179 related articles for article (PubMed ID: 23861142)
1. Smad-interacting protein 1 affects acute and tonic, but not chronic pain.
Pradier B; Jeub M; Markert A; Mauer D; Tolksdorf K; Van de Putte T; Seuntjens E; Gailus-Durner V; Fuchs H; Hrabě de Angelis M; Huylebroeck D; Beck H; Zimmer A; Rácz I
Eur J Pain; 2014 Feb; 18(2):249-57. PubMed ID: 23861142
[TBL] [Abstract][Full Text] [Related]
2. ZEB2 zinc-finger missense mutations lead to hypomorphic alleles and a mild Mowat-Wilson syndrome.
Ghoumid J; Drevillon L; Alavi-Naini SM; Bondurand N; Rio M; Briand-Suleau A; Nasser M; Goodwin L; Raymond P; Yanicostas C; Goossens M; Lyonnet S; Mowat D; Amiel J; Soussi-Yanicostas N; Giurgea I
Hum Mol Genet; 2013 Jul; 22(13):2652-61. PubMed ID: 23466526
[TBL] [Abstract][Full Text] [Related]
3. A novel long-range enhancer regulates postnatal expression of Zeb2: implications for Mowat-Wilson syndrome phenotypes.
El-Kasti MM; Wells T; Carter DA
Hum Mol Genet; 2012 Dec; 21(26):5429-42. PubMed ID: 23001561
[TBL] [Abstract][Full Text] [Related]
4. A case of Mowat-Wilson syndrome caused by a truncating mutation within exon 8 of the ZEB2 gene.
Meral C; Malbora B; Celikel F; Aydemir G; Süleymanoğlu S; Zollino M; Derbent M
Turk J Pediatr; 2012; 54(5):523-7. PubMed ID: 23427518
[TBL] [Abstract][Full Text] [Related]
5. De novo inbred heterozygous Zeb2/Sip1 mutant mice uniquely generated by germ-line conditional knockout exhibit craniofacial, callosal and behavioral defects associated with Mowat-Wilson syndrome.
Takagi T; Nishizaki Y; Matsui F; Wakamatsu N; Higashi Y
Hum Mol Genet; 2015 Nov; 24(22):6390-402. PubMed ID: 26319231
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. ZEB2 gene mutation and duplication of 22q11.23 in Mowat-Wilson syndrome.
Buraniqi E; Moodley M
J Child Neurol; 2015 Jan; 30(1):32-6. PubMed ID: 25028418
[TBL] [Abstract][Full Text] [Related]
8. Ophthalmologic abnormalities in Mowat-Wilson syndrome and a mutation in ZEB2.
Ariss M; Natan K; Friedman N; Traboulsi EI
Ophthalmic Genet; 2012 Sep; 33(3):159-60. PubMed ID: 22486326
[TBL] [Abstract][Full Text] [Related]
9. The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations.
Yamada Y; Nomura N; Yamada K; Matsuo M; Suzuki Y; Sameshima K; Kimura R; Yamamoto Y; Fukushi D; Fukuhara Y; Ishihara N; Nishi E; Imataka G; Suzumura H; Hamano S; Shimizu K; Iwakoshi M; Ohama K; Ohta A; Wakamoto H; Kajita M; Miura K; Yokochi K; Kosaki K; Kuroda T; Kosaki R; Hiraki Y; Saito K; Mizuno S; Kurosawa K; Okamoto N; Wakamatsu N
Am J Med Genet A; 2014 Aug; 164A(8):1899-908. PubMed ID: 24715670
[TBL] [Abstract][Full Text] [Related]
10. Clinical spectrum of eye malformations in four patients with Mowat-Wilson syndrome.
Bourchany A; Giurgea I; Thevenon J; Goldenberg A; Morin G; Bremond-Gignac D; Paillot C; Lafontaine PO; Thouvenin D; Massy J; Duncombe A; Thauvin-Robinet C; Masurel-Paulet A; Chehadeh SE; Huet F; Bron A; Creuzot-Garcher C; Lyonnet S; Faivre L
Am J Med Genet A; 2015 Jul; 167(7):1587-92. PubMed ID: 25899569
[TBL] [Abstract][Full Text] [Related]
11. Mowat-Wilson syndrome: neurological and molecular study in seven patients.
Paz JA; Kim CA; Goossens M; Giurgea I; Marques-Dias MJ
Arq Neuropsiquiatr; 2015 Jan; 73(1):12-7. PubMed ID: 25608121
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. SIP1 expression patterns in brain investigated by generating a SIP1-EGFP reporter knock-in mouse.
Nishizaki Y; Takagi T; Matsui F; Higashi Y
Genesis; 2014 Jan; 52(1):56-67. PubMed ID: 24243579
[TBL] [Abstract][Full Text] [Related]
14. Mowat-Wilson syndrome in a fetus with antenatal diagnosis of short corpus callosum: advocacy for standard autopsy.
Spaggiari E; Baumann C; Alison M; Oury JF; Belarbi N; Dupont C; Guimiot F; Delezoide AL
Eur J Med Genet; 2013 Jun; 56(6):297-300. PubMed ID: 23523603
[TBL] [Abstract][Full Text] [Related]
15. The behavioral phenotype of Mowat-Wilson syndrome.
Evans E; Einfeld S; Mowat D; Taffe J; Tonge B; Wilson M
Am J Med Genet A; 2012 Feb; 158A(2):358-66. PubMed ID: 22246645
[TBL] [Abstract][Full Text] [Related]
16. [Mowat-Wilson syndrome: a report of three Danish cases].
Nissen KB; Søndergaard C; Thelle T; Møller RS
Ugeskr Laeger; 2011 Sep; 173(36):2199-200. PubMed ID: 21893004
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases.
Wenger TL; Harr M; Ricciardi S; Bhoj E; Santani A; Adam MP; Barnett SS; Ganetzky R; McDonald-McGinn DM; Battaglia D; Bigoni S; Selicorni A; Sorge G; Monica MD; Mari F; Andreucci E; Romano S; Cocchi G; Savasta S; Malbora B; Marangi G; Garavelli L; Zollino M; Zackai EH
Am J Med Genet A; 2014 Oct; 164A(10):2557-66. PubMed ID: 25123255
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Epigenetic transcriptional activation of monocyte chemotactic protein 3 contributes to long-lasting neuropathic pain.
Imai S; Ikegami D; Yamashita A; Shimizu T; Narita M; Niikura K; Furuya M; Kobayashi Y; Miyashita K; Okutsu D; Kato A; Nakamura A; Araki A; Omi K; Nakamura M; James Okano H; Okano H; Ando T; Takeshima H; Ushijima T; Kuzumaki N; Suzuki T; Narita M
Brain; 2013 Mar; 136(Pt 3):828-43. PubMed ID: 23364351
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]