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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1995 2
1998 1
2000 3
2001 1
2002 1
2003 1
2004 3
2005 1
2006 3
2007 2
2009 1
2010 1
2011 1
2013 1
2024 1

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PubMed (cited) for id: 600543

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Page 1
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19.
Takahashi Y, Fukuda Y, Yoshimura J, Toyoda A, Kurppa K, Moritoyo H, Belzil VV, Dion PA, Higasa K, Doi K, Ishiura H, Mitsui J, Date H, Ahsan B, Matsukawa T, Ichikawa Y, Moritoyo T, Ikoma M, Hashimoto T, Kimura F, Murayama S, Onodera O, Nishizawa M, Yoshida M, Atsuta N, Sobue G; JaCALS; Fifita JA, Williams KL, Blair IP, Nicholson GA, Gonzalez-Perez P, Brown RH Jr, Nomoto M, Elenius K, Rouleau GA, Fujiyama A, Morishita S, Goto J, Tsuji S. Takahashi Y, et al. Am J Hum Genet. 2013 Nov 7;93(5):900-5. doi: 10.1016/j.ajhg.2013.09.008. Epub 2013 Oct 10. Am J Hum Genet. 2013. PMID: 24119685 Free PMC article.
Neuregulin-1 enhances depolarization-induced GABA release.
Woo RS, Li XM, Tao Y, Carpenter-Hyland E, Huang YZ, Weber J, Neiswender H, Dong XP, Wu J, Gassmann M, Lai C, Xiong WC, Gao TM, Mei L. Woo RS, et al. Neuron. 2007 May 24;54(4):599-610. doi: 10.1016/j.neuron.2007.04.009. Neuron. 2007. PMID: 17521572 Free article.
23 results