Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where authors phrase all words 'Tsujino, S' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 60 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Miyamoto, T; Kanazawa, N; Kato, S; Kawakami, M; Inoue, Y; Kuhara, T; Inoue, T; Takeshita, K; Tsujino, S
      Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis: a common mutation, R179X

      JOURNAL OF HUMAN GENETICS
    2. Shiroma, N; Kanazawa, N; Izumi, M; Sugai, K; Fukumizu, M; Sasaki, M; Hanaoka, S; Kaga, M; Tsujino, S
      Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis

      JOURNAL OF HUMAN GENETICS
    3. Tsujino, S; Huei, M; Kanazawa, N; Sugie, H; Goto, Y; Kawai, M; Nonaka, I; Hirschhorn, R; Sakuragawa, N
      Frequent mutations in Japanese patients with acid maltase deficiency

      NEUROMUSCULAR DISORDERS
    4. Tsujino, S; Allen, SJ; Thomas, M; Eckhause, T; Gwinn, E; Rufenacht, M; Zhang, JP; Speck, J; Sakaki, H
      Quantum confinement without walls

      SUPERLATTICES AND MICROSTRUCTURES
    5. Tsujino, S; Nonaka, I; DiMauro, S
      Glycogen storage myopathies

      NEUROLOGIC CLINICS
    6. Tsujino, S; Rufenacht, M; Miranda, P; Allen, SJ; Tamborenea, P; Schoendeld, W; Herold, G; Lupke, G; Lundstrom, T; Petroff, P; Metiu, H; Moses, D
      Quantum control of electron transfer

      PHYSICA STATUS SOLIDI B-BASIC RESEARCH
    7. Rufenacht, M; Tsujino, S; Allen, SJ; Schoenfeld, W; Petroff, P
      Coherent transfer and electron teleportation in semiconductor double quantum well

      PHYSICA STATUS SOLIDI B-BASIC RESEARCH
    8. Tsujino, S; Kanazawa, N; Ohashi, T; Eto, Y; Saito, T; Kira, J; Yamada, T
      Three novel mutations (G27E, insAAC, R179X) in the ORNT1 gene of Japanese patients with hyperornithinemia, hyperammonemia, and hyperammonemia syndrome

      ANNALS OF NEUROLOGY
    9. Tsujino, S; Rufenacht, M; Nakajima, H; Noda, T; Metzner, C; Sakaki, H
      Peak position of the intersubband absorption spectrum of quantum wells with controlled electron concentrations

      PHYSICAL REVIEW B
    10. Tsujino, S; Di Santo, JP; Takaoka, A; McKernan, TL; Noguchi, S; Taya, C; Yonekawa, H; Saito, T; Taniguchi, T; Fujii, H
      Differential requirement of the cytoplasmic subregions of gamma c chain inT cell development and function

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    11. Eckhause, TA; Tsujino, S; Lehnert, KW; Gwinn, EG; Allen, SJ; Thomas, M; Kroemer, H
      Midinfrared studies of the contact region at superconductor-semiconductor interfaces

      APPLIED PHYSICS LETTERS
    12. Pari, G; Crerar, MM; Nalbantoglu, J; Shoubridge, E; Jani, A; Tsujino, S; Shanske, S; DiMauro, S; Howell, JM; Karpati, G
      Myophosphorylase gene transfer in McArdle's disease myoblasts in vitro

      NEUROLOGY
    13. KOBAYASHI K; TSUJINO S; EZOE T; HAMAGUCHI H; NIHEI K; SAKURAGAWA N
      MISSENSE MUTATION (I143T) IN A JAPANESE PATIENT WITH CANAVAN-DISEASE

      Human mutation
    14. TSUJINO S; KINOSHITA N; TASHIRO T; IKEDA K; ICHIHARA N; KIKUCHI H; HAGIWARA Y; MIZUTANI M; KIKUCHI T; SAKURAGAWA N
      ADENOVIRUS-MEDIATED TRANSFER OF HUMAN ACID MALTASE GENE REDUCES GLYCOGEN ACCUMULATION IN SKELETAL-MUSCLE OF JAPANESE-QUAIL WITH ACID MALTASE DEFICIENCY

      Human gene therapy
    15. TSUJINO S; NAKAJIMA H; INOSHITA T; NODA T; SAKAKI H
      NEGATIVE VERTICAL PHOTOVOLTAIC RESPONSE OF 2-DIMENSIONAL ELECTRONS INTHE QUANTUM HALL REGIME

      Physica. B, Condensed matter
    16. RUFENACHT M; TSUJINO S; SAKAKI H
      TRANSIENT NEGATIVE PHOTOCONDUCTANCE IN A CHARGE-TRANSFER DOUBLE-QUANTUM-WELL UNDER OPTICAL INTERSUBBAND EXCITATION

      Physica. B, Condensed matter
    17. MIYAZAKI T; TAKAOKA A; NOGUEIRA L; DIKIC I; FUJII H; TSUJINO S; MITANI Y; MAEDA M; SCHLESSINGER J; TANIGUCHI T
      PYK2 IS A DOWNSTREAM MEDIATOR OF THE IL-2 RECEPTOR-COUPLED JAK SIGNALING PATHWAY

      Genes & development
    18. HUIE ML; TSUJINO S; BROOKS SS; ENGEL A; ELIAS E; BONTHRON DT; BESSLEY C; SHANSKE S; DIMAURO S; GOTO YI; HIRSCHHORN R
      GLYCOGEN-STORAGE-DISEASE TYPE-II - IDENTIFICATION OF 4 NOVEL MISSENSEMUTATIONS (D645N, G648S, R672W, R672Q) AND 2 INSERTIONS DELETIONS IN THE ACID ALPHA-GLUCOSIDASE LOCUS OF PATIENTS OF DIFFERING PHENOTYPE/

      Biochemical and biophysical research communications
    19. SASAGAWA R; SUGAWARA H; OHNO Y; NAKAJIMA H; TSUJINO S; AKIYAMA H; SAKAKI H
      ENHANCEMENT OF INTERSUBBAND TRANSITION ENERGIES IN GAAS QUANTUM-WELLSBY SI DELTA-DOPING OF HIGH-CONCENTRATION

      Applied physics letters
    20. Nishio, T; Sunohara, N; Nonaka, I; Tsujino, S; Sugie, H
      Myophosphorylase deficiency and limb-girdle muscular dystrophy in the samepedigree

      ACTA NEUROLOGICA SCANDINAVICA
    21. ELSCHAHAWI M; BRUNO C; TSUJINO S; SARRAZIN AM; SHANSKE S; LEROUX MG; DIMAURO S
      SUDDEN-INFANT-DEATH-SYNDROME (SIDS) IN A FAMILY WITH MYOPHOSPHORYLASEDEFICIENCY

      Neuromuscular disorders
    22. IKEDA K; TOHYAMA J; TSUJINO S; SATO K; OONO T; ARATA J; ENDO F; SAKURAGAWA N
      AMELIORATION OF PROLIDASE DEFICIENCY IN FIBROBLASTS USING ADENOVIRUS-MEDIATED GENE-TRANSFER

      Japanese journal of human genetics
    23. TSUJINO S; METZNER C; NODA T; SAKAKI H
      SATURATION OF INTERSUBBAND ABSORPTION BY REAL-SPACE TRANSFER IN MODULATION-DOPED SINGLE GAAS-ALAS QUANTUM-WELL

      Physica status solidi. b, Basic research
    24. ITO M; FENG JH; TSUJINO S; INAGAKI N; INAGAKI M; TANAKA J; ICHIKAWA K; HARTSHORNE DJ; NAKANO T
      INTERACTION OF SMOOTH-MUSCLE MYOSIN PHOSPHATASE WITH PHOSPHOLIPIDS

      Biochemistry
    25. INAGAKI N; NISHIZAWA M; ITO M; FUJIOKA M; NAKANO T; TSUJINO S; MATSUZAWA K; KIMURA K; KAIBUCHI K; INAGAKI M
      MYOSIN BINDING SUBUNIT OF SMOOTH-MUSCLE MYOSIN PHOSPHATASE AT THE CELL-CELL ADHESION SITES IN MDCK CELLS

      Biochemical and biophysical research communications
    26. RUFENACHT M; TSUJINO S; OHNO Y; SAKAKI H
      DELAYED LUMINESCENCE INDUCED BY INTERSUBBAND OPTICAL-EXCITATION IN A CHARGE-TRANSFER DOUBLE-QUANTUM-WELL STRUCTURE

      Applied physics letters
    27. HUIE ML; TSUJINO S; BEESLEY C; BONTHRON D; ENGEL A; SHANSKE S; DIMAURO S; HIRSCHHORN R
      MISSENSE MUTATIONS IN A CONSERVED REGION OF THE ACID ALPHA-GLUCOSIDASE GENE - GENOTYPE-PHENOTYPE

      American journal of human genetics
    28. TSUJINO S; SHANSKE S; VALBERG SJ; CARDINET GH; SMITH BP; DIMAURO S
      CLONING OF BOVINE MUSCLE GLYCOGEN-PHOSPHORYLASE CDNA AND IDENTIFICATION OF A MUTATION IN CATTLE WITH MYOPHOSPHORYLASE DEFICIENCY, AN ANIMAL-MODEL FOR MCARDLES-DISEASE

      Neuromuscular disorders
    29. TSUJINO S; KOBAYASHI K; TASHIRO T; IKEDA K; KIKUCHI H; ICHIHARA N; HAGIWARA Y; MIZUTANI M; KIKUCHI T; SAKURAGAWA N
      ADENOVIRUS-MEDIATED TRANSFER OF HUMAN ACID ALPHA-GLUCOSIDASE GENE-REDUCED GLYCOGEN ACCUMULATION IN MUSCLE OF JAPANESE-QUAIL WITH ACID ALPHA-GLUCOSIDASE DEFICIENCY

      Annals of neurology
    30. ISHII S; NISHIO T; SUNOHARA N; YOSHIHARA T; TAKEMURA K; HIKIJI K; TSUJINO S; SAKURAGAWA N
      SMALL INCREASE IN TRIPLET REPEAT LENGTH OF CEREBELLUM FROM PATIENTS WITH MYOTONIC-DYSTROPHY

      Human genetics
    31. ISHII T; TSUJINO S; MATSUNOBU S; ENDO F; SATO K; SAKURAGAWA N
      CLONING OF MOUSE PROLIDASE CDNA - PREDOMINANT EXPRESSION OF PROLIDASEMESSENGER-RNA IN KIDNEY

      Biochimica et biophysica acta, N. Gene structure and expression
    32. TOSCANO A; TSUJINO S; VITA G; SHANSKE S; MESSINA C; DIMAURO S
      MOLECULAR-BASIS OF MUSCLE PHOSPHOGLYCERATE MUTASE (PGAM-M) DEFICIENCYIN THE ITALIAN KINDRED

      Muscle & nerve
    33. ELSCHAHAWI M; TSUJINO S; SHANSKE S; DIMAURO S
      DIAGNOSIS OF MCARDLES-DISEASE BY MOLECULAR-GENETIC ANALYSIS OF BLOOD

      Neurology
    34. MARTINUZZI A; TSUJINO S; VERGANI L; SCHIEVANO G; CADALDINI M; BARTOLONI L; FANIN M; SICILIANO G; SHANSKE S; DIMAURO S; ANGELINI C
      MOLECULAR CHARACTERIZATION OF MYOPHOSPHORYLASE DEFICIENCY IN A GROUP OF PATIENTS FROM NORTHERN ITALY

      Journal of the neurological sciences
    35. TSUJINO S; SEKIMATA M; INAGAKI N; KAMEI Y; HIGASHIHARA M; KUROKAWA K; IMAJOHOHMI S; INAGAKI M
      PRIMARY STRUCTURE OF LIGHT AND HEAVY-CHAIN VARIABLE REGIONS OF ANTIBODIES RECOGNIZING PHOSPHORYLATED VIMENTINS

      Biochemical and biophysical research communications
    36. TSUJINO S; SHANSKE S; MARTINUZZI A; HEIMANPATTERSON T; DIMAURO S
      2 NOVEL MISSENSE MUTATIONS (E654K, L396P) IN CAUCASIAN PATIENTS WITH MYOPHOSPHORYLASE DEFICIENCY (MCARDLES-DISEASE)

      Human mutation
    37. TSUJINO S; SHANSKE S; CARROLL JE; SABINA RL; DIMAURO S
      DOUBLE TROUBLE - COMBINED MYOPHOSPHORYLASE AND AMP-DEAMINASE DEFICIENCY IN A CHILD HOMOZYGOUS FOR NONSENSE MUTATIONS AT BOTH LOCI

      Neuromuscular disorders
    38. ANGELOS S; VALBERG SJ; SMITH BP; MCQUARRIE PS; SHANSKE S; TSUJINO S; DIMAURO S; CARDINET GH
      MYOPHOSPHORYLASE DEFICIENCY ASSOCIATED WITH RHABDOMYOLYSIS AND EXERCISE INTOLERANCE IN 6 RELATED CHAROLAIS CATTLE

      Muscle & nerve
    39. DIMAURO S; TSUJINO S; SHANSKE S; ROWLAND LP
      BIOCHEMISTRY AND MOLECULAR-GENETICS OF HUMAN GLYCOGENOSES - AN OVERVIEW

      Muscle & nerve
    40. TSUJINO S; SHANSKE S; NONAKA I; DIMAURO S
      THE MOLECULAR-GENETIC BASIS OF MYOPHOSPHORYLASE DEFICIENCY (MCARDLES-DISEASE)

      Muscle & nerve
    41. TSUJINO S; SHANSKE S; DIMAURO S
      MOLECULAR-GENETIC HETEROGENEITY OF PHOSPHOGLYCERATE KINASE (PGK) DEFICIENCY

      Muscle & nerve
    42. TSUJINO S; SHANSKE S; SAKODA S; TOSCANO A; DIMAURO S
      MOLECULAR-GENETIC STUDIES IN MUSCLE PHOSPHOGLYCERATE MUTASE (PGAM-M) DEFICIENCY

      Muscle & nerve
    43. KAUFMANN P; TSUJINO S; SHANSKE S; TARONI F; DIDONATO SS; DIMAURO S
      GENETIC-CHARACTERIZATION OF AMERICAN PATIENTS WITH CPTII DEFICIENCY

      Neurology
    44. TSUJINO S; AKIYAMA H; SUGAWARA H; RUFENACHT M; KADOYA Y; NODA T; SAKAKI H
      EFFECT OF INTENSE INTERSUBBAND OPTICAL-EXCITATION ON THE ELECTRON-DISTRIBUTION IN GAAS ALAS QUANTUM-WELLS/

      JAPANESE JOURNAL OF APPLIED PHYSICS PART 1-REGULAR PAPERS SHORT NOTES & REVIEW PAPERS
    45. TSUJINO S; RUBIN LA; SHANSKE S; DIMAURO S
      AN A-TO-C SUBSTITUTION INVOLVING THE TRANSLATION INITIATION CODON IN A PATIENT WITH MYOPHOSPHORYLASE DEFICIENCY (MCARDLES-DISEASE)

      Human mutation
    46. TSUJINO S; SHANSKE S; GOTO Y; NONAKA I; DIMAURO S
      2 MUTATIONS, ONE NOVEL AND ONE FREQUENTLY OBSERVED, IN JAPANESE PATIENTS WITH MCARDLES-DISEASE

      Human molecular genetics
    47. HUIE ML; CHEN AS; TSUJINO S; SHANSKE S; DIMAURO S; ENGEL AG; HIRSCHHORN R
      ABERRANT SPLICING IN ADULT-ONSET GLYCOGEN-STORAGE-DISEASE TYPE-II (GSDII) - MOLECULAR-IDENTIFICATION OF AN IVS1 (-13T-]G) MUTATION IN A MAJORITY OF PATIENTS AND A NOVEL IVS10 (-]CT) MUTATION(1GT)

      Human molecular genetics
    48. TSUJINO S; SHANSKE S; BROWNELL AKW; HALLER RG; DIMAURO S
      MOLECULAR-GENETIC STUDIES OF MUSCLE LACTATE-DEHYDROGENASE DEFICIENCY IN WHITE PATIENTS

      Annals of neurology
    49. TSUJINO S; TONIN P; SHANSKE S; NOHRIA V; BOUSTANY RM; LEWIS D; CHEN YT; DIMAURO S
      A SPLICE JUNCTION MUTATION IN A NEW MYOPATHIC VARIANT OF PHOSPHOGLYCERATE KINASE-DEFICIENCY (PGK NORTH-CAROLINA)

      Annals of neurology
    50. TONIN P; SHANSKE S; TSUJINO S; DIMAURO S
      PHOSPHOGLYCERATE KINASE-DEFICIENCY - REPLY

      Neurology
    51. MARTINUZZI A; TSUJINO S; BARTOLONI L; CARROZZO R; SHANSKE S; DIMAURO S; ANGELINI C
      MOLECULAR CHARACTERIZATION OF MYOPHOSPHORYLASE DEFICIENCY IN ITALIAN PATIENTS

      Neurology
    52. TSUJINO S; SHANSKE S; BROWNELL AKW; HALLER RG; DIMAURO S
      2 NOVEL MUTATIONS IN CAUCASIAN PATIENTS WITH MUSCLE LACTATE-DEHYDROGENASE (LDH-A) DEFICIENCY

      Neurology
    53. KRISTJANSSON K; TSUJINO S; DIMAURO S
      MYOPHOSPHORYLASE DEFICIENCY - AN UNUSUALLY SEVERE FORM WITH MYOGLOBINURIA

      The Journal of pediatrics
    54. AKIYAMA H; SUGAWARA H; KADOYA Y; LORKE A; TSUJINO S; SAKAKI H
      CONTROL OF ELECTRON POPULATION BY INTERSUBBAND OPTICAL-EXCITATION IN POTENTIAL-INSERTED DOUBLE-QUANTUM-WELL STRUCTURES

      Applied physics letters
    55. TSUJINO S; SERVIDEI S; TONIN P; SHANSKE S; AZAN G; DIMAURO S
      IDENTIFICATION OF 3 NOVEL MUTATIONS IN NON-ASHKENAZI ITALIAN PATIENTSWITH MUSCLE PHOSPHOFRUCTOKINASE DEFICIENCY

      American journal of human genetics
    56. TSUJINO S; SHANSKE S; NONAKA I; ETO Y; MENDELL JR; FENICHEL GM; DIMAURO S
      3 NEW MUTATIONS IN PATIENTS WITH MYOPHOSPHORYLASE DEFICIENCY (MCARDLEDISEASE)

      American journal of human genetics
    57. HAYASHI H; SUGIYAMA S; SHIGEMOTO N; MIYAURA K; TSUJINO S; KAWASHIRO K; UEMURA S
      FORMATION OF AN INTERMETALLIC COMPOUND PD3TE WITH DEACTIVATION OF TE PD/C CATALYSTS FOR SELECTIVE OXIDATION OF SODIUM LACTATE TO PYRUVATE IN AQUEOUS-PHASE/

      Catalysis letters
    58. TSUJINO S; SHANSKE S; DIMAURO S
      MOLECULAR-GENETIC HETEROGENEITY OF MYOPHOSPHORYLASE DEFICIENCY (MCARDLES-DISEASE)

      The New England journal of medicine
    59. TOSCANO A; TSUJINO S; VITA G; SHANSKE S; DIMAURO S; MESSINA C
      MOLECULAR-BASIS OF MUSCLE PHOSPHOGLYCERATE MUTASE (PGAM-M) DEFICIENCYIN AN ITALIAN KINDRED

      Neurology
    60. TSUJINO S; SHANSKE S; DIMAURO S
      MOLECULAR-BASIS OF MYOPHOSPHORYLASE DEFICIENCY (MCARDLES DISEASE)

      Neurology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 25/10/20 alle ore 23:52:33