CPLX1 (Catalan Wikipedia)

Analysis of information sources in references of the Wikipedia article "CPLX1" in Catalan language version.

refsWebsite

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3sciencedirect.com

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1atlasgeneticsoncology.org

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1geneontology.org

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1sinobiological.com

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1frontiersin.org

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atlasgeneticsoncology.org

«CPLX1 (complexin 1)». Atlas of Genetics and Cytogenetics in Oncology and Haematology, 01-10-2016. [Consulta: 12 octubre 2012].

bgee.org

«Gene: CPLX1 (Homo Sapiens)». Bgee - Swiss Institute of Bioinformatics, 10-2020. [Consulta: 21 octubre 2023].

doi.org

dx.doi.org

McMahon, H. T.; Missler, M.; Li, C.; Südhof, T. C. «Complexins: cytosolic proteins that regulate SNAP receptor function». Cell, 83, 1, 06-10-1995, pàg. 111–119. DOI: 10.1016/0092-8674(95)90239-2. ISSN: 0092-8674. PMID: 7553862.
Bućan, M.; Zimmer, M.; Whaley, W. L.; Poustka, A.; Youngman, S. «Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation». Genomics, 6, 1, 01-1990, pàg. 1–15. DOI: 10.1016/0888-7543(90)90442-w. ISSN: 0888-7543. PMID: 2137426.
Engbers, H; van der Smagt, J; van ‘t Slot, R; Vermeesch, J; Hochstenbach, R «Wolf–Hirschhorn syndrome facial dysmorphic features in a patient with a terminal 4p16.3 deletion telomeric to the WHSCR and WHSCR 2 regions». European Journal of Human Genetics, 17, 1, 01-2009, pàg. 129–132. DOI: 10.1038/ejhg.2008.168. ISSN: 1476-5438.
Chen, X; Tomchick, D; Kovrigin, E; Araç, D; Machius, M «Three-dimensional structure of the complexin/SNARE complex». Neuron, 33, 3, 31-01-2002, pàg. 397–409. DOI: 10.1016/s0896-6273(02)00583-4. ISSN: 0896-6273. PMID: 11832227.
Hao, T; Feng, N; Gong, F; Yu, Y; Liu, J «Complexin-1 regulated assembly of single neuronal SNARE complex revealed by single-molecule optical tweezers». Communications Biology, 6, 1, 07-02-2023, pàg. 155. DOI: 10.1038/s42003-023-04506-w. ISSN: 2399-3642. PMC: 9905088. PMID: 36750663.
Gong, J; Lai, Y; Li, X; Wang, M; Leitz, J «C-terminal domain of mammalian complexin-1 localizes to highly curved membranes» (en anglès). Proceedings of the National Academy of Sciences, 113, 47, 22-11-2016. DOI: 10.1073/pnas.1609917113. ISSN: 0027-8424. PMC: PMC5127347. PMID: 27821736.
McMahon, H. T.; Missler, M.; Li, C.; Südhof, T. C. «Complexins: cytosolic proteins that regulate SNAP receptor function». Cell, 83, 1, 06-10-1995, pàg. 111–119. DOI: 10.1016/0092-8674(95)90239-2. ISSN: 0092-8674. PMID: 7553862.
Xue, M; Craig, T; Xu, J; Chao, H; Rizo, J «Binding of the complexin N terminus to the SNARE complex potentiates synaptic-vesicle fusogenicity». Nature Structural & Molecular Biology, 17, 5, 05-2010, pàg. 568–575. DOI: 10.1038/nsmb.1791. ISSN: 1545-9985. PMC: 3172005. PMID: 20400951.
Chen, X; Tomchick, D; Kovrigin, E; Araç, D; Machius, M «Three-Dimensional Structure of the Complexin/SNARE Complex». Neuron, 33, 3, 31-01-2002, pàg. 397–409. DOI: 10.1016/S0896-6273(02)00583-4. ISSN: 0896-6273.
Hu, K; Carroll, J; Rickman, C; Davletov, B «Action of Complexin on SNARE Complex*». Journal of Biological Chemistry, 277, 44, 01-11-2002, pàg. 41652–41656. DOI: 10.1074/jbc.M205044200. ISSN: 0021-9258.
Dulubova, I.; Sugita, S; Hill, S; Hosaka, M; Fernandez, I «A conformational switch in syntaxin during exocytosis: role of munc18». The EMBO Journal, 18, 16, 16-08-1999, pàg. 4372–4382. DOI: 10.1093/emboj/18.16.4372. PMC: PMC1171512. PMID: 10449403.
Xu, Y; Zhao, X; Liu, J; Wang, Y; Xiong, L «Complexin I knockout rats exhibit a complex neurobehavioral phenotype including profound ataxia and marked deficits in lifespan». Pflugers Archiv: European Journal of Physiology, 472, 1, 01-2020, pàg. 117–133. DOI: 10.1007/s00424-019-02337-5. ISSN: 1432-2013. PMID: 31875236.
Glynn, D; Drew, C; Reim, K; Brose, N; Morton, A «Profound ataxia in complexin I knockout mice masks a complex phenotype that includes exploratory and habituation deficits». Human Molecular Genetics, 14, 16, 15-08-2005, pàg. 2369–2385. DOI: 10.1093/hmg/ddi239. ISSN: 0964-6906. PMID: 16000319.
Glynn, D; Sizemore, R; Morton, A «Early motor development is abnormal in complexin 1 knockout mice». Neurobiology of Disease, 25, 3, 03-2007, pàg. 483–495. DOI: 10.1016/j.nbd.2006.10.011. ISSN: 0969-9961. PMID: 17188502.
Redler, S; Strom, T; Wieland, T; Cremer, K; Engels, H «Variants in CPLX1 in two families with autosomal-recessive severe infantile myoclonic epilepsy and ID». European Journal of Human Genetics, 25, 7, 07-2017, pàg. 889–893. DOI: 10.1038/ejhg.2017.52. ISSN: 1018-4813. PMC: 5520065. PMID: 28422131.
Karaca, E; Harel, T; Pehlivan, D; Jhangiani, S; Gambin, T «Genes that affect brain structure and function identified by rare variant analyses of Mendelian neurologic disease». Neuron, 88, 3, 04-11-2015, pàg. 499–513. DOI: 10.1016/j.neuron.2015.09.048. ISSN: 0896-6273. PMC: 4824012. PMID: 26539891.
Cali, E; Rocca, C; Salpietro, V; Houlden, H «Epileptic Phenotypes Associated With SNAREs and Related Synaptic Vesicle Exocytosis Machinery». Frontiers in Neurology, 12, 13-01-2022. DOI: 10.3389/fneur.2021.806506. ISSN: 1664-2295. PMC: PMC8792400. PMID: 35095745.
Khan, A; Akram, M; Daniyal, M; Zainab, R «Awareness and current knowledge of Parkinson's disease: a neurodegenerative disorder». The International Journal of Neuroscience, 129, 1, 01-2019, pàg. 55–93. DOI: 10.1080/00207454.2018.1486837. ISSN: 1563-5279. PMID: 29883227.
Huang, Y; Liu, Z; Li, N; Tian, C; Yang, H «Parkinson's Disease Derived Exosomes Aggravate Neuropathology in SNCA*A53T Mice». Annals of Neurology, 92, 2, 08-2022, pàg. 230–245. DOI: 10.1002/ana.26421. ISSN: 1531-8249. PMID: 35596947.
Lahut, S; Gispert, S; Ömür, Ö; Depboylu, C; Seidel, K «Blood RNA biomarkers in prodromal PARK4 and rapid eye movement sleep behavior disorder show role of complexin 1 loss for risk of Parkinson's disease». Disease Models & Mechanisms, 10, 5, 01-05-2017, pàg. 619–631. DOI: 10.1242/dmm.028035. ISSN: 1754-8411. PMC: 5451169. PMID: 28108469.
Gispert, S; Kurz, A; Brehm, N; Rau, K; Walter, M «Complexin-1 and Foxp1 Expression Changes Are Novel Brain Effects of Alpha-Synuclein Pathology». Molecular Neurobiology, 52, 1, 12-08-2014, pàg. 57–63. DOI: 10.1007/s12035-014-8844-0. ISSN: 0893-7648. PMC: 4510914. PMID: 25112678.
Lill, C; Roehr, J; McQueen, M; Kavvoura, F; Bagade, S «Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database». PLoS Genetics, 8, 3, 15-03-2012, pàg. e1002548. DOI: 10.1371/journal.pgen.1002548. ISSN: 1553-7390. PMC: 3305333. PMID: 22438815.
Tanaka, H; Kanda, M; Shimizu, D; Tanaka, C; Inokawa, Y «Transcriptomic profiling on localized gastric cancer identified CPLX1 as a gene promoting malignant phenotype of gastric cancer and a predictor of recurrence after surgery and subsequent chemotherapy» (en anglès). Journal of Gastroenterology, 57, 9, 01-09-2022, pàg. 640–653. DOI: 10.1007/s00535-022-01884-6. ISSN: 1435-5922.
Tolios, A.; De Las Rivas, J.; Hovig, E.; Trouillas, P.; Scorilas, A. «Computational approaches in cancer multidrug resistance research: Identification of potential biomarkers, drug targets and drug-target interactions». Drug Resistance Updates, 48, 01-01-2020, pàg. 100662. DOI: 10.1016/j.drup.2019.100662. ISSN: 1368-7646.

doi.org

Tanaka, H; Kanda, M; Shimizu, D; Tanaka, C; Inokawa, Y «Transcriptomic profiling on localized gastric cancer identified CPLX1 as a gene promoting malignant phenotype of gastric cancer and a predictor of recurrence after surgery and subsequent chemotherapy» (en anglès). Journal of Gastroenterology, 57, 9, 01-09-2022, pàg. 640–653. DOI: 10.1007/s00535-022-01884-6. ISSN: 1435-5922.

embopress.org

emboj.embopress.org

Dulubova, I.; Sugita, S; Hill, S; Hosaka, M; Fernandez, I «A conformational switch in syntaxin during exocytosis: role of munc18». The EMBO Journal, 18, 16, 16-08-1999, pàg. 4372–4382. DOI: 10.1093/emboj/18.16.4372. PMC: PMC1171512. PMID: 10449403.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000168993 - Ensembl, May 2017

feb2023.archive.ensembl.org

«Gene: CPLX1 (ENSG00000168993) - Summary - Homo_sapiens - Ensembl genome browser 109». Ensembl project, 02-2023. [Consulta: 21 octubre 2023].

frontiersin.org

Cali, E; Rocca, C; Salpietro, V; Houlden, H «Epileptic Phenotypes Associated With SNAREs and Related Synaptic Vesicle Exocytosis Machinery». Frontiers in Neurology, 12, 13-01-2022. DOI: 10.3389/fneur.2021.806506. ISSN: 1664-2295. PMC: PMC8792400. PMID: 35095745.

genecards.org

«CPLX1 Gene - Complexin 1». Gene Cards - The human gene database, 04-10-2023. [Consulta: 21 octubre 2023].

geneontology.org

amigo.geneontology.org

«AmiGO 2: Search CPLX1». AmiGO, Gene Ontology Consortium, 10-2023. [Consulta: 29 octubre 2023].

nature.com

Engbers, H; van der Smagt, J; van ‘t Slot, R; Vermeesch, J; Hochstenbach, R «Wolf–Hirschhorn syndrome facial dysmorphic features in a patient with a terminal 4p16.3 deletion telomeric to the WHSCR and WHSCR 2 regions». European Journal of Human Genetics, 17, 1, 01-2009, pàg. 129–132. DOI: 10.1038/ejhg.2008.168. ISSN: 1476-5438.

nih.gov

ncbi.nlm.nih.gov

«Human PubMed Reference:». National Center for Biotechnology Information, U.S. National Library of Medicine.
«Mouse PubMed Reference:». National Center for Biotechnology Information, U.S. National Library of Medicine.
McMahon, H. T.; Missler, M.; Li, C.; Südhof, T. C. «Complexins: cytosolic proteins that regulate SNAP receptor function». Cell, 83, 1, 06-10-1995, pàg. 111–119. DOI: 10.1016/0092-8674(95)90239-2. ISSN: 0092-8674. PMID: 7553862.
Bućan, M.; Zimmer, M.; Whaley, W. L.; Poustka, A.; Youngman, S. «Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation». Genomics, 6, 1, 01-1990, pàg. 1–15. DOI: 10.1016/0888-7543(90)90442-w. ISSN: 0888-7543. PMID: 2137426.
«CPLX1 complexin 1 [Homo sapiens (human) - Gene - NCBI]». National Library of Medicine, 10-10-2023. [Consulta: 12 octubre 2023].
Chen, X; Tomchick, D; Kovrigin, E; Araç, D; Machius, M «Three-dimensional structure of the complexin/SNARE complex». Neuron, 33, 3, 31-01-2002, pàg. 397–409. DOI: 10.1016/s0896-6273(02)00583-4. ISSN: 0896-6273. PMID: 11832227.
Hao, T; Feng, N; Gong, F; Yu, Y; Liu, J «Complexin-1 regulated assembly of single neuronal SNARE complex revealed by single-molecule optical tweezers». Communications Biology, 6, 1, 07-02-2023, pàg. 155. DOI: 10.1038/s42003-023-04506-w. ISSN: 2399-3642. PMC: 9905088. PMID: 36750663.
Gong, J; Lai, Y; Li, X; Wang, M; Leitz, J «C-terminal domain of mammalian complexin-1 localizes to highly curved membranes» (en anglès). Proceedings of the National Academy of Sciences, 113, 47, 22-11-2016. DOI: 10.1073/pnas.1609917113. ISSN: 0027-8424. PMC: PMC5127347. PMID: 27821736.
McMahon, H. T.; Missler, M.; Li, C.; Südhof, T. C. «Complexins: cytosolic proteins that regulate SNAP receptor function». Cell, 83, 1, 06-10-1995, pàg. 111–119. DOI: 10.1016/0092-8674(95)90239-2. ISSN: 0092-8674. PMID: 7553862.
Xue, M; Craig, T; Xu, J; Chao, H; Rizo, J «Binding of the complexin N terminus to the SNARE complex potentiates synaptic-vesicle fusogenicity». Nature Structural & Molecular Biology, 17, 5, 05-2010, pàg. 568–575. DOI: 10.1038/nsmb.1791. ISSN: 1545-9985. PMC: 3172005. PMID: 20400951.
Dulubova, I.; Sugita, S; Hill, S; Hosaka, M; Fernandez, I «A conformational switch in syntaxin during exocytosis: role of munc18». The EMBO Journal, 18, 16, 16-08-1999, pàg. 4372–4382. DOI: 10.1093/emboj/18.16.4372. PMC: PMC1171512. PMID: 10449403.
Xu, Y; Zhao, X; Liu, J; Wang, Y; Xiong, L «Complexin I knockout rats exhibit a complex neurobehavioral phenotype including profound ataxia and marked deficits in lifespan». Pflugers Archiv: European Journal of Physiology, 472, 1, 01-2020, pàg. 117–133. DOI: 10.1007/s00424-019-02337-5. ISSN: 1432-2013. PMID: 31875236.
Glynn, D; Drew, C; Reim, K; Brose, N; Morton, A «Profound ataxia in complexin I knockout mice masks a complex phenotype that includes exploratory and habituation deficits». Human Molecular Genetics, 14, 16, 15-08-2005, pàg. 2369–2385. DOI: 10.1093/hmg/ddi239. ISSN: 0964-6906. PMID: 16000319.
Glynn, D; Sizemore, R; Morton, A «Early motor development is abnormal in complexin 1 knockout mice». Neurobiology of Disease, 25, 3, 03-2007, pàg. 483–495. DOI: 10.1016/j.nbd.2006.10.011. ISSN: 0969-9961. PMID: 17188502.
Redler, S; Strom, T; Wieland, T; Cremer, K; Engels, H «Variants in CPLX1 in two families with autosomal-recessive severe infantile myoclonic epilepsy and ID». European Journal of Human Genetics, 25, 7, 07-2017, pàg. 889–893. DOI: 10.1038/ejhg.2017.52. ISSN: 1018-4813. PMC: 5520065. PMID: 28422131.
Karaca, E; Harel, T; Pehlivan, D; Jhangiani, S; Gambin, T «Genes that affect brain structure and function identified by rare variant analyses of Mendelian neurologic disease». Neuron, 88, 3, 04-11-2015, pàg. 499–513. DOI: 10.1016/j.neuron.2015.09.048. ISSN: 0896-6273. PMC: 4824012. PMID: 26539891.
Cali, E; Rocca, C; Salpietro, V; Houlden, H «Epileptic Phenotypes Associated With SNAREs and Related Synaptic Vesicle Exocytosis Machinery». Frontiers in Neurology, 12, 13-01-2022. DOI: 10.3389/fneur.2021.806506. ISSN: 1664-2295. PMC: PMC8792400. PMID: 35095745.
Khan, A; Akram, M; Daniyal, M; Zainab, R «Awareness and current knowledge of Parkinson's disease: a neurodegenerative disorder». The International Journal of Neuroscience, 129, 1, 01-2019, pàg. 55–93. DOI: 10.1080/00207454.2018.1486837. ISSN: 1563-5279. PMID: 29883227.
Huang, Y; Liu, Z; Li, N; Tian, C; Yang, H «Parkinson's Disease Derived Exosomes Aggravate Neuropathology in SNCA*A53T Mice». Annals of Neurology, 92, 2, 08-2022, pàg. 230–245. DOI: 10.1002/ana.26421. ISSN: 1531-8249. PMID: 35596947.
Lahut, S; Gispert, S; Ömür, Ö; Depboylu, C; Seidel, K «Blood RNA biomarkers in prodromal PARK4 and rapid eye movement sleep behavior disorder show role of complexin 1 loss for risk of Parkinson's disease». Disease Models & Mechanisms, 10, 5, 01-05-2017, pàg. 619–631. DOI: 10.1242/dmm.028035. ISSN: 1754-8411. PMC: 5451169. PMID: 28108469.
Gispert, S; Kurz, A; Brehm, N; Rau, K; Walter, M «Complexin-1 and Foxp1 Expression Changes Are Novel Brain Effects of Alpha-Synuclein Pathology». Molecular Neurobiology, 52, 1, 12-08-2014, pàg. 57–63. DOI: 10.1007/s12035-014-8844-0. ISSN: 0893-7648. PMC: 4510914. PMID: 25112678.
Lill, C; Roehr, J; McQueen, M; Kavvoura, F; Bagade, S «Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database». PLoS Genetics, 8, 3, 15-03-2012, pàg. e1002548. DOI: 10.1371/journal.pgen.1002548. ISSN: 1553-7390. PMC: 3305333. PMID: 22438815.

pubmed.ncbi.nlm.nih.gov

McMahon, H. T.; Missler, M.; Li, C.; Südhof, T. C. «Complexins: cytosolic proteins that regulate SNAP receptor function». Cell, 83, 1, 06-10-1995, pàg. 111–119. DOI: 10.1016/0092-8674(95)90239-2. ISSN: 0092-8674. PMID: 7553862.
Bućan, M.; Zimmer, M.; Whaley, W. L.; Poustka, A.; Youngman, S. «Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation». Genomics, 6, 1, 01-1990, pàg. 1–15. DOI: 10.1016/0888-7543(90)90442-w. ISSN: 0888-7543. PMID: 2137426.
Chen, X; Tomchick, D; Kovrigin, E; Araç, D; Machius, M «Three-dimensional structure of the complexin/SNARE complex». Neuron, 33, 3, 31-01-2002, pàg. 397–409. DOI: 10.1016/s0896-6273(02)00583-4. ISSN: 0896-6273. PMID: 11832227.
Hao, T; Feng, N; Gong, F; Yu, Y; Liu, J «Complexin-1 regulated assembly of single neuronal SNARE complex revealed by single-molecule optical tweezers». Communications Biology, 6, 1, 07-02-2023, pàg. 155. DOI: 10.1038/s42003-023-04506-w. ISSN: 2399-3642. PMC: 9905088. PMID: 36750663.
McMahon, H. T.; Missler, M.; Li, C.; Südhof, T. C. «Complexins: cytosolic proteins that regulate SNAP receptor function». Cell, 83, 1, 06-10-1995, pàg. 111–119. DOI: 10.1016/0092-8674(95)90239-2. ISSN: 0092-8674. PMID: 7553862.
Xue, M; Craig, T; Xu, J; Chao, H; Rizo, J «Binding of the complexin N terminus to the SNARE complex potentiates synaptic-vesicle fusogenicity». Nature Structural & Molecular Biology, 17, 5, 05-2010, pàg. 568–575. DOI: 10.1038/nsmb.1791. ISSN: 1545-9985. PMC: 3172005. PMID: 20400951.
Xu, Y; Zhao, X; Liu, J; Wang, Y; Xiong, L «Complexin I knockout rats exhibit a complex neurobehavioral phenotype including profound ataxia and marked deficits in lifespan». Pflugers Archiv: European Journal of Physiology, 472, 1, 01-2020, pàg. 117–133. DOI: 10.1007/s00424-019-02337-5. ISSN: 1432-2013. PMID: 31875236.
Glynn, D; Drew, C; Reim, K; Brose, N; Morton, A «Profound ataxia in complexin I knockout mice masks a complex phenotype that includes exploratory and habituation deficits». Human Molecular Genetics, 14, 16, 15-08-2005, pàg. 2369–2385. DOI: 10.1093/hmg/ddi239. ISSN: 0964-6906. PMID: 16000319.
Glynn, D; Sizemore, R; Morton, A «Early motor development is abnormal in complexin 1 knockout mice». Neurobiology of Disease, 25, 3, 03-2007, pàg. 483–495. DOI: 10.1016/j.nbd.2006.10.011. ISSN: 0969-9961. PMID: 17188502.
Khan, A; Akram, M; Daniyal, M; Zainab, R «Awareness and current knowledge of Parkinson's disease: a neurodegenerative disorder». The International Journal of Neuroscience, 129, 1, 01-2019, pàg. 55–93. DOI: 10.1080/00207454.2018.1486837. ISSN: 1563-5279. PMID: 29883227.
Huang, Y; Liu, Z; Li, N; Tian, C; Yang, H «Parkinson's Disease Derived Exosomes Aggravate Neuropathology in SNCA*A53T Mice». Annals of Neurology, 92, 2, 08-2022, pàg. 230–245. DOI: 10.1002/ana.26421. ISSN: 1531-8249. PMID: 35596947.
Lahut, S; Gispert, S; Ömür, Ö; Depboylu, C; Seidel, K «Blood RNA biomarkers in prodromal PARK4 and rapid eye movement sleep behavior disorder show role of complexin 1 loss for risk of Parkinson's disease». Disease Models & Mechanisms, 10, 5, 01-05-2017, pàg. 619–631. DOI: 10.1242/dmm.028035. ISSN: 1754-8411. PMC: 5451169. PMID: 28108469.

pnas.org

Gong, J; Lai, Y; Li, X; Wang, M; Leitz, J «C-terminal domain of mammalian complexin-1 localizes to highly curved membranes» (en anglès). Proceedings of the National Academy of Sciences, 113, 47, 22-11-2016. DOI: 10.1073/pnas.1609917113. ISSN: 0027-8424. PMC: PMC5127347. PMID: 27821736.

sciencedirect.com

Chen, X; Tomchick, D; Kovrigin, E; Araç, D; Machius, M «Three-Dimensional Structure of the Complexin/SNARE Complex». Neuron, 33, 3, 31-01-2002, pàg. 397–409. DOI: 10.1016/S0896-6273(02)00583-4. ISSN: 0896-6273.
Hu, K; Carroll, J; Rickman, C; Davletov, B «Action of Complexin on SNARE Complex*». Journal of Biological Chemistry, 277, 44, 01-11-2002, pàg. 41652–41656. DOI: 10.1074/jbc.M205044200. ISSN: 0021-9258.
Tolios, A.; De Las Rivas, J.; Hovig, E.; Trouillas, P.; Scorilas, A. «Computational approaches in cancer multidrug resistance research: Identification of potential biomarkers, drug targets and drug-target interactions». Drug Resistance Updates, 48, 01-01-2020, pàg. 100662. DOI: 10.1016/j.drup.2019.100662. ISSN: 1368-7646.

sinobiological.com

«CPLX1 Protein Overview: Sequence, Structure, Function and Protein Interaction». SinoBiological, 03-2023. [Consulta: 21 octubre 2023].

worldcat.org

McMahon, H. T.; Missler, M.; Li, C.; Südhof, T. C. «Complexins: cytosolic proteins that regulate SNAP receptor function». Cell, 83, 1, 06-10-1995, pàg. 111–119. DOI: 10.1016/0092-8674(95)90239-2. ISSN: 0092-8674. PMID: 7553862.
Bućan, M.; Zimmer, M.; Whaley, W. L.; Poustka, A.; Youngman, S. «Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation». Genomics, 6, 1, 01-1990, pàg. 1–15. DOI: 10.1016/0888-7543(90)90442-w. ISSN: 0888-7543. PMID: 2137426.
Engbers, H; van der Smagt, J; van ‘t Slot, R; Vermeesch, J; Hochstenbach, R «Wolf–Hirschhorn syndrome facial dysmorphic features in a patient with a terminal 4p16.3 deletion telomeric to the WHSCR and WHSCR 2 regions». European Journal of Human Genetics, 17, 1, 01-2009, pàg. 129–132. DOI: 10.1038/ejhg.2008.168. ISSN: 1476-5438.
Chen, X; Tomchick, D; Kovrigin, E; Araç, D; Machius, M «Three-dimensional structure of the complexin/SNARE complex». Neuron, 33, 3, 31-01-2002, pàg. 397–409. DOI: 10.1016/s0896-6273(02)00583-4. ISSN: 0896-6273. PMID: 11832227.
Hao, T; Feng, N; Gong, F; Yu, Y; Liu, J «Complexin-1 regulated assembly of single neuronal SNARE complex revealed by single-molecule optical tweezers». Communications Biology, 6, 1, 07-02-2023, pàg. 155. DOI: 10.1038/s42003-023-04506-w. ISSN: 2399-3642. PMC: 9905088. PMID: 36750663.
Gong, J; Lai, Y; Li, X; Wang, M; Leitz, J «C-terminal domain of mammalian complexin-1 localizes to highly curved membranes» (en anglès). Proceedings of the National Academy of Sciences, 113, 47, 22-11-2016. DOI: 10.1073/pnas.1609917113. ISSN: 0027-8424. PMC: PMC5127347. PMID: 27821736.
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