نتایج جستجو برای: cardiac muscle

تعداد نتایج: 575312  

Journal: :The Biochemical journal 1989
F Wuytack Y Kanmura J A Eggermont L Raeymaekers J Verbist D Hartweg K Gietzen R Casteels

Smooth muscle expresses in its endoplasmic reticulum an isoform of the Ca2+-transport ATPase that is very similar to or identical with that of the cardiac-muscle/slow-twitch skeletal-muscle form. However, this enzyme differs from that found in fast-twitch skeletal muscle. This conclusion is based on two independent sets of observations, namely immunological observations and phosphorylation expe...

Journal: :Molecular and cellular biology 1989
J E Johnson B J Wold S D Hauschka

Muscle creatine kinase (MCK) is expressed at high levels only in skeletal and cardiac muscle tissues. Previous in vitro transfection studies of skeletal muscle myoblasts and fibroblasts had identified two MCK enhancer elements and one proximal promoter element, each of which exhibited expression only in differentiated skeletal muscle. In this study, we have identified several regions of the mou...

2005
Eric N. Olson Robert A. Welch

The two striated muscle cell types, skeletal and cardiac muscle, express overlapping sets of muscle-specific genes. Activation of muscle-specific transcription in skeletal muscle is controlled by the MyoD family of regulatory factors, which are expressed exclusively in skeletal muscle. Members of the MyoD family share homology within a basic helix-loop-helix (HLH) motif that mediates DNA bindin...

Journal: :Circulation research 1993
E N Olson

The two striated muscle cell types, skeletal and cardiac muscle, express overlapping sets of muscle-specific genes. Activation of muscle-specific transcription in skeletal muscle is controlled by the MyoD family of regulatory factors, which are expressed exclusively in skeletal muscle. Members of the MyoD family share homology within a basic helix-loop-helix (HLH) motif that mediates DNA bindin...

Journal: :Journal of applied physiology 2004
Loring B Rowell

This perspective examines origins of some key ideas central to major issues to be addressed in five subsequent mini-reviews related to Skeletal and Cardiac Muscle Blood Flow. The questions discussed are as follows. 1). What causes vasodilation in skeletal and cardiac muscle and 2). might the mechanisms be the same in both? 3). How important is muscle's mechanical contribution (via muscle pumpin...

2002
T. Tokuyasu T. Koyama G. Sakaguchi M. Komeda

AbstructFor operation planning before the cardiac plastic surgery, a cardiac surgeon needs to touch the cardiac muscle to know where thin and soft regions of the muscular wall due to myocardial infraction and dilate cardiomyopathy are located. Since the opportunity to palpate the cardiac muscle of the diseased heart is limited to the operative scene, young, inexperienced cardiac surgeons strong...

Journal: :Circulation research 2011
Michela Noseda Tessa Peterkin Filipa C Simões Roger Patient Michael D Schneider

Cardiac muscle creation during embryogenesis requires extracellular instructive signals that are regulated precisely in time and space, intersecting with intracellular genetic programs that confer or fashion the ability of the cells to respond. Unmasking the essential signals for cardiac lineage decisions has paramount importance for cardiac development and regenerative medicine, including the ...

Journal: :Pharmacology and clinical pharmacy research 2022

Curcumin, the active compound found in turmeric, is believed to delay development of diabetes through several mechanisms. This study aimed investigate if an aqueous extract turmeric can improve glucose uptake and uric acid mouse tissues vitro, after inclusion diet for four weeks. Fourteen adult male Swiss mice were divided into three groups. The first group was control (n=6) that given clean wa...

Journal: :Circulation research 2009
Daniel E Michele Zhyldyz Kabaeva Sarah L Davis Robert M Weiss Kevin P Campbell

RATIONALE Genetic mutations in a number of putative glycosyltransferases lead to the loss of glycosylation of dystroglycan and loss of its laminin-binding activity in genetic forms of human muscular dystrophy. Human patients and glycosylation defective myd mice develop cardiomyopathy with loss of dystroglycan matrix receptor function in both striated and smooth muscle. OBJECTIVE To determine ...

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