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    1. Sunada, Y; Ohi, H; Hase, A; Ohi, H; Hosono, T; Arata, S; Higuchi, S; Matsumura, K; Shimizu, T
      Transgenic mice expressing mutant caveolin-3 show severe myopathy associated with increased nNOS activity

      HUMAN MOLECULAR GENETICS
    2. Sunada, Y
      Glomerulopathy in MELAS syndrome

      INTERNAL MEDICINE
    3. Kobayashi, K; Sasaki, J; Kondo-Iida, E; Fukuda, Y; Kinoshita, M; Sunada, Y; Nakamura, Y; Toda, T
      Structural organization, complete genomic sequences and mutational analyses of the Fukuyama-type congenital muscular dystrophy gene, fukutin

      FEBS LETTERS
    4. Tachibana, H; Sunada, Y; Miyase, T; Sano, M; Maeda-Yamamoto, M; Yamada, K
      Identification of a methylated tea catechin as an inhibitor of degranulation in human basophilic KU812 cells

      BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
    5. Masaki, T; Matsumura, K; Saito, F; Sunada, Y; Shimizu, T; Yorifuji, H; Motoyoshi, K; Kamakura, K
      Expression of dystroglycan and laminin-2 in peripheral nerve under axonal degeneration and regeneration

      ACTA NEUROPATHOLOGICA
    6. Gu, JY; Wakizono, Y; Sunada, Y; Hung, P; Nonaka, M; Sugano, M; Yamada, K
      Dietary effect of tocopherols and tocotrienols on the immune function of spleen and mesenteric lymph node lymphocytes in Brown Norway rats

      BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
    7. Rinoie, K; Hata, K; Shirai, Y; Sunada, Y
      Velocity bias corrections of laser Doppler anemometry for separated flow measurements

      TRANSACTIONS OF THE JAPAN SOCIETY FOR AERONAUTICAL AND SPACE SCIENCES
    8. Matsumura, K; Saito, F; Yamada, H; Hase, A; Sunada, Y; Shimizu, T
      Sarcoglycan complex: A muscular supporter of dystroglycan-dystrophin interplay?

      CELLULAR AND MOLECULAR BIOLOGY
    9. Saito, F; Masaki, T; Kamakura, K; Anderson, LVB; Fujita, S; Fukuta-Ohi, H; Sunada, Y; Shimizu, T; Matsumura, K
      Characterization of the transmembrane molecular architecture of the dystroglycan complex in Schwann cells

      JOURNAL OF BIOLOGICAL CHEMISTRY
    10. NAKAGAWA H; ANDO Y; TAKANO K; SUNADA Y
      DIFFERENTIAL PRODUCTION OF CHEMOKINES AND THEIR ROLE IN NEUTROPHIL INFILTRATION IN RAT ALLERGIC INFLAMMATION

      International archives of allergy and immunology
    11. DUCLOS F; BROUX O; BOURG N; STRAUB V; FELDMAN GL; SUNADA Y; LIM LE; PICCOLO F; CUTSHALL S; GARY F; QUETIER F; KAPLAN JC; JACKSON CE; BECKMANN JS; CAMPBELL KP
      BETA-SARCOGLYCAN - GENOMIC ANALYSIS AND IDENTIFICATION OF A NOVEL MISSENSE MUTATION IN THE LGMD2E AMISH ISOLATE

      Neuromuscular disorders
    12. SUNADA Y; SAITO F; MATSUMURA K; SHIMIZU T
      DIFFERENTIAL EXPRESSION OF THE PARKIN GENE IN THE HUMAN BRAIN AND PERIPHERAL LEUKOCYTES

      Neuroscience letters
    13. NAKAGAWA H; SUNADA Y; ANDO Y
      BIOLOGICAL-ACTIVITIES OF C3-BETA-C, A NOVEL NEUTROPHIL CHEMOATTRACTANT DERIVED FROM THE BETA-CHAIN OF RAT COMPLEMENT C3

      Immunology
    14. WILLIAMSON RA; HENRY MD; DANIELS KJ; HRSTKA RF; LEE JC; SUNADA Y; IBRAGHIMOVBESKROVNAYA O; CAMPBELL KP
      DYSTROGLYCAN IS ESSENTIAL FOR EARLY EMBRYONIC-DEVELOPMENT - DISRUPTION OF REICHERTS-MEMBRANE IN DAG1-NULL MICE

      Human molecular genetics
    15. ALLAMAND V; SUNADA Y; SALIH MAM; STRAUB V; OZO CO; ALTURAIKI MHS; AKBAR M; KOLO T; COLOGNATO H; ZHANG X; SOROKIN LM; YURCHENCO PD; TRYGGVASON K; CAMPBELL KP
      MILD CONGENITAL MUSCULAR-DYSTROPHY IN 2 PATIENTS WITH AN INTERNALLY DELETED LAMININ ALPHA-2-CHAIN

      Human molecular genetics
    16. MATSUMURA K; YAMADA H; SAITO F; SUNADA Y; SHIMIZU T
      PERIPHERAL-NERVE INVOLVEMENT IN MEROSIN-DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY AND DY MOUSE

      Neuromuscular disorders
    17. MATSUMURA K; YAMADA H; SAITO F; SUNADA Y; SHIMIZU T
      THE ROLE OF DYSTROGLYCAN, A NOVEL RECEPTOR OF LAMININ AND AGRIN, IN CELL-DIFFERENTIATION

      Histology and histopathology
    18. CARRIE A; PICCOLO F; LETURCQ F; DETOMA C; AZIBI K; BELDJORD C; VALLAT JM; MERLINI L; VOIT T; SEWRY C; URTIZBEREA JA; ROMERO N; TOME FMS; FARDEAU M; SUNADA Y; CAMPBELL KP; KAPLAN JC; JEANPIERRE M
      MUTATIONAL DIVERSITY AND HOT-SPOTS IN THE ALPHA-SARCOGLYCAN GENE IN AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY (LGMD2D)

      Journal of Medical Genetics
    19. SAITO F; YAMADA H; SUNADA Y; HORI H; SHIMIZU T; MATSUMURA K
      CHARACTERIZATION OF A 30-KDA PERIPHERAL-NERVE GLYCOPROTEIN THAT BINDSLAMININ AND HEPARIN

      The Journal of biological chemistry
    20. CLEMENS PR; KOCHANEK S; SUNADA Y; CHAN S; CHEN HH; CAMPBELL KP; CASKEY CT
      IN-VIVO MUSCLE GENE-TRANSFER OF FULL-LENGTH DYSTROPHIN WITH AN ADENOVIRAL VECTOR THAT LACKS ALL VIRAL GENES

      Gene therapy
    21. BECKMANN JS; RICHARD I; BROUX O; FOUGEROUSSE F; ALLAMAND V; CHIANNILKULCHAI N; LIM LE; DUCLOS F; BOURG N; BRENGUIER L; PASTURAUD P; QUETIER F; ROUDAUT C; SUNADA Y; MEYER J; DINCER P; LEFRANC G; MERLINI L; TOPALOGLU H; TOME FMS; COHEN D; JACKSON CE; CAMPBELL KP; FARDEAU M
      IDENTIFICATION OF MUSCLE-SPECIFIC CALPAIN AND BETA-SARCOGLYCAN GENES IN PROGRESSIVE AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHIES

      Neuromuscular disorders
    22. JEANPIERRE M; CARRIE A; PICCOLO F; LETURCQ F; AZIBI K; DETOMA C; BELDJORD C; MERLINI L; VOIT T; ROMERO N; SUNADA Y; TOME FMS; FARDEAU M; CAMPBELL KP; KAPLAN JC
      FROM ADHALINOPATHIES TO ALPHA-SARCOGLYCANOPATHIES - AN OVERVIEW

      Neuromuscular disorders
    23. SALIH MAM; SUNADA Y; ALNASSER M; OZO CO; ALTURAIKI MHS; AKBAR M; CAMPBELL KP
      MUSCULAR-DYSTROPHY ASSOCIATED WITH BETA-DYSTROGLYCAN DEFICIENCY

      Annals of neurology
    24. MORANDI L; BARRESI R; DIBLASI C; JUNG D; SUNADA Y; CONFALONIERI V; DWORZAK F; MANTEGAZZA R; ANTOZZI C; JARRE L; PINI A; GOBBI G; BIANCHI C; CORNELIO F; CAMPBELL KP; MORA M
      CLINICAL HETEROGENEITY OF ADHALIN DEFICIENCY

      Annals of neurology
    25. SEIDAHMED MZ; SUNADA Y; OZO CO; HAMID F; CAMPBELL KP; SALIH MAM
      LETHAL CONGENITAL MUSCULAR-DYSTROPHY IN 2 SIBS WITH ARTHROGRYPOSIS MULTIPLEX - NEW ENTITY OR VARIANT OF COBBLESTONE LISSENCEPHALY SYNDROME

      Neuropediatrics
    26. FADIC R; SUNADA Y; WACLAWIK AJ; BUCK S; LEWANDOSKI PJ; CAMPBELL KP; LOTZ BP
      BRIEF REPORT - DEFICIENCY OF A DYSTROPHIN-ASSOCIATED GLYCOPROTEIN (ADHALIN) IN A PATIENT WITH MUSCULAR-DYSTROPHY AND CARDIOMYOPATHY

      The New England journal of medicine
    27. MORA M; MORANDI L; BARRESI R; DIBLASI C; CONFALONIERI V; MANTEGAZZA R; ANTOZZI C; CORNELIO F; JUNG D; SUNADA Y; CAMPBELL KP
      CLINICAL PHENOTYPES IN ADHALIN DEFICIENCY

      Neurology
    28. JUNG D; DUCLOS F; APOSTOL B; STRAUB V; LEE JC; ALLAMAND V; VENZKE DP; SUNADA Y; MOOMAW CR; LEVEILLE CJ; SLAUGHTER CA; CRAWFORD TO; MCPHERSON JD; CAMPBELL KP
      CHARACTERIZATION OF DELTA-SARCOGLYCAN, A NOVEL COMPONENT OF THE OLIGOMERIC SARCOGLYCAN COMPLEX INVOLVED IN LIMB-GIRDLE MUSCULAR-DYSTROPHY

      The Journal of biological chemistry
    29. JUNG D; LETURCQ F; SUNADA Y; DUCLOS F; TOME FMS; MOOMAW C; MERLINI L; AZIBI K; CHAOUCH M; SLAUGHTER C; FARDEAU M; KAPLAN JC; CAMPBELL KP
      ABSENCE OF GAMMA-SARCOGLYCAN (35-DAG) IN AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY LINKED TO CHROMOSOME 13Q12

      FEBS letters
    30. SUNADA Y; CAMPBELL KP
      DYSTROPHIN-GLYCOPROTEIN COMPLEX - MOLECULAR-ORGANIZATION AND CRITICALROLES IN SKELETAL-MUSCLE

      Current opinion in neurology
    31. LIM LE; DUCLOS F; BROUX O; BOURG N; SUNADA Y; ALLAMAND V; MEYER J; RICHARD IZ; MOOMAW C; SLAUGHTER C; TOME FMS; FARDEAU M; JACKSON CE; BECKMANN JS; CAMPBELL KP
      BETA-SARCOGLYCAN - CHARACTERIZATION AND ROLE IN LIMB-GIRDLE MUSCULAR-DYSTROPHY LINKED TO 4Q12

      Nature genetics
    32. PAUNIO T; SUNADA Y; KIURU S; MAKISHITA H; IKEDA S; WEISSENBACH J; PALO J; PELTONEN L
      HAPLOTYPE ANALYSIS IN GELSOLIN-RELATED AMYLOIDOSIS REVEALS INDEPENDENT ORIGIN OF IDENTICAL MUTATION (G654A) OF GELSOLIN IN FINLAND AND JAPAN

      Human mutation
    33. LIM LE; DUCLOS F; BROUX O; BOURG N; SUNADA Y; ALLAMAND V; MEYER J; RICHARD I; MOOMAW C; SLAUGHTER C; JACKSON CE; BECKMANN JS; CAMPBELL KP
      CHARACTERIZATION OF A 43 KDA COMPONENT OF THE DYSTROPHIN-GLYCOPROTEINCOMPLEX AND INVOLVEMENT IN A NOVEL FORM OF RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHY

      Molecular biology of the cell
    34. DANIELS K; SOLURSH M; CAMPBELL K; SUNADA Y; RUSSO A
      EXPRESSION OF ALPHA-DYSTROGLYCAN AND BETA-DYSTROGLYCAN BY NONMUSCLE AVIAN AND MURINE EMBRYONIC-TISSUES AND MIGRATING NEURAL CREST

      Molecular biology of the cell
    35. WELLS DJ; WELLS KE; ASANTE EA; TURNER G; SUNADA Y; CAMPBELL KP; WALSH FS; DICKSON G
      EXPRESSION OF HUMAN FULL-LENGTH AND MINIDYSTROPHIN IN TRANSGENIC MDX MICE - IMPLICATIONS FOR GENE-THERAPY OF DUCHENNE MUSCULAR-DYSTROPHY

      Human molecular genetics
    36. SUNADA Y; BERNIER SM; UTANI A; YAMADA Y; CAMPBELL KP
      IDENTIFICATION OF A NOVEL MUTANT TRANSCRIPT OF LAMININ ALPHA-2 CHAIN GENE RESPONSIBLE FOR MUSCULAR-DYSTROPHY AND DYSMYELINATION IN DY(2J) MICE

      Human molecular genetics
    37. MILLS KA; SUNADA Y; CAMPBELL KP; MATHEWS KD
      A SYNTROPHIN GENE MAPS TO MOUSE CHROMOSOME-8 AND IS NOT THE MYODYSTROPHY GENE

      Mammalian genome
    38. DUCLOS F; LIM LE; SUNADA Y; MEYER J; CAMPBELL KP; BROUX O; BOURG N; ALLAMAND V; RICHARD I; BECKMANN JS; MOOMAW C; SLAUGHTER C; TOME FMS; FARDEAU M; JACKSON CE
      BETA-SARCOGLYCAN - A PROTEIN OF THE DYSTR OPHIN-GLYCOPROTEINS COMPLEX, IS RESPONSIBLE FOR RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHY

      MS. Medecine sciences
    39. TODA T; WATANABE T; MATSUMURA K; SUNADA Y; YAMADA H; NAKANO I; MANNEN T; KANAZAWA I; SHIMIZU T
      3-DIMENSIONAL MR-IMAGING OF BRAIN SURFACE ANOMALIES IN FUKUYAMA TYPE CONGENITAL MUSCULAR-DYSTROPHY

      Muscle & nerve
    40. FADIC R; LOTZ BP; WACLAWIK AJ; BUCK S; SUNADA Y; CAMPBELL KP
      50-KILODALTON DYSTROPHIN-ASSOCIATED GLYCOPROTEIN DEFICIENCY PRESENTING WITH MUSCULAR-DYSTROPHY AND END-STAGE CARDIOMYOPATHY IN A NORTH-AMERICAN BOY

      Neurology
    41. SUNADA Y; EDGAR TS; LOTZ BP; RUST RS; CAMPBELL KP
      MEROSIN-NEGATIVE CONGENITAL MUSCULAR-DYSTROPHY ASSOCIATED WITH EXTENSIVE BRAIN ABNORMALITIES

      Neurology
    42. WILLIAMSON RA; IBRAGHIMOYBESKROVNAYA O; HRSTKA R; LEE J; SUNADA Y; CAMPBELL KP
      INACTIVATION OF THE MURINE DYSTROGLYCAN GENE PRODUCES AN EARLY MIDGESTATION EMBRYONIC LETHAL

      American journal of human genetics
    43. KAPLAN JC; CARRIE A; PICCOLO F; SUNADA Y; LETURCQ F; AZIBI K; ELKERCH F; BELDJORD C; MERLINI L; VOIT T; ROMERO N; TOME FMS; FARDEAU M; CAMPBELL KP; JEANPIERRE M
      ALLELIC AND PHENOTYPIC HETEROGENEITY OF PRIMARY ADHALINOPATHIES

      American journal of human genetics
    44. SUNADA Y; PICCOLO F; JUNG D; DUCLOS F; LIM LE; KAPLAN JC; CAMPBELL KP
      CHARACTERIZATION OF HETEROGENEOUS ADHALIN-DEFICIENT LIMB-GIRDLE MUSCULAR IN THE UNITED-STATES

      American journal of human genetics
    45. SATO J; SUNADA Y
      EXPERIMENTAL RESEARCH ON BLUNT TRAILING-EDGE AIRFOIL SECTIONS AT LOW REYNOLDS-NUMBERS

      AIAA journal
    46. COX GA; SUNADA Y; CAMPBELL KP; CHAMBERLAIN JS
      DP71 CAN RESTORE THE DYSTROPHIN-ASSOCIATED GLYCOPROTEIN COMPLEX IN MUSCLE BUT FAILS TO PREVENT DYSTROPHY

      Nature genetics
    47. GREENBERG DS; SUNADA Y; CAMPBELL KP; YAFFE D; NUDEL U
      EXOGENOUS DP71 RESTORES THE LEVELS OF DYSTROPHIN-ASSOCIATED PROTEINS BUT DOES NOT ALLEVIATE MUSCLE DAMAGE IN MDX MICE

      Nature genetics
    48. RAFAEL JA; SUNADA Y; COLE NM; CAMPBELL KP; FAULKNER JA; CHAMBERLAIN JS
      PREVENTION OF DYSTROPHIC PATHOLOGY IN MDX MICE BY A TRUNCATED DYSTROPHIN ISOFORM

      Human molecular genetics
    49. IDE T; MURATA M; SUNADA Y
      TRIACYLGLYCEROL AND FATTY-ACID SYNTHESIS IN HEPATOCYTES IN SUSPENSIONISOLATED FROM RATS FED SOYBEAN PHOSPHOLIPID

      Bioscience, biotechnology, and biochemistry
    50. TOME FMS; EVANGELISTA T; LECLERC A; SUNADA Y; MANOLE E; ESTOURNET B; BAROIS A; CAMPBELL KP; FARDEAU M
      CONGENITAL MUSCULAR-DYSTROPHY WITH MEROSIN DEFICIENCY

      Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie
    51. ITOH T; SUNADA Y; KANNARI F
      ENHANCEMENT OF KR2 EXCIMER GENERATION IN A PULSED RARE-GAS JET DISCHARGE WITH H-2 GAS CONTACT COOLING

      IEEE transactions on plasma science
    52. HITOSHI S; KUSUNOKI S; CHIBA A; TAKATSU R; SUNADA Y; NUKINA N; TAI T; KANAZAWA I
      CEREBELLAR-ATAXIA AND POLYNEUROPATHY IN A PATIENT WITH IGM M-PROTEIN SPECIFIC TO THE GAL(BETA-1-3)GALNAC EPITOPE

      Journal of the neurological sciences
    53. HITOSHI S; KUSUNOKI S; CHIBA A; TAKATSU R; SUNADA Y; NUKINA N; TAI T; KANAZAWA I
      CEREBELLAR-ATAXIA AND POLYNEUROPATHY IN A PATIENT WITH IGM M-PROTEIN SPECIFIC TO THE GAL(BETA-1-3)GALNAC EPITOPE

      Journal of the neurological sciences
    54. SUNADA Y; BERNIER SM; KOZAK CA; YAMADA Y; CAMPBELL KP
      DEFICIENCY OF MEROSIN IN DYSTROPHIC DY MICE AND GENETIC-LINKAGE OF LAMININ M-CHAIN GENE TO DY LOCUS

      The Journal of biological chemistry
    55. ASAOKA T; AMANO S; SUNADA Y; SAWA M
      LATTICE CORNEAL-DYSTROPHY TYPE-II WITH FAMILIAL AMYLOID POLYNEUROPATHY TYPE-IV

      Japanese Journal of Ophthalmology


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Documento generato il 26/01/21 alle ore 14:29:59