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@ARTICLE{Rapan:904691,
      author       = {Rapan, Lucija and Niu, Meiqi and Zhao, Ling and Funck,
                      Thomas and Amunts, Katrin and Zilles, Karl and
                      Palomero-Gallagher, Nicola},
      title        = {{R}eceptor architecture of macaque and human early visual
                      areas: not equal, but comparable},
      journal      = {Brain structure $\&$ function},
      volume       = {227},
      issn         = {0044-2232},
      address      = {Heidelberg},
      publisher    = {Springer},
      reportid     = {FZJ-2022-00040},
      pages        = {1247–1263},
      year         = {2022},
      abstract     = {Existing cytoarchitectonic maps of the human and macaque
                      posterior occipital cortex differ in the number of areas
                      they display, thus hampering identification of homolog
                      structures. We applied quantitative in vitro receptor
                      autoradiography to characterize the receptor architecture of
                      the primary visual and early extrastriate cortex in macaque
                      and human brains, using previously published
                      cytoarchitectonic criteria as starting point of our
                      analysis. We identified 8 receptor architectonically
                      distinct areas in the macaque brain (mV1d, mV1v, mV2d, mV2v,
                      mV3d, mV3v, mV3A, mV4v), and their respective counterpart
                      areas in the human brain (hV1d, hV1v, hV2d, hV2v, hV3d,
                      hV3v, hV3A, hV4v). Mean densities of 14 neurotransmitter
                      receptors were quantified in each area, and ensuing receptor
                      fingerprints used for multivariate analyses. The 1st
                      principal component segregated macaque and human early
                      visual areas differ. However, the 2nd principal component
                      showed that within each species, area-specific differences
                      in receptor fingerprints were associated with the
                      hierarchical processing level of each area. Subdivisions of
                      V2 and V3 were found to cluster together in both species and
                      were segregated from subdivisions of V1 and from V4v. Thus,
                      comparative studies like this provide valuable architectonic
                      insights into how differences in underlying microstructure
                      impact evolutionary changes in functional processing of the
                      primate brain and, at the same time, provide strong
                      arguments for use of macaque monkey brain as a suitable
                      animal model for translational studies.},
      cin          = {INM-1},
      ddc          = {610},
      cid          = {I:(DE-Juel1)INM-1-20090406},
      pnm          = {5251 - Multilevel Brain Organization and Variability
                      (POF4-525) / HBP SGA3 - Human Brain Project Specific Grant
                      Agreement 3 (945539) / HIBALL - Helmholtz International
                      BigBrain Analytics and Learning Laboratory (HIBALL)
                      (InterLabs-0015) / 3D-MMA - Gradienten der Verteilung
                      multipler Transmitterrezeptoren in der Hirnrinde als
                      Grundlage verteilter kognitiver, sensorischer und
                      motorischer Funktionen. (01GQ1902)},
      pid          = {G:(DE-HGF)POF4-5251 / G:(EU-Grant)945539 /
                      G:(DE-HGF)InterLabs-0015 / G:(BMBF)01GQ1902},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:34931262},
      UT           = {WOS:000731815800001},
      doi          = {10.1007/s00429-021-02437-y},
      url          = {https://juser.fz-juelich.de/record/904691},
}