239 related articles for article (PubMed ID: 36980900)
1. Zeb2 DNA-Binding Sites in Neuroprogenitor Cells Reveal Autoregulation and Affirm Neurodevelopmental Defects, Including in Mowat-Wilson Syndrome.
Birkhoff JC; Korporaal AL; Brouwer RWW; Nowosad K; Milazzo C; Mouratidou L; van den Hout MCGN; van IJcken WFJ; Huylebroeck D; Conidi A
Genes (Basel); 2023 Mar; 14(3):. PubMed ID: 36980900
[TBL] [Abstract][Full Text] [Related]
2. ZEB2, the Mowat-Wilson Syndrome Transcription Factor: Confirmations, Novel Functions, and Continuing Surprises.
Birkhoff JC; Huylebroeck D; Conidi A
Genes (Basel); 2021 Jul; 12(7):. PubMed ID: 34356053
[TBL] [Abstract][Full Text] [Related]
3. Targeted chromatin conformation analysis identifies novel distal neural enhancers of ZEB2 in pluripotent stem cell differentiation.
Birkhoff JC; Brouwer RWW; Kolovos P; Korporaal AL; Bermejo-Santos A; Boltsis I; Nowosad K; van den Hout MCGN; Grosveld FG; van IJcken WFJ; Huylebroeck D; Conidi A
Hum Mol Genet; 2020 Aug; 29(15):2535-2550. PubMed ID: 32628253
[TBL] [Abstract][Full Text] [Related]
4. Zeb2 Regulates Cell Fate at the Exit from Epiblast State in Mouse Embryonic Stem Cells.
Stryjewska A; Dries R; Pieters T; Verstappen G; Conidi A; Coddens K; Francis A; Umans L; van IJcken WF; Berx G; van Grunsven LA; Grosveld FG; Goossens S; Haigh JJ; Huylebroeck D
Stem Cells; 2017 Mar; 35(3):611-625. PubMed ID: 27739137
[TBL] [Abstract][Full Text] [Related]
5. Requirement of the Mowat-Wilson Syndrome Gene Zeb2 in the Differentiation and Maintenance of Non-photoreceptor Cell Types During Retinal Development.
Wei W; Liu B; Jiang H; Jin K; Xiang M
Mol Neurobiol; 2019 Mar; 56(3):1719-1736. PubMed ID: 29922981
[TBL] [Abstract][Full Text] [Related]
6. Multifaceted actions of Zeb2 in postnatal neurogenesis from the ventricular-subventricular zone to the olfactory bulb.
Deryckere A; Stappers E; Dries R; Peyre E; van den Berghe V; Conidi A; Zampeta FI; Francis A; Bresseleers M; Stryjewska A; Vanlaer R; Maas E; Smal IV; van IJcken WFJ; Grosveld FG; Nguyen L; Huylebroeck D; Seuntjens E
Development; 2020 May; 147(10):. PubMed ID: 32253238
[TBL] [Abstract][Full Text] [Related]
7. Zeb2 regulates the balance between retinal interneurons and Müller glia by inhibition of BMP-Smad signaling.
Menuchin-Lasowski Y; Dagan B; Conidi A; Cohen-Gulkar M; David A; Ehrlich M; Giladi PO; Clark BS; Blackshaw S; Shapira K; Huylebroeck D; Henis YI; Ashery-Padan R
Dev Biol; 2020 Dec; 468(1-2):80-92. PubMed ID: 32950463
[TBL] [Abstract][Full Text] [Related]
8. Functional characterization of the ZEB2 regulatory landscape.
Bar Yaacov R; Eshel R; Farhi E; Shemuluvich F; Kaplan T; Birnbaum RY
Hum Mol Genet; 2019 May; 28(9):1487-1497. PubMed ID: 30590588
[TBL] [Abstract][Full Text] [Related]
9. Mowat-Wilson syndrome factor ZEB2 controls early formation of human neural crest through BMP signaling modulation.
Charney RM; Prasad MS; Juan-Sing C; Patel LJ; Hernandez JC; Wu J; García-Castro MI
Stem Cell Reports; 2023 Nov; 18(11):2254-2267. PubMed ID: 37890485
[TBL] [Abstract][Full Text] [Related]
10. ZEB2 haploinsufficient Mowat-Wilson syndrome induced pluripotent stem cells show disrupted GABAergic transcriptional regulation and function.
Schuster J; Klar J; Khalfallah A; Laan L; Hoeber J; Fatima A; Sequeira VM; Jin Z; Korol SV; Huss M; Nordgren A; Anderlid BM; Gallant C; Birnir B; Dahl N
Front Mol Neurosci; 2022; 15():988993. PubMed ID: 36353360
[TBL] [Abstract][Full Text] [Related]
11. Role of Zeb2/Sip1 in neuronal development.
Epifanova E; Babaev A; Newman AG; Tarabykin V
Brain Res; 2019 Feb; 1705():24-31. PubMed ID: 30266271
[TBL] [Abstract][Full Text] [Related]
12. Mowat-Wilson Syndrome: Case Report and Review of
St Peter C; Hossain WA; Lovell S; Rafi SK; Butler MG
Int J Mol Sci; 2024 Feb; 25(5):. PubMed ID: 38474085
[TBL] [Abstract][Full Text] [Related]
13. Age-dependent epileptic encephalopathy associated with an unusual co-occurrence of ZEB2 and SCN1A variants.
Nardello R; Fontana A; Mangano GD; Efthymiou S; Salpietro V; Houlden H; Mangano S
Epileptic Disord; 2020 Feb; 22(1):111-115. PubMed ID: 32031527
[TBL] [Abstract][Full Text] [Related]
14. Transcriptional Regulator ZEB2 Is Essential for Bergmann Glia Development.
He L; Yu K; Lu F; Wang J; Wu LN; Zhao C; Li Q; Zhou X; Liu H; Mu D; Xin M; Qiu M; Lu QR
J Neurosci; 2018 Feb; 38(6):1575-1587. PubMed ID: 29326173
[TBL] [Abstract][Full Text] [Related]
15. Neurological Phenotype of Mowat-Wilson Syndrome.
Cordelli DM; Di Pisa V; Fetta A; Garavelli L; Maltoni L; Soliani L; Ricci E
Genes (Basel); 2021 Jun; 12(7):. PubMed ID: 34199024
[TBL] [Abstract][Full Text] [Related]
16. The Role of ZEB2 in Human CD8 T Lymphocytes: Clinical and Cellular Immune Profiling in Mowat-Wilson Syndrome.
Frith K; Munier CML; Hastings L; Mowat D; Wilson M; Seddiki N; Macintosh R; Kelleher AD; Gray P; Zaunders JJ
Int J Mol Sci; 2021 May; 22(10):. PubMed ID: 34070208
[TBL] [Abstract][Full Text] [Related]
17. Clinical characteristics of Polish patients with molecularly confirmed Mowat-Wilson syndrome.
Jakubiak A; Szczałuba K; Badura-Stronka M; Kutkowska-Kaźmierczak A; Jakubiuk-Tomaszuk A; Chilarska T; Pilch J; Braun-Walicka N; Castaneda J; Wołyńska K; Wiśniewska M; Kugaudo M; Bielecka M; Pesz K; Wierzba J; Latos-Bieleńska A; Obersztyn E; Krajewska-Walasek M; Śmigiel R
J Appl Genet; 2021 Sep; 62(3):477-485. PubMed ID: 33982229
[TBL] [Abstract][Full Text] [Related]
18. ETS1 is coexpressed with ZEB2 and mediates ZEB2-induced epithelial-mesenchymal transition in human tumors.
Yalim-Camci I; Balcik-Ercin P; Cetin M; Odabas G; Tokay N; Sayan AE; Yagci T
Mol Carcinog; 2019 Jun; 58(6):1068-1081. PubMed ID: 30790340
[TBL] [Abstract][Full Text] [Related]
19. Novel Zeb2 gene variation in the Mowat Wilson syndrome (MWS).
Moore SW; Fieggen K; Honey E; Zaahl M
J Pediatr Surg; 2016 Feb; 51(2):268-71. PubMed ID: 26852091
[TBL] [Abstract][Full Text] [Related]
20. Genome-wide analysis of endogenously expressed ZEB2 binding sites reveals inverse correlations between ZEB2 and GalNAc-transferase GALNT3 in human tumors.
Balcik-Ercin P; Cetin M; Yalim-Camci I; Odabas G; Tokay N; Sayan AE; Yagci T
Cell Oncol (Dordr); 2018 Aug; 41(4):379-393. PubMed ID: 29516288
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
