FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W1993264807> ?p ?o ?g. }

• W1993264807 endingPage "371" @default.
• W1993264807 startingPage "347" @default.
• W1993264807 abstract "The organization of the subcortical connections of caudate nucleus and putamen in the squirrel monkey was studied using horseradish peroxidase conjugated to wheat germ agglutinin as anterograde and retrograde neuronal tracer. The tracer was injected in similar quantities in the putamen on the left side and in the caudate nucleus on the right side in 10 monkeys, and its presence was revealed by means of the tetramethylbenzidine method. The study of anterogradely labeled fibers visualized after such injections shows that putaminofugal fibers terminate massively in the ventral two-thirds of the globus pallidus, where they display a band-like arrangement, and much less abundantly in the caudal third of the substantia nigra. In contrast, caudatofugal fibers occupy only the dorsal third of globus pallidus but arborize profusely in the rostral two-thirds of substantia nigra. In the pars reticulata of the substantia nigra the caudatonigral fibers form a highly complex network composed of fiber trabeculae while the putaminonigral fibers occur as more discrete fascicles confined to the dorsolateral region of the structure. In the pars compacta of the substantia nigra the retrogradely labeled cells occur in the form of clusters that are closely intermingled with clusters of unlabeled neurons. The labeled-cell clusters are particularly dense on the putamen-injected side and more loosely organized on the caudate-injected side. On both sides, however, the striatonigral fibers that reach the substantia nigra pars compacta can be seen to terminate almost exclusively upon clusters composed of retrogradely labeled cells, suggesting the existence of a precise reciprocal link between nigral and striatal neuronal aggregates. At thalamic levels the retrogradely labeled cells are distributed according to a strikingly asymmetric pattern. For instance, a prominent labeling of neurons in the central superior lateral nucleus is seen only on the caudate-injected side. Furthermore, in the centromedian/parafascicular complex retrograde cell labeling is seen exclusively in parafascicular nucleus on the caudate-injected side and only in the centromedian nucleus, except its lateralmost portion, on the putamen-injected side. Control experiments involving injection of the tracer in cerebral cortex overlying the striatum reveal that the neurons in the lateral segment of the centromedian, which do not project to striatum, are in fact reciprocally connected with the cerebral cortex. In addition, our data show that some of the so-called “specific” thalamic nuclei contribute significantly to the thalamostriatal projection in monkey. A particularly prominent projection arises in the ventral anteriorventral lateral nuclei where neurons projecting either to putamen or caudate nucleus occupy different territories. Finally, a significant number of striatal afferent neurons also occurs in midbrain raphe nuclei, pedunculopontine nucleus and amygdala. These various findings indicate that the subcortical connections of caudate nucleus and putamen in primates are organized according to patterns that are markedly different but also largely complementary to one another." @default.
• W1993264807 created "2016-06-24" @default.
• W1993264807 creator A5024165143 @default.
• W1993264807 creator A5051289855 @default.
• W1993264807 date "1986-06-01" @default.
• W1993264807 modified "2023-10-02" @default.
• W1993264807 title "Differential connections of caudate nucleus and putamen in the squirrel monkey (Saimiri sciureus)" @default.
• W1993264807 cites W1580411261 @default.
• W1993264807 cites W1634329394 @default.
• W1993264807 cites W1963674691 @default.
• W1993264807 cites W1964534260 @default.
• W1993264807 cites W1969833202 @default.
• W1993264807 cites W1972620910 @default.
• W1993264807 cites W1973350511 @default.
• W1993264807 cites W1973586919 @default.
• W1993264807 cites W1978802875 @default.
• W1993264807 cites W1980208993 @default.
• W1993264807 cites W1981453016 @default.
• W1993264807 cites W1984044818 @default.
• W1993264807 cites W1986683725 @default.
• W1993264807 cites W1988048218 @default.
• W1993264807 cites W1989686587 @default.
• W1993264807 cites W1990335809 @default.
• W1993264807 cites W1990421638 @default.
• W1993264807 cites W1992587213 @default.
• W1993264807 cites W1993126311 @default.
• W1993264807 cites W1995416377 @default.
• W1993264807 cites W1997504468 @default.
• W1993264807 cites W2000569019 @default.
• W1993264807 cites W2001789121 @default.
• W1993264807 cites W2002099931 @default.
• W1993264807 cites W2003289804 @default.
• W1993264807 cites W2004776903 @default.
• W1993264807 cites W2008110966 @default.
• W1993264807 cites W2016033342 @default.
• W1993264807 cites W2023196735 @default.
• W1993264807 cites W2023971191 @default.
• W1993264807 cites W2024618140 @default.
• W1993264807 cites W2025302838 @default.
• W1993264807 cites W2030033126 @default.
• W1993264807 cites W2030385412 @default.
• W1993264807 cites W2032242647 @default.
• W1993264807 cites W2034577726 @default.
• W1993264807 cites W2040365012 @default.
• W1993264807 cites W2040879740 @default.
• W1993264807 cites W2044011743 @default.
• W1993264807 cites W2044530383 @default.
• W1993264807 cites W2045614444 @default.
• W1993264807 cites W2047304621 @default.
• W1993264807 cites W2050448984 @default.
• W1993264807 cites W2050537245 @default.
• W1993264807 cites W2050780026 @default.
• W1993264807 cites W2051643483 @default.
• W1993264807 cites W2056183996 @default.
• W1993264807 cites W2056940283 @default.
• W1993264807 cites W2058572430 @default.
• W1993264807 cites W2069209764 @default.
• W1993264807 cites W2070577084 @default.
• W1993264807 cites W2070895732 @default.
• W1993264807 cites W2076792446 @default.
• W1993264807 cites W2077701484 @default.
• W1993264807 cites W2080337239 @default.
• W1993264807 cites W2081023593 @default.
• W1993264807 cites W2083027279 @default.
• W1993264807 cites W2085066179 @default.
• W1993264807 cites W2087258862 @default.
• W1993264807 cites W2090091967 @default.
• W1993264807 cites W2094336126 @default.
• W1993264807 cites W2095693723 @default.
• W1993264807 cites W2120125170 @default.
• W1993264807 cites W2144974041 @default.
• W1993264807 cites W2148019425 @default.
• W1993264807 cites W2151364442 @default.
• W1993264807 cites W2291916750 @default.
• W1993264807 cites W2413769716 @default.
• W1993264807 cites W4211192417 @default.
• W1993264807 cites W4229515813 @default.
• W1993264807 doi "https://doi.org/10.1016/0306-4522(86)90159-4" @default.
• W1993264807 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/3736862" @default.
• W1993264807 hasPublicationYear "1986" @default.
• W1993264807 type Work @default.
• W1993264807 sameAs 1993264807 @default.
• W1993264807 citedByCount "300" @default.
• W1993264807 countsByYear W19932648072012 @default.
• W1993264807 countsByYear W19932648072013 @default.
• W1993264807 countsByYear W19932648072014 @default.
• W1993264807 countsByYear W19932648072015 @default.
• W1993264807 countsByYear W19932648072016 @default.
• W1993264807 countsByYear W19932648072017 @default.
• W1993264807 countsByYear W19932648072018 @default.
• W1993264807 countsByYear W19932648072019 @default.
• W1993264807 countsByYear W19932648072020 @default.
• W1993264807 countsByYear W19932648072021 @default.
• W1993264807 countsByYear W19932648072022 @default.
• W1993264807 countsByYear W19932648072023 @default.
• W1993264807 crossrefType "journal-article" @default.
• W1993264807 hasAuthorship W1993264807A5024165143 @default.
• W1993264807 hasAuthorship W1993264807A5051289855 @default.

• next