The DOI matches its Crossref record; 73 of the 74 references it cites were found in a registry or an index.
The genomic basis of circadian and circalunar timing adaptations in a midge
Open accessAbstract
Organisms use endogenous clocks to anticipate regular environmental cycles, such as days and tides. Natural variants resulting in differently timed behaviour or physiology, known as chronotypes in humans, have not been well characterized at the molecular level. We sequenced the genome of Clunio marinus, a marine midge whose reproduction is timed by circadian and circalunar clocks. Midges from different locations show strain-specific genetic timing adaptations. We examined genetic variation in five C. marinus strains from different locations and mapped quantitative trait loci for circalunar and circadian chronotypes. The region most strongly associated with circadian chronotypes generates strain-specific differences in the abundance of calcium/calmodulin-dependent kinase II.1 (CaMKII.1) splice variants. As equivalent variants were shown to alter CaMKII activity in Drosophila melanogaster, and C. marinus (Cma)-CaMKII.1 increases the transcriptional activity of the dimer of the circadian proteins Cma-CLOCK and Cma-CYCLE, we suggest that modulation of alternative splicing is a mechanism for natural adaptation in circadian timing.
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.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Interestingly, one of the two quantitative trait loci (QTLs) linked to circalunar timing overlaps largely with one of the two circadian QTLs [46]”
From The Still Dark Side of the Moon: Molecular Mechanisms of Lunar-Controlled Rhythms and Clocks (2020) · cites this paper as [46]
In the citing paper
“However, the mapping of all known genes with key roles in circadian timing or light input pathways revealed their complete absence from these QTLs [46]”
From The Still Dark Side of the Moon: Molecular Mechanisms of Lunar-Controlled Rhythms and Clocks (2020) · cites this paper as [46]
In the citing paper
“Genetic linkage analysis identified two specific chromosomal regions responsible for diurnal emergence and two related to lunar timing.”
From The Still Dark Side of the Moon: Molecular Mechanisms of Lunar-Controlled Rhythms and Clocks (2020) · cites this paper as [46]
In the citing paper
“Interestingly, the current analysis in the midge is consistent with the idea that circadian and circalunar timing mechanisms are distinct, as none of the core circadian clock genes is involved in circalunar timing variation (29).”
From An Overview of Monthly Rhythms and Clocks (2017) · cites this paper as [29]
In the citing paper
“Combining rigorous genetic mapping of these differences with a high-resolution genome for this insect, as well as re-sequencing of distinct chronotypes, has recently allowed the identification of several candidate genes modulating circalunar (and circadian) timing in distinct C. marinus timing strains (29).”
From An Overview of Monthly Rhythms and Clocks (2017) · cites this paper as [29]
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
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
Livak, K. J., & Schmittgen, T. D. (2001) · Methods · doi:10.1006/meth.2001.1262 · Cited by 180,860
The Sequence Alignment/Map format and SAMtools
Li, H., Handsaker, B., Wysoker, A., Fennell, T., Ruan, J., Homer, N., Marth, G., Abecasis, G., Durbin, R., & 1000 Genome Project Data Processing Subgroup (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp352 · Cited by 62,041
Fast and accurate short read alignment with Burrows-Wheeler transform
Li, H., & Durbin, R. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp324 · Cited by 58,607
Cutadapt removes adapter sequences from high-throughput sequencing reads
Martin, M. (2011) · EMBnet.journal · doi:10.14806/ej.17.1.200 · Cited by 33,889
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
McKenna, A., Hanna, M., Banks, E., Sivachenko, A., Cibulskis, K., Kernytsky, A., Garimella, K., Altshuler, D., Gabriel, S., Daly, M., et al. (2010) · Genome Research · doi:10.1101/gr.107524.110 · Cited by 27,895
A Simple Sequentially Rejective Multiple Test Procedure
(1979) · Scandinavian Journal of Statistics · doi:10.2307/4615733 · Cited by 21,526
Full-length transcriptome assembly from RNA-Seq data without a reference genome
Grabherr, M. G., Haas, B. J., Yassour, M., Levin, J. Z., Thompson, D. A., Amit, I., Adiconis, X., Fan, L., Raychowdhury, R., Zeng, Q., et al. (2011) · Nature Biotechnology · doi:10.1038/nbt.1883 · Cited by 21,201
Cingolani, P., Platts, A., Wang, L. L., Coon, M., Nguyen, T., Wang, L., Land, S. J., Lu, X., & Ruden, D. M. (2012) · Fly · doi:10.4161/fly.19695 · Cited by 11,816
Circos: An information aesthetic for comparative genomicsPreprint
Krzywinski, M. I., Schein, J. E., Birol, İ., Connors, J. M., Gascoyne, R. D., Horsman, D. E., Jones, S. J. M., & Marra, M. A. (2009) · Genome Research · doi:10.1101/gr.092759.109 · Cited by 11,073
Velvet: Algorithms for de novo short read assembly using de Bruijn graphsPreprint
Zerbino, D. R., & Birney, E. (2008) · Genome Research · doi:10.1101/gr.074492.107 · Cited by 9,587
Crawley, M. J. (2007) · Medical Entomology and Zoology · Cited by 5,431
Mutation of the mouse klotho gene leads to a syndrome resembling ageing
Kuro-o, M., Matsumura, Y., Aizawa, H., Kawaguchi, H., Suga, T., Utsugi, T., Ohyama, Y., Kurabayashi, M., Kaname, T., Kume, E., et al. (1997) · Nature · doi:10.1038/36285 · Cited by 3,837
Korf, I. F. (2004) · BMC Bioinformatics · doi:10.1186/1471-2105-5-59 · Cited by 3,228
DELLY: structural variant discovery by integrated paired-end and split-read analysis
Rausch, T., Zichner, T., Schlattl, A., Stütz, A. M., Beneš, V., & Korbel, J. O. (2012) · Bioinformatics · doi:10.1093/bioinformatics/bts378 · Cited by 2,438
Scaffolding pre-assembled contigs using SSPACE.
Boetzer, M., Henkel, C. V., Jansen, H. J., Butler, D., & Pirovano, W. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btq683 · Cited by 2,337
Holt, C., & Yandell, M. (2011) · BMC Bioinformatics · doi:10.1186/1471-2105-12-491 · Cited by 2,118
Insights into social insects from the genome of the honeybee Apis mellifera
Weinstock, G. M., Gibbs, R. A., Worley, K. C., Sodergren, E. J., Milosavljević, A., Richards, S., Miller, J., Jiang, H., Zhang, L., Wei, X., et al. (2006) · Nature · doi:10.1038/nature05260 · Cited by 1,914
Gene prediction with a hidden Markov model and a new intron submodel
Stanke, M., & Waack, S. (2003) · Bioinformatics · doi:10.1093/bioinformatics/btg1080 · Cited by 1,439
The genome of the model beetle and pest Tribolium castaneum
Richards, S., Gibbs, R. A., Weinstock, G. M., Gibbs, R. A., Muzny, D. M., Attaway, T., Bell, S., Buhay, C., Chandrabose, M. N., Chavez, D., et al. (2008) · Nature · doi:10.1038/nature06784 · Cited by 1,378
Toward almost closed genomes with GapFiller
Boetzer, M., & Pirovano, W. (2012) · Genome biology · doi:10.1186/gb-2012-13-6-r56 · Cited by 1,123
Sleep and circadian rhythm disruption in psychiatric and neurodegenerative disease
Wulff, K., Gatti, S., Wettstein, J. G., & Foster, R. G. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2868 · Cited by 1,055
Kofler, R., Pandey, R. V., & Schlötterer, C. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr589 · Cited by 815
Sun, P., Enslen, H., Myung, P. S., & Maurer, R. A. (1994) · Genes & Development · doi:10.1101/gad.8.21.2527 · Cited by 744
The Monarch Butterfly Genome Yields Insights into Long-Distance Migration
Zhan, S., Merlin, C., Boore, J. L., & Reppert, S. M. (2011) · Cell · doi:10.1016/j.cell.2011.09.052 · Cited by 597
Kofler, R., Orozco‐terWengel, P., Maio, N. D., Pandey, R. V., Nolte, V., Futschik, A., Kosiol, C., & Schlötterer, C. (2011) · PLoS ONE · doi:10.1371/journal.pone.0015925 · Cited by 576
Comparative Genome and Proteome Analysis of Anopheles gambiae and Drosophila melanogaster
Zdobnov, E. M., von Mering, C., Letunic, I., Torrents, D., Suyama, M., Copley, R. R., Christophides, G. K., Thomasova, D., Holt, R. A., Subramanian, G. M., et al. (2002) · Science · doi:10.1126/science.1077061 · Cited by 553
Depression scores associate with chronotype and social jetlag in a rural population
Levandovski, R., Dantas, G., Fernandes, L. C., Caumo, W., Torres, I., Roenneberg, T., Hidalgo, M. P. L., & Allebrandt, K. V. (2011) · Chronobiology International · doi:10.3109/07420528.2011.602445 · Cited by 527
NextGenMap: fast and accurate read mapping in highly polymorphic genomes
Sedlazeck, F. J., Rescheneder, P., & von Haeseler, A. (2013) · Bioinformatics · doi:10.1093/bioinformatics/btt468 · Cited by 429
Self-citationCaMKII: Claiming Center Stage in Postsynaptic Function and Organization
Hell, J. W. (2014) · Neuron · doi:10.1016/j.neuron.2013.12.024 · Cited by 364
Hu, Y., Shmygelska, A., Tran, D., Eriksson, N., Tung, J. Y., & Hinds, D. A. (2016) · Nature Communications · doi:10.1038/ncomms10448 · Cited by 321
Natural Variation in a Drosophila Clock Gene and Temperature Compensation
Sawyer, L., Hennessy, J. M., Peixoto, A. A., Rosato, E., Parkinson, H., Costa, R., & Kyriacou, C. P. (1997) · Science · doi:10.1126/science.278.5346.2117 · Cited by 320
Lane, J. M., Vlasac, I., Anderson, S. G., Kyle, S. D., Dixon, W. G., Bechtold, D. A., Gill, S., Little, M. A., Luik, A., Loudon, A., et al. (2016) · Nature Communications · doi:10.1038/ncomms10889 · Cited by 312
Molecular insights into human daily behavior
Brown, S. A., Kunz, D., Dumas, A., Westermark, P. O., Vanselow, K., Tilmann-Wahnschaffe, A., Herzel, H., & Kramer, A. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0707772105 · Cited by 270
Chao, L. H., Stratton, M. M., Lee, I., Rosenberg, O. S., Levitz, J., Mandell, D. J., Kortemme, T., Groves, J. T., Schulman, H., & Kuriyan, J. (2011) · Cell · doi:10.1016/j.cell.2011.07.038 · Cited by 258
Another place, another timer: marine species and the rhythms of life
Tessmar‐Raible, K., Raible, F., & Arboleda, E. (2011) · BioEssays · doi:10.1002/bies.201000096 · Cited by 208
Self-citationA Molecular Basis for Natural Selection at the timeless Locus in Drosophila melanogaster
Sandrelli, F., Tauber, E., Pegoraro, M., Mazzotta, G., Cisotto, P., Landskron, J., Stanewsky, R., Piccin, A., Rosato, E., Zordan, M., et al. (2007) · Science · doi:10.1126/science.1138426 · Cited by 205
Preparation and purification of DNA from insects for AFLP analysis
Reineke, A., Karlovský, P., & Zebitz, C. P. W. (1998) · Insect Molecular Biology · doi:10.1046/j.1365-2583.1998.71048.x · Cited by 189
Compact genome of the Antarctic midge is likely an adaptation to an extreme environment
Kelley, J. L., Peyton, J. T., Fiston-Lavier, A.-S., Teets, N. M., Yee, M.-C., Johnston, J. S., Bustamante, C. D., Lee, R. E., & Denlinger, D. L. (2014) · Nature Communications · doi:10.1038/ncomms5611 · Cited by 171
Hamblen, M. J., Wheeler, D. A., Rutila, J. E., Rosbash, M., & Hall, J. C. (1992) · Journal of Insect Behavior · doi:10.1007/bf01058189 · Cited by 167
Nawathean, P., & Rosbash, M. (2004) · Molecular Cell · doi:10.1016/s1097-2765(03)00503-3 · Cited by 161
Logan, R. W., Edgar, N. M., Gillman, A. G., Hoffman, D., Zhu, X., & McClung, C. A. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.01.011 · Cited by 160
Emerging role of CaMKII in neuropsychiatric disease
Robison, A. J. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.07.001 · Cited by 150
Circadian and circalunar clock interactions in a marine annelid
Zantke, J., Ishikawa-Fujiwara, T., Arboleda, E., Lohs, C., Schipany, K., Hallay, N., Straw, A. D., Todo, T., & Tessmar-Raible, K. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.08.031 · Cited by 148
Self-citationThe Drosophila dCREB2 Gene Affects the Circadian Clock
Belvin, M. P., Zhou, H., & Yin, J. C. P. (1999) · Neuron · doi:10.1016/s0896-6273(00)80736-9 · Cited by 141
Gusev, O., Suetsugu, Y., Cornette, R., Kawashima, T., Logacheva, M. D., Kondrashov, A. S., Penin, A. A., Hatanaka, R., Kikuta, S., Shimura, S., et al. (2014) · Nature Communications · doi:10.1038/ncomms5784 · Cited by 138
Intracellular Ca2+Regulates Free-Running Circadian Clock OscillationIn Vivo
Harrisingh, M. C., Wu, Y., Lnenicka, G. A., & Nitabach, M. N. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3680-07.2007 · Cited by 132
Intersubunit capture of regulatory segments is a component of cooperative CaMKII activation
Chao, L. H., Pellicena, P., Deindl, S., Barclay, L. A., Schulman, H., & Kuriyan, J. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1751 · Cited by 119
Coactivation of the CLOCK–BMAL1 complex by CBP mediates resetting of the circadian clock
Lee, Y., Lee, J., Kwon, I., Nakajima, Y., Ohmiya, Y., Son, G. H., Lee, K. H., & Kim, K. (2010) · Journal of Cell Science · doi:10.1242/jcs.070300 · Cited by 116
Neumann, D. (1966) · Zeitschrift f�r Vergleichende Physiologie · doi:10.1007/bf00343045 · Cited by 116
Evolution and Phylogeny of the Diptera: A Molecular Phylogenetic Analysis Using 28S rDNA Sequences
Friedrich, M., & Tautz, D. (1997) · Systematic Biology · doi:10.1093/sysbio/46.4.674 · Cited by 114
Wu, X., & McMurray, C. T. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m006727200 · Cited by 106
LDx: Estimation of Linkage Disequilibrium from High-Throughput Pooled Resequencing Data
Feder, A. F., Petrov, D. A., & Bergland, A. O. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048588 · Cited by 91
Drosophila timeless2 Is Required for Chromosome Stability and Circadian Photoreception
Benna, C., Bonaccorsi, S., Wülbeck, C., Helfrich‐Förster, C., Gatti, M., Kyriacou, C. P., Costa, R., & Sandrelli, F. (2010) · Current Biology · doi:10.1016/j.cub.2009.12.048 · Cited by 82
Genetic basis of human circadian rhythm disorders
Jones, C. R., Huang, A. L., Ptáček, L. J., & Fu, Y. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.07.012 · Cited by 79
Rhythmic U2af26 Alternative Splicing Controls PERIOD1 Stability and the Circadian Clock in Mice
Preußner, M., Wilhelmi, I., Schultz, A.-S., Finkernagel, F., Michel, M., Möröy, T., & Heyd, F. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.04.015 · Cited by 74
Self-citationKon, N., Yoshikawa, T., Honma, S., Yamagata, Y., Yoshitane, H., Shimizu, K., Sugiyama, Y., Hara, C., Kameshita, I., Honma, K., et al. (2014) · Genes & Development · doi:10.1101/gad.237511.114 · Cited by 74
Second messenger and Ras/MAPK signalling pathways regulate CLOCK/CYCLE‐dependent transcription
Weber, F., Hung, H., Maurer, C., & Kay, S. A. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03865.x · Cited by 61
Signaling Mechanisms in Cortical Axon Growth, Guidance, and Branching
Kalil, K., Li, L., & Hutchins, B. I. (2011) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2011.00062 · Cited by 56
Functional Role of CREB-Binding Protein in the Circadian Clock System of Drosophila melanogaster
Lim, C., Lee, J., Choi, C., Kim, J., Doh, E., & Choe, J. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.02155-06 · Cited by 50
Kaiser, T. S., Neumann, D., & Heckel, D. G. (2011) · BMC Genetics · doi:10.1186/1471-2156-12-49 · Cited by 47
Self-citationKaiser, T. S., & Heckel, D. G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032092 · Cited by 37
Self-citationGenetic adaptation in emergence time ofClunio populations to different tidal conditions
Neumann, D. (1967) · Helgoländer Wissenschaftliche Meeresuntersuchungen · doi:10.1007/bf01618620 · Cited by 36
Kaiser, T. S., NEUMANN, D., Heckel, D. G., & Berendonk, T. U. (2010) · Molecular Ecology · doi:10.1111/j.1365-294x.2010.04706.x · Cited by 34
Self-citationSNP2GO: Functional Analysis of Genome-Wide Association Studies
Szkiba, D., Kapun, M., von Haeseler, A., & Gallach, M. (2014) · Genetics · doi:10.1534/genetics.113.160341 · Cited by 32
Self-citationChironomid Midges (Diptera, Chironomidae) Show Extremely Small Genome Sizes
Cornette, R., Gusev, O., Nakahara, Y., Shimura, S., Kikawada, T., & Okuda, T. (2015) · ZOOLOGICAL SCIENCE · doi:10.2108/zs140166 · Cited by 31
Signaling to the microtubule cytoskeleton: An unconventional role for C a MKII
McVicker, D. P., Millette, M. M., & Dent, E. W. (2014) · Developmental Neurobiology · doi:10.1002/dneu.22227 · Cited by 27
Guptaroy, B., Marwaha, N., Pla, M., Wang, Z., Nelson, H. B., Beckingham, K., & Griffith, L. C. (2000) · Molecular Brain Research · doi:10.1016/s0169-328x(00)00115-7 · Cited by 26
Structural plasticity of the circadian timing system. An overview from flies to mammals
Bosler, O., Girardet, C., Franc, J., Becquet, D., & François‐Bellan, A. (2015) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2015.02.001 · Cited by 22
Temperature compensation of circasemilunar timing in the intertidal insectClunio
Neumann, D. (1988) · Journal of Comparative Physiology A · doi:10.1007/bf00603851 · Cited by 21
Promoter Analysis for Daily Expression of Drosophila timeless Gene
Okada, T., Sakai, T., Murata, T., Kako, K., Sakamoto, K., Ohtomi, M., Katsura, T., & Ishida, N. (2001) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2001.4793 · Cited by 20
Circadian Clock Dysfunction and Psychiatric Disease: Could Fruit Flies have a Say?
Zordan, M. A., & Sandrelli, F. (2015) · Frontiers in Neurology · doi:10.3389/fneur.2015.00080 · Cited by 18
Scaffolder - software for manual genome scaffolding
Barton, M. D., & Barton, H. A. (2012) · Source Code for Biology and Medicine · doi:10.1186/1751-0473-7-4 · Cited by 14
Molecular Evolution of a Pervasive Natural Amino-Acid Substitution in Drosophila cryptochrome
Pegoraro, M., Noreen, S., Bhavnani, S., Tsolou, A., Schmid, R., Kyriacou, C. P., & Tauber, E. (2014) · PLoS ONE · doi:10.1371/journal.pone.0086483 · Cited by 11
Flagged first, then by citations
1 of the 74 references couldn’t be matched to a known paper.
Research works printed but not linked: 3
- Crawley, M. J. The R Book. (John Wiley & Sons Ltd., 2007)
- Honegger, H. W. An automatic device for the investigation of the rhythmic emergence pattern of Clunio marinus. Int. J. Chronobiol. 4, 217–221 (1977)
- Heimbach, F. Semilunare und diurnale Schlüpfrhythmen südenglischer und norwegischer Clunio-Populationen (Diptera, Chironomidae) PhD thesis, Universität Köln (1976)
Cited by
Sorted by citations
Fuentes‐Pardo, A. P., & Ruzzante, D. E. (2017) · Molecular Ecology · doi:10.1111/mec.14264 · Cited by 417
The origins and evolution of sleep
Keene, A. C., & Duboué, E. R. (2018) · Journal of Experimental Biology · doi:10.1242/jeb.159533 · Cited by 235
Two sides of a coin: ecological and chronobiological perspectives of timing in the wild
Helm, B., Visser, M. E., Schwartz, W. J., Kronfeld‐Schor, N., Gerkema, M. P., Piersma, T., & Bloch, G. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0246 · Cited by 216
Model and Non-model Insects in Chronobiology
Beer, K., & Helfrich‐Förster, C. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.601676 · Cited by 125
An Overview of Monthly Rhythms and Clocks
Raible, F., Takekata, H., & Tessmar-Raible, K. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00189 · Cited by 121
Self-citation
Metadata
- Authors
- Kaiser, T. S., Poehn, B., Szkiba, D., Preussner, M., Sedlazeck, F. J., Zrim, A., Neumann, T., Nguyen, L.-T., Betancourt, A. J., Hummel, T., Vogel, H., Dorner, S., Heyd, F., von Haeseler, A., & Tessmar-Raible, K.
- Affiliations
- University of Vienna (AT)
- Freie Universität Berlin (DE)
- University of Veterinary Medicine Vienna (AT)
- Max Planck Institute for Chemical Ecology (DE)
- Corresponding author
- Kaiser, Tobias S.
- ORCID
- Venue
- Nature
- Published
- 2016-11-21
- Volume
- 540
- Issue
- 7631
- Pages
- 69-73
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC5133387
- OpenAlex
- W2555773426
- Cited by
- 109
- References
- 74
- Citations by year
- 2026: 2 · 2025: 13 · 2024: 9 · 2023: 7 · 2022: 19 · 2021: 16 · 2020: 11 · 2019: 12 · 2018: 11 · 2017: 9
- FWCI
- 6.79
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Nature (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion, other-oa)
- RePEc: Research Papers in Economics (submittedVersion)
- Max Planck Digital Library (submittedVersion)
- Max Planck Digital Library (submittedVersion, other-oa)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Refubium (Universitätsbibliothek der Freien Universität Berlin) (submittedVersion, cc-by)
- Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver (cc-by)
- Funders
- Deutsche Forschungsgemeinschaft (FP7/2007–2013, HE5398/4)
- Austrian Science Fund (#AY0041321)
- Universität Wien (I059-N)
- FP7 Ideas: European Research Council (337011)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Physical Sciences › Environmental Science › Ecology › Physiological and biochemical adaptations
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
- Keywords
- Clunio marinus, circadian clock, chronotype, alternative splicing, calcium/calmodulin-dependent kinase II, quantitative trait loci, natural genetic variation, Drosophila melanogaster
- MeSH terms
- Acclimatization, Animals, Chironomidae, Circadian Rhythm, Drosophila melanogaster, Male, Phenotype, Reproduction, Species Specificity, Time Factors, Transcription, Genetic, Genetic Variation, Moon, Alternative Splicing, Genomics, Quantitative Trait Loci, Genome, Insect, Calcium-Calmodulin-Dependent Protein Kinase Type 2, Tidal Waves, Genetic Association Studies, CLOCK Proteins, Circadian Clocks
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