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Striated Muscle

In vivo analysis of two striated muscle actin promoters reveals combinations of multiple regulatory modules required for skeletal and cardiac muscle specific gene expression

In vivo analysis of two striated muscle actin promoters reveals combinations of multiple regulatory modules required for skeletal and cardiac muscle specific gene expression

... for muscle actin gene expression in cardiac ...cardiac muscle, and any other putative trans-acting factors that would bind to E box in cardiac muscle have not been ...cardiac muscle, an ...

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Modelling oxygen capillary supply to striated muscle tissues

Modelling oxygen capillary supply to striated muscle tissues

... a striated muscle with spatially uniform oxygen uptake ...cardiac muscle, they found that DOM accurately capture the predicted flux lines ...all striated muscle tissues, especially in ...

7

The homeobox gene Msx in development and transdifferentiation of jellyfish striated muscle

The homeobox gene Msx in development and transdifferentiation of jellyfish striated muscle

... the striated and smooth muscles of the ...differentiated striated muscle of the medusa in vivo and in ...isolated striated muscle undergoing transdifferentiation, to be upregulated ...

7

Mechanical properties of myosin cross bridges in frog striated muscle

Mechanical properties of myosin cross bridges in frog striated muscle

... MECHANICAL PROPERTIES OF MYOSIN CROSSBRIDGES IN FROG STRIATED MUSCLE David Graham Hirst A Thesis Submitted for the Degree of PhD at the University of St Andrews.. 1975 Full metadata for [r] ...

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Fusion of bone marrow–derived stem cells with striated muscle may not be sufficient to activate muscle genes

Fusion of bone marrow–derived stem cells with striated muscle may not be sufficient to activate muscle genes

... in striated muscle (10) and in normal developing muscle cells faithfully reflects expression of the endogenous myosin gene ...skeletal muscle dif- ferentiation from unfractionated bone ...

5

Myosin accumulation and striated muscle myopathy result from the loss of muscle RING finger 1 and 3

Myosin accumulation and striated muscle myopathy result from the loss of muscle RING finger 1 and 3

... DKO muscle but are clearly not sufficient for complete MHC degrada- ...DKO muscle and worsen the phenotype by producing substrates for UPS-dependent ...

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A Region of the Myosin Rod Important for Interaction With Paramyosin in Caenorhabditis elegans Striated Muscle

A Region of the Myosin Rod Important for Interaction With Paramyosin in Caenorhabditis elegans Striated Muscle

... Figure 5.—(A) The 322-residue region of the C-terminal MHC A rod is required for e73 suppression activity. All five rod chimeras diagrammed here contain MHC B sequences within the critical region at the rod C terminus, ...

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Ultrastructural and molecular changes in striated muscle during post mortem shortening

Ultrastructural and molecular changes in striated muscle during post mortem shortening

... Muscle stored at 2° and sampled 2h hours post-mortem After 2k hours of post-mortem storage at 2°, the muscle observed was supercontracted and was similar to the structure observed in neu[r] ...

96

Effects of Na+ on Sugar and Amino Acid Transport in Striated Muscle

Effects of Na+ on Sugar and Amino Acid Transport in Striated Muscle

... Subsequently, Csaky and Zollicoffer acid AIB is Na+ dependent; 3 transport sys2, 3, using rat and toad intestinal preparations, tems requiring Na+ are inhibited by the glycoside, reporte[r] ...

10

Mechanical Power output from Striated Muscle during Cyclic Contraction

Mechanical Power output from Striated Muscle during Cyclic Contraction

... At a peak-to-peak amplitude of 5—6 % rest length the excursion amplitude giving maximum work in a stimulated muscle the work absorbed per cycle is 0-1—0-25 J kg" 1 , which is about one-t[r] ...

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Force Maintenance with Reduced Ability to Shorten Actively in Barnacle Striated Muscle

Force Maintenance with Reduced Ability to Shorten Actively in Barnacle Striated Muscle

... Force changes in response to a quick restretch following a quick release To characterize further the relaxation phase of the mechanical response, in which the ability to shorten actively[r] ...

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The Ionic Basis of the Resting Potential in a Cross Striated Muscle of the Aquatic Snail Lymnaea Stagnalis

The Ionic Basis of the Resting Potential in a Cross Striated Muscle of the Aquatic Snail Lymnaea Stagnalis

... The chloride dependence of the resting potential The membrane potential of Lymnaea heart ventricle muscle cells did not change by the predicted amount during the reduction or subsequent [r] ...

10

Exercise related changes in protein turnover in mammalian striated muscle

Exercise related changes in protein turnover in mammalian striated muscle

... Age-related changes in the fractional rates of protein synthesis and degradation in four striated muscles of the rat Fractional rate of protein synthesis % day - 1 Foetal age days Muscl[r] ...

22

Myoglobin: an essential hemoprotein in striated muscle

Myoglobin: an essential hemoprotein in striated muscle

... skeletal muscle function were significantly impaired by pharmacological or chemical agents that reduced the levels of oxymyoglobin (Wittenberg and Wittenberg, 1975; Doeller and Wittenberg, 1991), additional ...

6

Membrane Properties of the Somatic Muscle (Obliquely Striated Muscle) of the Earthworm

Membrane Properties of the Somatic Muscle (Obliquely Striated Muscle) of the Earthworm

... Typical patterns of membrane activity recorded from the longitudinal muscle cells of earthworm, a The initial discharges with high frequency was generated by mechanical stimulation and t[r] ...

17

ELECTROLYTE CHANGES IN HUMAN STRIATED MUSCLE IN ACIDOSIS AND ALKALOSIS

ELECTROLYTE CHANGES IN HUMAN STRIATED MUSCLE IN ACIDOSIS AND ALKALOSIS

... Inasmuch as direct studies of human tissues during states of potassium depletion have not been reported, the present studies were undertaken in an attempt to define the composition of th[r] ...

6

Identification of novel monosodium urate crystal regulated mRNAs by transcript profiling of dissected murine air pouch membranes

Identification of novel monosodium urate crystal regulated mRNAs by transcript profiling of dissected murine air pouch membranes

... leukocyte count had returned close to its original level at the end of the 50-hour time course (Figure 1b), IL-6 mRNA also returned to near baseline by 50 hours. The mRNAs encoding IL-1β, tumour necrosis factor (TNF)-α, ...

13

Leukotrienes as mediators in ischemia reperfusion injury in a microcirculation model in the hamster

Leukotrienes as mediators in ischemia reperfusion injury in a microcirculation model in the hamster

... in striated muscle in awake hamsters and sequential RP-HPLC and RIA for leukotrienes, we demonstrate in this study that (a) the leukotrienes (LT)B4 and LTD4 elicit leukocyte/endothelium interaction and ...

7

Histological Evaluation of Decellularized Skeletal Muscle Tissue Using Two Different Decellularization Agents

Histological Evaluation of Decellularized Skeletal Muscle Tissue Using Two Different Decellularization Agents

... skeletal muscle tissue ap- peared almost translucent in SDS protocol; Triton protocol did not affect a muscle so well and we could observe cy- toplasmic debris in the ...skeletal muscle tissue which ...

6

Contractile properties of the striated adductor muscle in the bay scallop Argopecten irradians at several temperatures

Contractile properties of the striated adductor muscle in the bay scallop Argopecten irradians at several temperatures

... the striated (‘fast’) portion of the single adductor muscle (Lowy, 1954), which is morphologically distinct and much larger than the adjacent smooth ...The muscle is attached directly to the valves ...

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