PubMed (OMIM) for id: 1600

Year	Number of Results
1997	3
1998	1
1999	2
2000	1
2001	1
2002	1
2003	1
2004	1
2005	1
2006	1
2008	1
2010	1
2013	1
2017	1
2018	2
2024	0

1

Endothelial Dab1 signaling orchestrates neuro-glia-vessel communication in the central nervous system.

Segarra M, Aburto MR, Cop F, Llaó-Cid C, Härtl R, Damm M, Bethani I, Parrilla M, Husainie D, Schänzer A, Schlierbach H, Acker T, Mohr L, Torres-Masjoan L, Ritter M, Acker-Palmer A. Segarra M, et al. Science. 2018 Aug 24;361(6404):eaao2861. doi: 10.1126/science.aao2861. Science. 2018. PMID: 30139844

2

Clinical, genetic and neuropathological characterization of spinocerebellar ataxia type 37.

Corral-Juan M, Serrano-Munuera C, Rábano A, Cota-González D, Segarra-Roca A, Ispierto L, Cano-Orgaz AT, Adarmes AD, Méndez-Del-Barrio C, Jesús S, Mir P, Volpini V, Alvarez-Ramo R, Sánchez I, Matilla-Dueñas A. Corral-Juan M, et al. Brain. 2018 Jul 1;141(7):1981-1997. doi: 10.1093/brain/awy137. Brain. 2018. PMID: 29939198 Free article.

3

A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia.

Seixas AI, Loureiro JR, Costa C, Ordóñez-Ugalde A, Marcelino H, Oliveira CL, Loureiro JL, Dhingra A, Brandão E, Cruz VT, Timóteo A, Quintáns B, Rouleau GA, Rizzu P, Carracedo Á, Bessa J, Heutink P, Sequeiros J, Sobrido MJ, Coutinho P, Silveira I. Seixas AI, et al. Am J Hum Genet. 2017 Jul 6;101(1):87-103. doi: 10.1016/j.ajhg.2017.06.007. Am J Hum Genet. 2017. PMID: 28686858 Free PMC article.

4

New subtype of spinocerebellar ataxia with altered vertical eye movements mapping to chromosome 1p32.

Serrano-Munuera C, Corral-Juan M, Stevanin G, San Nicolás H, Roig C, Corral J, Campos B, de Jorge L, Morcillo-Suárez C, Navarro A, Forlani S, Durr A, Kulisevsky J, Brice A, Sánchez I, Volpini V, Matilla-Dueñas A. Serrano-Munuera C, et al. JAMA Neurol. 2013 Jun;70(6):764-71. doi: 10.1001/jamaneurol.2013.2311. JAMA Neurol. 2013. PMID: 23700170

5

Reelin and stk25 have opposing roles in neuronal polarization and dendritic Golgi deployment.

Matsuki T, Matthews RT, Cooper JA, van der Brug MP, Cookson MR, Hardy JA, Olson EC, Howell BW. Matsuki T, et al. Cell. 2010 Nov 24;143(5):826-36. doi: 10.1016/j.cell.2010.10.029. Cell. 2010. PMID: 21111240 Free PMC article.

6

Disabled-1 is a large common fragile site gene, inactivated in multiple cancers.

McAvoy S, Zhu Y, Perez DS, James CD, Smith DI. McAvoy S, et al. Genes Chromosomes Cancer. 2008 Feb;47(2):165-74. doi: 10.1002/gcc.20519. Genes Chromosomes Cancer. 2008. PMID: 18008369

7

Mouse Disabled1 (DAB1) is a nucleocytoplasmic shuttling protein.

Honda T, Nakajima K. Honda T, et al. J Biol Chem. 2006 Dec 15;281(50):38951-65. doi: 10.1074/jbc.M609061200. Epub 2006 Oct 23. J Biol Chem. 2006. PMID: 17062576 Free article.

8

Signaling through Disabled 1 requires phosphoinositide binding.

Huang Y, Shah V, Liu T, Keshvara L. Huang Y, et al. Biochem Biophys Res Commun. 2005 Jun 17;331(4):1460-8. doi: 10.1016/j.bbrc.2005.04.064. Biochem Biophys Res Commun. 2005. PMID: 15883038

9

Disabled-1-regulated adhesion of migrating neurons to radial glial fiber contributes to neuronal positioning during early corticogenesis.

Sanada K, Gupta A, Tsai LH. Sanada K, et al. Neuron. 2004 Apr 22;42(2):197-211. doi: 10.1016/s0896-6273(04)00222-3. Neuron. 2004. PMID: 15091337 Free article.

10

The gene encoding disabled-1 (DAB1), the intracellular adaptor of the Reelin pathway, reveals unusual complexity in human and mouse.

Bar I, Tissir F, Lambert de Rouvroit C, De Backer O, Goffinet AM. Bar I, et al. J Biol Chem. 2003 Feb 21;278(8):5802-12. doi: 10.1074/jbc.M207178200. Epub 2002 Nov 21. J Biol Chem. 2003. PMID: 12446734 Free article.

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