Topics

No keywords indexed for this article. Browse by subject →

References
71
[1]
Aggleton JP, Desimone R, Mishkin M (1986) The origin, course, and termination of the hippocampothalamic projections in the macaque. J Comp Neurol 243:09–421. https://doi.org/10.1002/cne.902430310 10.1002/cne.902430310
[2]
Aggleton AP, Pralus A, Nelson AJD, Hornberger M (2016) Thalamic pathology and memory loss in early Alzheimer’s disease: moving the focus from the medial temporal lobe to Papez circuit. Brain 139:1877–1890. https://doi.org/10.1093/brain/aww083 10.1093/brain/aww083
[3]
The evolution of episodic memory

Timothy A. Allen, Norbert J. Fortin

Proceedings of the National Academy of Sciences 2013 10.1073/pnas.1301199110
[4]
Amaral DG, Cowan WM (1980) Subcortical afferents to the hippocampal formation in the monkey. J Comp Neurol 189:573–591. https://doi.org/10.1002/cne.901890402 10.1002/cne.901890402
[5]
How to correct susceptibility distortions in spin-echo echo-planar images: application to diffusion tensor imaging

Jesper L.R. Andersson, Stefan Skare, John Ashburner

NeuroImage 2003 10.1016/s1053-8119(03)00336-7
[6]
Symmetric diffeomorphic image registration with cross-correlation: Evaluating automated labeling of elderly and neurodegenerative brain

B AVANTS, C EPSTEIN, M GROSSMAN et al.

Medical Image Analysis 2008 10.1016/j.media.2007.06.004
[7]
Behrens TEJ, Johansen-Ber H, Woolrich MW, Smith SM, Wheeler-Kingshott CAM, Boulby PA, Barker GJ, Sillery EL, Sheehan K, Ciccarelli O, Thompson AJ, Brady JM, Matthews PM (2003) Non-invasive mapping of the connections between human thalamus and cortex using diffusion imaging. Nat Neurosci 6:750–757. https://doi.org/10.1038/nn1075 10.1038/nn1075
[8]
Bertram EH, Mangan PS, Zhang D, Scott CA, Williamson JM (2001) The midline thalamus: alterations and a potential role in limbic epilepsy. Epilepsia 8:967–978. https://doi.org/10.1046/j.1528-1157.2001.042008967.x 10.1046/j.1528-1157.2001.042008967.x
[9]
Neuropathological stageing of Alzheimer-related changes

H. Braak, E. Braak

Acta Neuropathologica 1991 10.1007/bf00308809
[10]
Braak H, Braak E (1991b) Alzheimer’s disease affects limbic nuclei of the thalamus. Acta Neuropathol 81:261–268. https://doi.org/10.1007/BF00305867 10.1007/bf00305867
[11]
Brown EC, Clark DL, Hassel S, MacQueen G, Ramasubbu R (2017) Thalamocortical connectivity in major depressive disorder. J Affect Disord 217:125–131. https://doi.org/10.1016/j.jad2017.04.004 10.1016/j.jad2017.04.004
[12]
Dahl RE (2004) Adolescent brain development: a period of vulnerabilities and opportunities. Ann NY Acad Sci 1021:1–22. https://doi.org/10.1196/annals.1308.001 10.1196/annals.1308.001
[13]
Descoteaux M, Deriche R, Knosche TR, Anwander A (2009) Deterministic and probabilistic tractography based on complex fibre orientation distributions. IEEE Trans Med Imag 28(2):269–286. https://doi.org/10.1109/TMI.2008.2004424 10.1109/tmi.2008.2004424
[14]
DeVito JL (1980) Subcortical projections to the hippocampal formation in squirrel monkey (Saimiri sciureus). Brain Res Bull 5:285–289. https://doi.org/10.1016/0361-9230(80)90170-7 10.1016/0361-9230(80)90170-7
[15]
Comprehensive cellular‐resolution atlas of the adult human brain

Song‐Lin Ding, Joshua J. Royall, Susan M. Sunkin et al.

Journal of Comparative Neurology 2016 10.1002/cne.24080
[16]
Dolleman-van der Weel MJ, Witter MP (1996) Projections from the nucleus reuniens thalami to the entorhinal cortex, hippocampal field NA1, and the subiculum in the rat arise from different populations of neurons. J Comp Neurol 364(4):635–650. https://doi.org/10.1002/(SICI)1096-9861(19960122)364:4%3c637::AID-CNE3%3e3.0.CO;2-4 10.1002/(sici)1096-9861(19960122)364:4<637::aid-cne3>3.0.co;2-4
[17]
Dolleman-van der Weel MJ, Griffin L, Ito HT, Shapiro ML, Witter MP, Vertes RP, Allen TA (2019) The nucleus reuniens of the thalamus sits at the nexus of a hippocampus and medial prefrontal cortex circuit enabling memory and behavior. Learn Mem 26:191–205. https://doi.org/10.1101/lm.048389.118 10.1101/lm.048389.118
[18]
Do-Monte FH, Quinones-Laracuente K, Quirk GJ (2015) A temporal shift in circuits mediating retrieval of fear memory. Nature 519:460–463. https://doi.org/10.1038/nature14030 10.1038/nature14030
[19]
Dyrby TB, Søgaard LV, Parker GJ, Alexander DC, Lind NM, Baaré WFC, Hay-Schmidt AH, Eriksen N, Pakkenberg B, Paulson OB, Jelsing J (2007) Validation of in vitro probabilistic tractography. Neuroimage 37(4):1267–1277. https://doi.org/10.1016/j.neuroimage.2007.06.022 10.1016/j.neuroimage.2007.06.022
[20]
Freiman TM, Gimbel K, Honegger J, Volk B, Zentner J, Frotscher M, Deller T (2002) Anterograde tracing of human hippocampus in vitro—a neuroanatomical tract tracing technique for the analysis of local fiber tracts in human brain. J Neurosci Methods 120(1):95–103. https://doi.org/10.1016/s0165-0270(02)00187-5 10.1016/s0165-0270(02)00187-5
[21]
Greicius MD, Flores BH, Menon V, Glover GH, Solvason HB, Kenna H, Reiss AL, Schatzberg AF (2007) Resting-state functional connectivity in major depression: abnormally increased contributions from subgenual cingulate cortex and thalamus. Biol Psychiatry 62(5):429–437 10.1016/j.biopsych.2006.09.020
[22]
Hallock HL, Wang A, Shaw CL, Griffin AL (2013) Transient inactivation of the thalamic nucleus reuniens and rhomboid nucleus produces deficits of a working-memory dependent tactile-visual conditional discrimination task. Behav Neurosci 127(6):860–866. https://doi.org/10.1037/a0034653 10.1037/a0034653
[23]
Hauer BE, Pagliardini S, Dickson CT (2019) The reuniens nucleus of the thalamus has essential role in coordinating slow-wave activity between neocortex and hippocampus. eNeuro. 6(5):1–17. https://doi.org/10.1523/eneuro.0365-19.2019 10.1523/eneuro.0365-19.2019
[24]
Heller AS, Casey BJ (2016) The neurodynamics of emotion: Delineating typical and atypical emotional processes during adolescence. Dev Sci 19(1):3–18. https://doi.org/10.1111/desc.12373 10.1111/desc.12373
[25]
Hsu DT, Price JL (2007) Midline and intralaminar thalamic connections with the orbital and medial prefrontal networks in macaque monkeys. J Comp Neurol 5–4(2):89–111. https://doi.org/10.1002/cne.21440 10.1002/cne.21440
[26]
Hsu DT, Price JL (2009) The paraventricular thalamic nucleus: Subcortical connections and innervation by serotonin, orexin, and corticotropin releasing hormone in macaque monkeys. J Comp Neurol 512:825–848. https://doi.org/10.1002/cne.21934 10.1002/cne.21934
[27]
Hsu DT, Kirouac GJ, Zubieta J, Bhatnagar S (2014) Contrubutions of the paraventricular thalamic nucleus in the regulation of stress, motivation, and mood. Front Behav Neurosci 8:1–10. https://doi.org/10.3389/fnbeh.2014.00 10.3389/fnbeh.2014.00
[28]
A probabilistic atlas of the human thalamic nuclei combining ex vivo MRI and histology

Juan Eugenio Iglesias, Ricardo Insausti, Garikoitz Lerma-Usabiaga et al.

NeuroImage 2018 10.1016/j.neuroimage.2018.08.012
[29]
Inutsuka A, Yamanaka A, Vaudry H, De Lecea L (2013) The physiological role of orexin/hypocretin neurons in the regulation of sleep/wakefulness and neuroendocrine functions. Front Endocrinol 4(18):1–10. https://doi.org/10.3389/fendo.2013.00018 10.3389/fendo.2013.00018
[30]
Ito SHT, Zhang SJ, Witter MP, Moser EI, Moser MB (2015) A prefrontal-thalamo-hippocampal circuit for goal directed spatial navigation. Nature 522:50–55. https://doi.org/10.1038/nature14396 10.1038/nature14396
[31]
Jayachandran M, Linley SB, Schlecht M, Mahler SV, Vertes RP, Allen TA (2019) Prefrontal pathways provide top-down control of memory for sequences of events. Cell Rep 28(3):1–15. https://doi.org/10.1016/j.celrep.2019.06.053 10.1016/j.celrep.2019.06.053
[32]
Model‐based analysis of multishell diffusion MR data for tractography: How to get over fitting problems

Saad Jbabdi, Stamatios N. Sotiropoulos, Alexander M. Savio et al.

Magnetic Resonance in Medicine 2012 10.1002/mrm.24204
[33]
Joyce MKP, Marshall LG, Banik SL, Wang J, Xiao D, Bunce JG, Barbas H (2022) Pathways for memory, cognition, and emotional context: hippocampal, subgenual area 25, and the amygdalar axons show unique interactions in the primate thalamic reuniens nucleus. J Neurosci 42(6):1068–1089. https://doi.org/10.1523/JNEUROSCI.1724-21.2021 10.1523/jneurosci.1724-21.2021
[34]
Kark SM, Birnie MT, Baram TZ, Yassa MA (2021) Functional connectivity of the human paraventricular thalamic nucleus: Insights from high field functional MRI. Front Interg Neurosci 15:1–18. https://doi.org/10.3389/fnint.2021.662293 10.3389/fnint.2021.662293
[35]
Kelley AE, Stinus L (1984) The distribution of the projection from the parataenial nucleus of the thalamus to the nucleus accumbens in the rat: an autoradiographic study. Exp Brain Res 54:499–512. https://doi.org/10.1007/BF00235475 10.1007/bf00235475
[36]
Klein JC, Rushworth MFS, Behrens TEJ, Mackay CE, Creshpigny AJ, D’Arceuil D, Johansen-Berg H (2010) Topography of connections between human prefrontal cortex and mediodorsal thalamus studied with diffusion tractography. Neuroimage 51(2):555–564 10.1016/j.neuroimage.2010.02.062
[37]
Krauth A, Blanc R, Poveda A, Jeanmonod D, Morel A, Szekely G (2010) A mean three-dimensional atlas of the human thalamus: generation from multiple histological data. Neuroimage 49(3):2052–2062 10.1016/j.neuroimage.2009.10.042
[38]
Lambert C, Simon H, Colman J, Barrick TR (2017) Defining thalamic nuclei and topographic connectivity gradients in vivo. Neuroimage 158:446–479. https://doi.org/10.1016/j.neuroimage.2016.08.028 10.1016/j.neuroimage.2016.08.028
[39]
Laubach M, Amaranthe LM, Swanson K, White SR (2018) What, if anything, is rodent prefrontal cortex? eNeuro. 5(5):1–14. https://doi.org/10.1523/eneuro.0315-18.2018 10.1523/eneuro.0315-18.2018
[40]
Li S, Kirouac GJ (2008) Projections from the paraventricular nucleus of the thalamus to the forebrain, with special emphasis on the extended amygdala. J Comp Neurol 506(2):263–287. https://doi.org/10.1002/cne.21502 10.1002/cne.21502
[41]
Manns JR, Eichenbaum H (2006) Evolution of declarative memory. Hippocampus 19(6):795–808. https://doi.org/10.1002/hipo.20205 10.1002/hipo.20205
[42]
Martin RE, Ochsner KN (2016) The neuroscience of emotion regulation development: implication for education. Curr Opin Behav Sci 10:142–148. https://doi.org/10.1016/j.cobeha.2016.06.006 10.1016/j.cobeha.2016.06.006
[43]
McKenna JT, Vertes RP (2004) Afferent projections to nucleus reuniens of the thalamus. J Comp Neurol 480(2):115–142. https://doi.org/10.1002/cne.20342 10.1002/cne.20342
[44]
McMakin DL, Kimbler A, Tustison NJ, Pettit JW, Mattfeld AT (2020) Negative overgeneralization is associated with anxiety and mechanisms of pattern completion in peripubertal youth. Spc Cogn Affect Neurosci 17(2):231–240. https://doi.org/10.1093/scan/nsab089 10.1093/scan/nsab089
[45]
Mitchell AS (2015) The medial dorsal nucleus as a higher order thalamic relay nucleus important for learning and decision making. Neurosci Biobehav Rev 54:76–88 10.1016/j.neubiorev.2015.03.001
[46]
Mitchell AS, Chakraborty S (2013) What does the mediodorsal thalamus do? Front Syst Neurosci. https://doi.org/10.3389/fnsys.2013.00037 10.3389/fnsys.2013.00037
[47]
Multiarchitectonic and stereotactic atlas of the human thalamus

Anne Morel, Michel Magnin, Daniel Jeanmonod

Journal of Comparative Neurology 1997 10.1002/(sici)1096-9861(19971103)387:4<588::aid-cne8>3.0.co;2-z
[48]
Neumeister A, Nugent AC, Waldeck T, Geraci M, Schwarz M, Bonne O, Bain EE, Luckenbaugh DA, Herscovitch P, Charney DS, Drevets WC (2004) Neural and behavioral responses to tryptophan depletion in unmedicated patients with remitted major depressive disorder and controls. Arch Gen Psychiatry 61(8):765–773. https://doi.org/10.1001/archpsyc.61.8.765 10.1001/archpsyc.61.8.765
[49]
Padilla-Coreano N, Do-Monte FH, Quirk GJ (2012) A time-dependent role of midline thalamic nuclei in the retrieval of fear memory. Neuropharmacology 62:457–463. https://doi.org/10.1016/j.neuropharm.2011.08.037 10.1016/j.neuropharm.2011.08.037
[50]
Parsons MP, Li S, Kirouac GJ (2007) Functional and anatomical connection between the paraventricular nucleus of the thalamus and dopamine fibers of the nucleus accumbens. J Comp Neurol 500(6):1050–1063. https://doi.org/10.1002/cne.21224 10.1002/cne.21224

Showing 50 of 71 references

Metrics
9
Citations
71
References
Details
Published
Jan 04, 2023
Vol/Issue
228(8)
Pages
1835-1847
License
View
Funding
Feinberg Foundation
Cite This Article
Puck C. Reeders, M. Vanessa Rivera Núñez, Robert P. Vertes, et al. (2023). Identifying the midline thalamus in humans in vivo. Brain Structure and Function, 228(8), 1835-1847. https://doi.org/10.1007/s00429-022-02607-6
Related

You May Also Like