Immunohistochemical localization and biochemical characterization of hypocretin/orexin-related peptides in the central nervous system of the frogRana ridibunda

2000 ◽  
Vol 429 (2) ◽  
pp. 242-252 ◽  
Author(s):  
Ludovic Galas ◽  
Hubert Vaudry ◽  
Benedicte Braun ◽  
Anthony N. Van Den Pol ◽  
Luis De Lecea ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Biochemical Characterization ◽  
Immunohistochemical Localization ◽  
The Central Nervous System

Biochemical Characterization of Myelin Isolated from the Central Nervous System of Xenopus Tadpoles

1980 ◽  
Vol 34 (5) ◽  
pp. 1241-1246 ◽  
Author(s):  
Bruce D. Trapp ◽  
Laurence J. McIntyre ◽  
Richard H. Quarles ◽  
Genïchro Nonaka ◽  
Ann Moser ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Biochemical Characterization ◽  
The Central Nervous System

scholarly journals Crystal Structure and Biochemical Characterization of Human Kallikrein 6 Reveals That a Trypsin-like Kallikrein Is Expressed in the Central Nervous System

2002 ◽  
Vol 277 (27) ◽  
pp. 24562-24570 ◽  
Author(s):  
Matthew J. Bernett ◽  
Sachiko I. Blaber ◽  
Isobel A. Scarisbrick ◽  
Pushparani Dhanarajan ◽  
Steven M. Thompson ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Central Nervous System ◽  
Nervous System ◽  
Biochemical Characterization ◽  
The Central Nervous System ◽  
Kallikrein 6

scholarly journals Molecular cloning and analysis of l(1)ogre, a locus of Drosophila melanogaster with prominent effects on the postembryonic development of the central nervous system.

Genetics ◽  
1990 ◽  
Vol 126 (4) ◽  
pp. 1033-1044 ◽  
Author(s):  
T Watanabe ◽  
D R Kankel
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Postembryonic Development ◽  
P Element ◽  
Reading Frame ◽  
Isolation And Characterization ◽  
The Central Nervous System ◽  
Highly Hydrophobic ◽  
Conceptual Translation

Abstract Previous genetic studies have shown that wild-type function of the l(1)ogre (lethal (1) optic ganglion reduced) locus is essential for the generation and/or maintenance of the postembryonic neuroblasts including those from which the optic lobe is descended. In the present study molecular isolation and characterization of the l(1)ogre locus was carried out to study the structure and expression of this gene in order to gain information about the nature of l(1)ogre function and its relevance to the development of the central nervous system. About 70 kilobases (kb) of genomic DNA were isolated that spanned the region where l(1)ogre was known to reside. Southern analysis of a l(1)ogre mutation and subsequent P element-mediated DNA transformation mapped the l(1)ogre+ function within a genomic fragment of 12.5 kb. Northern analyses showed that a 2.9-kb message transcribed from this 12.5-kb region represented l(1)ogre. A 2.15-kb portion of a corresponding cDNA clone was sequenced. An open reading frame (ORF) of 1,086 base paris was found, and a protein sequence of 362 amino acids with one highly hydrophobic segment was deduced from conceptual translation of this ORF.

scholarly journals Detection and Characterization of Autoantibodies to Neuronal Cell-Surface Antigens in the Central Nervous System

2016 ◽  
Vol 9 ◽  
Author(s):  
Marleen H. van Coevorden-Hameete ◽  
Maarten J. Titulaer ◽  
Marco W. J. Schreurs ◽  
Esther de Graaff ◽  
Peter A. E. Sillevis Smitt ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Cell Surface ◽  
Neuronal Cell ◽  
Surface Antigens ◽  
Cell Surface Antigens ◽  
The Central Nervous System

Characterization of placental luteinizing hormone-relasing factor-like material

1981 ◽  
Vol 96 (3) ◽  
pp. 394-397 ◽  
Author(s):  
Jau-Nan Lee ◽  
Markku Seppälä ◽  
Tim Chard
Keyword(s):  
Central Nervous System ◽  
High Pressure ◽  
Nervous System ◽  
Acetic Acid ◽  
Liquid Chromatography ◽  
Luteinizing Hormone ◽  
Human Placenta ◽  
The Central Nervous System ◽  
Inhibition Curve

Abstract. High pressure liquid chromatography (HPLC) and radioimmunoassay were employed to characterize luteinizing hormone-releasing factor (LRF)-like material in the human placenta. Methanol extracts of the placenta were washed with acetic acid and chloroform, further purified on coarse octadecylsilane columns, fractionated on HPLC, and tested by radioimmunoassay. In HPLC, placental LRF had the same retention time as synthetic LRF, and such fractions gave an inhibition curve which was parallel to that of synthetic LRF in radioimmunoassav. It is concluded that human placental I.RF is similar or identical to LRF in the central nervous system.

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