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    1. Henry, MD; Cohen, MB; Campbell, KP
      Reduced expression of dystroglycan in breast and prostate cancer

      HUMAN PATHOLOGY
    2. Ahern, CA; Arikkath, J; Vallejo, P; Gurnett, CA; Powers, PA; Campbell, KP; Coronado, R
      Intramembrane charge movements and excitation-contraction coupling expressed by two-domain fragments of the Ca2+ channel

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    3. Smelt, SC; Borrow, P; Kunz, S; Cao, W; Tishon, A; Lewicki, H; Campbell, KP; Oldstone, MBA
      Differences in affinity of binding of lymphocytic choriomeningitis virus strains to the cellular receptor alpha-dystroglycan correlate with viral tropism and disease kinetics

      JOURNAL OF VIROLOGY
    4. Cohn, RD; Durbeej, M; Moore, SA; Coral-Vazquez, R; Prouty, S; Campbell, KP
      Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex

      JOURNAL OF CLINICAL INVESTIGATION
    5. Henry, MD; Satz, JS; Brakebusch, C; Costell, M; Gustafsson, E; Fassler, R; Campbell, KP
      Distinct roles for dystroglycan, beta 1 integrin and perlecan in cell surface laminin organization

      JOURNAL OF CELL SCIENCE
    6. Kunz, S; Sevilla, N; McGavern, DB; Campbell, KP; Oldstone, MBA
      Molecular analysis of the interaction of LCMV with its cellular receptor alpha-dystroglycan

      JOURNAL OF CELL BIOLOGY
    7. Kang, MG; Chen, CC; Felix, R; Letts, VA; Frankel, WN; Mori, Y; Campbell, KP
      Biochemical and biophysical evidence for gamma(2) subunit association withneuronal voltage-activated Ca2+ channels

      JOURNAL OF BIOLOGICAL CHEMISTRY
    8. Durbeej, M; Cohn, RD; Hrstka, RF; Moore, SA; Allamand, V; Davidson, BL; Williamson, RA; Campbell, KP
      Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity oflimb-girdle muscular dystrophy type 2E

      MOLECULAR CELL
    9. Allamand, V; Donahue, KM; Straub, V; Davisson, RL; Davidson, BL; Campbell, KP
      Early adenovirus-mediated gene transfer effectively prevents muscular dystrophy in alpha-sarcoglycan-deficient mice

      GENE THERAPY
    10. Allamand, V; Campbell, KP
      Animal models for muscular dystrophy: valuable tools for the development of therapies

      HUMAN MOLECULAR GENETICS
    11. Crosbie, RH; Lim, LE; Moore, SA; Hirano, M; Hays, AP; Maybaum, SW; Collin, H; Dovico, SA; Stolle, CA; Fardeau, M; Tome, FMS; Campbell, KP
      Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions

      HUMAN MOLECULAR GENETICS
    12. Ertel, EA; Campbell, KP; Harpold, MM; Hofmann, F; Mori, Y; Perez-Reyes, E; Schwartz, A; Snutch, TP; Tanabe, T; Birnbaumer, L; Tsien, RW; Catterall, WA
      Nomenclature of voltage-gated calcium channels

      NEURON
    13. Grady, RM; Zhou, H; Cunningham, JM; Henry, MD; Campbell, KP; Sanes, JR
      Maturation and maintenance of the neuromuscular synapse: Genetic evidence for roles of the dystrophin-glycoprotein complex

      NEURON
    14. Straub, V; Donahue, KM; Allamand, V; Davisson, RL; Kim, YR; Campbell, KP
      Contrast agent-enhanced magnetic resonance imaging of skeletal muscle damage in animal models of muscular dystrophy

      MAGNETIC RESONANCE IN MEDICINE
    15. Piccolo, F; Moore, SA; Ford, GC; Campbell, KP
      Intracellular accumulation and reduced sarcolemmal expression of dysferlinin limb-girdle muscular dystrophies

      ANNALS OF NEUROLOGY
    16. Flanigan, KM; Kerr, M; Bromberg, MB; Leonard, C; Tsuruda, J; Zhang, P; Gonzalez-Gomez, I; Cohn, R; Campbell, KP; Leppert, M
      Congenital muscular dystrophy with rigid spine syndrome: A clinical, pathological, radiological, and genetic study

      ANNALS OF NEUROLOGY
    17. 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
    18. Cohn, RD; Campbell, KP
      Molecular basis of muscular dystrophies

      MUSCLE & NERVE
    19. Leschziner, A; Moukhles, H; Lindenbaum, M; Gee, SH; Butterworth, J; Campbell, KP; Carbonetto, S
      Neural regulation of alpha-dystroglycan biosynthesis and glycosylation in skeletal muscle

      JOURNAL OF NEUROCHEMISTRY
    20. Sevilla, N; Kunz, S; Holz, A; Lewicki, H; Homann, D; Yamada, H; Campbell, KP; de la Torre, JC; Oldstone, MBA
      Immunosuppression and resultant viral persistence by specific viral targeting of dendritic cells

      JOURNAL OF EXPERIMENTAL MEDICINE
    21. Crawford, GE; Faulkner, JA; Crosbie, RH; Campbell, KP; Froehner, SC; Chamberlain, JS
      Assembly of the dystrophin-associated protein complex does not require thedystrophin COOH-terminal domain

      JOURNAL OF CELL BIOLOGY
    22. Barresi, R; Moore, SA; Stolle, CA; Mendell, JR; Campbell, KP; Campbell, P
      Expression of gamma-sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex

      JOURNAL OF BIOLOGICAL CHEMISTRY
    23. Holt, KH; Crosbie, RH; Venzke, DP; Campbell, KP
      Biosynthesis of dystroglycan: processing of a precursor propeptide

      FEBS LETTERS
    24. Heathcote, RD; Ekman, JM; Campbell, KP; Godfrey, EW
      Dystroglycan overexpression in vivo alters acetylcholine receptor aggregation at the neuromuscular junction

      DEVELOPMENTAL BIOLOGY
    25. Badorff, C; Lee, GH; Lamphear, BJ; Martone, ME; Campbell, KP; Rhoads, RE; Knowlton, KU
      Enteroviral protease 2A cleaves dystrophin: Evidence of cytoskeletal disruption in an acquired cardiomyopathy

      NATURE MEDICINE
    26. Burgess, DL; Biddlecome, GH; McDonough, SI; Diaz, ME; Zilinski, CA; Bean, BP; Campbell, KP; Noebels, JL
      beta subunit reshuffling modifies N- and P/Q-type Ca2+ channel subunit compositions in lethargic mouse brain

      MOLECULAR AND CELLULAR NEUROSCIENCE
    27. Henry, MD; Campbell, KP
      Dystroglycan inside and out

      CURRENT OPINION IN CELL BIOLOGY
    28. Coral-Vazquez, R; Cohn, RD; Moore, SA; Hill, JA; Weiss, RM; Davisson, RL; Straub, V; Barresi, R; Bansal, D; Hrstka, RF; Williamson, R; Campbell, KP
      Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle:A novel mechanism for cardiomyopathy and muscular dystrophy

      CELL
    29. Johnston, JC; Gasmi, M; Lim, LE; Elder, JH; Yee, JK; Jolly, DJ; Campbell, KP; Davidson, BL; Sauter, SL
      Minimum requirements for efficient transduction of dividing and nondividing cells by feline immunodeficiency virus vectors

      JOURNAL OF VIROLOGY
    30. Brown, SC; Fassati, A; Popplewell, L; Page, AM; Henry, MD; Campbell, KP; Dickson, G
      Dystrophic phenotype induced in vitro by antibody blockade of muscle alpha-dystroglycan-laminin interaction

      JOURNAL OF CELL SCIENCE
    31. Brown, SC; Fassati, A; Popplewell, L; Page, AM; Henry, MD; Campbell, KP; Dickson, G
      Dystrophic phenotype induced in vitro by antibody blockade of muscle alpha-dystroglycan-laminin interaction (vol 112, pg 209, 1999)

      JOURNAL OF CELL SCIENCE
    32. Crosbie, RH; Lebakken, CS; Holt, KH; Venzke, DP; Straub, V; Lee, JC; Grady, RM; Chamberlain, JS; Sanes, JR; Campbell, KP
      Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex

      JOURNAL OF CELL BIOLOGY
    33. Straub, V; Ettinger, AJ; Durbeej, M; Venzke, DP; Cutshall, S; Sanes, JR; Campbell, KP
      epsilon-sarcoglycan replaces alpha-sarcoglycan in smooth muscle to form a unique dystrophin-glycoprotein complex

      JOURNAL OF BIOLOGICAL CHEMISTRY
    34. Durbeej, M; Campbell, KP
      Biochemical characterization of the epithelial dystroglycan complex

      JOURNAL OF BIOLOGICAL CHEMISTRY
    35. LIM LE; CAMPBELL KP
      THE SARCOGLYCAN COMPLEX IN LIMB-GIRDLE MUSCULAR-DYSTROPHY

      Current opinion in neurology
    36. HOLT KH; LIM LE; STRAUB V; VENZKE DP; DUCLOS F; ANDERSON RD; DAVIDSON BL; CAMPBELL KP
      FUNCTIONAL RESCUE OF THE SARCOGLYCAN COMPLEX IN THE BIO-14.6 HAMSTER USING DELTA-SARCOGLYCAN GENE-TRANSFER

      MOLECULAR CELL
    37. LETTS VA; FELIX R; BIDDLECOME GH; ARIKKATH J; MAHAFFEY CL; VALENZUELA A; BARTLETT FS; MORI Y; CAMPBELL KP; FRANKEL WN
      THE MOUSE STARGAZER GENE ENCODES A NEURONAL CA2-CHANNEL GAMMA-SUBUNIT()

      Nature genetics
    38. HENRY MD; CAMPBELL KP
      A ROLE FOR DYSTROGLYCAN IN THE FORMATION OF BASEMENT-MEMBRANES

      Molecular biology of the cell
    39. CROSBIE RH; STRAUB V; YUN HY; LEE JC; RAFAEL JA; CHAMBERLAIN JS; DAWSON VL; DAWSON TM; CAMPBELL KP
      MDX MUSCLE PATHOLOGY IS INDEPENDENT OF NNOS PERTURBATION

      Human molecular genetics
    40. 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
    41. DURBEEJ M; HENRY MD; CAMPBELL KP
      DYSTROGLYCAN IN DEVELOPMENT AND DISEASE

      Current opinion in cell biology
    42. SCOTT VES; FELIX R; ARIKKATH J; CAMPBELL KP
      EVIDENCE FOR A 95 KDA SHORT-FORM OF THE ALPHA(1A) SUBUNIT ASSOCIATED WITH THE OMEGA-CONOTOXIN MVIIC RECEPTOR OF THE P Q-TYPE CA2+ CHANNELS/

      The Journal of neuroscience
    43. Salih, MAM; Al Rayess, M; Cutshall, S; Urtizberea, JA; Al-Turaiki, MHS; Ozo, CO; Straub, V; Akbar, M; Abid, M; Andeejani, A; Campbell, KP
      A novel form of familial congenital muscular dystrophy in two adolescents

      NEUROPEDIATRICS
    44. Henry, MD; Campbell, KP
      A role for dystroglycan in basement membrane assembly

      CELL
    45. Rambukkana, A; Yamada, H; Zanazzi, G; Mathus, T; Salzer, JL; Yurchenco, PD; Campbell, KP; Fischetti, VA
      Role of alpha-dystroglycan as a Schwann cell receptor for Mycobacterium leprae

      SCIENCE
    46. Cao, W; Henry, MD; Borrow, P; Yamada, H; Elder, JH; Ravkov, EV; Nichol, ST; Compans, RW; Campbell, KP; Oldstone, MBA
      Identification of alpha-dystroglycan as a receptor for lymphocytic choriomeningitis virus and lassa fever virus

      SCIENCE
    47. Dinsmore, AJ; Rees-Blanchard, W; Bentley, P; Lewis, T; Kahl, SD; McPherson, PS; Mullinnix, MJ; Campbell, KP; Windass, JD; Earley, FGP
      Characterisation of antibody models of the ryanodine receptor for use in high-throughput screening

      PESTICIDE SCIENCE
    48. MUSSELL HG; ALLAMAND V; CAMPBELL KP; OH SJ
      LATE-ONSET MEROSIN DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY

      Neurology
    49. MATHEWS KD; STRAUB VW; CAMPBELL KP
      EVANS BLUE UPTAKE DEMONSTRATES SARCOLEMMAL DISRUPTION IN THE MYODYSTROPHY MOUSE

      Neurology
    50. DING JM; BUCHANAN GF; TISCHKAU SA; CHEN D; KURIASHKINA L; FAIMAN LE; ALSTER JM; MCPHERSON PS; CAMPBELL KP; GILLETTE MU
      A NEURONAL RYANODINE RECEPTOR MEDIATES LIGHT-INDUCED PHASE DELAYS OF THE CIRCADIAN CLOCK

      Nature
    51. DURBEEJ M; HENRY MD; FERLETTA M; CAMPBELL KP; EKBLOM P
      DISTRIBUTION OF DYSTROGLYCAN IN NORMAL ADULT-MOUSE TISSUES

      The Journal of histochemistry and cytochemistry
    52. DUCLOS F; STRAUB V; MOORE SA; VENZKE DP; HRSTKA RF; CROSBIE RH; DURBEEJ M; LEBAKKEN CS; ETTINGER AJ; VANDERMEULEN J; HOLT KH; LIM LE; SANES JR; DAVIDSON BL; FAULKNER JA; WILLIAMSON R; CAMPBELL KP
      PROGRESSIVE MUSCULAR-DYSTROPHY IN ALPHA-SARCOGLYCAN-DEFICIENT MICE

      The Journal of cell biology
    53. WALKER D; BICHET D; CAMPBELL KP; DEWAARD M
      A BETA(4) ISOFORM-SPECIFIC INTERACTION SITE IN THE CARBOXYL-TERMINAL REGION OF THE VOLTAGE-DEPENDENT CA2+ CHANNEL ALPHA(1A) SUBUNIT

      The Journal of biological chemistry
    54. Holt, KH; Campbell, KP
      Assembly of the sarcoglycan complex - Insights for muscular dystrophy

      JOURNAL OF BIOLOGICAL CHEMISTRY
    55. CROSBIE RH; YAMADA H; VENZKE DP; LISANTI MP; CAMPBELL KP
      CAVEOLIN-3 IS NOT AN INTEGRAL COMPONENT OF THE DYSTROPHIN-GLYCOPROTEIN COMPLEX

      FEBS letters
    56. STRAUB V; DUCLOS F; VENZKE DP; LEE JC; CUTSHALL S; LEVEILLE CJ; CAMPBELL KP
      MOLECULAR PATHOGENESIS OF MUSCLE DEGENERATION IN THE DELTA-SARCOGLYCAN-DEFICIENT HAMSTER

      The American journal of pathology
    57. STRAUB V; CAMPBELL KP
      MUSCULAR-DYSTROPHIES AND THE DYSTROPHIN-GLYCOPROTEIN COMPLEX

      Current opinion in neurology
    58. 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
    59. 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
    60. CAMPBELL KP
      MOLECULAR PATHOGENESIS OF MUSCULAR-DYSTROPHY

      The FASEB journal
    61. CROSBIE RH; STRAUB V; VENZKE DP; YUN HY; CHAMBERLAIN JS; DAWSON VL; DAWSON TM; CAMPBELL KP
      DYSTROPHIN AND NNOS DOUBLE KNOCKOUT MICE MAINTAIN DYSTROPHIC PHENOTYPE

      The FASEB journal
    62. CAMPBELL KP
      HOT PAPERS - GENETICS - BETA-SARCOGLYCAN - CHARACTERIZATION AND ROLE IN LIMB-GIRDLE MUSCULAR-DYSTROPHY LINKED TO 4Q12 BY LIM,L.E., DUCLOS,F., BROUX,O., BOURG,N., SUNADA,Y., ALLAMAND,V., MEYER,J., RICHARD,I., MOOMAW,C., SLAUGHTER,C., TOME,F.M.S., FARDEAU,M., JACKSON,C.E., BECKMANN,J.S., CAMPBELL,K.P. - COMMENTS

      The Scientist
    63. DINCER P; LETURCQ F; RICHARD I; PICCOLO F; YALNIZOGLU D; DETOMA C; AKCOREN Z; BROUX O; DEBURGRAVE N; BRENGUIER L; ROUDAUT C; URTIZBEREA JA; JUNG D; TAN E; JEANPIERRE M; CAMPBELL KP; KAPLAN JC; BECKMANN JS; TOPALOGLU H
      A BIOCHEMICAL, GENETIC, AND CLINICAL SURVEY OF AUTOSOMAL RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHIES IN TURKEY

      Annals of neurology
    64. FELIX R; GURNETT CA; DEWAARD M; CAMPBELL KP
      DISSECTION OF FUNCTIONAL DOMAINS OF THE VOLTAGE-DEPENDENT CA2+ CHANNEL ALPHA(2)DELTA SUBUNIT

      The Journal of neuroscience
    65. EYMARD B; ROMERO NB; LETURCQ F; PICCOLO F; CARRIE A; JEANPIERRE M; COLLIN H; DEBURGRAVE N; AZIBI K; CHAOUCH M; MERLINI L; THEMARNOEL C; PENISSON I; MAYER M; TANGUY O; CAMPBELL KP; KAPLAN JC; TOME FMS; FARDEAU M
      PRIMARY ADHALINOPATHY (ALPHA-SARCOGLYCANOPATHY) - CLINICAL, PATHOLOGICAL, AND GENETIC CORRELATION IN 20 PATIENTS WITH AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY

      Neurology
    66. MATHEWS KD; MOORE SA; STRAUB VW; MILLS KA; CAMPBELL KP
      IMMUNOHISTOCHEMICAL ANALYSIS OF MYODYSTROPHY MOUSE MUSCLE

      Neurology
    67. DEWAARD M; LIU HY; WALKER D; SCOTT VES; GURNETT CA; CAMPBELL KP
      DIRECT BINDING OF G-PROTEIN BETA-GAMMA COMPLEX TO VOLTAGE-DEPENDENT CALCIUM CHANNELS

      Nature
    68. BIES RD; MAEDA M; ROBERDS SL; HOLDER E; BOHLMEYER T; YOUNG JB; CAMPBELL KP
      A 5'-DYSTROPHIN DUPLICATION MUTATION CAUSES MEMBRANE DEFICIENCY OF ALPHA-DYSTROGLYCAN IN A FAMILY WITH X-LINKED CARDIOMYOPATHY

      Journal of Molecular and Cellular Cardiology
    69. 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
    70. FAHLKE C; KNITTLE T; GURNETT CA; CAMPBELL KP; GEORGE AL
      SUBUNIT STOICHIOMETRY OF HUMAN MUSCLE CHLORIDE CHANNELS

      The Journal of general physiology
    71. STRAUB V; RAFAEL JA; CHAMBERLAIN JS; CAMPBELL KP
      ANIMAL-MODELS FOR MUSCULAR-DYSTROPHY SHOW DIFFERENT PATTERNS OF SARCOLEMMAL DISRUPTION

      The Journal of cell biology
    72. CROSBIE RH; HEIGHWAY J; VENZKE DP; LEE JC; CAMPBELL KP
      SARCOSPAN, THE 25-KDA TRANSMEMBRANE COMPONENT OF THE DYSTROPHIN-GLYCOPROTEIN COMPLEX

      The Journal of biological chemistry
    73. GURNETT CA; FELIX R; CAMPBELL KP
      EXTRACELLULAR INTERACTION OF THE VOLTAGE-DEPENDENT CA2+ CHANNEL ALPHA(2)DELTA AND ALPHA(1) SUBUNITS

      The Journal of biological chemistry
    74. MATSUMURA K; CHIBA A; YAMADA H; FUKUTAOHI H; FUJITA S; ENDO T; KOBATA A; ANDERSON LVB; KANAZAWA I; CAMPBELL KP; SHIMIZU T
      A ROLE OF DYSTROGLYCAN IN SCHWANNOMA CELL-ADHESION TO LAMININ

      The Journal of biological chemistry
    75. DURBEEJ M; JUNG D; HJALT T; CAMPBELL KP; EKBLOM P
      TRANSIENT EXPRESSION OF DP140, A PRODUCT OF THE DUCHENNE MUSCULAR-DYSTROPHY LOCUS, DURING KIDNEY TUBULOGENESIS

      Developmental biology
    76. LIU H; DEWAARD M; FELIX R; CAMPBELL KP
      DIRECT INTERACTION BETWEEN VOLTAGE-DEPENDENT CA2-PROTEIN BETA-GAMMA COMPLEX( CHANNELS AND G)

      Biophysical journal
    77. GURNETT CA; FELIX R; CAMPBELL KP
      CHARACTERIZATION OF INTERACTION DOMAINS BETWEEN THE VOLTAGE-DEPENDENTCALCIUM-CHANNEL ALPHA(2)DELTA AND ALPHA(1) SUBUNITS

      Biophysical journal
    78. CROSBIE RH; HEIGHWAY J; VENZKE DP; CAMPBELL KP
      SARCOSPAN - A NOVEL 25KDA COMPONENT OF THE DYSTROPHIN-GLYCOPROTEIN COMPLEX MAPS TO HUMAN-CHROMOSOME 12P11.2

      American journal of human genetics
    79. HOLT KH; LIM LE; STRAUB VW; DUCLOS F; VENZKE DP; LEE JC; ANDERSON RD; DAVIDSON BL; CAMPBELL KP
      FUNCTIONAL RESTORATION OF THE SARCOGLYCAN AND DYSTROGLYCAN COMPLEXES IN THE CARDIOMYOPATHIC HAMSTER

      American journal of human genetics
    80. STRAUB V; CROSBIE R; HENRY MD; CHAMBERLAIN JS; CAMPBELL KP
      ANIMAL-MODELS FOR MUSCULAR-DYSTROPHY SHOW DIFFERENT PATTERNS OF SARCOLEMMAL DISRUPTION

      Molecular biology of the cell
    81. 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
    82. PICCOLO F; JEANPIERRE M; LETURCQ F; DODE C; AZIBI K; TOUTAIN A; MERLINI L; JARRE L; NAVARRO C; KRISHNAMOORTHY R; TOME FMS; URTIZBEREA JA; BECKMANN JS; CAMPBELL KP; KAPLAN JC
      A FOUNDER MUTATION IN THE GAMMA-SARCOGLYCAN GENE OF GYPSIES POSSIBLY PREDATING THEIR MIGRATION OUT OF INDIA

      Human molecular genetics
    83. 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
    84. 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
    85. HENRY MD; CAMPBELL KP
      DYSTROGLYCAN - AN EXTRACELLULAR-MATRIX RECEPTOR-LINKED TO THE CYTOSKELETON

      Current opinion in cell biology
    86. TIAN M; JACOBSON C; GEE SH; CAMPBELL KP; CARBONETTO S; JUCKER M
      DYSTROGLYCAN IN THE CEREBELLUM IS A LAMININ ALPHA-2-CHAIN BINDING-PROTEIN AT THE GLIAL-VASCULAR INTERFACE AND IS EXPRESSED IN PURKINJE-CELLS

      European journal of neuroscience
    87. GURNETT CA; DEWAARD M; CAMPBELL KP
      DUAL FUNCTION OF THE VOLTAGE-DEPENDENT CA2+ CHANNEL ALPHA(2)DELTA SUBUNIT IN CURRENT STIMULATION AND SUBUNIT INTERACTION

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

      Annals of neurology
    89. 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
    90. CULLEN MJ; WALSH J; ROBERDS SL; CAMPBELL KP
      ULTRASTRUCTURAL-LOCALIZATION OF ADHALIN, ALPHA-DYSTROGLYCAN AND MEROSIN IN NORMAL AND DYSTROPHIC MUSCLE

      Neuropathology and applied neurobiology
    91. LIU HY; FELIX R; GURNETT CA; DEWAARD M; WITCHER DR; CAMPBELL KP
      EXPRESSION AND SUBUNIT INTERACTION OF VOLTAGE-DEPENDENT CA2+ CHANNELSIN PC12 CELLS

      The Journal of neuroscience
    92. 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
    93. OEXLE K; HERRMANN R; DODE C; LETURCQ F; HUBNER C; KAPLAN JC; MIZUNO Y; OZAWA E; CAMPBELL KP; VOIT T
      NEUROSENSORY HEARING-LOSS IN SECONDARY ADHALINOPATHY

      Neuropediatrics
    94. YAMADA H; CHIBA A; ENDO T; KOBATA A; KANAZAWA I; CAMPBELL KP; SHIMIZU T; MATSUMURA K
      CHARACTERIZATION OF DYSTROGLYCAN-LAMININ INTERACTION IN PERIPHERAL-NERVE

      Journal of muscle research and cell motility
    95. CULLEN MJ; WALSH J; ROBERDS SL; CAMPBELL KP
      IMMUNOGOLD LOCALIZATION OF ADHALIN AND ALPHA-DYSTROGLYCAN IN NORMAL AND DYSTROPHIC SKELETAL-MUSCLE

      Journal of muscle research and cell motility
    96. 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
    97. 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
    98. EYMARD B; ROMERO NB; LETURCQ F; CARRIE A; PICCOLO F; COLLIN H; KAPLAN JC; TOME FMS; FARDEAU M; AZIBI K; CHAOUCH M; MERLINI L; PENISSON I; SEFIANI A; CAMPBELL KP
      ADHALIN-DEFICIENT MUSCULAR-DYSTROPHIES - CLINICAL, PATHOLOGICAL, AND GENETIC CORRELATIONS

      Neurology
    99. CAMPBELL KP; CROSBIE RH
      MUSCULAR-DYSTROPHY - UTROPHIN TO THE RESCUE

      Nature
    100. YAMADA H; CHIBA A; ENDO T; KOBATA A; ANDERSON VB; HORI H; FUKUTAOHI H; KANAZAWA I; CAMPBELL KP; SHIMIZU T; MATSUMURA K
      CHARACTERIZATION OF DYSTROGLYCAN - LAMININ INTERACTION IN PERIPHERAL-NERVE

      Journal of neurochemistry


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 18/01/21 alle ore 18:50:52