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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
   
   Y. Sunada et al., "Transgenic mice expressing mutant caveolin-3 show severe myopathy associated with increased nNOS activity", HUM MOL GEN, 10(3), 2001, pp. 173-178
2. Sunada, Y
   Glomerulopathy in MELAS syndrome
   INTERNAL MEDICINE
   
   Y. Sunada, "Glomerulopathy in MELAS syndrome", INTERN MED, 40(7), 2001, pp. 561-562
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
   
   K. Kobayashi et al., "Structural organization, complete genomic sequences and mutational analyses of the Fukuyama-type congenital muscular dystrophy gene, fukutin", FEBS LETTER, 489(2-3), 2001, pp. 192-196
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
   
   H. Tachibana et al., "Identification of a methylated tea catechin as an inhibitor of degranulation in human basophilic KU812 cells", BIOS BIOT B, 64(2), 2000, pp. 452-454
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
   
   T. Masaki et al., "Expression of dystroglycan and laminin-2 in peripheral nerve under axonal degeneration and regeneration", ACT NEUROP, 99(3), 2000, pp. 289-295
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
   
   J.Y. Gu et al., "Dietary effect of tocopherols and tocotrienols on the immune function of spleen and mesenteric lymph node lymphocytes in Brown Norway rats", BIOS BIOT B, 63(10), 1999, pp. 1697-1702
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
   
   K. Rinoie et al., "Velocity bias corrections of laser Doppler anemometry for separated flow measurements", T JPN SOC A, 42(137), 1999, pp. 147-149
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
   
   K. Matsumura et al., "Sarcoglycan complex: A muscular supporter of dystroglycan-dystrophin interplay?", CELL MOL B, 45(6), 1999, pp. 751-762
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
   
   F. Saito et al., "Characterization of the transmembrane molecular architecture of the dystroglycan complex in Schwann cells", J BIOL CHEM, 274(12), 1999, pp. 8240-8246
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
    
    H. Nakagawa et al., "DIFFERENTIAL PRODUCTION OF CHEMOKINES AND THEIR ROLE IN NEUTROPHIL INFILTRATION IN RAT ALLERGIC INFLAMMATION", International archives of allergy and immunology, 115(2), 1998, pp. 137-143
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
    
    F. Duclos et al., "BETA-SARCOGLYCAN - GENOMIC ANALYSIS AND IDENTIFICATION OF A NOVEL MISSENSE MUTATION IN THE LGMD2E AMISH ISOLATE", Neuromuscular disorders, 8(1), 1998, pp. 30-38
12. SUNADA Y; SAITO F; MATSUMURA K; SHIMIZU T
    DIFFERENTIAL EXPRESSION OF THE PARKIN GENE IN THE HUMAN BRAIN AND PERIPHERAL LEUKOCYTES
    Neuroscience letters
    
    Y. Sunada et al., "DIFFERENTIAL EXPRESSION OF THE PARKIN GENE IN THE HUMAN BRAIN AND PERIPHERAL LEUKOCYTES", Neuroscience letters, 254(3), 1998, pp. 180-182
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
    
    H. Nakagawa et al., "BIOLOGICAL-ACTIVITIES OF C3-BETA-C, A NOVEL NEUTROPHIL CHEMOATTRACTANT DERIVED FROM THE BETA-CHAIN OF RAT COMPLEMENT C3", Immunology, 94(2), 1998, pp. 253-257
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
    
    R.A. Williamson et al., "DYSTROGLYCAN IS ESSENTIAL FOR EARLY EMBRYONIC-DEVELOPMENT - DISRUPTION OF REICHERTS-MEMBRANE IN DAG1-NULL MICE", Human molecular genetics, 6(6), 1997, pp. 831-841
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
    
    V. Allamand et al., "MILD CONGENITAL MUSCULAR-DYSTROPHY IN 2 PATIENTS WITH AN INTERNALLY DELETED LAMININ ALPHA-2-CHAIN", Human molecular genetics, 6(5), 1997, pp. 747-752
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
    
    K. Matsumura et al., "PERIPHERAL-NERVE INVOLVEMENT IN MEROSIN-DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY AND DY MOUSE", Neuromuscular disorders, 7(1), 1997, pp. 7-12
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
    
    K. Matsumura et al., "THE ROLE OF DYSTROGLYCAN, A NOVEL RECEPTOR OF LAMININ AND AGRIN, IN CELL-DIFFERENTIATION", Histology and histopathology, 12(1), 1997, pp. 195-203
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
    
    A. Carrie et al., "MUTATIONAL DIVERSITY AND HOT-SPOTS IN THE ALPHA-SARCOGLYCAN GENE IN AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY (LGMD2D)", Journal of Medical Genetics, 34(6), 1997, pp. 470-475
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
    
    F. Saito et al., "CHARACTERIZATION OF A 30-KDA PERIPHERAL-NERVE GLYCOPROTEIN THAT BINDSLAMININ AND HEPARIN", The Journal of biological chemistry, 272(42), 1997, pp. 26708-26713
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
    
    P.R. Clemens et al., "IN-VIVO MUSCLE GENE-TRANSFER OF FULL-LENGTH DYSTROPHIN WITH AN ADENOVIRAL VECTOR THAT LACKS ALL VIRAL GENES", Gene therapy, 3(11), 1996, pp. 965-972
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
    
    J.S. Beckmann et al., "IDENTIFICATION OF MUSCLE-SPECIFIC CALPAIN AND BETA-SARCOGLYCAN GENES IN PROGRESSIVE AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHIES", Neuromuscular disorders, 6(6), 1996, pp. 455-462
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
    
    M. Jeanpierre et al., "FROM ADHALINOPATHIES TO ALPHA-SARCOGLYCANOPATHIES - AN OVERVIEW", Neuromuscular disorders, 6(6), 1996, pp. 463-465
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
    
    M.A.M. Salih et al., "MUSCULAR-DYSTROPHY ASSOCIATED WITH BETA-DYSTROGLYCAN DEFICIENCY", Annals of neurology, 40(6), 1996, pp. 925-928
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
    
    L. Morandi et al., "CLINICAL HETEROGENEITY OF ADHALIN DEFICIENCY", Annals of neurology, 39(2), 1996, pp. 196-202
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
    
    M.Z. Seidahmed et al., "LETHAL CONGENITAL MUSCULAR-DYSTROPHY IN 2 SIBS WITH ARTHROGRYPOSIS MULTIPLEX - NEW ENTITY OR VARIANT OF COBBLESTONE LISSENCEPHALY SYNDROME", Neuropediatrics, 27(6), 1996, pp. 305-310
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
    
    R. Fadic et al., "BRIEF REPORT - DEFICIENCY OF A DYSTROPHIN-ASSOCIATED GLYCOPROTEIN (ADHALIN) IN A PATIENT WITH MUSCULAR-DYSTROPHY AND CARDIOMYOPATHY", The New England journal of medicine, 334(6), 1996, pp. 362-366
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
    
    M. Mora et al., "CLINICAL PHENOTYPES IN ADHALIN DEFICIENCY", Neurology, 46(2), 1996, pp. 4085-4085
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
    
    D. Jung et al., "CHARACTERIZATION OF DELTA-SARCOGLYCAN, A NOVEL COMPONENT OF THE OLIGOMERIC SARCOGLYCAN COMPLEX INVOLVED IN LIMB-GIRDLE MUSCULAR-DYSTROPHY", The Journal of biological chemistry, 271(50), 1996, pp. 32321-32329
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
    
    D. Jung et al., "ABSENCE OF GAMMA-SARCOGLYCAN (35-DAG) IN AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY LINKED TO CHROMOSOME 13Q12", FEBS letters, 381(1-2), 1996, pp. 15-20
30. SUNADA Y; CAMPBELL KP
    DYSTROPHIN-GLYCOPROTEIN COMPLEX - MOLECULAR-ORGANIZATION AND CRITICALROLES IN SKELETAL-MUSCLE
    Current opinion in neurology
    
    Y. Sunada e K.P. Campbell, "DYSTROPHIN-GLYCOPROTEIN COMPLEX - MOLECULAR-ORGANIZATION AND CRITICALROLES IN SKELETAL-MUSCLE", Current opinion in neurology, 8(5), 1995, pp. 379-384
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
    
    L.E. Lim et al., "BETA-SARCOGLYCAN - CHARACTERIZATION AND ROLE IN LIMB-GIRDLE MUSCULAR-DYSTROPHY LINKED TO 4Q12", Nature genetics, 11(3), 1995, pp. 257-265
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
    
    T. Paunio et al., "HAPLOTYPE ANALYSIS IN GELSOLIN-RELATED AMYLOIDOSIS REVEALS INDEPENDENT ORIGIN OF IDENTICAL MUTATION (G654A) OF GELSOLIN IN FINLAND AND JAPAN", Human mutation, 6(1), 1995, pp. 60-65
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
    
    L.E. Lim et al., "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, 6, 1995, pp. 881-881
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
    
    K. Daniels et al., "EXPRESSION OF ALPHA-DYSTROGLYCAN AND BETA-DYSTROGLYCAN BY NONMUSCLE AVIAN AND MURINE EMBRYONIC-TISSUES AND MIGRATING NEURAL CREST", Molecular biology of the cell, 6, 1995, pp. 1876-1876
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
    
    D.J. Wells et al., "EXPRESSION OF HUMAN FULL-LENGTH AND MINIDYSTROPHIN IN TRANSGENIC MDX MICE - IMPLICATIONS FOR GENE-THERAPY OF DUCHENNE MUSCULAR-DYSTROPHY", Human molecular genetics, 4(8), 1995, pp. 1245-1250
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
    
    Y. Sunada et al., "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, 4(6), 1995, pp. 1055-1061
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
    
    K.A. Mills et al., "A SYNTROPHIN GENE MAPS TO MOUSE CHROMOSOME-8 AND IS NOT THE MYODYSTROPHY GENE", Mammalian genome, 6(9), 1995, pp. 664-665
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
    
    F. Duclos et al., "BETA-SARCOGLYCAN - A PROTEIN OF THE DYSTR OPHIN-GLYCOPROTEINS COMPLEX, IS RESPONSIBLE FOR RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHY", MS. Medecine sciences, 11(12), 1995, pp. 1732-1738
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
    
    T. Toda et al., "3-DIMENSIONAL MR-IMAGING OF BRAIN SURFACE ANOMALIES IN FUKUYAMA TYPE CONGENITAL MUSCULAR-DYSTROPHY", Muscle & nerve, 18(5), 1995, pp. 508-517
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
    
    R. Fadic et al., "50-KILODALTON DYSTROPHIN-ASSOCIATED GLYCOPROTEIN DEFICIENCY PRESENTING WITH MUSCULAR-DYSTROPHY AND END-STAGE CARDIOMYOPATHY IN A NORTH-AMERICAN BOY", Neurology, 45(4), 1995, pp. 183-184
41. SUNADA Y; EDGAR TS; LOTZ BP; RUST RS; CAMPBELL KP
    MEROSIN-NEGATIVE CONGENITAL MUSCULAR-DYSTROPHY ASSOCIATED WITH EXTENSIVE BRAIN ABNORMALITIES
    Neurology
    
    Y. Sunada et al., "MEROSIN-NEGATIVE CONGENITAL MUSCULAR-DYSTROPHY ASSOCIATED WITH EXTENSIVE BRAIN ABNORMALITIES", Neurology, 45(11), 1995, pp. 2084-2089
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
    
    R.A. Williamson et al., "INACTIVATION OF THE MURINE DYSTROGLYCAN GENE PRODUCES AN EARLY MIDGESTATION EMBRYONIC LETHAL", American journal of human genetics, 57(4), 1995, pp. 55-55
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
    
    J.C. Kaplan et al., "ALLELIC AND PHENOTYPIC HETEROGENEITY OF PRIMARY ADHALINOPATHIES", American journal of human genetics, 57(4), 1995, pp. 103-103
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
    
    Y. Sunada et al., "CHARACTERIZATION OF HETEROGENEOUS ADHALIN-DEFICIENT LIMB-GIRDLE MUSCULAR IN THE UNITED-STATES", American journal of human genetics, 57(4), 1995, pp. 1325-1325
45. SATO J; SUNADA Y
    EXPERIMENTAL RESEARCH ON BLUNT TRAILING-EDGE AIRFOIL SECTIONS AT LOW REYNOLDS-NUMBERS
    AIAA journal
    
    J. Sato e Y. Sunada, "EXPERIMENTAL RESEARCH ON BLUNT TRAILING-EDGE AIRFOIL SECTIONS AT LOW REYNOLDS-NUMBERS", AIAA journal, 33(11), 1995, pp. 2001-2005
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
    
    G.A. Cox et al., "DP71 CAN RESTORE THE DYSTROPHIN-ASSOCIATED GLYCOPROTEIN COMPLEX IN MUSCLE BUT FAILS TO PREVENT DYSTROPHY", Nature genetics, 8(4), 1994, pp. 333-339
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
    
    D.S. Greenberg et al., "EXOGENOUS DP71 RESTORES THE LEVELS OF DYSTROPHIN-ASSOCIATED PROTEINS BUT DOES NOT ALLEVIATE MUSCLE DAMAGE IN MDX MICE", Nature genetics, 8(4), 1994, pp. 340-344
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
    
    J.A. Rafael et al., "PREVENTION OF DYSTROPHIC PATHOLOGY IN MDX MICE BY A TRUNCATED DYSTROPHIN ISOFORM", Human molecular genetics, 3(10), 1994, pp. 1725-1733
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
    
    T. Ide et al., "TRIACYLGLYCEROL AND FATTY-ACID SYNTHESIS IN HEPATOCYTES IN SUSPENSIONISOLATED FROM RATS FED SOYBEAN PHOSPHOLIPID", Bioscience, biotechnology, and biochemistry, 58(4), 1994, pp. 699-702
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
    
    F.M.S. Tome et al., "CONGENITAL MUSCULAR-DYSTROPHY WITH MEROSIN DEFICIENCY", Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 317(4), 1994, pp. 351-357
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
    
    T. Itoh et al., "ENHANCEMENT OF KR2 EXCIMER GENERATION IN A PULSED RARE-GAS JET DISCHARGE WITH H-2 GAS CONTACT COOLING", IEEE transactions on plasma science, 22(2), 1994, pp. 210-216
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
    
    S. Hitoshi et al., "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, 126(2), 1994, pp. 219-224
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
    
    S. Hitoshi et al., "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, 126(2), 1994, pp. 219-224
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
    
    Y. Sunada et al., "DEFICIENCY OF MEROSIN IN DYSTROPHIC DY MICE AND GENETIC-LINKAGE OF LAMININ M-CHAIN GENE TO DY LOCUS", The Journal of biological chemistry, 269(19), 1994, pp. 13729-13732
55. ASAOKA T; AMANO S; SUNADA Y; SAWA M
    LATTICE CORNEAL-DYSTROPHY TYPE-II WITH FAMILIAL AMYLOID POLYNEUROPATHY TYPE-IV
    Japanese Journal of Ophthalmology
    
    T. Asaoka et al., "LATTICE CORNEAL-DYSTROPHY TYPE-II WITH FAMILIAL AMYLOID POLYNEUROPATHY TYPE-IV", Japanese Journal of Ophthalmology, 37(4), 1993, pp. 426-431