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For: Schulte D, Geerts D. MEIS transcription factors in development and disease. Development 2019;146:dev174706. [PMID: 31416930 DOI: 10.1242/dev.174706] [Cited by in Crossref: 28] [Cited by in F6Publishing: 31] [Article Influence: 9.3] [Reference Citation Analysis]
Number Citing Articles
1 Roussel J, Larcher R, Sicard P, Bideaux P, Richard S, Marmigère F, Thireau J. The autism-associated Meis2 gene is necessary for cardiac baroreflex regulation in mice. Sci Rep 2022;12:20150. [DOI: 10.1038/s41598-022-24616-5] [Reference Citation Analysis]
2 Diaz C, de la Torre MM, Rubenstein JLR, Puelles L. Dorsoventral Arrangement of Lateral Hypothalamus Populations in the Mouse Hypothalamus: a Prosomeric Genoarchitectonic Analysis. Mol Neurobiol 2022. [DOI: 10.1007/s12035-022-03043-7] [Reference Citation Analysis]
3 Roussel J, Larcher R, Sicard P, Bideaux P, Richard S, Marmigere F, Thireau J. The autism-associated Meis2 gene is necessary for cardiac baroreflex regulation in mice.. [DOI: 10.21203/rs.3.rs-2065006/v1] [Reference Citation Analysis]
4 Roussel J, Larcher R, Sicard P, Bideaux P, Richard S, Marmigère F, Thireau J. The autism-associated Meis2 gene is necessary for cardiac baroreflex regulation in mice.. [DOI: 10.1101/2022.09.14.507907] [Reference Citation Analysis]
5 Owa T, Shiraishi R, Adachi T, Miyashita S, Ichijo K, Nishioka T, Taya S, Kaibuchi K, Hoshino M. Homeodomain-less MEIS1 suppresses CUL3-dependent ATOH1 degradation to regulate cerebellar granule cell development.. [DOI: 10.1101/2022.08.17.504235] [Reference Citation Analysis]
6 Zhang B, Tarkhov AE, Ratzan W, Ying K, Moqri M, Poganik JR, Barre B, Trapp A, Zoller JA, Haghani A, Horvath S, Peshkin L, Gladyshev VN. Epigenetic profiling and incidence of disrupted development point to gastrulation as aging ground zero in Xenopus laevis.. [DOI: 10.1101/2022.08.02.502559] [Reference Citation Analysis]
7 Bae T, Fasching L, Wang Y, Shin JH, Suvakov M, Jang Y, Norton S, Dias C, Mariani J, Jourdon A, Wu F, Panda A, Pattni R, Chahine Y, Yeh R, Roberts RC, Huttner A, Kleinman JE, Hyde TM, Straub RE, Walsh CA, Urban AE, Leckman JF, Weinberger DR, Vaccarino FM, Abyzov A, Walsh CA, Park PJ, Sestan N, Weinberger D, Moran JV, Gage FH, Vaccarino FM, Gleeson J, Mathern G, Courchesne E, Roy S, Chess AJ, Akbarian S, Bizzotto S, Coulter M, Dias C, D'Gama A, Ganz J, Hill R, Huang AY, Khoshkhoo S, Kim S, Lee A, Lodato M, Maury EA, Miller M, Borges-Monroy R, Rodin R, Zhou Z, Bohrson C, Chu C, Cortes-Ciriano I, Dou Y, Galor A, Gulhan D, Kwon M, Luquette J, Sherman M, Viswanadham V, Jones A, Rosenbluh C, Cho S, Langmead B, Thorpe J, Erwin J, Jaffe A, McConnell M, Narurkar R, Paquola A, Shin J, Straub R, Abyzov A, Bae T, Jang Y, Wang Y, Molitor C, Peters M, Linker S, Reed P, Wang M, Urban A, Zhou B, Zhu X, Pattni R, Serres Amero A, Juan D, Lobon I, Marques-Bonet T, Solis Moruno M, Garcia Perez R, Povolotskaya I, Soriano E, Antaki D, Averbuj D, Ball L, Breuss M, Yang X, Chung C, Emery SB, Flasch DA, Kidd JM, Kopera HC, Kwan KY, Mills RE, Moldovan JB, Sun C, Zhao X, Zhou W, Frisbie TJ, Cherskov A, Fasching L, Jourdon A, Pochareddy S, Scuderi S; Brain Somatic Mosaicism Network§. Analysis of somatic mutations in 131 human brains reveals aging-associated hypermutability. Science 2022;377:511-7. [PMID: 35901164 DOI: 10.1126/science.abm6222] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
8 Zhong M, Huang Z, Wang X, Cai D, Li C, Gao F, Wu X, Wang W. A Transcription Factor Signature Can Identify the CMS4 Subtype and Stratify the Prognostic Risk of Colorectal Cancer. Front Oncol 2022;12:902974. [DOI: 10.3389/fonc.2022.902974] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Le Nabec A, Blotas C, Briset A, Collobert M, Férec C, Moisan S. 3D Chromatin Organization Involving MEIS1 Factor in the cis-Regulatory Landscape of GJB2. IJMS 2022;23:6964. [DOI: 10.3390/ijms23136964] [Reference Citation Analysis]
10 Isogai E, Okumura K, Saito M, Tokunaga Y, Wakabayashi Y. Meis1 plays roles in cortical development through regulation of cellular proliferative capacity in the embryonic cerebrum. Biomed Res 2022;43:91-7. [PMID: 35718449 DOI: 10.2220/biomedres.43.91] [Reference Citation Analysis]
11 Gutierrez J, Davis BA, Nevonen KA, Ward S, Carbone L, Maslen CL. DNA Methylation Analysis of Turner Syndrome BAV. Front Genet 2022;13:872750. [PMID: 35711915 DOI: 10.3389/fgene.2022.872750] [Reference Citation Analysis]
12 Prummel KD, Crowell HL, Nieuwenhuize S, Brombacher EC, Daetwyler S, Soneson C, Kresoja-Rakic J, Kocere A, Ronner M, Ernst A, Labbaf Z, Clouthier DE, Firulli AB, Sánchez-Iranzo H, Naganathan SR, O'Rourke R, Raz E, Mercader N, Burger A, Felley-Bosco E, Huisken J, Robinson MD, Mosimann C. Hand2 delineates mesothelium progenitors and is reactivated in mesothelioma. Nat Commun 2022;13:1677. [PMID: 35354817 DOI: 10.1038/s41467-022-29311-7] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
13 Fritsche K, Boccellato F, Schlaermann P, Koeppel M, Denecke C, Gut I, Meyer TF, Berger H. DNA methylation in human gastric epithelial cells allows cell type-related plasticity and defines regional identity.. [DOI: 10.1101/2022.03.29.486203] [Reference Citation Analysis]
14 Bae T, Fasching L, Wang Y, Shin JH, Suvakov M, Jang Y, Norton S, Dias C, Mariani J, Jourdon A, Wu F, Panda A, Roberts RC, Huttner A, Kleinman JE, Hyde TM, Straub RE, Walsh CA, Urban A, Leckman JF, Weinberger DR, Vaccarino FM, Abyzov A, Brain Somatic Mosaicism Network. Somatic mutations reveal hypermutable brains and are associated with neuropsychiatric disorders.. [DOI: 10.1101/2022.02.09.22269114] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Meriç N, Kocabaş F. The Historical Relationship Between Meis1 and Leukemia. Advances in Experimental Medicine and Biology 2022. [DOI: 10.1007/5584_2021_705] [Reference Citation Analysis]
16 Zhang B, Liu M, Fong C, Iqbal MA. MEIS2 (15q14) gene deletions in siblings with mild developmental phenotypes and bifid uvula: documentation of mosaicism in an unaffected parent. Mol Cytogenet 2021;14. [DOI: 10.1186/s13039-021-00570-1] [Reference Citation Analysis]
17 Lam DD, Nikolic AA, Zhao C, Mirza-Schreiber N, Krężel W, Oexle K, Winkelmann J. Intronic elements associated with insomnia and restless legs syndrome exhibit cell type-specific epigenetic features contributing to MEIS1 regulation. Hum Mol Genet 2021:ddab355. [PMID: 34888668 DOI: 10.1093/hmg/ddab355] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
18 Liu A, Han N, Munoz-muriedas J, Bender A. Deriving time-concordant event cascades from gene expression data: A case study for Drug-Induced Liver Injury (DILI).. [DOI: 10.1101/2021.09.23.461089] [Reference Citation Analysis]
19 Lam DD, Nikolic AA, Zhao C, Mirza-schreiber N, Krężel W, Oexle K, Winkelmann J. Intronic elements associated with insomnia and restless legs syndrome exhibit cell type-specific epigenetic features contributing to MEIS1 regulation.. [DOI: 10.1101/2021.09.03.458823] [Reference Citation Analysis]
20 Fabik J, Psutkova V, Machon O. The Mandibular and Hyoid Arches-From Molecular Patterning to Shaping Bone and Cartilage. Int J Mol Sci 2021;22:7529. [PMID: 34299147 DOI: 10.3390/ijms22147529] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
21 Durán Alonso MB, Vendrell V, López-Hernández I, Alonso MT, Martin DM, Giráldez F, Carramolino L, Giovinazzo G, Vázquez E, Torres M, Schimmang T. Meis2 Is Required for Inner Ear Formation and Proper Morphogenesis of the Cochlea. Front Cell Dev Biol 2021;9:679325. [PMID: 34124068 DOI: 10.3389/fcell.2021.679325] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
22 Dupacova N, Antosova B, Paces J, Kozmik Z. Meis homeobox genes control progenitor competence in the retina. Proc Natl Acad Sci U S A 2021;118:e2013136118. [PMID: 33723039 DOI: 10.1073/pnas.2013136118] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
23 Reichlmeir M, Elias L, Schulte D. Posttranslational Modifications in Conserved Transcription Factors: A Survey of the TALE-Homeodomain Superclass in Human and Mouse. Front Cell Dev Biol 2021;9:648765. [PMID: 33768097 DOI: 10.3389/fcell.2021.648765] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
24 Meng L, Tian Z, Wang J, Liu X, Zhang W, Hu M, Wang M, Zhang Y. Effect of myeloid ecotropic viral integration site (MEIS) family genes on tumor microenvironment remodeling and its potential therapeutic effect. Transl Androl Urol 2021;10:594-608. [PMID: 33718062 DOI: 10.21037/tau-20-1163] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
25 Winkelmann J, Schormair B. The genetics of restless legs syndrome. Reference Module in Neuroscience and Biobehavioral Psychology 2021. [DOI: 10.1016/b978-0-12-822963-7.00279-6] [Reference Citation Analysis]
26 Prummel KD, Crowell HL, Nieuwenhuize S, Brombacher EC, Daetwyler S, Soneson C, Kresoja-rakic J, Ronner M, Kocere A, Ernst A, Labbaf Z, Clouthier DE, Firulli AB, Sánchez-iranzo H, Naganathan SR, O’rourke R, Raz E, Mercader N, Burger A, Felley-bosco E, Huisken J, Robinson MD, Mosimann C. Hand2 delineates mesothelium progenitors and is reactivated in mesothelioma.. [DOI: 10.1101/2020.11.11.355693] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
27 Fabik J, Kovacova K, Kozmik Z, Machon O. Neural crest cells require Meis2 for patterning the mandibular arch via the Sonic hedgehog pathway. Biol Open 2020;9:bio052043. [PMID: 32616504 DOI: 10.1242/bio.052043] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
28 Yan W, Laboulaye MA, Tran NM, Whitney IE, Benhar I, Sanes JR. Mouse Retinal Cell Atlas: Molecular Identification of over Sixty Amacrine Cell Types. J Neurosci 2020;40:5177-95. [PMID: 32457074 DOI: 10.1523/JNEUROSCI.0471-20.2020] [Cited by in Crossref: 92] [Cited by in F6Publishing: 98] [Article Influence: 46.0] [Reference Citation Analysis]
29 Berenguer M, Meyer KF, Yin J, Duester G. Discovery of genes required for body axis and limb formation by global identification of retinoic acid-regulated epigenetic marks. PLoS Biol 2020;18:e3000719. [PMID: 32421711 DOI: 10.1371/journal.pbio.3000719] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 6.0] [Reference Citation Analysis]
30 Wang L, Tang Q, Xu J, Li H, Yang T, Li L, Machon O, Hu T, Chen Y. The transcriptional regulator MEIS2 sets up the ground state for palatal osteogenesis in mice. J Biol Chem 2020;295:5449-60. [PMID: 32169905 DOI: 10.1074/jbc.RA120.012684] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
31 Yan W, Laboulaye MA, Tran NM, Whitney IE, Benhar I, Sanes JR. Molecular identification of sixty-three amacrine cell types completes a mouse retinal cell atlas.. [DOI: 10.1101/2020.03.10.985770] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
32 Markitantova Y, Simirskii V. Inherited Eye Diseases with Retinal Manifestations through the Eyes of Homeobox Genes. Int J Mol Sci 2020;21:E1602. [PMID: 32111086 DOI: 10.3390/ijms21051602] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 7.5] [Reference Citation Analysis]