The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
A putative flip–flop switch for control of REM sleep
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Narcolepsy in orexin Knockout Mice
Chemelli, R. M., Willie, J. T., Sinton, C. M., Elmquist, J. K., Scammell, T., Lee, C., Richardson, J. A., Williams, S. C., Xiong, Y., Kisanuki, Y., et al. (1999) · Cell · doi:10.1016/s0092-8674(00)81973-x · Cited by 3,095
Self-citationHypothalamic regulation of sleep and circadian rhythms
Saper, C. B., Scammell, T. E., & Lu, J. (2005) · Nature · doi:10.1038/nature04284 · Cited by 2,804
Self-citationAston-Jones, G., & Bloom, F. (1981) · The Journal of Neuroscience · doi:10.1523/jneurosci.01-08-00876.1981 · Cited by 1,960
Differential expression of orexin receptors 1 and 2 in the rat brain
Marcus, J. N., Aschkenasi, C. J., Lee, C. E., Chemelli, R. M., Saper, C. B., Yanagisawa, M., & Elmquist, J. K. (2001) · Journal of Comparative Neurology · doi:10.1002/cne.1190 · Cited by 1,659
Self-citationCritical role of dorsomedial hypothalamic nucleus in a wide range of behavioral circadian rhythms
Chou, T. C., Scammell, T. E., Gooley, J. J., Gaus, S. E., Saper, C. B., & Lu, J. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-33-10691.2003 · Cited by 576
Self-citationKayama, Y., Ohta, M., & Jodo, E. (1992) · Brain Research · doi:10.1016/0006-8993(92)90632-j · Cited by 247
Postnatal phenotype and localization of spinal cord V1 derived interneurons
Alvarez, F. J., Jonas, P. C., Sapir, T., Hartley, R., Berrocal, M. C., Geiman, E. J., Todd, A. J., & Goulding, M. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20711 · Cited by 243
Research works printed but not linked: 32
- McCarley, R. W. Mechanisms and models of REM sleep control. Arch. Ital. Biol. 142, 429–467 (2004)
- Steriade, M., Pare, D., Datta, S., Oakson, G. & Curro Dossi, R. Different cellular types in mesopontine cholinergic nuclei related to ponto-geniculo-occipital waves. J. Neurosci. 10, 2560–2579 (1990) · DOI
- Wu, M. F. et al. Activity of dorsal raphe cells across the wake–sleep cycle and during cataplexy in narcoleptic dogs. J. Physiol. (Lond.) 554, 202–215 (2004) · DOI
- Hobson, J. A., McCarley, R. W. & Nelson, J. P. Location and spike-train characteristics of cells in anterodorsal pons having selective decreases in firing rate during desynchronized sleep. J. Neurophysiol. 50, 770–783 (1983) · DOI
- Kubin, L. Carbachol models of REM sleep: recent developments and new directions. Arch. Ital. Biol. 139, 147–168 (2001)
- Coleman, C. G., Lydic, R. & Baghdoyan, H. A. M2 muscarinic receptors in pontine reticular formation of C57BL/6J mouse contribute to rapid eye movement sleep generation. Neuroscience 126, 821–830 (2004) · DOI
- Wilson, S. & Argyropoulos, S. Antidepressants and sleep: a qualitative review of the literature. Drugs 65, 927–947 (2005) · DOI · Paper page
- Jones, B. E., Harper, S. T. & Halaris, A. E. Effects of locus coeruleus lesions upon cerebral monoamine content, sleep–wakefulness states and the response to amphetamine in the cat. Brain Res. 124, 473–496 (1977) · DOI · Paper page
- Mouret, J. & Coindet, J. Polygraphic evidence against a critical role of the raphe nuclei in sleep in the rat. Brain Res. 186, 273–287 (1980) · DOI
- Shouse, M. N. & Siegel, J. M. Pontine regulation of REM sleep components in cats: integrity of the pedunculopontine tegmentum (PPT) is important for phasic events but unnecessary for atonia during REM sleep. Brain Res. 571, 50–63 (1992) · DOI
- Lee, M. G., Hassani, O. K. & Jones, B. E. Discharge of identified orexin/hypocretin neurons across the wake–sleep cycle. J. Neurosci. 25, 6716–6720 (2005) · DOI · Paper page
- Mileykovskiy, B. Y., Kiyashchenko, L. I. & Siegel, J. M. Behavioral correlates of activity in identified hypocretin/orexin neurons. Neuron 46, 787–798 (2005) · DOI · Paper page
- Thannickal, T. C. et al. Reduced number of hypocretin neurons in human narcolepsy. Neuron 27, 469–474 (2000) · DOI · Paper page
- Lu, J. et al. Selective activation of the extended ventrolateral preoptic nucleus during rapid eye movement sleep. J. Neurosci. 22, 4568–4576 (2002) · DOI · Paper page
- Sastre, J. P., Buda, C., Kitahama, K. & Jouvet, M. Importance of the ventrolateral region of the periaqueductal gray and adjacent tegmentum in the control of paradoxical sleep as studied by muscimol microinjections in the cat. Neuroscience 74, 415–426 (1996) · DOI
- Boissard, R. et al. The rat ponto-medullary network responsible for paradoxical sleep onset and maintenance: a combined microinjection and functional neuroanatomical study. Eur. J. Neurosci. 16, 1959–1973 (2002) · DOI · Paper page
- Sakai, K., Crochet, S. & Onoe, H. Pontine structures and mechanisms involved in the generation of paradoxical (REM) sleep. Arch. Ital. Biol. 139, 93–107 (2001)
- Onoe, H. & Sakai, K. Kainate receptors: a novel mechanism in paradoxical (REM) sleep generation. Neuroreport 6, 353–356 (1995) · DOI
- Boissard, R. et al. Localization of the GABAergic and non-GABAergic neurons projecting to the sublaterodorsal nucleus and potentially gating paradoxical sleep onset. Eur. J. Neurosci. 18, 1627–1639 (2003) · DOI
- Saper, C. B., Chou, T. C. & Scammell, T. E. The sleep switch: hypothalamic control of sleep and wakefulness. Trends Neurosci. 24, 726–731 (2001) · DOI · Paper page
- Sastre, J. P. & Jouvet, M. Oneiric behavior in cats. Physiol. Behav. 22, 979–989 (1979) · DOI
- Sanford, L. D. et al. Sleep patterning and behaviour in cats with pontine lesions creating REM without atonia. J. Sleep Res. 3, 233–240 (1994) · DOI
- Plazzi, G. et al. Pontine lesions in idiopathic narcolepsy. Neurology 46, 1250–1254 (1996) · DOI
- Rye, D. B. et al. Medullary and spinal efferents of the pedunculopontine tegmental nucleus and adjacent mesopontine tegmentum in the rat. J. Comp. Neurol. 269, 315–341 (1988) · DOI · Paper page
- Sastre, J. P., Sakai, K. & Jouvet, M. Are the gigantocellular tegmental field neurons responsible for paradoxical sleep? Brain Res. 229, 147–161 (1981) · DOI
- Taal, W. & Holstege, J. C. GABA and glycine frequently colocalize in terminals on cat spinal motoneurons. Neuroreport 5, 2225–2228 (1994) · DOI
- Chase, M. H., Soja, P. J. & Morales, F. R. Evidence that glycine mediates the postsynaptic potentials that inhibit lumbar motoneurons during the atonia of active sleep. J. Neurosci. 9, 743–751 (1989) · DOI
- Kapas, L. et al. The effects of immunolesions of nerve growth factor-receptive neurons by 192 IgG–saporin on sleep. Brain Res. 712, 53–59 (1996) · DOI
- Gerashchenko, D., Salin-Pascual, R. & Shiromani, P. J. Effects of hypocretin–saporin injections into the medial septum on sleep and hippocampal theta. Brain Res. 913, 106–115 (2001) · DOI
- Manford, M. & Andermann, F. Complex visual hallucinations. Clinical and neurobiological insights. Brain 21, 1819–1840 (1998) · DOI · Paper page
- Kimura, K. et al. A discrete pontine ischemic lesion could cause REM sleep behavior disorder. Neurology 55, 894–895 (2000) · DOI
- Braak, H. et al. Parkinson's disease: affection of brain stem nuclei controlling premotor and motor neurons of the somatomotor system. Acta Neuropathol. (Berl.) 99, 489–495 (2000) · DOI
Cited by
Pathophysiology of Sleep Apnea
Dempsey, J. A., Veasey, S. C., Morgan, B. J., & O'Donnell, C. P. (2010) · Physiological Reviews · doi:10.1152/physrev.00043.2008 · Cited by 2,243
Pathophysiology of migraine: a disorder of sensory processing
Goadsby, P. J., Holland, P. R., Martins-Oliveira, M., Hoffmann, J., Schankin, C., & Akerman, S. (2017) · Physiological Reviews · doi:10.1152/physrev.00034.2015 · Cited by 1,998
The hyperarousal model of insomnia: A review of the concept and its evidence
Riemann, D., Spiegelhalder, K., Feige, B., Voderholzer, U., Berger, M., Perlis, M., & Nissen, C. (2010) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2009.04.002 · Cited by 1,789
Control of sleep and wakefulness
Brown, R. E., Basheer, R., McKenna, J. T., Strecker, R. E., & McCarley, R. W. (2012) · Physiological Reviews · doi:10.1152/physrev.00032.2011 · Cited by 1,477
Saper, C. B., Fuller, P. M., Pedersen, N. P., Lu, J., & Scammell, T. E. (2010) · Neuron · doi:10.1016/j.neuron.2010.11.032 · Cited by 1,404
Self-citationGeneral anaesthesia: from molecular targets to neuronal pathways of sleep and arousal
Franks, N. P. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2372 · Cited by 1,295
Neural Circuitry of Wakefulness and Sleep
Scammell, T. E., Arrigoni, E., & Lipton, J. O. (2017) · Neuron · doi:10.1016/j.neuron.2017.01.014 · Cited by 966
How (and why) the immune system makes us sleep
Imeri, L., & Opp, M. R. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2576 · Cited by 710
The cortisol awakening response: More than a measure of HPA axis function
Clow, A., Hucklebridge, F., Stalder, T., Evans, P., & Thorn, L. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.12.011 · Cited by 635
REM sleep and dreaming: towards a theory of protoconsciousness
Hobson, J. A. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2716 · Cited by 625
Jhou, T. C., Geisler, S., Marinelli, M., Degarmo, B. A., & Zahm, D. S. (2009) · Journal of Comparative Neurology · doi:10.1002/cne.21891 · Cited by 503
Reassessment of the structural basis of the ascending arousal system
Fuller, P., Sherman, D., Pedersen, N. P., Saper, C. B., & Lu, J. (2011) · Journal of Comparative Neurology · doi:10.1002/cne.22559 · Cited by 465
Self-citationOpp, M. R. (2005) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2005.01.002 · Cited by 393
Wake–sleep circuitry: an overview
Saper, C. B., & Fuller, P. M. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.03.021 · Cited by 383
Self-citationCircadian Rhythms, Sleep, and Disorders of Aging
Mattis, J., & Sehgal, A. (2016) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2016.02.003 · Cited by 369
Peever, J., & Fuller, P. M. (2017) · Current Biology · doi:10.1016/j.cub.2017.10.026 · Cited by 360
Phantasia–The psychological significance of lifelong visual imagery vividness extremes
Zeman, A., Milton, F., Della Sala, S., Dewar, M., Frayling, T., Gaddum, J., Hattersley, A., Heuerman-Williamson, B., Jones, K., MacKisack, M., et al. (2020) · Cortex · doi:10.1016/j.cortex.2020.04.003 · Cited by 336
Restoration of normal motor control in Parkinson’s disease during REM sleep
De Cock, V. C., Vidailhet, M., Leu, S., Texeira, A., Apartis, E., Elbaz, A., Roze, E., Willer, J. C., Derenne, J. P., Agid, Y., et al. (2007) · Brain · doi:10.1093/brain/awl363 · Cited by 321
Optogenetic activation of cholinergic neurons in the PPT or LDT induces REM sleep
Van Dort, C. J., Zachs, D. P., Kenny, J. D., Zheng, S., Goldblum, R. R., Gelwan, N. A., Ramos, D. M., Nolan, M. A., Wang, K., Weng, F.-J., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1423136112 · Cited by 296
The neurobiological basis of narcolepsy
Mahoney, C. E., Cogswell, A., Koralnik, I. J., & Scammell, T. E. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0097-x · Cited by 289
Slow waves, sharp waves, ripples, and REM in sleeping dragons
Shein-Idelson, M., Ondracek, J. M., Liaw, H.-P., Reiter, S., & Laurent, G. (2016) · Science · doi:10.1126/science.aaf3621 · Cited by 274
Oscillating circuitries in the sleeping brain
Adamantidis, A. R., Gutierrez Herrera, C., & Gent, T. C. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0223-4 · Cited by 281
Paraventricular hypothalamic nucleus: Axonal projections to the brainstem
Geerling, J. C., Shin, J., Chimenti, P. C., & Loewy, A. D. (2010) · Journal of Comparative Neurology · doi:10.1002/cne.22283 · Cited by 273
Galanin neurons in the ventrolateral preoptic area promote sleep and heat loss in mice
Kroeger, D., Absi, G., Gagliardi, C., Bandaru, S. S., Madara, J. C., Ferrari, L. L., Arrigoni, E., Münzberg, H., Scammell, T. E., Saper, C. B., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06590-7 · Cited by 276
Self-citationDescending command neurons in the brainstem that halt locomotion
Bouvier, J., Caggiano, V., Leiras, R., Caldeira, V., Bellardita, C., Balueva, K., Fuchs, A., & Kiehn, O. (2015) · Cell · doi:10.1016/j.cell.2015.10.074 · Cited by 259
Circadian Variation of Heart Rate Variability Across Sleep Stages
Boudreau, P., Yeh, W.-H., Dumont, G. A., & Boivin, D. B. (2013) · Sleep · doi:10.5665/sleep.3230 · Cited by 235
The Neurobiology of Sleep and Wakefulness
Schwartz, M. D., & Kilduff, T. S. (2015) · Psychiatric Clinics of North America · doi:10.1016/j.psc.2015.07.002 · Cited by 207
REM sleep characteristics in narcolepsy and REM sleep behavior disorder
Dauvilliers, Y., Rompré, S., Gagnon, J.-F., Vendette, M., Petit, D., & Montplaisir, J. (2007) · Sleep · doi:10.1093/sleep/30.7.844 · Cited by 197
Synaptic plasticity in sleep: learning, homeostasis and disease
Wang, G., Grone, B., Colas, D., Appelbaum, L., & Mourrain, P. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.07.005 · Cited by 172
NREM and REM Sleep: Complementary Roles in Recovery after Wakefulness
Vyazovskiy, V. V., & Delogu, A. (2014) · The Neuroscientist · doi:10.1177/1073858413518152 · Cited by 169
Parallel preoptic pathways for thermoregulation
Yoshida, K., Li, X., Cano, G., Lazarus, M., & Saper, C. B. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2643-09.2009 · Cited by 160
Self-citationThe supramammillary nucleus and the claustrum activate the cortex during REM sleep
Renouard, L., Billwiller, F., Ogawa, K., Clément, O., Camargo, N., Abdelkarim, M., Gay, N., Scoté-Blachon, C., Touré, R., Libourel, P.-A., et al. (2015) · Science Advances · doi:10.1126/sciadv.1400177 · Cited by 152
Selective activation of cholinergic basal forebrain neurons induces immediate sleep-wake transitions
Han, Y., Shi, Y.-F., Xi, W., Zhou, R., Tan, Z.-B., Wang, H., Li, X.-M., Chen, Z., Feng, G., Luo, M., et al. (2014) · Current Biology · doi:10.1016/j.cub.2014.02.011 · Cited by 137
Kristensson, K., Nygård, M., Bertini, G., & Bentivoglio, M. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.12.001 · Cited by 140
Calcium imaging of sleep-wake related neuronal activity in the dorsal pons
Cox, J., Pinto, L., & Dan, Y. (2016) · Nature Communications · doi:10.1038/ncomms10763 · Cited by 133
Siclari, F., Khatami, R., Urbaniok, F., Nobili, L., Mahowald, M. W., Schenck, C. H., Cramer Bornemann, M. A., & Bassetti, C. L. (2010) · Brain · doi:10.1093/brain/awq296 · Cited by 131
Amygdala lesions reduce cataplexy in orexin knock-out mice
Burgess, C. R., Oishi, Y., Mochizuki, T., Peever, J. H., & Scammell, T. E. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5632-12.2013 · Cited by 108
State-dependent and reflex drives to the upper airway: basic physiology with clinical implications
Horner, R. L., Hughes, S. W., & Malhotra, A. (2014) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00531.2013 · Cited by 104
Physiological Mechanisms of Upper Airway Hypotonia during REM Sleep
McSharry, D. G., Saboisky, J. P., DeYoung, P., Jordan, A. S., Trinder, J., Smales, E., Hess, L., Chamberlin, N. L., & Malhotra, A. (2014) · Sleep · doi:10.5665/sleep.3498 · Cited by 102
Physiological arousal: a role for hypothalamic systems
Adamantidis, A., & de Lecea, L. (2008) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-008-7521-8 · Cited by 95
Non-circadian direct effects of light on sleep and alertness: Lessons from transgenic mouse models
Hubbard, J., Ruppert, E., Gropp, C.-M., & Bourgin, P. (2013) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2012.12.004 · Cited by 94
REM sleep behavior disorder (RBD)
Hu, M. T. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.104996 · Cited by 93
Neural and Homeostatic Regulation of REM Sleep
Park, S.-H., & Weber, F. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2020.01662 · Cited by 82
Joiner, W. J., Friedman, E. B., Hung, H.-T., Koh, K., Sowcik, M., Sehgal, A., & Kelz, M. B. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003605 · Cited by 82
REM sleep-active hypothalamic neurons may contribute to hippocampal social-memory consolidation
Qin, H., Fu, L., Jian, T., Jin, W., Liang, M., Li, J., Chen, Q., Yang, X., Du, H., Liao, X., et al. (2022) · Neuron · doi:10.1016/j.neuron.2022.09.004 · Cited by 78
The retinal iprgc-preoptic circuit mediates the acute effect of light on sleep
Zhang, Z., Beier, C., Weil, T., & Hattar, S. (2021) · Nature Communications · doi:10.1038/s41467-021-25378-w · Cited by 75
REM sleep is associated with distinct global cortical dynamics and controlled by occipital cortex
Wang, Z., Fei, X., Liu, X., Wang, Y., Hu, Y., Peng, W., Wang, Y.-W., Zhang, S., & Xu, M. (2022) · Nature Communications · doi:10.1038/s41467-022-34720-9 · Cited by 73
Skopin, M. D., Kabadi, S. V., Viechweg, S. S., Mong, J. A., & Faden, A. I. (2015) · Journal of Neurotrauma · doi:10.1089/neu.2014.3664 · Cited by 71
Cortical regulation of two-stage rapid eye movement sleep
Dong, Y., Li, J., Zhou, M., Du, Y., & Liu, D. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01195-2 · Cited by 60
Sleep stage dynamics in neocortex and hippocampus
Durán, E., Oyanedel, C. N., Niethard, N., Inostroza, M., & Born, J. (2018) · Sleep · doi:10.1093/sleep/zsy060 · Cited by 52
Molecular Mechanisms of REM Sleep
Yamada, R. G., & Ueda, H. R. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01402 · Cited by 49
Probabilistic sleep architecture models in patients with and without sleep apnea
BIANCHI, M. T., EISEMAN, N. A., CASH, S. S., MIETUS, J., PENG, C., & THOMAS, R. J. (2012) · Journal of Sleep Research · doi:10.1111/j.1365-2869.2011.00937.x · Cited by 44
“The main conceptual model of sleep transitions draws analogy to a flip-flop switch controlling transitions between wake and sleep, and between REM and NREM sleep (Fuller et al., 2007; Lu et al., 2006).”
Sepsis-induced alterations in sleep of rats
Baracchi, F., Ingiosi, A. M., Raymond, R. M., & Opp, M. R. (2011) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00354.2011 · Cited by 42
Chiaro, G., Calandra-Buonaura, G., Cecere, A., Mignani, F., Sambati, L., Loddo, G., Cortelli, P., & Provini, F. (2018) · Clinical Autonomic Research · doi:10.1007/s10286-017-0460-4 · Cited by 42
Memory corticalization triggered by REM sleep: mechanisms of cellular and systems consolidation
Almeida-Filho, D. G., Queiroz, C. M., & Ribeiro, S. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2886-9 · Cited by 38
The gut–brain axis in early Parkinson’s disease: from prodrome to prevention
Oliver, P. J., Civitelli, L., & Hu, M. T. (2025) · Journal of Neurology · doi:10.1007/s00415-025-13138-5 · Cited by 42
“…because α-synucleinopathies are associated with cell loss in the neuronal structures regulating REM sleep atonia, which animal studies have localized to the pontine sub-coeruleus and central medulla of the brainstem, thought to contain a putative ‘flip-flop’ switch for REM sleep control [40, 41].”
Deep imaging in the brainstem reveals functional heterogeneity in V2a neurons controlling locomotion
Schwenkgrub, J., Harrell, E. R., Bathellier, B., & Bouvier, J. (2020) · Science Advances · doi:10.1126/sciadv.abc6309 · Cited by 27
Fifel, K., Piggins, H., & Deboer, T. (2016) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2015.02.005 · Cited by 30
Acetylcholine and metacognition during sleep
Gott, J. A., Stücker, S., Kanske, P., Haaker, J., & Dresler, M. (2024) · Consciousness and Cognition · doi:10.1016/j.concog.2023.103608 · Cited by 25
Lu, H.-C., Pollack, H., Lefante, J. J., Mills, A. A., & Tian, D. (2019) · Sleep · doi:10.1093/sleep/zsy253 · Cited by 22
Lanir-Azaria, S., Meiri, G., Avigdor, T., Minert, A., & Devor, M. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.12.035 · Cited by 20
Self-citationLlewellyn, S. (2016) · Consciousness and Cognition · doi:10.1016/j.concog.2016.09.018 · Cited by 17
Large-scale functional brain networks for consciousness
Han, M.-E., Park, S. Y., & Oh, S.-O. (2021) · Anatomy & Cell Biology · doi:10.5115/acb.20.305 · Cited by 9
Metadata
- Authors
- Lu, J., Sherman, D., Devor, M., & Saper, C. B.
- Venue
- Nature
- Published
- 2006-05-10
- Volume
- 441
- Issue
- 7093
- Pages
- 589-594
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2027429673
- Cited by
- 1,215
- References
- 7
- FWCI
- 30.40
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.