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    1. Matsubara, M; Yamagata, H; Kamino, K; Nomura, T; Kohara, K; Kondo, I; Miki, T
      Genetic association between Alzheimer disease and the alpha-synuclein gene

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    2. Meguro, M; Kashiwagi, A; Mitsuya, K; Nakao, M; Kondo, I; Saitoh, S; Oshimura, M
      A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome

      NATURE GENETICS
    3. Kohno, M; Ohmori, K; Wada, Y; Kondo, I; Noma, T; Fujita, N; Mizushige, K; Mandal, AK
      Inhibition by eicosapentaenoic acid of oxidized-LDL- and lysophosphatidylcholine-induced human coronary artery smooth muscle cell production of endothelin

      JOURNAL OF VASCULAR RESEARCH
    4. Obata, K; Fukuda, T; Morishita, R; Abe, S; Asakawa, S; Yamaguchi, S; Yoshino, M; Ihara, K; Murayama, K; Shigemoto, K; Shimizu, N; Kondo, I
      Human biotin-containing subunit of 3-methylcrotonyl-CoA carboxylase gene (MCCA): cDNA sequence, genomic organization, localization to chromosomal band 3q27, and expression

      GENOMICS
    5. Kamijo, Y; Kondo, I; Soma, K; Imaizumi, H; Ohwada, T
      Alkaline esophagitis evaluated by endoscopic ultrasound

      JOURNAL OF TOXICOLOGY-CLINICAL TOXICOLOGY
    6. Kondo, I; Mizushige, K; Hirao, K; Nozaki, S; Tsuji, T; Masugata, H; Kohno, M; Matsuo, H
      Ultrasonographic assessment of coronary flow reserve and abdominal fat in obesity

      ULTRASOUND IN MEDICINE AND BIOLOGY
    7. Gocho, K; Kondo, I; Yamaki, K
      Identification of autoreactive T cells in Vogt-Koyanagi-Harada disease

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    8. Sato, Y; Asoh, T; Kondo, I; Satoh, K
      Vitamin D deficiency and risk of hip fractures among disabled elderly stroke patients

      STROKE
    9. Sato, Y; Kondo, I; Ishida, S; Motooka, H; Takayama, K; Tomita, Y; Maeda, H; Satoh, K
      Decreased bone mass and increased bone turnover with valproate therapy in adults with epilepsy

      NEUROLOGY
    10. Kondo, I; Hosokawa, K; Soma, M; Iwata, M; Maltais, D
      Protocol to prevent shoulder-hand syndrome after stroke

      ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION
    11. Ueda, T; Mizushige, K; Yukiiri, K; Aoyama, T; Kondo, I; Kohno, M; Matsuo, H
      Contrast harmonic power Doppler imaging of congenital ventricular diverticulum - A case report

      ANGIOLOGY
    12. Horibe, M; Kondo, I; Damron, DS; Murray, PA
      Propofol attenuates capacitative calcium entry in pulmonary artery smooth muscle cells

      ANESTHESIOLOGY
    13. Yamazaki, I; Koizumi, W; Kondo, I; Saigenji, K
      Role of regenerative mucosa in primary gastric cancer treated by chemotherapy

      ONCOLOGY REPORTS
    14. Kawano, Y; Ohmori, K; Wada, Y; Kondo, I; Mizushige, K; Senda, S; Nozaki, S; Kohno, M
      A novel color M-mode Doppler echocardiographic index for left ventricular relaxation: depth of the maximal velocity point of left ventricular inflow in early diastole

      HEART AND VESSELS
    15. Yoshizawa, Y; Sakurada, J; Sakurai, S; Machida, K; Kondo, I; Masuda, S
      An exfoliative toxin A-converting phage isolated from Staphylococcus aureus strain ZM

      MICROBIOLOGY AND IMMUNOLOGY
    16. Yasuda, T; Yamaguchi, N; Kobayashi, K; Nishi, I; Horinouchi, H; Jalil, MA; Li, MX; Ushikai, M; Iijima, M; Kondo, I; Saheki, T
      Identification of two novel mutations in the SLC25A13 gene and detection of seven mutations in 102 patients with adult-onset type II citrullinemia

      HUMAN GENETICS
    17. Shigemoto, K; Kubo, S; Maruyama, N; Yamada, S; Obata, K; Kikuchi, K; Kondo, I
      Identification and characterization of 5 ' extension of mammalian agrin cDNA, the exons and the promoter sequences

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    18. Kondo, I; Mizushige, K; Nozaki, S; Hirao, K; Iwado, Y; Ohmori, K; Matsuo, H
      Effect of cibenzoline on regional left ventricular function in hypertrophic obstructive cardiomyopathy

      CLINICAL CARDIOLOGY
    19. Obata, K; Matsuishi, T; Yamashita, Y; Fukuda, T; Kuwajima, K; Horiuchi, I; Nagamitsu, S; Iwanaga, R; Kimura, A; Omori, I; Endo, S; Mori, K; Kondo, I
      Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome

      JOURNAL OF MEDICAL GENETICS
    20. Yamaki, K; Gocho, K; Hayakawa, K; Kondo, I; Sakuragi, S
      Tyrosinase family proteins are antigens specific to Vogt-Koyanagi-Harada disease

      JOURNAL OF IMMUNOLOGY
    21. Ebisawa, T; Kondo, I; Masaki, E; Hori, S; Kawamura, M
      Capacitative calcium entry is involved in steroidogenesis in bovine adrenocortical fasciculata cells

      JOURNAL OF ENDOCRINOLOGY
    22. Kondo, I
      Protein kinase C potentiates capacitative Ca2+ entry that links to steroidogenesis in bovine adrenocortical cells

      JAPANESE JOURNAL OF PHARMACOLOGY
    23. Yamaki, K; Kondo, I; Nakamura, H; Miyano, M; Konno, S; Sakuragi, S
      Ocular and extraocular inflammation induced by immunization of tyrosinase related protein 1 and 2 in Lewis rats

      EXPERIMENTAL EYE RESEARCH
    24. Masaki, E; Ebisawa, T; Kondo, I; Hayashida, K; Matsumoto, Y; Kawamura, M
      P2-purinergic receptor antagonists reduce the minimum alveolar concentration of inhaled volatile anesthetics

      BRAIN RESEARCH
    25. Mizushige, K; Tokudome, T; Seki, M; Kondo, I; Hirao, K; Nozaki, S; Miki, S; Yuasa, S; Matsuo, H
      Sensitive detection of myocardial contraction abnormality in chronic hemodialysis patients by ultrasonic tissue characterization with integrated backscatter

      ANGIOLOGY
    26. Mizugishi, K; Kuwajima, K; Obata, K; Kondo, I
      An AciI polymorphism in the 3 ' untranslated region of the human phosphomannomutase 2 (PMM2) gene

      JOURNAL OF HUMAN GENETICS
    27. Kobayashi, K; Sinasac, DS; Iijima, M; Boright, AP; Begum, L; Lee, JR; Yasuda, T; Ikeda, S; Hirano, R; Terazono, H; Crackower, MA; Kondo, I; Tsui, LC; Scherer, SW; Saheki, T
      The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein

      NATURE GENETICS
    28. Numao, N; Hirota, Y; Iwahori, A; Kidokoro, S; Sasatsu, M; Kondo, I; Itoh, S; Itoh, E; Katoh, T; Shimozono, N; Yamazaki, A; Takao, K; Kobayashi, S
      Biological activities of 1,1,6-trisubstituted indanes: Beyond magainin 2

      BIOLOGICAL & PHARMACEUTICAL BULLETIN
    29. Mizugishi, K; Yamanaka, K; Kuwajima, K; Yuasa, I; Shigemoto, K; Kondo, I
      Missense mutations in the phosphomannomutase 2 gene of two Japanese siblings with carbohydrate-deficient glycoprotein syndrome type I

      BRAIN & DEVELOPMENT
    30. Mizushige, K; Kondo, I; Ohmori, K; Hirao, K; Matsuo, H
      Enhancement of ultrasound-accelerated thrombolysis by echo contrast agents: Dependence on microbubble structure

      ULTRASOUND IN MEDICINE AND BIOLOGY
    31. Matsumuro, A; Takada, Y; Takahashi, Y; Senoo, M; Kondo, I
      Consolidation of C-60 powder by a high-pressure technique up to 5.4 GPa and its mechanical properties

      JOURNAL OF MATERIALS SCIENCE LETTERS
    32. Kondo, I; Mizushige, K; Ueda, T; Masugata, H; Ohmori, K; Matsuo, H
      Histological observations and the process of ultrasound contrast agent enhancement of tissue plasminogen activator thrombolysis with ultrasound exposure

      JAPANESE CIRCULATION JOURNAL-ENGLISH EDITION
    33. Plaster, NM; Uyama, E; Uchino, M; Ikeda, T; Flanigan, KM; Kondo, I; Ptacek, LJ
      Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24

      NEUROLOGY
    34. Tanaka, Y; Yamaguchi, M; Ijiri, R; Kondo, I
      Malignant large cell calcifying Sertoli cell tumor with endocrine overactivity

      JOURNAL OF UROLOGY
    35. Mizushima, K; Watanabe, M; Kondo, I; Okamoto, K; Shizuka, M; Abe, K; Aoki, M; Shoji, M
      Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)(1-2) polymorphism and contribution to founder effect

      JOURNAL OF MEDICAL GENETICS
    36. Kondo, I; Mizugishi, K; Yoneda, Y; Hashimoto, T; Kuwajima, K; Yuasa, I; Shigemoto, K; Kuroda, Y
      Missense mutations in phosphomannomutase 2 gene in two Japanese families with carbohydrate-deficient glycoprotein syndrome type 1

      CLINICAL GENETICS
    37. Masaki, E; Kondo, I
      Methylene blue, a soluble guanylyl cyclase inhibitor, reduces the sevoflurane minimum alveolar anesthetic concentration and decreases the brain cyclic guanosine monophosphate content in rats

      ANESTHESIA AND ANALGESIA
    38. MIZUGISHI K; YAMANAKA K; KUWAJIMA K; KONDO I
      INTERSTITIAL DELETION OF CHROMOSOME 7Q IN A PATIENT WITH WILLIAMS-SYNDROME AND INFANTILE SPASMS

      JOURNAL OF HUMAN GENETICS
    39. TANAKA T; TAMARI N; KONDO I; IWASA M
      FABRICATION OF 3-DIMENSIONAL TYRANNO FIBER-REINFORCED SIC COMPOSITE BY THE POLYMER PRECURSOR METHOD

      Ceramics international
    40. TSUKAHARA M; OKAMOTO N; OHASHI H; KUWAJIMA K; KONDO I; SUGIE H; NAGAI T; NARITOMI K; HASEGAWA T; FUKUSHIMA Y; MASUNO M; KUROKI Y
      BRACHMANN-DE-LANGE-SYNDROME AND CONGENITAL HEART-DISEASE

      American journal of medical genetics
    41. Kinbara, A; Kusano, E; Kondo, I
      Fundamentals of plasma and sputtering processes

      VACUUM
    42. Kusano, E; Kashiwagi, N; Kobayashi, T; Nanto, H; Kondo, I; Kinbara, A
      Effects of CH4 addition to Ar-O-2 discharge gases on resistivity and structure of ITO coatings

      VACUUM
    43. KINBARA A; KUSANO E; KAMIYA T; KONDO I; TAKENAKA O
      EVALUATION OF ADHESION STRENGTH OF TI FILMS ON SI(100) BY THE INTERNAL-STRESS METHOD

      Thin solid films
    44. KONDO I; EBISAWA K; KAWAMURA M
      CAPACITATIVE CALCIUM-ENTRY LINKS TO STEROIDOGENESIS IN BOVINE ADRENOCORTICAL-CELLS

      Naunyn-Schmiedeberg's archives of pharmacology
    45. EBISAWA T; KONDO I; OHNO Y; KAWAMURA M
      INTRACELLULAR CALCIUM MOBILIZATION CAUSED BY EXTRACELLULAR ATP IS ASSOCIATED WITH CAPACITATIVE CALCIUM-ENTRY IN BOVINE ADRENOCORTICAL-CELLS

      Naunyn-Schmiedeberg's archives of pharmacology
    46. MASAKI E; KONDO I; UTSUGI K; KAWAMURA M
      HALOGENATED VOLATILE ANESTHETICS INHIBIT CO-STIMULATED SOLUBLE GUANYLYL CYCLASE ACTIVITY IN RAT-BRAIN

      Naunyn-Schmiedeberg's archives of pharmacology
    47. YAMAGATA H; KINOSHITA M; KOMORI T; KONDO I; MIKI T
      MOLECULAR ANALYSIS OF 2 PRE-MUTATIONS IN MYOTONIC-DYSTROPHY

      Clinical genetics
    48. KONDO I; YAMAMOTO M
      GENETIC-POLYMORPHISM OF PARAOXONASE-1 (PON1) AND SUSCEPTIBILITY TO PARKINSONS-DISEASE

      Brain research
    49. MASAKI E; KATO F; KONDO I; KAWAMURA M
      P2X PURINERGIC RECEPTORS AS A POSSIBLE SITE OF ACTION OF SEVOFLURANE

      Anesthesiology
    50. KUMAGAI M; AHMED AAK; OZAKI M; KONDO I; AMAKI Y
      EFFECT OF SEVOFLURANE EXPOSURE TIME ON NEUROMUSCULAR BLOCKING ACTION OF VECURONIUM

      Anesthesiology
    51. KUNO N; MIZUTANI S; OHNO Y; GOTO K; ITAKURA A; KONDO I; KURAUCHI O; KIKKAWA F; TOMODA Y
      POSSIBLE INVOLVEMENT OF PLACENTAL PROTEASES IN BRADYKININ (BK) DEGRADATION

      Reproduction, fertility and development
    52. NUMAO N; IWAHORI A; HIROTA Y; SASATSU M; KONDO I; ONIMURA K; SAMPE R; YAMANE S; ITOH S; KATOH T; KOBAYASHI S
      ANTIBACTERIAL ACTIVITY OF 2 ALKYLAMINES INTEGRATED ON AN INDANE SCAFFOLD - MIMICRY OF A COMPLEMENTARY UNIT ON MAGAININ-2

      Biological & pharmaceutical bulletin
    53. IWAHORI A; HIROTA Y; SAMPE R; MIYANO S; TAKAHASHI N; SASATSU M; KONDO I; NUMAO N
      ON THE ANTIBACTERIAL ACTIVITY OF NORMAL AND REVERSED MAGAININ-2 ANALOGS AGAINST HELICOBACTER-PYLORI

      Biological & pharmaceutical bulletin
    54. NUMAO N; HIROTA Y; IWAHORI A; SASATSU M; KONDO I; TAKAO K; KOBAYASHI S
      ANTIBACTERIAL ACTIVITY OF (+ -)6-BENZYL-1-(3-CARBOXYPROPYL) INDANE - A POSSIBLE WAY TO IDENTIFY LEADING NOVEL ANTI-H-PYLORI AGENTS/

      Biological & pharmaceutical bulletin
    55. NAMBA N; MORI R; TANAKA H; KONDO I; NARAHARA K; SEINO Y
      THE INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR2.2V (KCNJN1) MAPS TO 17P11.2-]P11.1

      Cytogenetics and cell genetics
    56. KIMURA T; ARAKAWA Y; INOUE S; FUKUSHIMA Y; KONDO I; KOYAMA K; HOSOI T; ORIMO A; MURAMATSU M; NAKAMURA Y; ABE T; INAZAWA J
      THE BRAIN FINGER PROTEIN GENE (ZNF179), A MEMBER OF THE RING FINGER FAMILY, MAPS WITHIN THE SMITH-MAGENIS SYNDROME REGION AT 17P11.2

      American journal of medical genetics
    57. SAITOH S; BUITING K; CASSIDY SB; CONROY JM; DRISCOLL DJ; GABRIEL JM; GILLESSENKAESBACH G; GLENN CC; GREENSWAG LR; HORSTHEMKE B; KONDO I; KUWAJIMA K; NIIKAWA N; ROGAN PK; SCHWARTZ S; SEIP J; WILLIAMS CA; NICHOLLS RD
      CLINICAL SPECTRUM AND MOLECULAR DIAGNOSIS OF ANGELMAN AND PRADER-WILLI-SYNDROME PATIENTS WITH AN IMPRINTING MUTATION

      American journal of medical genetics
    58. YAMASHIKI M; KOSAKA Y; KONDO I; NOMOTO M
      IMPAIRED CYTOKINE PRODUCTION BY PERIPHERAL T-LYMPHOCYTES IN LOW RESPONDERS TO HEPATITIS-B VACCINATION

      Clinical science
    59. KUSANO E; KINBARA A; KONDO I
      FORMATION OF COMPOSITIONALLY GRADED MULTILAYER FILMS BY DISCHARGE GAS-FLOW MODULATION IN MAGNETRON SPUTTERING

      Journal of non-crystalline solids
    60. ASADA Y; HASHIBA Y; YAMAHARA N; OKAMURA N; MORIWAKI T; ANDO T; TAKEMURA K; KONDO I; SUGANUMA N
      ANALYSIS FOR Y-CHROMOSOME MICRODELETIONS IN INFERTILE MALE-PATIENTS UNDERGOING INTRACYTOPLASMIC SPERM INJECTION

      Fertility and sterility
    61. HATTORI H; HIGUCHI Y; OKUNO T; ASATO R; FUKUMOTO M; KONDO I
      EARLY-CHILDHOOD PROGRESSIVE MYOCLONUS EPILEPSY PRESENTING AS PARTIAL SEIZURES IN DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY

      Epilepsia
    62. YAMAMOTO M; KONDO I; OGAWA N; ASANUMA M; YAMASHITA Y; MIZUNO Y
      GENETIC ASSOCIATION BETWEEN SUSCEPTIBILITY TO PARKINSONS-DISEASE AND ALPHA(1)-ANTICHYMOTRYPSIN POLYMORPHISM

      Brain research
    63. MIZUGISHI K; YAMANAKA K; KUWAJIMA K; KONDO I
      INTERSTITIAL DELETION OF CHROMOSOME 7Q IN A PATIENT WITH THE WILLIAMS-SYNDROME AND INFANTILE SPASMS

      American journal of human genetics
    64. KONDO I; MIZUGISHI K; YAMANAKA K; SHIGEMOTO K; YUASA I; KUWAJIMA K
      PHOSPHOMANNOMUTASE-2 (PMM2) MUTATIONS IN JAPANESE SIBLINGS WITH CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME-1 (CDG1)

      American journal of human genetics
    65. KONDO I; SUGANUMA N; ANDO PL; ASADA Y; FURUHASHI M; TOMODA Y
      CLINICAL FACTORS FOR SUCCESSFUL CRYOPRESERVED-THAWED EMBRYO-TRANSFER

      Journal of assisted reproduction and genetics
    66. ANDO T; SUGANUMA N; FURUHASHI M; ASADA Y; KONDO I; TOMODA Y
      SUCCESSFUL GLUCOCORTICOID TREATMENT FOR PATIENTS WITH ABNORMAL AUTOIMMUNITY ON IN-VITRO FERTILIZATION AND EMBRYO-TRANSFER

      Journal of assisted reproduction and genetics
    67. SUGANUMA N; TSUKAHARA S; KITAGAWA T; FURUHASHI M; ASADA Y; KONDO I
      A CONTROLLED OVARIAN HYPERSTIMULATION REGIMEN INVOLVING INTERMITTENT GONADOTROPIN ADMINISTRATION WITH A SHORT PROTOCOL OF GONADOTROPIN-RELEASING-HORMONE AGONIST FOR IN-VITRO FERTILIZATION

      Journal of assisted reproduction and genetics
    68. YANAGISAWA H; FUJII K; NAGAFUCHI S; NAKAHORI Y; NAKAGOME Y; AKANE A; NAKAMURA M; SANO A; KOMURE O; KONDO I; JIN DK; SORENSEN SA; POTTER NT; YOUNG SR; NAKAMURA K; NUKINA N; NAGAO Y; TADOKORO K; OKUYAMA T; MIYASHITA T; INOUE T; KANAZAWA I; YAMADA M
      A UNIQUE ORIGIN AND MULTISTEP PROCESS FOR THE GENERATION OF EXPANDED DRPLA TRIPLET REPEATS

      Human molecular genetics
    69. TAKAKUBO F; KUWANO A; KONDO I
      EVIDENCE THAT POOR METABOLIZERS OF (S)-MEPHENYTOIN COULD BE IDENTIFIED BY HAPLOTYPES OF CYP2C19 IN JAPANESE

      Pharmacogenetics
    70. TATE S; SUGANUMA N; FURUHASHI M; ANDO T; ASADA Y; KONDO I; KIKKAWA F; TOMODA Y
      DIRECT EFFECTS OF ESTRADIOL AND TAMOXIFEN ON GENE EXPRESSIONS OF INHIBIN ALPHA-SUBUNIT AND BETA-A-SUBUNIT IN RAT GRANULOSA-CELLS IN-VITRO

      Endocrine journal
    71. INAOKA T; KAGOSHIMAMAEZONO M; KUWANO S; KONDO I; KUMEGAWA M; KOKUBO T
      HUMAN CATHEPSIN-K - GENE ISOLATION, GENOMIC ORGANIZATION, AND CHROMOSOMAL LOCALIZATION

      Journal of bone and mineral research
    72. MIYAZAKI M; HASHIMOTO T; NAKAGAWA R; YONEDA Y; TAYAMA M; KAWANO N; MURAYAMA N; KONDO I; KURODA Y
      CHARACTERISTIC EVOKED-POTENTIALS IN CHILDHOOD-ONSET DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY

      Brain & development
    73. MIYAZAKI M; HASHIMOTO T; YONEDA Y; TAYAMA M; HARADA M; MIYOSHI H; KAWANO N; MURAYAMA N; KONDO I; KURODA Y
      PROTON MAGNETIC-RESONANCE SPECTROSCOPY ON CHILDHOOD-ONSET DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY (DRPLA)

      Brain & development
    74. UYAMA E; TOKUNAGA M; MURAKAMI T; KUWANO A; KONDO I; UCHINO M
      FAMILIAL ADULT MYOCLONUS EPILEPSY - A NEW PHENOTYPE OF AUTOSOMAL-DOMINANT MYOCLONUS EPILEPSY

      Annals of neurology
    75. KUWANO A; MORIMOTO Y; NAGAI T; FUKUSHIMA Y; OHASHI H; HASEGAWA T; KONDO I
      PRECISE CHROMOSOMAL LOCATIONS OF THE GENES FOR DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY (DRPLA), VON-WILLEBRAND-FACTOR (F8VWF) AND PARATHYROID HORMONE-LIKE HORMONE (PTHLH) IN HUMAN-CHROMOSOME 12P BY DELETION MAPPING

      Human genetics
    76. TAKAKUBO F; YAMAMOTO M; OGAWA N; YAMASHITA Y; MIZUNO Y; KONDO I
      GENETIC ASSOCIATION BETWEEN CYTOCHROME P450IA1 GENE AND SUSCEPTIBILITY TO PARKINSONS-DISEASE

      Journal of neural transmission
    77. JUYAL RC; KUWANO A; KONDO I; ZARA F; BALDINI A; PATEL PI
      MOSAICISM FOR DEL(17)(P11.2P11.2) UNDERLYING THE SMITH-MAGENIS SYNDROME

      American journal of medical genetics
    78. KUBOTA Y; KONDO I; HARADA M; NOGUCHI S; HOSAKA M
      DO THE WORST HISTOLOGICAL ELEMENTS IN NEEDLE-BIOPSY SPECIMENS OF PROSTATE-CANCER PREDICT PROGNOSIS

      Lancet
    79. NORITAKE C; KONDO I; KONDO K; TAKENAKA O; KINBARA A
      DIFFERENCE OF SI NODULES PRECIPITATING FROM AL-X WT-PERCENT SI (X=0.5-SIMILAR-TO-3.3)

      Thin solid films
    80. YANAGIHARA D; KONDO I
      NITRIC-OXIDE PLAYS A KEY ROLE IN ADAPTIVE-CONTROL OF LOCOMOTION IN CAT

      Proceedings of the National Academy of Sciences of the United Statesof America
    81. KUWANO A; TAKAKUBO F; MORIMOTO Y; UYAMA E; UCHINO M; ANDO M; YASUDA T; TERAO A; HAYAMA T; KOBAYASHI R; KONDO I
      BENIGN ADULT FAMILIAL MYOCLONUS EPILEPSY (BAFME) - AN AUTOSOMAL-DOMINANT FORM NOT LINKED TO THE DENTATORUBRAL PALLIDOLUYSIAN ATROPHY (DRPLA) GENE

      Journal of Medical Genetics
    82. IKEDA I; MIURA T; KONDO I; KAMEDA Y
      NEURILEMOMA OF THE KIDNEY

      British Journal of Urology
    83. IKEDA I; MIURA T; KONDO I
      PYRIDINIUM CROSS-LINKS AS URINARY MARKERS OF BONE METASTASES IN PATIENTS WITH PROSTATE-CANCER

      British Journal of Urology
    84. RICHARDS RI; CRAWFORD J; NARAHARA K; MANGELSDORF M; FRIEND K; STAPLES A; DENTON M; EASTEAL S; HORI TA; KONDO I; JENKINS T; GOLDMAN A; PANICH V; FERAKOVA E; SUTHERLAND GR
      DYNAMIC MUTATION LOCI - ALLELE DISTRIBUTIONS IN DIFFERENT POPULATIONS

      Annals of Human Genetics
    85. INAMOTO Y; HAMANAKA S; HAMANAKA Y; NAGATE T; KONDO I; TAKEMOTO T; OKITA K
      LIPID-COMPOSITION AND FATTY-ACID ANALYSIS OF HELICOBACTER-PYLORI

      Journal of gastroenterology
    86. KUWANO A; KONDO I; KISHI F; SUMINAMI Y; KATO H
      ASSIGNMENT OF THE SQUAMOUS-CELL CARCINOMA ANTIGEN LOCUS (SCC) TO 18Q21 BY IN-SITU HYBRIDIZATION

      Genomics
    87. KONDO I
      NONRADIOACTIVE DNA DIAGNOSIS FOR THE FRAGILE-X SYNDROME IN JAPANESE MENTALLY-RETARDED MALES - COMMENT

      Brain & development
    88. KATO A; NAKAMURA H; TAMARI N; TANAKA T; KONDO I
      USEFULNESS OF ALUMINA-COATED SIC WHISKERS IN THE PREPARATION OF WHISKER-REINFORCED ALUMINA CERAMICS

      Ceramics international
    89. MIYAZAKI M; KATO T; HASHIMOTO T; HARADA M; KONDO I; KURODA Y
      MR OF CHILDHOOD-ONSET DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY

      American journal of neuroradiology
    90. MORIMOTO Y; MURAYAMA N; KUWANO A; KONDO I; YAMASHITA Y; MIZUNO Y
      ASSOCIATION ANALYSIS OF A POLYMORPHISM OF THE MONOAMINE-OXIDASE-B GENE WITH PARKINSONS-DISEASE IN A JAPANESE POPULATION

      American journal of medical genetics
    91. NORITAKE C; KONDO I; KONDO K; TAKENAKA O; KINBARA A
      GROWTH-MECHANISM OF SI NODULES ON BPSG

      Thin solid films
    92. KOMURE O; SANO A; NISHINO N; YAMAUCHI N; UENO S; KONDOH K; SANO N; TAKAHASHI M; MURAYAMA N; KONDO I; NAGAFUCHI S; YAMADA M; KANAZAWA I
      DNA ANALYSIS IN HEREDITARY DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY - CORRELATION BETWEEN CAG REPEAT LENGTH AND PHENOTYPIC VARIATION AND THE MOLECULAR-BASIS OF ANTICIPATION

      Neurology
    93. IKEDA I; MIURA T; KONDO I
      CASE OF VESICO-APPENDICEAL FISTULA SECONDARY TO MUCINOUS ADENOCARCINOMA OF THE APPENDIX

      The Journal of urology
    94. UYAMA E; KONDO I; UCHINO M; FUKUSHIMA T; MURAYAMA N; KUWANO A; INOKUCHI N; OHTANI Y; ANDO M
      DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY (DRPLA) - CLINICAL, GENETIC, ANDNEURORADIOLOGIC STUDIES IN A FAMILY

      Journal of the neurological sciences
    95. MASUDA N; GOTO J; MURAYAMA N; WATANABE M; KONDO I; KANAZAWA I
      ANALYSIS OF TRIPLET REPEATS IN THE HUNTINGTIN GENE IN JAPANESE FAMILIES AFFECTED WITH HUNTINGTONS-DISEASE

      Journal of Medical Genetics
    96. KONDO I; KUWANO A; TAKAKUBO F; MORIMOTO Y; UYAMA E; UCHINO M; ANDO M; YASUDA T; TERAO A
      FAMILIAL DOMINANT FORM OF MYOCLONUS EPILEPSY NOT LINKED TO DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY

      Epilepsia
    97. MORIMOTO Y; MURAYAMA N; KUWANO A; YOSHIMURA O; KONDO I
      A BAMHI POLYMORPHISM IN THE HUMAN CYTOCHROME-P450 GENE, CYP2D6

      Clinical genetics
    98. MAGUCHI M; NISHIDA W; KOHARA K; KUWANO A; KONDO I; HIWADA K
      MOLECULAR-CLONING AND GENE-MAPPING OF HUMAN BASIC AND ACIDIC CALPONINS

      Biochemical and biophysical research communications
    99. KONDO I; TAKAKUBO F; KUWANO A; MORIMOTO Y; TAKAHASHI M; YOSHIZAWA T; KANAZAWA I
      SEGREGATION OF EXPANDED CAG ALLELES IN THE DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY (DRPLA) PEDIGREES

      American journal of human genetics
    100. KUWANO A; MORIMOTO Y; TAKAKUBO F; OHASHI H; FUKUSHIMA Y; KONDO I
      EXPRESSION STUDY OF THE PRADER-WILLI-SYNDROME ASSOCIATED WITH METHYLATED GENES IN PATIENTS WITH INV DUP (15Q)

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 13/08/20 alle ore 11:24:10