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La ricerca find articoli where soggetti phrase all words 'ALPHA-TROPOMYOSIN' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 246 riferimenti
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    1. Hernandez, OM; Housmans, PR; Potter, JD
      Plasticity in skeletal cardiac, and smooth muscle - Invited review: Pathophysiology of cardiac muscle contraction and relaxation as a result of alterations in thin filament regulation

      JOURNAL OF APPLIED PHYSIOLOGY
    2. Watkins, H
      Hypertrophic cardiomyopathy: from molecular and genetic mechanisms to clinical management

      EUROPEAN HEART JOURNAL SUPPLEMENTS
    3. Naimi, B; Harrison, A; Cummins, M; Nongthomba, U; Clark, S; Canal, I; Ferrus, A; Sparrow, JC
      A tropomyosin-2 mutation suppresses a troponin I myopathy in Drosophila

      MOLECULAR BIOLOGY OF THE CELL
    4. Hasegawa, Y
      Complete nucleotide sequences of cDNA encoding for tropomyosin isoforms from the catch muscle of scallop Patinopecten yessoensis

      FISHERIES SCIENCE
    5. Ochiai, Y; Ahmed, K; Ahsan, MN; Funabara, D; Nakaya, M; Watabe, S
      cDNA cloning and deduced amino acid sequence of tropomyosin from fast skeletal muscle of white croaker Pennahia argentata

      FISHERIES SCIENCE
    6. Erdmann, J; Raible, J; Maki-Abadi, J; Hummel, M; Hammann, J; Wollnik, B; Frantz, E; Fleck, E; Hetzer, R; Regitz-Zagrosek, V
      Spectrum of clinical phenotypes and gene variants in cardiac myosin-binding protein C mutation carriers with hypertrophic cardiomyopathy

      JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
    7. Marian, AJ
      On genetic and phenotypic variability of hypertrophic cardiomyopathy: Nature versus nurture

      JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
    8. Dalloz, F; Osinska, H; Robbins, J
      Genetically modified animal models in cardiovascular research

      REVISTA ESPANOLA DE CARDIOLOGIA
    9. Fujino, N; Shimizu, M; Ino, H; Okeie, K; Yamaguchi, M; Yasuda, T; Kokado, H; Mabuchi, H
      Cardiac troponin T Arg92Trp mutation and progression from hypertrophic to dilated cardiomyopathy

      CLINICAL CARDIOLOGY
    10. Franz, WM; Muller, OJ; Katus, HA
      Cardiomyopathies: from genetics to the prospect of treatment

      LANCET
    11. Aharinejad, S; Schafer, R; Hofbauer, R; Abraham, D; Blumer, R; Miksovsky, A; Traxler, H; Pullirsch, D; Alexandrowicz, R; Taghavi, S; Kocher, A; Laufer, G
      Impact of cardiac transplantation on molecular pathology of ET-1, VEGF-C, and mitochondrial metabolism and morphology in dilated versus ischemic cardiomyopathic patients

      TRANSPLANTATION
    12. Stewart, M
      Structural basis for bending tropomyosin around actin in muscle thin filaments

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    13. Brown, JH; Kim, KH; Jun, G; Greenfield, NJ; Dominguez, R; Volkmann, N; Hitchcock-DeGregori, SE; Cohen, C
      Deciphering the design of the tropomyosin molecule

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    14. Anyanful, A; Sakube, Y; Takuwa, K; Kagawa, H
      The third and fourth tropomyosin isoforms of Caenorhabditis elegans are expressed in the pharynx and intestines and are essential for development andmorphology

      JOURNAL OF MOLECULAR BIOLOGY
    15. Marian, AJ; Roberts, R
      The molecular genetic basis for hypertrophic cardiomyopathy

      JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
    16. Dalloz, F; Osinska, H; Robbins, J
      Manipulating the contractile apparatus: Genetically defined animal models of cardiovascular disease

      JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
    17. Mogensen, J; Andersen, PS; Steffensen, U; Christiansen, M; Egeblad, H; Gregersen, N; Borglum, AD
      Development and application of linkage analysis in genetic diagnosis of familial hypertrophic cardiomyopathy

      JOURNAL OF MEDICAL GENETICS
    18. Miller, T; Szczesna, D; Housmans, PR; Zhao, JJ; de Freitas, F; Gomes, AV; Culbreath, L; McCue, J; Wang, Y; Xu, YY; Glenn, W; Kerrick, L; Potter, JD
      Abnormal contractile function in transgenic mice expressing a familial hypeptrophic cardiomyopathy-linked troponin T (I79N) mutation

      JOURNAL OF BIOLOGICAL CHEMISTRY
    19. Strand, J; Nili, M; Homsher, E; Tobacman, LS
      Modulation of myosin function by isoform-specific properties of Saccharomyces cerevisiae and muscle tropomyosins

      JOURNAL OF BIOLOGICAL CHEMISTRY
    20. Szczesna, D; Ghosh, D; Gomes, AV; Guzman, G; Arana, C; Zhi, G; Stull, JT; Potter, JD
      Familial hypertrophic cardiomyopathy mutations in the regulatory light chains of myosin affect their structure, Ca2+ binding, and phosphorylation

      JOURNAL OF BIOLOGICAL CHEMISTRY
    21. Takahashi-Yanaga, F; Ohtsuki, I; Morimoto, S
      Effects of troponin T mutations in familial hypertrophic cardiomyopathy onregulatory functions of other troponin subunits

      JOURNAL OF BIOCHEMISTRY
    22. Huang, XH; Song, L; Ma, AQ; Gao, JH; Zheng, WY; Zhou, XL; Zhang, Q; Liu, YL; Hu, RT
      A malignant phenotype of hypertrophic cardiomyopathy caused by Arg719Gln cardiac beta-myosin heavy-chain mutation in a Chinese family

      CLINICA CHIMICA ACTA
    23. Li, DX; Czernuszewicz, GZ; Gonzalez, O; Tapscott, T; Karibe, A; Durand, JB; Brugada, R; Hill, R; Gregoritch, JM; Anderson, JL; Quinones, M; Bachinski, LL; Roberts, R
      Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy

      CIRCULATION
    24. Varnava, AM; Elliott, PM; Baboonian, C; Davison, F; Davies, MJ; McKenna, WJ
      Hypertrophic cardiomyopathy - Histopathological features of sudden death in cardiac troponin T disease

      CIRCULATION
    25. Palm, T; Graboski, S; Hitchcock-DeGregori, SE; Greenfield, NJ
      Disease-causing mutations in cardiac troponin T: Identification of a critical tropomyosin-binding region

      BIOPHYSICAL JOURNAL
    26. Hitchcock-DeGregori, SE; Song, Y; Moraczewska, J
      Importance of internal regions and the overall length of tropomyosin for actin binding and regulatory function

      BIOCHEMISTRY
    27. Suarez, MC; Lehrer, SS; Silva, JL
      Local heterogeneity in the pressure denaturation of the coiled-coil tropomyosin because of subdomain folding units

      BIOCHEMISTRY
    28. Maytum, R; Konrad, M; Lehrer, SS; Geeves, MA
      Regulatory properties of tropomyosin effects of length, isoform, and N-terminal sequence

      BIOCHEMISTRY
    29. Hilario, E; Lataro, RC; Alegria, MC; Lavarda, SCS; Ferro, JA; Bertolini, MC
      High-level production of functional muscle alpha-tropomyosin in Pichia pastoris

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    30. Lee, WH; Hwang, TH; Kimura, A; Park, SW; Satoh, M; Nishi, H; Harada, H; Toyama, J; Park, JE
      Different expressivity of a ventricular essential myosin light chain gene Ala57Gly mutation in familial hypertrophic cardiomyopathy

      AMERICAN HEART JOURNAL
    31. Sorajja, P; Elliott, PM; McKenna, WJ
      The molecular genetics of hypertrophic cardiomyopathy: prognostic implications

      EUROPACE
    32. Shah, G; Roberts, R
      Molecular genetics of cardiomyopathies

      JOURNAL OF NUCLEAR CARDIOLOGY
    33. Michele, DE; Metzger, JM
      Contractile dysfunction in hypertrophic cardiomyopathy: Elucidating primary defects of mutant contractile proteins by gene transfer

      TRENDS IN CARDIOVASCULAR MEDICINE
    34. Michele, DE; Metzger, JM
      Physiological consequences of tropomyosin mutations associated with cardiac and skeletal myopathies

      JOURNAL OF MOLECULAR MEDICINE-JMM
    35. Whitby, FG; Phillips, GN
      Crystal structure of tropomyosin at 7 Angstroms resolution

      PROTEINS-STRUCTURE FUNCTION AND GENETICS
    36. Li, ST; Tack, CJ; Fananapazir, L; Goldstein, DS
      Myocardial perfusion and sympathetic innervation in patients with hypertrophic cardiomyopathy

      JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
    37. Eidem, BW; Jones, C; Cetta, F
      Unusual association of hypertrophic cardiomyopathy with complete atrioventricular canal defect and Down syndrome

      TEXAS HEART INSTITUTE JOURNAL
    38. Wendel, B; Reinhard, R; Wachtendorf, U; Zacharzowsky, UB; Osterziel, KJ; Schulte, HD; Haase, H; Hoehe, MR; Morano, I
      The human beta-myosin heavy chain gene: Sequence diversity and functional characteristics of the protein

      JOURNAL OF CELLULAR BIOCHEMISTRY
    39. Evans, CC; Pena, JR; Phillips, RM; Muthuchamy, M; Wieczorek, DF; Solaro, RJ; Wolska, BM
      Altered hemodynamics in transgenic mice harboring mutant tropomyosin linked to hypertrophic cardiomyopathy

      AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
    40. Zajdel, RW; McLean, MD; Isitmangil, G; Lemanski, LF; Wieczorek, DF; Dube, DK
      Alteration of cardiac myofibrillogenesis by liposome-mediated delivery of exogenous proteins and nucleic acids into whole embryonic hearts

      ANATOMY AND EMBRYOLOGY
    41. King-Briggs, KE; Shanahan, CM
      TGF-beta superfamily members do not promote smooth muscle-specific alternative splicing, a late marker of vascular smooth muscle cell differentiation

      DIFFERENTIATION
    42. McKenna, WJ; Iglesias, LM
      Identification and treatment of patients with hypertrophhic cardiomyopathyat risk of sudden death

      REVISTA ESPANOLA DE CARDIOLOGIA
    43. Thierfelder, L
      Genetic aspects of arrhythmias

      ZEITSCHRIFT FUR KARDIOLOGIE
    44. Muller-Hocker, J; Schafer, S; Mendel, B; Lochmuller, H; Pongratz, D
      Nemaline cardiomyopathy in a young adult: An ultraimmunohistochemical study and review of the literature

      ULTRASTRUCTURAL PATHOLOGY
    45. Watkins, H
      Sudden death in hypertrophic cardiomyopathy.

      NEW ENGLAND JOURNAL OF MEDICINE
    46. Lehman, W; Hatch, V; Korman, V; Rosol, M; Thomas, L; Maytum, R; Geeves, MA; Van Eyk, JE; Tobacman, LS; Craig, R
      Tropomyosin and actin isoforms modulate the localization of tropomyosin strands on actin filaments

      JOURNAL OF MOLECULAR BIOLOGY
    47. Moolman-Smook, J; De Lange, W; Corfield, V; Brink, P
      Expression of HCM causing mutations: lessons learnt from genotype-phenotype studies of the South African founder MYH7 A797T mutation

      JOURNAL OF MEDICAL GENETICS
    48. Seidman, C
      Hypertrophic cardiomyopathy: from man to mouse

      JOURNAL OF CLINICAL INVESTIGATION
    49. Wen, KK; Kuang, B; Rubenstein, PA
      Tropomyosin-dependent filament formation by a polymerization-defective mutant yeast actin (V266G,L267G)

      JOURNAL OF BIOLOGICAL CHEMISTRY
    50. Oliveira, DM; Nakaie, CR; Sousa, AD; Farah, CS; Reinach, FC
      Mapping the domain of troponin T responsible for the activation of actomyosin ATPase activity - Identification of residues involved in binding to actin

      JOURNAL OF BIOLOGICAL CHEMISTRY
    51. Ogut, O; Jin, JP
      Cooperative interaction between developmentally regulated troponin T and tropomyosin isoforms in the absence of F-actin

      JOURNAL OF BIOLOGICAL CHEMISTRY
    52. Szczesna, D; Zhang, R; Zhao, JJ; Jones, M; Guzman, G; Potter, JD
      Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy

      JOURNAL OF BIOLOGICAL CHEMISTRY
    53. Takahashi-Yanaga, F; Morimoto, S; Ohtsuki, I
      Effect of Arg145Gly mutation in human cardiac troponin I on the ATPase activity of cardiac myofibrils

      JOURNAL OF BIOCHEMISTRY
    54. Harada, K; Takahashi-Yanaga, F; Minakami, R; Morimoto, S; Ohtsuki, I
      Functional consequences of the deletion mutation Delta Glu160 in human cardiac troponin T

      JOURNAL OF BIOCHEMISTRY
    55. Singer, JM; Hermann, GJ; Shaw, JM
      Suppressors of mdm20 in yeast identify new alleles of ACT1 and TPM1 predicted to enhance actin-tropomyosin interactions

      GENETICS
    56. Hirano, K; Hirano, M; Eto, W; Nishimura, J; Kanaide, H
      Mitogen-induced up-regulation of non-smooth muscle isoform of alpha-tropomyosin in rat aortic smooth muscle cells

      EUROPEAN JOURNAL OF PHARMACOLOGY
    57. Levitsky, DI; Rostkova, EV; Orlov, VN; Nikolaeva, OP; Moiseeva, LN; Teplova, MV; Gusev, NB
      Complexes of smooth muscle tropomyosin with F-actin studied by differential scanning calorimetry

      EUROPEAN JOURNAL OF BIOCHEMISTRY
    58. Sano, K; Maeda, K; Taniguchi, H; Maeda, Y
      Amino-acid replacements in an internal region of tropomyosin alter the properties of the entire molecule

      EUROPEAN JOURNAL OF BIOCHEMISTRY
    59. Redwood, C; Lohmann, K; Bing, W; Esposito, GM; Elliott, K; Abdulrazzak, H; Knott, A; Purcell, I; Marston, S; Watkins, H
      Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy - Ca2+ regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein

      CIRCULATION RESEARCH
    60. Kokado, H; Shimizu, M; Yoshio, H; Ino, H; Okeie, K; Emoto, Y; Matsuyama, T; Yamaguchi, M; Yasuda, T; Fujino, N; Ito, H; Mabuchi, H
      Clinical features of hypertrophic cardiomyopathy caused by a Lys183 deletion mutation in the cardiac troponin I gene

      CIRCULATION
    61. Ho, CY; Lever, HM; DeSanctis, R; Farver, CF; Seidman, JG; Seidman, CE
      Homozygous mutation in cardiac troponin T - Implications for hypertrophic cardiomyopathy

      CIRCULATION
    62. Moolman, JA; Reith, S; Uhl, K; Bailey, S; Gautel, M; Jeschke, B; Fischer, C; Ochs, J; McKenna, WJ; Klues, H; Vosberg, HP
      A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetrance

      CIRCULATION
    63. Atiga, WL; Fananapazir, L; McAreavey, D; Calkins, H; Berger, RD
      Temporal repolarization lability in hypertrophic cardiomyopathy caused by beta-myosin heavy-chain gene mutations

      CIRCULATION
    64. Frey, N; Franz, WM; Gloeckner, K; Degenhardt, M; Muller, M; Muller, O; Merz, H; Katus, HA
      Transgenic rat hearts expressing a human cardiac troponin T deletion reveal diastolic dysfunction and ventricular arrhythmias

      CARDIOVASCULAR RESEARCH
    65. Lin, TL; Ichihara, S; Yamada, Y; Nagasaka, T; Ishihara, H; Nakashima, N; Yokota, M
      Phenotypic variation of familial hypertrophic: cardiomyopathy caused by the Phe110 -> IIe mutation in cardiac troponin T

      CARDIOLOGY
    66. Moraczewska, J; Greenfield, NJ; Liu, YD; Hitchcock-DeGregori, SE
      Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation

      BIOPHYSICAL JOURNAL
    67. Rosol, M; Lehman, W; Craig, R; Landis, C; Butters, C; Tobacman, LS
      Three-dimensional reconstruction of thin filaments containing mutant tropomyosin

      BIOPHYSICAL JOURNAL
    68. Maytum, R; Geeves, MA; Konrad, M
      Actomyosin regulatory properties of yeast tropomyosin are dependent upon N-terminal modification

      BIOCHEMISTRY
    69. Pieples, K; Wieczorek, DF
      Tropomyosin 3 increases striated muscle isoform diversity

      BIOCHEMISTRY
    70. Moraczewska, J; Hitchcock-DeGregori, SE
      Independent functions for the N- and C-termini in the overlap region of tropomyosin

      BIOCHEMISTRY
    71. Laing, NG
      Inherited disorders of sarcomeric proteins

      CURRENT OPINION IN NEUROLOGY
    72. Yu, QT; Zhao, GL; Marian, AJ
      In vivo short-term expression of a hypertrophic cardiomyopathy mutation inadult rabbit myocardium: Myofibrillar incorporation without early disarray

      PROCEEDINGS OF THE ASSOCIATION OF AMERICAN PHYSICIANS
    73. Cregg, N; Cheng, DCH; Karski, JM; Williams, WG; Webb, G; Wigle, ED
      Morbidity outcome in patients with hypertrophic obstructive cardiomyopathyundergoing cardiac septal myectomy: Early-extubation anesthesia versus high-dose opioid anesthesia technique

      JOURNAL OF CARDIOTHORACIC AND VASCULAR ANESTHESIA
    74. Ren, DT; Liu, AX; Yan, LF
      Immunochemical identification and immunofluorescent localization of tropomyosin in germinated pollen of Lilium davidii

      PROGRESS IN NATURAL SCIENCE
    75. Amack, JD; Paguio, AP; Mahadevan, MS
      Cis and trans effects of the myotonic dystrophy (DM) mutation in a cell culture model

      HUMAN MOLECULAR GENETICS
    76. Tan, P; Briner, J; Boltshauser, E; Davis, MR; Wilton, SD; North, K; Wallgren-Pettersson, C; Laing, NG
      Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy

      NEUROMUSCULAR DISORDERS
    77. Hardy, S; Hamon, S; Cooper, B; Mohun, T; Thiebaud, P
      Two skeletal alpha-tropomyosin transcripts with distinct 3 ' UTR have different temporal and spatial patterns of expression in the striated muscle lineages of Xenopus laevis

      MECHANISMS OF DEVELOPMENT
    78. Inoue, A; Ojima, T; Nishita, K
      Cloning and sequencing of cDNA for akazara scallop tropomyosin

      FISHERIES SCIENCE
    79. Krohn, K
      TGF-beta 1-dependent differential expression of a rat homolog for latent TGF-beta binding protein in astrocytes and C6 glioma cells

      GLIA
    80. Barton, PJR; Cullen, ME; Townsend, PJ; Brand, NJ; Mullen, AJ; Norman, DAM; Bhavsar, PK; Yacoub, MH
      Close physical linkage of human troponin genes: Organization, sequence, and expression of the locus encoding cardiac troponin I acid slow skeletal troponin T

      GENOMICS
    81. Eisenberg, I; Thiel, C; Levi, T; Tiram, E; Argov, Z; Sadeh, M; Jackson, CL; Thierfelder, L; Mitrani-Rosenbaum, S
      Fine-structure mapping of the hereditary inclusion body myopathy locus

      GENOMICS
    82. Elliott, PM; Sharma, S; Varnava, A; Poloniecki, J; Rowland, E; McKenna, WJ
      Survival after cardiac arrest or sustained ventricular tachycardia in patients with hypertrophic cardiomyopathy

      JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
    83. Nakaura, H; Morimoto, S; Yanaga, F; Nakata, M; Nishi, H; Imaizumi, T; Ohtsuki, I
      Functional changes in troponin T by a splice donor site mutation that causes hypertrophic cardiomyopathy

      AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
    84. Durand, JB
      Genetic basis of cardiomyopathy

      CURRENT OPINION IN CARDIOLOGY
    85. Waddleton, DM; Jackman, DM; Bieger, T; Heeley, DH
      Characterisation of troponin-T from salmonid fish

      JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY
    86. Das, K; Ashby, KD; Smirnov, AV; Reinach, FC; Petrich, JW; Farah, CS
      Fluorescence properties of recombinant tropomyosin containing tryptophan, 5-hydroxytryptophan and 7-azatryptophan

      PHOTOCHEMISTRY AND PHOTOBIOLOGY
    87. Kochilas, LK; Li, J; Jin, F; Buck, CA; Epstein, JA
      P57(Kip2) expression is enhanced during mid-cardiac murine development andis restricted to trabecular myocardium

      PEDIATRIC RESEARCH
    88. Huang, QQ; Brozovich, FV; Jin, JP
      Fast skeletal muscle troponin T increases the cooperativity of transgenic mouse cardiac muscle contraction

      JOURNAL OF PHYSIOLOGY-LONDON
    89. Jaaskelainen, P; Miettinen, R; Silvennoinen, K; Vauhkonen, I; Laakso, M; Kuusisto, J
      The cardiac troponin I gene is not associated with hypertrophic cardiomyopathy in patients from eastern Finland

      JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
    90. Groger, H; Callaerts, P; Gehring, WJ; Schmid, V
      Gene duplication and recruitment of a specific tropomyosin into striated muscle cells in the jellyfish Podocoryne carnea

      JOURNAL OF EXPERIMENTAL ZOOLOGY
    91. Tardiff, JC; Hewett, TE; Palmer, BM; Olsson, C; Factor, SM; Moore, RL; Robbins, J; Leinwand, LA
      Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy

      JOURNAL OF CLINICAL INVESTIGATION
    92. Rust, EM; Albayya, FP; Metzger, JM
      Identification of a contractile deficit in adult cardiac myocytes expressing hypertrophic cardiomyopathy-associated mutant troponin T proteins

      JOURNAL OF CLINICAL INVESTIGATION
    93. Helfman, DM; Berthier, C; Grossman, J; Leu, M; Ehler, E; Perriard, E; Perriard, JC
      Nonmuscle tropomyosin-4 requires coexpression with other low molecular weight isoforms for binding to thin filaments in cardiomyocytes

      JOURNAL OF CELL SCIENCE
    94. Hart, MC; Cooper, JA
      Vertebrate isoforms of actin capping protein beta have distinct functions in vivo

      JOURNAL OF CELL BIOLOGY
    95. Landis, C; Back, N; Homsher, E; Tobacman, LS
      Effects of tropomyosin internal deletions on thin filament function

      JOURNAL OF BIOLOGICAL CHEMISTRY
    96. Tobacman, LS; Lin, D; Butters, C; Landis, C; Back, N; Pavlov, D; Homsher, E
      Functional consequences of troponin T mutations found in hypertrophic cardiomyopathy

      JOURNAL OF BIOLOGICAL CHEMISTRY
    97. Almenar-Queralt, A; Lee, A; Conley, CA; de Pouplana, LR; Fowler, VM
      Identification of a novel tropomodulin isoform, skeletal tropomodulin, that caps actin filament pointed ends in fast skeletal muscle

      JOURNAL OF BIOLOGICAL CHEMISTRY
    98. Minamisawa, S; Gu, YS; Ross, J; Chien, KR; Chen, J
      A post-transcriptional compensatory pathway in heterozygous ventricular myosin light chain 2-deficient mice results in lack of gene dosage effect during normal cardiac growth or hypertrophy

      JOURNAL OF BIOLOGICAL CHEMISTRY
    99. Yanaga, F; Morimoto, S; Ohtsuki, I
      Ca2+ sensitization and potentiation of the maximum level of myofibrillar ATPase activity caused by mutations of troponin T found in familial hypertrophic cardiomyopathy

      JOURNAL OF BIOLOGICAL CHEMISTRY
    100. Hinkle, A; Goranson, A; Butters, CA; Tobacman, LS
      Roles for the troponin tail domain in thin filament assembly and regulation - A deletional study of cardiac troponin T

      JOURNAL OF BIOLOGICAL CHEMISTRY


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/01/21 alle ore 22:41:34