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  Vol. 55 No. 6, June 1998 TABLE OF CONTENTS
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  Basic Science Seminars in Neurology
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Complementary DNA Libraries and Neurological Disease

Benjamin Joseph, BA; Henry Furneaux, PhD

Arch Neurol. 1998;55:785-788.

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

INTRODUCTION

The DNA in our cell nuclei contains all the information necessary to direct our biological functions. The gene is 1 unit of such information that usually specifies the expression of 1 protein product. A detailed knowledge of each gene will enable us to understand disease at the molecular level. To study each gene we must purify and study it in isolation. This process is usually described as gene cloning. However, this is a difficult task since most of the human genome is junk DNA that does not encode genes. Messenger RNA (mRNA), on the other hand, is representative of only that DNA that has been transcribed. More to the point, within each tissue or cell type, only mRNA that is important for the function of the selected cells will be present. Indeed, different cell types, developmental stages, and many disease states arise because of . . . [Full Text of this Article]

CLONING A GENE USING A cDNA LIBRARY

CLONING BY DNA ANNEALING: ISOLATION OF THE SCRAPIE GENE

CLONING AN ANTIGEN: THE PARANEOPLASTIC ENCEPHALOMYELITIS ANTIGEN

INTERACTION CLONING: THE HUNTINGTIN-ASSOCIATED PROTEIN

SUMMARY AND FUTURE DEVELOPMENTS

From the Program in Molecular Pharmacology and Therapeutics, Memorial Sloan Kettering Cancer Center, New York, NY.







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