C384-394i1996j
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Kokai YCKaneko HCIizuka KCMatsuura A and Fujimoto JFInhibition of resistance to hemopoietic allo-grafts in granulocyte colony-stimulating factor transgenic miceDEuropean Journal of Immunology 26C115-119i1996j
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Kaneko HCInoue RCYamada UCKasahara KCTakami TCKondo NFAtaxia telangiectasia syndrome with B cell lymphomaDClinical Genetics 49C331-332i1996j
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Kaneko HCKatagiri-Kawade MCMotoyoshi FCTashita HCTeramoto TCKondo NFAbnormal B cell response of protein kinase C in some common variable immunodeficiencyDExperimental and Clinical Immunogenetics 13C36-42i1996j
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Kaneko HCInoue RCYamada YCSukegawa KCFukao TCTashita HCTeramoto TCKasahara KCTakami TCKondo NFMicrosatellite instability in B-cell lymphoma originating from Bloom syndromeDInternational Journal of Cancer 69C480-483i1996j
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Uchida YCKondo NCOrii TCHashimoto TFPurification and properties of rat liver peroxisomal very-long-chain acyl-CoA synthetaseDJ Biochem 119C565-571i1996j
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Fukuda SCTomatsu SCMasuno MCOgawa TCYamagishi ACRezvi G M MCSukegawa KCShimozawa NCSuzuki YCKondo NCImaizumi KCKuroki KCOkabe TCOrii TFMucopolysaccharidosis VIACSubmicroscopic deletion of 16q24C3 and a novel R386C mutation of N-acetylgalactosamine-‚U-sulfate sulfatase gene in a classical Morquio diseaseDHuman Mutation 7i2jC123-134i1996j
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Fukuda SCShimozawa NCSuzuki YCZhang ZCTomatsu SCTsukamoto TCHashiguchi NCOsumi TCMasuno MCImaizumi KCKuroki YCFujiki YCOrii TCKondo NFHuman peroxisome assembly factor-2iPAF-2jCA gene responsible for group C peroxisome biogenesis disorders in humansDAm J Hum Genet 59C1210-1220i1996j
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Fukuda SCTomatsu SCAlan CooperCJDEDWraithCKato ZCYamda NCIsogai KCSukegawa KCKondo NCOrii TFMucopolysaccharidosis IVAiMorquio AjCThree novel small deletions in the N-acetylgalactosamine-‚U-sulfate sulftase geneDHuman Mutation 8C187-190i1996j
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Imamura ACSuzuki YCSong X-QCFukao TCShimozawa NCOrii TCKondo NFPrenatal Diagnosis of Adrenoleukodystrophy by means of mutation analysisDPrenatal Diagnosis 16C259-261i1996j
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Shinbara MCKondo NCAgata HCFukutomi OCKuwabara NCKobayashi YCMiura MCOrii TFInterferon-ƒÁ and interleukin-4 production of ovalbuminstimulated lymphocytes in egg-sensitive childrenDAnn Allergy Asthma Immunol 77C60-66i1996j
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Yamagishi ACTomatsu SCFukuda SCUchiyama ACShimozawa NCSuzuki YCKondo NCSukegawa KCOrii TFMucopolysaccharidosis type ECidentification of common mutations that cause Hurler and Scheie syndromes in Japanese populationsDHuman Mutation 7C23-29i1996j
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Rezvi G M MCTomatsu SCFukuda SCYamagishi ACCooper ACWraith J ECIwata HCKato ZCYamada NCSukegawa KCShimozawa NCSuzuki YCKondo NCOrii TFMucopolysaccharidosis IVACa comparative study of polymorphic DNA haplotypes in the Caucasian and Japanese populationsDJ Inher Metab Dis 19C301-308i1996j
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Orii KECAoyama TCSouri MCJiang L-LCOrii KOCHayashi SCYamaguchi SCKondo NCOrii TCHashimoto TFFormation of the enzyme complex in mitochondria is required for function of trifunctional beta-oxidation proteinDBiochem Biophys Res Commun 219C773-777i1996j
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Aoyama TCWakui KCFukushima YCOrii KECHashimoto TFAssignment of the human mitochondrial very-long-chain acyl-CoA dehydrogenase geneiLCACDjto 17p13 by in situ hybridizationDGenomics 37C144-145i1996j
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Souri MCAoyama TCOrii KOCYamaguchi SCHashimoto TFMutation analysis of very-long-chain acyl-coenzyme A dehydrogenaseiVLCADjdeficiencyFIdentification and characterization of mutant VLCAD cDNAs from four patientsDAm J Hum Genet 58C97-106i1996j
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Shinoda SCAgata HCFukutomi OCKondo NFCombination of IgE values and lymphcyte proliferative responses for consideration of the clinical course of infantile hen's egg-senstive atopic dermatitisDInt Arch Allergy Immunol 112C163-168i1997j
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Agata HCKondo NCFukutomi OCTakemura MCTashita HCKobayashi YCShinoda SCNishida TCShinbara MCOrii TFPulmonary hemosiderosis with hypersensitivity to buckwheatDAnn Allergy Asthma Immunol 78C233-237i1997j
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Tsukamoto TCBogaki ACOkumoto KCTateishi KCFujiki YCShimozawa NCSuzuki YCKondo NCOsumi TFIsolation of a new peroxisome-deficient CHO cell mutant defectivein peroxisome targeting signal-1 receptorDBiochem Biophysical Res Commun 230C402-406i1997j
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Kondo NCInoue RDKasahara KCFukao TCKaneko HCTashita HCTeramoto TFReduced expression of the interferon-gamma messenger RNA in IgG‚Q deficiencyDScand J Immunol 45C227-230i1997j
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Fukao TCSong X-QCYamaguchi SCKondo NCOrii TCMatthieu J-MCBachmann CCHashimoto TFIdentification of three novel frameshift mutationsi83 del ATC754 ind CTCand 435{‚PG to Ajof mitochondrial acetoacetyl-coenzyme A thiolase gene in two Swiss patients with CRM-negative beta-ketothiolase deficiencyDHum Mutat 9C277-279i1997j
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Kondo NCFukutomi OCAgata HCYokoyama YFProliferative responses of lymphocytes to food antigens are useful for detection of allergens in nonimmediate type of food allergyDJ Invest Allergol Clin Immunol 7C122-126i1997j
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Takahashi YCSuzuki YCKumazaki KCTanabe YCAkaboshi SCMiura KCShimozawa NCKondo NCNishiguchi TCTerada KCOrii TFEpilepsy in peroxisomal diseasesDEpilepsia 38C182-188i1997j
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Song XQCFukao TCMitchell GACKassovska-Bratinoba SCUgarte MCWanders RJACHirayama KCShintaku HCChurchill PCWatanabe HCOrii TCKondo NFSuccinyl-CoAC3-ketoacid coenzyme A transferaseiSCOTjCdevelopment of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiencyDBiochim Biophys Acta 1360C151-156i1997j
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Takahashi YCWatanabe MCFujiwara TCYagi KCKondo NCOrii TCSeino MFTwo different pathological conditions of photoparoxysmal responses in hereditary dentatorubral-pallidoluysian atrophyDBrain & Development 19C285-289i1997j
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Fukuda SCYamada YCNishimura MCIsogai KCTerada TCIwata MCShimozawa NCSuzuki YCKondo NFMarinesco-sjogren syndrome associated with acute myeloblastic leukemiaDClin Genet 51C278-280i1997j
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Mayumi MCKatamura KCTamura TCIto SCHirao TCAkutagawa HCMorikawa ACKondo NFInvolvement of genetic factors in early development of bronchial asthma in Japanese infants with atopic dermatitisCResults of a 1 year follow-up studyDAllergology International 46C83-89i1997j
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Orii KECAoyama TCWakui KCFukushima YCMiyajima HCYamaguchi SCOrii TCKondo NCHashimoto TFGenomic and mutational analysis of the mitochondrial trifunctional protein-subunitiHADHBjgene in patients with trifunctional protein deficiencyDHum Mol Genet 6C1215-1224i1997j
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Fukuda SCYamada NCTomatsu SCSukegawa KCMontano AMCHopwood JJCMuller VCOrii TCKondo NFMucopolysaccharidosis IVACa novel splice acceptor site mutation in intron 4 of the N-acetylgalactosamine- 6 -sulfate sulfatase gene in an Afghanistan girl with classical Morquio diseaseDJpn J Human Genet 42C317-322i1997j
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Orii KOCAoyama TCSaito-Ohara FCIkeuchi TCOrii TCKondo NCHashimoto TFMolecular characterization of the mouse very-long-chain acyl-CoA dehydrogenase geneCMammalian Genome 8C516-518i1997j
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Orii KOCSaito-Ohara FCIkeuchi TCOrii TCKondo NCAoyama TCHashimoto TFAssignment of the gene for very-long-chain acyl-CoA dehydrogenaseiAcadvljto mouse chromosome band 11B 2-5 by in situ hybridizationDCytogenet and Cell Genet 78C25i1997j
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Imamura ACSuzuki YCSong XQCFukao TCUchiyama ACShimozawa NCKamijo KCHashimoto TCOrii TCKondo NFTwo novel missense mutation in the ATP-binding domain of the adrenoleukodystrophy geneCimmunoblotting and immunocytological study of two patientsDClin Genet 51C322-325i1997j
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Fukao TCSong XQCMitchell GACYamaguchi SCSukegawa KCOrii TCKondo NFEnzymes of ketone body utilization in human tissuesFprotein and mRNA levels of succinyl-coenzyme AiCoAjC3-ketoacid CoA transferase and mitochondorial and cytosolic acetoacetyl-CoA thiolasesDPediatr Res 42C498-502i1997j
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Kaneko HCInoue RCYamada YCFukao TCKondo NFManagement of malignant lymphoma in two siblings with Bloom's syndromeDOncology Reports 4C1281-1283i1997j
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Kondo NCShinbara MCInoue RCFukao TCKaneko HCTeramoto TCTashita HFInhibition of interferon-ƒÁ production from lymphocytes stimulated with food antigens by a ƒÀ2-agonistCprocaterolCin patients with food-sensitive atopic dermatitisDJ Invest Allergol Clin Immunol 7C225-228i1997j
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Iwata SCSukegawa KCSasaki TCKokuryu MCYamashita SCNoma ACIwasa SCKondo NCOrii TFMass screening test for mucopolysaccharidoses using the 1C9-dimethylmethylene blue methodCPositive interference from paper diapersDClin Chim Acta 264C245-250i1997j
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Tateishi KCOkumoto KCShimozawa NCTsukamoto TCOsumi TCSuzuki YCKondo NCOkano ICFujiki YFNewly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammalsDEur J Cell Biol 73C352-359i1997j
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Inoue RCMatsuoka TCKondo NCNishimura YCMatsushita SFIdentification of dermatophagoides farinae-2-Derived peptides and classEHLA molecules recognized by T cell from atopic individualsDInt Arch Allergy Immunol 114C354-360i1997j
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Sukegawa KCSong XQCMasuno MCFukao TCShimozawa NCFukuda SCIsogai KCNishio HCMatsuo MCTomatsu SCKondo NCOrii TFHunter disease in a girl caused by R468Q mutation in the iduronate-2-sulfatase gene and skewed inactivation of the X chromosome carrying the normal alleleDHum Mutat 10C361-367i1997j
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Tomatsu SCFukuda SCCooper ACWraith JECFerreira PCNatale PDCTortora PCFujimoto ACKato ZCYamada NCIsogai KCYamagishi ACSukegawa KCSuzuki YCShimozawa NCKondo NCSly WSCOrii TFFourteen novel mucopolysaccharidosis IVA producing mutations in