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Cell Communication & Adhesion Volume 10, 2003 - Issue 1
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Research Article

Expression Profiles of the Novel Human Connexin Genes hCx30.2, hCx40.1, and hCx62 Differ from Their Putative Mouse Orthologues

Goran Söhl Institut für Genetik, Abteilung Molekulargenetik, Universität Bonn, Bonn, Germany
,
Peter A. Nielsen Department of Cell Biology, The Scripps Research Institute, La Jolla, CA, USA
,
Jürgen Eiberger Institut für Genetik, Abteilung Molekulargenetik, Universität Bonn, Bonn, Germany
&
Klaus Willecke Institut für Genetik, Abteilung Molekulargenetik, Universität Bonn, Bonn, Germany
Pages 27-36 | Published online: 11 Jul 2009

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Véronique Cruciani, Karen-Marie Heintz, Trine Husøy, Eivind Hovig, David J. Warren & Svein-Ole Mikalsen. (2004) The Detection of Hamster Connexins: A Comparison of Expression Profiles with Wild-Type Mouse and the Cancer-Prone Min Mouse. Cell Communication & Adhesion 11:5-6, pages 155-171.
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Goran Söhl & Klaus Willecke. (2003) An Update on Connexin Genes and their Nomenclature in Mouse and Man. Cell Communication & Adhesion 10:4-6, pages 173-180.
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Articles from other publishers (16)

Sergiu A. Lucaciu, Stephanie E. Leighton, Alexandra Hauser, Ryan Yee & Dale W. Laird. (2023) Diversity in connexin biology. Journal of Biological Chemistry 299:11, pages 105263.
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Xuewen Wu, Wenjuan Zhang, Yihui Li & Xi Lin. (2019) Structure and Function of Cochlear Gap Junctions and Implications for the Translation of Cochlear Gene Therapies. Frontiers in Cellular Neuroscience 13.
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Xuan Tao, Yan Liang, Xuemei Yang, Jianhui Pang, Zhijun Zhong, Xiaohui Chen, Yuekui Yang, Kai Zeng, Runming Kang, Yunfeng Lei, Sancheng Ying, Jianjun Gong, Yiren Gu & Xuebin Lv. (2017) Transcriptomic profiling in muscle and adipose tissue identifies genes related to growth and lipid deposition. PLOS ONE 12:9, pages e0184120.
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Hui Ram Kim, Se-Kyung Oh, Eun-Shil Lee, Soo-Young Choi, Seung-Eon Roh, Sang Jeong Kim, Tomitake Tsukihara, Kyu-Yup Lee, Chang-Jin Jeon & Un-Kyung Kim. (2016) The pathological effects of connexin 26 variants related to hearing loss by in silico and in vitro analysis. Human Genetics 135:3, pages 287-298.
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Andrew Marsh, Katherine Casey-Green, Fay Probert, David Withall, Daniel A. Mitchell, Suzanne J. Dilly, Sean James, Wade Dimitri, Sweta R. Ladwa, Paul C. Taylor & Donald R. J. Singer. (2016) Simvastatin Sodium Salt and Fluvastatin Interact with Human Gap Junction Gamma-3 Protein. PLOS ONE 11:2, pages e0148266.
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Donglin Bai. (2016) Structural analysis of key gap junction domains—Lessons from genome data and disease-linked mutants. Seminars in Cell & Developmental Biology 50, pages 74-82.
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Lyubov Avshalumova, Jordan Fabrikant & Angie Koriakos. (2014) Overview of skin diseases linked to connexin gene mutations. International Journal of Dermatology 53:2, pages 192-205.
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Ching-Chyuan Su, Shuan-Yow Li, Yung-Chang Yen, Jhih-Hao Nian, Wei-Guang Liang & Jiann-Jou Yang. (2012) Mechanism of Two Novel Human GJC3 Missense Mutations in Causing Non-Syndromic Hearing Loss. Cell Biochemistry and Biophysics 66:2, pages 277-286.
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Hiromi Hirata, Hua Wen, Yu Kawakami, Yuriko Naganawa, Kazutoyo Ogino, Kenta Yamada, Louis Saint-Amant, Sean E. Low, Wilson W. Cui, Weibin Zhou, Shawn M. Sprague, Kazuhide Asakawa, Akira Muto, Koichi Kawakami & John Y. Kuwada. (2012) Connexin 39.9 Protein Is Necessary for Coordinated Activation of Slow-twitch Muscle and Normal Behavior in Zebrafish. Journal of Biological Chemistry 287:2, pages 1080-1089.
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Goran Söhl, Antonia Joussen, Norbert Kociok & Klaus Willecke. (2010) Expression of connexin genes in the human retina. BMC Ophthalmology 10:1.
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Alessandro De Luca, Anna Sarkozy, Federica Consoli, Andrea De Zorzi, Rita Mingarelli, Maria Cristina Digilio, Bruno Marino & Bruno Dallapiccola. (2010) Exclusion of Cx43 gene mutation as a major cause of criss-cross heart anomaly in man. International Journal of Cardiology 144:2, pages 300-302.
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Jack R. Lee & Thomas W. White. (2009) Connexin-26 mutations in deafness and skin disease. Expert Reviews in Molecular Medicine 11.
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Maria M. Kreuzberg, Marcus Liebermann, Sara Segschneider, Radoslaw Dobrowolski, Halina Dobrzynski, Riyaz Kaba, Giselle Rowlinson, Emmanuel Dupont, Nicholas J. Severs & Klaus Willecke. (2009) Human connexin31.9, unlike its orthologous protein connexin30.2 in the mouse, is not detectable in the human cardiac conduction system. Journal of Molecular and Cellular Cardiology 46:4, pages 553-559.
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Radoslaw DobrowolskiKlaus Willecke. (2009) Connexin-Caused Genetic Diseases and Corresponding Mouse Models. Antioxidants & Redox Signaling 11:2, pages 283-296.
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Daniel B. Gros, Sébastien Alcoléa, Laurent Dupays, Sonia Meysen, Magali Théveniau-Ruissy, Birgit E.J. Teunissen & Marti F.A. Bierhuizen. 2005. Gap Junctions in Development and Disease. Gap Junctions in Development and Disease 29 55 .
Goran Söhl, Benjamin Odermatt, Stephan Maxeiner, Joachim Degen & Klaus Willecke. (2004) New insights into the expression and function of neural connexins with transgenic mouse mutants. Brain Research Reviews 47:1-3, pages 245-259.
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