PubMed (OMIM) for id: 4094

Year	Number of Results
1974	1
1983	1
1989	1
1996	2
1997	1
1998	1
1999	1
2000	1
2002	3
2003	1
2006	1
2007	3
2009	1
2011	1
2012	1
2014	1
2015	2
2018	1
2024	0

1

Induction and transcriptional regulation of the co-inhibitory gene module in T cells.

Chihara N, Madi A, Kondo T, Zhang H, Acharya N, Singer M, Nyman J, Marjanovic ND, Kowalczyk MS, Wang C, Kurtulus S, Law T, Etminan Y, Nevin J, Buckley CD, Burkett PR, Buenrostro JD, Rozenblatt-Rosen O, Anderson AC, Regev A, Kuchroo VK. Chihara N, et al. Nature. 2018 Jun;558(7710):454-459. doi: 10.1038/s41586-018-0206-z. Epub 2018 Jun 13. Nature. 2018. PMID: 29899446 Free PMC article.

2

Mutations Impairing GSK3-Mediated MAF Phosphorylation Cause Cataract, Deafness, Intellectual Disability, Seizures, and a Down Syndrome-like Facies.

Niceta M, Stellacci E, Gripp KW, Zampino G, Kousi M, Anselmi M, Traversa A, Ciolfi A, Stabley D, Bruselles A, Caputo V, Cecchetti S, Prudente S, Fiorenza MT, Boitani C, Philip N, Niyazov D, Leoni C, Nakane T, Keppler-Noreuil K, Braddock SR, Gillessen-Kaesbach G, Palleschi A, Campeau PM, Lee BH, Pouponnot C, Stella L, Bocchinfuso G, Katsanis N, Sol-Church K, Tartaglia M. Niceta M, et al. Am J Hum Genet. 2015 May 7;96(5):816-25. doi: 10.1016/j.ajhg.2015.03.001. Epub 2015 Apr 9. Am J Hum Genet. 2015. PMID: 25865493 Free PMC article.

3

The long intergenic noncoding RNA landscape of human lymphocytes highlights the regulation of T cell differentiation by linc-MAF-4.

Ranzani V, Rossetti G, Panzeri I, Arrigoni A, Bonnal RJ, Curti S, Gruarin P, Provasi E, Sugliano E, Marconi M, De Francesco R, Geginat J, Bodega B, Abrignani S, Pagani M. Ranzani V, et al. Nat Immunol. 2015 Mar;16(3):318-325. doi: 10.1038/ni.3093. Epub 2015 Jan 26. Nat Immunol. 2015. PMID: 25621826 Free PMC article.

4

Identification of a novel missense mutation of MAF in a Japanese family with congenital cataract by whole exome sequencing: a clinical report and review of literature.

Narumi Y, Nishina S, Tokimitsu M, Aoki Y, Kosaki R, Wakui K, Azuma N, Murata T, Takada F, Fukushima Y, Kosho T. Narumi Y, et al. Am J Med Genet A. 2014 May;164A(5):1272-6. doi: 10.1002/ajmg.a.36433. Epub 2014 Mar 24. Am J Med Genet A. 2014. PMID: 24664492 Review.

5

The transcription factor c-Maf controls touch receptor development and function.

Wende H, Lechner SG, Cheret C, Bourane S, Kolanczyk ME, Pattyn A, Reuter K, Munier FL, Carroll P, Lewin GR, Birchmeier C. Wende H, et al. Science. 2012 Mar 16;335(6074):1373-6. doi: 10.1126/science.1214314. Epub 2012 Feb 16. Science. 2012. PMID: 22345400

6

Marked induction of c-Maf protein during Th17 cell differentiation and its implication in memory Th cell development.

Sato K, Miyoshi F, Yokota K, Araki Y, Asanuma Y, Akiyama Y, Yoh K, Takahashi S, Aburatani H, Mimura T. Sato K, et al. J Biol Chem. 2011 Apr 29;286(17):14963-71. doi: 10.1074/jbc.M111.218867. Epub 2011 Mar 14. J Biol Chem. 2011. PMID: 21402704 Free PMC article.

7

MafB/c-Maf deficiency enables self-renewal of differentiated functional macrophages.

Aziz A, Soucie E, Sarrazin S, Sieweke MH. Aziz A, et al. Science. 2009 Nov 6;326(5954):867-71. doi: 10.1126/science.1176056. Science. 2009. PMID: 19892988

8

Novel MAF mutation in a family with congenital cataract-microcornea syndrome.

Hansen L, Eiberg H, Rosenberg T. Hansen L, et al. Mol Vis. 2007 Oct 18;13:2019-22. Mol Vis. 2007. PMID: 17982426

9

Syndrome of congenital cataracts, sensorineural deafness, Down syndrome-like facial appearance, short stature, and mental retardation: two additional cases.

Keppler-Noreuil K, Welch J, Baker-Lange K. Keppler-Noreuil K, et al. Am J Med Genet A. 2007 Nov 1;143A(21):2581-7. doi: 10.1002/ajmg.a.31990. Am J Med Genet A. 2007. PMID: 17935251

10

A heterozygous c-Maf transactivation domain mutation causes congenital cataract and enhances target gene activation.

Perveen R, Favor J, Jamieson RV, Ray DW, Black GC. Perveen R, et al. Hum Mol Genet. 2007 May 1;16(9):1030-8. doi: 10.1093/hmg/ddm048. Epub 2007 Mar 20. Hum Mol Genet. 2007. PMID: 17374726

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