Molecular Basis of Neurological Disorders and Their Treatment
cyhemical techniques (ICC) which provide a useful adjunct to investigations by immunoblotting. A particular advantage of a cyhemical approach to the investigation of mihondrial disorders is that it allows the mosaic distribution of certain of these defects to be detected, whereas the tissue homogeniza­ tion involved in conventional enzyme assays or immunoblotting precludes this. A further advantage of MEA or ICC is that only small amounts of tissue are needed, which is important since many of the affected patients are infants or small children. The main aim of this communication is to outline ways in which these techniques can be used in the diagnosis and further investigation of mihondrial disorders. Reference will be made not only to those situations in which MEA and ICC offer advantages over standard enzyme asays and immunoblotting but also to contexts in which the reverse applies. 4. 2 MATERIALS AND METHODS Muscle biopsies for cyhemical investigation were snap-frozen using isopentane cooled to - 150°C in liquid nitrogen. Samples were stored in heat-sealed polythene packets in the vapour phase of liquid nitrogen containers. 4. 2. 1 Microphotometric enzyme assays Frozen sections 8 Jlm thick were cut using a Reichert-J ung Frigocut cryostat microtome equipped with motor-driven cutting action to maintain maximal reproducibility of section thickness. Sections were picked up on microscope slides and air-dried for 15 min at room temperature.
1101498135
Molecular Basis of Neurological Disorders and Their Treatment
cyhemical techniques (ICC) which provide a useful adjunct to investigations by immunoblotting. A particular advantage of a cyhemical approach to the investigation of mihondrial disorders is that it allows the mosaic distribution of certain of these defects to be detected, whereas the tissue homogeniza­ tion involved in conventional enzyme assays or immunoblotting precludes this. A further advantage of MEA or ICC is that only small amounts of tissue are needed, which is important since many of the affected patients are infants or small children. The main aim of this communication is to outline ways in which these techniques can be used in the diagnosis and further investigation of mihondrial disorders. Reference will be made not only to those situations in which MEA and ICC offer advantages over standard enzyme asays and immunoblotting but also to contexts in which the reverse applies. 4. 2 MATERIALS AND METHODS Muscle biopsies for cyhemical investigation were snap-frozen using isopentane cooled to - 150°C in liquid nitrogen. Samples were stored in heat-sealed polythene packets in the vapour phase of liquid nitrogen containers. 4. 2. 1 Microphotometric enzyme assays Frozen sections 8 Jlm thick were cut using a Reichert-J ung Frigocut cryostat microtome equipped with motor-driven cutting action to maintain maximal reproducibility of section thickness. Sections were picked up on microscope slides and air-dried for 15 min at room temperature.
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Molecular Basis of Neurological Disorders and Their Treatment

Molecular Basis of Neurological Disorders and Their Treatment

Molecular Basis of Neurological Disorders and Their Treatment

Molecular Basis of Neurological Disorders and Their Treatment

Paperback(Softcover reprint of the original 1st ed. 1991)

$219.99 
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Overview

cyhemical techniques (ICC) which provide a useful adjunct to investigations by immunoblotting. A particular advantage of a cyhemical approach to the investigation of mihondrial disorders is that it allows the mosaic distribution of certain of these defects to be detected, whereas the tissue homogeniza­ tion involved in conventional enzyme assays or immunoblotting precludes this. A further advantage of MEA or ICC is that only small amounts of tissue are needed, which is important since many of the affected patients are infants or small children. The main aim of this communication is to outline ways in which these techniques can be used in the diagnosis and further investigation of mihondrial disorders. Reference will be made not only to those situations in which MEA and ICC offer advantages over standard enzyme asays and immunoblotting but also to contexts in which the reverse applies. 4. 2 MATERIALS AND METHODS Muscle biopsies for cyhemical investigation were snap-frozen using isopentane cooled to - 150°C in liquid nitrogen. Samples were stored in heat-sealed polythene packets in the vapour phase of liquid nitrogen containers. 4. 2. 1 Microphotometric enzyme assays Frozen sections 8 Jlm thick were cut using a Reichert-J ung Frigocut cryostat microtome equipped with motor-driven cutting action to maintain maximal reproducibility of section thickness. Sections were picked up on microscope slides and air-dried for 15 min at room temperature.

Product Details

ISBN-13: 9789401053792
Publisher: Springer Netherlands
Publication date: 10/08/2012
Edition description: Softcover reprint of the original 1st ed. 1991
Pages: 337
Product dimensions: 6.10(w) x 9.25(h) x 0.03(d)

Table of Contents

1 Towards a molecular model of the acetylcholine receptor channel.- 2 Proton-motive ATP synthase and energy transfer in the cell.- 3 Comparative analysis of the amount of subunit I and subunit IV of the cyhrome c oxidase mRNAs in the cerebral hemispheres of senescent rat and effect of acetyl-l-carnitine.- 4 Cyhemical and immunocyhemical investigation of respiratory complexes in individual fibres of human skeletal muscle.- 5 Native myelin proteins and myelin assembly in the central nervous system.- 6 Regulation of immune cells by serine phospholipids.- 7 Cell adhesion molecules belonging to the immunoglobulin superfamily.- 8 Neurogenic control of cerebral blood vessels.- 9 The fine structural aspects of brain oedema and associated microvascular and glial changes.- 10 Image-guided localized nuclear magnetic resonance spectroscopy of human brain tumours.- 11 Neuroimaging study of frontal lobes.- 12 Biochemical indicators of ischaemic brain damage.- 13 Molecular basis of astroglial reaction to brain injury; regulation of glial fibrillary acidic protein mRNA in rat cerebral cortex and in primary astroglial cell cultures.- 14 Tissue plasminogen activator; acute thrombotic stroke.- 15 Lysosomal storage of a mihondrial protein in Batten’s disease (ceroid lipofuscinosis).- 16 Leber’s hereditary optic neuropathy; from the clinical to the new biochemical and molecular findings for understanding the pathogenesis of the disorder.- 17 Types and mechanism of mihondrial DNA mutations in mihondrial myopathy and related diseases.- 18 Direct tandem duplications of mihondrial DNA in mihondrial myopathy.- 19 Mutations of mihondrial DNA; the molecular basis of mihondrial encephalomyopathies and ageing.- 20 Analysis of giant deletions of human mihondrialDNA in progressive external opthalmoplegia.- 21 Biochemical and genetic investigations in eleven cases of mihondrial myopathies.- 22 Familiar cases of mihondrial myopathies; mihondrial DNA deletions and genetic analysis.- 23 The correlation between pathology, biochemistry and molecular genetics in mihondrial encephalomyopathies.- 24 Various clinical presentation of myhondriopathies; clinical and therapeutic considerations.- 25 Voltage-gated sodium channels as target for pharmacologic agents.- 26 A K+ channel opener in vascular smooth muscle; pharmacology and mechanism of action of cromakalim.- 27 Molecular and cellular mechanisms involves in high resistance neonatal brain resistance to anoxia.- 28 Metabolic activation and mechanisms of MPTP toxicity.- 29 Neurochemical changes produced by perinatal exposure to lead.- 30 Electrophoretic studies of the interaction of neuroleptic drugs with brain tissue.
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