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La ricerca find articoli where soggetti phrase all words 'SARCOGLYCAN COMPLEX' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 37 riferimenti
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    1. Lynch, GS
      Novel therapies for muscular dystrophy and other muscle wasting conditions

      EXPERT OPINION ON THERAPEUTIC PATENTS
    2. Takeda, S; Miyagoe-Suzuki, Y
      Gene therapy for muscular dystrophies - Current status and future prospects

      BIODRUGS
    3. Enigk, RE; Maimone, MM
      Cellular and molecular properties of alpha-dystrobrevin in skeletal muscle

      FRONTIERS IN BIOSCIENCE
    4. Ozawa, E; Nishino, I; Nonaka, I
      Sarcolemmopathy: Muscular dystrophies with cell membrane defects

      BRAIN PATHOLOGY
    5. Yamada, H; Saito, F; Fukuta-Ohi, H; Zhong, D; Hase, A; Arai, K; Okuyama, A; Maekawa, R; Shimizu, T; Matsumura, K
      Processing of beta-dystroglycan by matrix metalloproteinase disrupts the link between the extracellular matrix and cell membrane via the dystroglycancomplex

      HUMAN MOLECULAR GENETICS
    6. Romero, NB; De Lonlay, P; Llense, S; Leturcq, F; Touati, G; Urtizberea, JA; Saudubray, JM; Munnich, A; Kaplan, JC; Recan, D
      Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomaticcarrier with 'de novo' duplication of dystrophin gene

      NEUROMUSCULAR DISORDERS
    7. Pogue, R; Anderson, LVB; Pyle, A; Sewry, C; Pollitt, C; Johnson, MA; Davison, K; Moss, JA; Mercuri, E; Muntoni, F; Bushby, KMD
      Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies

      NEUROMUSCULAR DISORDERS
    8. de Paula, F; Vainzof, M; Bernardino, ALF; McNally, E; Kunkel, LM; Zatz, M
      Mutations in the caveolin-3 gene: When are they pathogenic?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    9. Draviam, R; Billington, L; Senchak, A; Hoffman, EP; Watkins, SC
      Confocal analysis of the dystrophin protein complex in muscular dystrophy

      MUSCLE & NERVE
    10. Rando, TA
      The dystrophin-glycoprotein complex, cellular signaling, and the regulation of cell survival in the muscular dystrophies

      MUSCLE & NERVE
    11. Kawada, T; Sakamoto, A; Nakazawa, M; Urabe, M; Masuda, F; Hemmi, C; Wang, Y; Shin, WS; Nakatsuru, Y; Sato, H; Ozawa, K; Toyo-oka, T
      Morphological and physiological restorations of hereditary form of dilatedcardiomyopathy by somatic gene therapy

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    12. Sewry, CA
      Immunocytochemical analysis of human muscular dystrophy

      MICROSCOPY RESEARCH AND TECHNIQUE
    13. Hartigan-O'Connor, D; Chamberlain, JS
      Developments in gene therapy for muscular dystrophy

      MICROSCOPY RESEARCH AND TECHNIQUE
    14. Lebakken, CS; Venzke, DP; Hrstka, RF; Consolino, CM; Faulkner, JA; Williamson, RA; Campbell, KP
      Sarcospan-deficient mice maintain normal muscle function

      MOLECULAR AND CELLULAR BIOLOGY
    15. Xiao, X; Li, J; Tsao, YP; Dressman, D; Hoffman, EP; Watchko, JF
      Full functional rescue of a complete muscle (TA) in dystrophic hamsters byadeno-associated virus vector-directed gene therapy

      JOURNAL OF VIROLOGY
    16. Lidov, HGW
      The molecular neuropathology of the muscular dystrophies: A review and update

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    17. Holt, KH; Crosbie, RH; Venzke, DP; Campbell, KP
      Biosynthesis of dystroglycan: processing of a precursor propeptide

      FEBS LETTERS
    18. Biral, D; Jakubiec-Puka, A; Ciechomska, I; Sandri, M; Rossini, K; Carraro, U; Betto, R
      Loss of dystrophin and some dystrophin-associated proteins with concomitant signs of apoptosis in rat leg muscle overworked in extension

      ACTA NEUROPATHOLOGICA
    19. Laing, NG; Mastaglia, FL
      Inherited skeletal muscle disorders

      ANNALS OF HUMAN BIOLOGY
    20. Ozawa, E; Hagiwara, Y; Yoshida, M
      Creatine kinase, cell membrane and Duchenne muscular dystrophy

      MOLECULAR AND CELLULAR BIOCHEMISTRY
    21. Tsao, CY; Mendell, JR
      The childhood muscular dystrophies: Making order out of chaos

      SEMINARS IN NEUROLOGY
    22. Kakulas, BA; Laing, NG; Johnsen, RD
      The contribution of molecular genetics in the diagnosis and management of neuromuscular disorders

      SCANDINAVIAN JOURNAL OF REHABILITATION MEDICINE
    23. Durbeej, M; Campbell, KP
      Biochemical characterization of the epithelial dystroglycan complex

      JOURNAL OF BIOLOGICAL CHEMISTRY
    24. 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
    25. Bartoloni, L; Horrigan, SK; Viles, KD; Gilchrist, JM; Stajich, JM; Vance, JM; Yamaoka, LH; Pericak-Vance, MA; Westbrook, CA; Speer, MC
      Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31

      GENOMICS
    26. ANGELINI C; FANIN M; MENEGAZZO E; FREDA MP; DUGGAN DJ; HOFFMAN EP
      HOMOZYGOUS ALPHA-SARCOGLYCAN MUTATION IN 2 SIBLINGS - ONE ASYMPTOMATIC AND ONE STEROID-RESPONSIVE MILD LIMB-GIRDLE MUSCULAR-DYSTROPHY PATIENT

      Muscle & nerve
    27. OZAWA E; NOGUCHI S; MIZUNO Y; HAGIWARA Y; YOSHIDA M
      INVITED REVIEW - FROM DYSTROPHINOPATHY TO SARCOGLYCANOPATHY - EVOLUTION OF A CONCEPT OF MUSCULAR-DYSTROPHY

      Muscle & nerve
    28. Illarioshkin, SN; Ivanova-Smolenskaya, IA
      Molecular basis of progressing muscular dystrophias

      ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA
    29. BUSHBY K; ANDERSON LVB; POLLITT C; NAOM I; MUNTONI F; BINDOFF L
      ABNORMAL MEROSIN IN ADULTS - A NEW FORM OF LATE-ONSET MUSCULAR-DYSTROPHY NOT LINKED TO CHROMOSOME 6Q2

      Brain
    30. PRELLE A; COMI GP; TANCREDI L; RIGOLETTO C; CISCATO P; FORTUNATO F; NESTI S; SCIACCO M; ROBOTTI M; BAZZI P; FELISARI G; MOGGIO M; SCARLATO G
      SARCOGLYCAN DEFICIENCY IN A LARGE ITALIAN POPULATION OF MYOPATHIC PATIENTS

      Acta Neuropathologica
    31. NIGRO V; OKAZAKI Y; BELSITO A; PILUSO G; MATSUDA Y; POLITANO L; NIGRO G; VENTURA C; ABBONDANZA C; MOLINARI AM; ACAMPORA D; NISHIMURA M; HAYASHIZAKI Y; PUCA GA
      IDENTIFICATION OF THE SYRIAN-HAMSTER CARDIOMYOPATHY GENE

      Human molecular genetics
    32. COX GF; KUNKEL LM
      DYSTROPHIES AND HEART-DISEASE

      Current opinion in cardiology
    33. TOPALOGLU H; DINCER P; RICHARD I; AKCOREN Z; ALEHAN D; OZME S; CAGLAR M; KARADUMAN A; URTIZBEREA JA; BECKMANN JS
      CALPAIN-3 DEFICIENCY CAUSES A MILD MUSCULAR-DYSTROPHY IN CHILDHOOD

      Neuropediatrics
    34. VAINZOF M; COSTA CS; MARIE SK; MOREIRA ES; REED U; PASSOSBUENO MR; BEGGS AH; ZATZ M
      DEFICIENCY OF ALPHA-ACTININ-3 (ACTN3) OCCURS IN DIFFERENT FORMS OF MUSCULAR-DYSTROPHY

      Neuropediatrics
    35. FANIN M; DUGGAN DJ; MOSTACCIUOLO ML; MARTINELLO F; FREDA MP; SORARU G; TREVISAN CP; HOFFMAN EP
      GENETIC EPIDEMIOLOGY OF MUSCULAR-DYSTROPHIES RESULTING FROM SARCOGLYCAN GENE-MUTATIONS

      Journal of Medical Genetics
    36. LIU L; VACHON PH; KUANG W; XU H; WEWER UM; KYLSTEN P; ENGVALL E
      MOUSE ADHALIN - PRIMARY STRUCTURE AND EXPRESSION DURING LATE STAGES OF MUSCLE DIFFERENTIATION IN-VITRO

      Biochemical and biophysical research communications
    37. 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


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 29/10/20 alle ore 15:56:16