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Molekuliarnaia biologiia, ISSN 0026-8984, 05/2019, Volume 53, Issue 3, pp. 497 - 501
Journal Article
European journal of medical genetics, ISSN 1769-7212, 02/2019, p. 103627
Myeloid ecotropic insertion site 2 (MEIS2) gene, encoding a homeodomain-containing transcription factor, has been recently related to syndromic intellectual... 
Journal Article
Journal Article
Nature, ISSN 0028-0836, 2014, Volume 512, Issue 1, pp. 49 - 53
Journal Article
by Wang, MG and Wang, HT and Wen, YQ and Chen, XY and Liu, X and Gao, J and Su, P and Xu, YF and Zhou, W and Shi, LH and Zhou, JX
STEM CELL RESEARCH & THERAPY, ISSN 1757-6512, 12/2018, Volume 9, Issue 1, pp. 340 - 13
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 09/2018, Volume 176, Issue 9, pp. 1845 - 1851
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 02/2019, Volume 509, Issue 2, pp. 455 - 461
Calcific aortic valve disease (CAVD) is the most common valvular disease worldwide. The osteoblastic transdifferentiation of aortic valve interstitial cells... 
Aortic valve interstitial cells | Meis2 | Osteoblastic transdifferentiation | Calcific aortic valve disease | Notch1 | TRANSFORMATION | CLEFT-PALATE | ACTIVATION | ZEBRAFISH | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSCRIPTION | CARDIAC DEVELOPMENT | HOX | BIOPHYSICS | DISEASE | REGULATORS | LINEAGE
Journal Article
EXPERIMENTAL EYE RESEARCH, ISSN 0014-4835, 06/2013, Volume 111, pp. 112 - 121
Forkhead box C1 (FOXC1) is a transcription factor that affects eye development. FOXC1 is implicated in the etiology of glaucoma because mutations in the gene... 
TRANSCRIPTION FACTORS | FOXC1 | PROTEIN | ITG beta 1 | INTRAOCULAR-PRESSURE | MEIS2 | OPTIMEDIN | MISSENSE MUTATIONS | trabecular meshwork | AXENFELD-RIEGER-SYNDROME | GENE | OPHTHALMOLOGY | MiR-204 | PITX2 | GLAUCOMA | EXPRESSION
Journal Article
by Guan, L and Li, T and Ai, NP and Wang, W and He, B and Bai, YX and Yu, ZC and Li, MY and Dong, SS and Zhu, QG and Ding, XX and Zhang, SM and Li, M and Tang, GB and Xia, XC and Zhao, J and Lin, S and Yao, S and Zhang, L and Chen, G and Liu, FE and Li, XY and Zhang, HQ
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, ISSN 1756-9966, 10/2019, Volume 38, Issue 1, pp. 1 - 14
Background MEIS2 has been identified as one of the key transcription factors in the gene regulatory network in the development and pathogenesis of human... 
BREAST-CANCER | Alternative splicing | ONCOLOGY | CDC-73 | Hippo | PROSTATE-CANCER | GENE-EXPRESSION | HCC | TALE TRANSCRIPTION FACTORS | PROLIFERATION | Wnt | MEIS2 | Liver cancer | Medical prognosis | Genes | Cell division | Tumorigenesis | Neuroblastoma | Localization | Prostate | Patients | Binding sites | Deoxyribonucleic acid--DNA | Ovarian cancer
Journal Article
Journal of Ophthalmic and Vision Research, ISSN 2008-2010, 10/2017, Volume 12, Issue 4, pp. 407 - 412
We aimed to assess whether the transcription factor PAX6 affects transcription of . PAX6 is a transcription factor with significant roles in development of the... 
Glaucoma | Cytoskeleton | Care and treatment | Transcription factors | Research | Analysis | Medical research | Disease | Genomics | Genomes | Gene expression | Metabolism | Kinases | Studies | Proteins | Software | Mutation | Bioinformatics | Endocrinology | Binding sites | University colleges | FOXC1 | FMNL2 | PAX6 | Original | MEIS2 | Trabecular Meshwork | FMNL2; FOXC1; Glaucoma; MEIS2; PAX6; Trabecular Meshwork
Journal Article
国际眼科杂志:英文版, ISSN 2222-3959, 2017, Volume 10, Issue 3, pp. 361 - 365
AIM:To identify the expression of lens-related micro RNAs(miRNAs)in the central epithelium of transparent infant lenses and congenital cataract.... 
MiR-204 | Lens-related miRNAs | Meis2 | Congenital cataract | EYE | miR-204 | MUTATION | lens-related miRNAs | OPHTHALMOLOGY | congenital cataract | PROLIFERATION
Journal Article
Oncology Reports, ISSN 1021-335X, 07/2019, Volume 42, Issue 1, pp. 213 - 223
Colorectal cancer (CRC) is one of the most common types of malignancy worldwide. Distant metastasis is a key cause of CRC-associated mortality. MEIS2 has been... 
Prognosis | MEIS2 | Migration | Invasion | Colorectal cancer | SURVIVAL | PI3K/AKT/MTOR | colorectal cancer | METASTASIS | invasion | BIOMARKER | ONCOLOGY | migration | PROTEINS | prognosis | EXPRESSION
Journal Article
Nature Genetics, ISSN 1061-4036, 01/2019, Volume 51, Issue 1, pp. 106 - 116
We combined de novo mutation (DNM) data from 10,927 individuals with developmental delay and autism to identify 253 candidate neurodevelopmental disease genes... 
INTELLECTUAL DISABILITY | AUTISM | MOUSE MODEL | GENETICS & HEREDITY | MISSENSE MUTATION | SEGMENTAL DUPLICATIONS | DEVELOPMENTAL DELAY | SPECTRUM | TRUNCATING MUTATIONS | CLINICAL-SIGNIFICANCE | HAPLOINSUFFICIENCY | Autistic Disorder - genetics | Humans | Mi-2 Nucleosome Remodeling and Deacetylase Complex - genetics | DNA Copy Number Variations - genetics | Developmental Disabilities - genetics | Neurodevelopmental Disorders - genetics | Mutation - genetics | Intellectual Disability - genetics | Exome - genetics | Phenotype | Animals | Chromosome Aberrations | Polymorphism, Single Nucleotide - genetics | Mice | Intracellular Signaling Peptides and Proteins - genetics | Gene mutations | Copy number variations | Analysis | Nervous system | Degeneration | Genetic aspects | Research | Morbidity | Neurosciences | Intellectual disabilities | Copy number | Genes | Disorders | Likelihood ratio | Genomes | Gene deletion | Neurodevelopmental disorders | Spiny neurons | Autism | Missense mutation | Clonal deletion | Reproduction (copying) | Neostriatum | Deletion | Gene duplication | Mutation | Chromosome 16 | TRIO | MYT1L | HNRNPU | EHMT1 | ENO3 | CAPN15 | SUV420H1 | PPP1CB | EFTUD2 | COL4A3BP | SYNGAP1 | PPP2R1A | POGZ | EP300 | KCNH1 | SOX5 | MAP2K1 | MEF2C | CSNK2A1 | TMEM178A | DYRK1A | CASK | FOXP1 | KAT6B | TBL1XR1 | KAT6A | SCN8A | HECW2 | KCNQ2 | EEF1A2 | KCNQ3 | ADNP | Genetics of Developmental Delay | DLX3 | SET | KMT2A | SRCAP | ANP32A | STXBP1 | CUL3 | FOXG1 | ANKRD11 | ITPR1 | de novo Mutation | HIVEP3 | SNX5 | ZBTB18 | CREBBP | IQSEC2 | BCL11A | NONO | UPF3B | BRAF | ADAP1 | GRIN2B | SMARCA2 | SMARCA4 | MED13L | GNAO1 | AGO4 | DLG4 | CAPRIN1 | Neurodevelopmental Disorders | TCF4 | CDK13 | SCN2A | GABRB2 | KDM5B | SETD5 | DDX3X | CHD8 | PTEN | TCF20 | CTCF | CHD3 | CHD2 | WDR45 | SLC6A1 | MECP2 | SNAPC5 | SYNCRIP | TLK2 | CHAMP1 | KIF1A | RAC1 | TNPO2 | DNMT3A | MSL3 | PPP2R5D | ASH1L | SMC1A | ARID1B | CNKSR2 | PACS2 | SETBP1 | PIK3CA | PACS1 | WAC | ZMYND11 | SHANK3 | AHDC1 |