Citations for
1EML1
EML1 is essential for retinal photoreceptor migration and survival.
Poria D, Sun C, Santeford A, Kielar M, Apte RS, Kisselev OG, Chen S, Kefalov VJ.
Sci Rep. Feb 21;12(1):2897. doi: 10.1038/s41598-022-06571-3. 2022
2EML1, H4C5
Genetic variants of EML1 and HIST1H4E in myeloid cell-related pathway genes independently predict cutaneous melanoma-specific survival
He Y, Liu H, Luo S, Amos CI, Lee JE, Yang K, Qureshi AA, Han J, Wei Q.
Am J Cancer Res. Jun 15;11(6):3252-3262. 2021
3EML1, OVGRH
A novel missense variant in the EML1 gene associated with bilateral ribbon-like subcortical heterotopia leads to ciliary defects
Markus F, Kannengießer A, Näder P, Atigbire P, Scholten A, Vössing C, Bültmann E, Korenke GC, Owczarek-Lipska M, Neidhardt J.
J Hum Genet. Dec;66(12):1159-1167. doi: 10.1038/s10038-021-00947-5. Epub 2021 Jul 1. 2021
4EML1
Disruption in murine Eml1 perturbs retinal lamination during early development.
Collin GB, Won J, Krebs MP, Hicks WJ, Charette JR, Naggert JK, Nishina PM.
Sci Rep. Mar 27;10(1):5647. doi: 10.1038/s41598-020-62373-5. 2020
5EML1, OVGRH
EML1-associated brain overgrowth syndrome with ribbon-like heterotopia.
Oegema R, McGillivray G, Leventer R, Le Moing AG, Bahi-Buisson N, Barnicoat A, Mandelstam S, Francis D, Francis F, Mancini GMS, Savelberg S, van Haaften G, Mankad K, Lequin MH.
Am J Med Genet C Semin Med Genet. Dec;181(4):627-637. doi: 10.1002/ajmg.c.31751. Epub 2019 Nov 11. 2019
6EML1
Mutations in the Heterotopia Gene Eml1/EML1 Severely Disrupt the Formation of Primary Cilia
Uzquiano A, Cifuentes-Diaz C, Jabali A, Romero DM, Houllier A, Dingli F, Maillard C, Boland A, Deleuze JF, Loew D, Mancini GMS, Bahi-Buisson N, Ladewig J, Francis F.
Cell Rep. Aug 6;28(6):1596-1611.e10. doi: 10.1016/j.celrep.2019.06.096. 2019
7EML1
Eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex
Bizzotto S, Uzquiano A, Dingli F, Ershov D, Houllier A, Arras G, Richards M, Loew D, Minc N, Croquelois A, Houdusse A, Francis F.
Sci Rep. Dec 11;7(1):17308. doi: 10.1038/s41598-017-15253-4. 2017
8EML1
The genetic landscape of familial congenital hydrocephalus
Shaheen R, Sebai MA, Patel N, Ewida N, Kurdi W, Altweijri I, Sogaty S, Almardawi E, Seidahmed MZ, Alnemri A, Madirevula S, Ibrahim N, Abdulwahab F, Hashem M, Al-Sheddi T, Alomar R, Alobeid E, Sallout B, AlBaqawi B, AlAali W, Ajaji N, Lesmana H, Hopkin RJ, Dupuis L, Mendoza-Londono R, Al Rukban H, Yoon G, Faqeih E, Alkuraya FS.
Ann Neurol. Jun;81(6):890-897. doi: 10.1002/ana.24964 2017
9EML1, OVGRH
Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human
Kielar M, Tuy FP, Bizzotto S, Lebrand C, de Juan Romero C, Poirier K, Oegema R, Mancini GM, Bahi-Buisson N, Olaso R, Le Moing AG, Boutourlinsky K, Boucher D, Carpentier W, Berquin P, Deleuze JF, Belvindrah R, Borrell V, Welker E, Chelly J, Croquelois A, Francis F.
Nat Neurosci. Jul;17(7):923-33. doi: 10.1038/nn.3729. Epub 2014 May 25 2014
10EML1
EML1 (CNG-modulin) controls light sensitivity in darkness and under continuous illumination in zebrafish retinal cone photoreceptors
Korenbrot JI, Mehta M, Tserentsoodol N, Postlethwait JH, Rebrik TI.
J Neurosci. Nov 6;33(45):17763-76. doi: 10.1523/JNEUROSCI.2659-13.2013 2013
11ABL1, EML1
ABL1 fusion genes in hematological malignancies: a review.
De Braekeleer E, Douet-Guilbert N, Rowe D, Bown N, Morel F, Berthou C, Férec C, De Braekeleer M.
Eur J Haematol. May;86(5):361-71. doi: 10.1111/j.1600-0609.2011.01586.x. Epub 2011 Mar 23. 2011
12NUP214, ABL1, EML1
Fusion of EML1 to ABL1 in T-cell acute lymphoblastic leukemia with cryptic t(9;14)(q34;q32).
De Keersmaecker K, Graux C, Odero MD, Mentens N, Somers R, Maertens J, Wlodarska I, Vandenberghe P, Hagemeijer A, Marynen P, Cools J.
Blood 105(12):4849-52. Epub 2005 Feb 15. 2005
13EML1
Identification of rat EMAP, a delta-glutamate receptor binding protein.
Ly CD, Roche KW, Lee HK, Wenthold RJ.
Biochem Biophys Res Commun 291(1):85-90. 2002
14EML1, EML2
Sequence and expression patterns of a human EMAP-related protein-2 (HuEMAP-2).
Lepley DM, Palange JM, Suprenant KA.
Gene 237(2):343-9. 1999
15EML1, USH1A
Isolation of a novel human homologue of the gene coding for echinoderm microtubule-associated protein (EMAP) from the Usher syndrome type 1a locus at 14q32.
Eudy JD, Ma-Edmonds M, Yao SF, Talmadge CB, Kelley PM, Weston MD, Kimberling WJ, Sumegi J.
Genomics 43(1):104-6. 1997