Similar articles for PMID: 15006694

Year	Number of Results
1953	1
1961	2
1962	1
1963	1
1995	1
1998	1
2000	1
2001	6
2002	6
2003	7
2004	14
2005	9
2006	8
2007	9
2008	4
2009	3
2010	4
2011	2
2013	2
2014	2
2015	3
2018	2
2019	2
2020	1
2024	0

1

Pleiotropic and diverse expression of ZFHX1B gene transcripts during mouse and human development supports the various clinical manifestations of the "Mowat-Wilson" syndrome.

Bassez G, Camand OJ, Cacheux V, Kobetz A, Dastot-Le Moal F, Marchant D, Catala M, Abitbol M, Goossens M. Bassez G, et al. Neurobiol Dis. 2004 Mar;15(2):240-50. doi: 10.1016/j.nbd.2003.10.004. Neurobiol Dis. 2004. PMID: 15006694

2

Neural crest-specific removal of Zfhx1b in mouse leads to a wide range of neurocristopathies reminiscent of Mowat-Wilson syndrome.

Van de Putte T, Francis A, Nelles L, van Grunsven LA, Huylebroeck D. Van de Putte T, et al. Hum Mol Genet. 2007 Jun 15;16(12):1423-36. doi: 10.1093/hmg/ddm093. Epub 2007 May 3. Hum Mol Genet. 2007. PMID: 17478475

3

ZFHX1B mutations in patients with Mowat-Wilson syndrome.

Dastot-Le Moal F, Wilson M, Mowat D, Collot N, Niel F, Goossens M. Dastot-Le Moal F, et al. Hum Mutat. 2007 Apr;28(4):313-21. doi: 10.1002/humu.20452. Hum Mutat. 2007. PMID: 17203459

4

Genetic interaction between Sox10 and Zfhx1b during enteric nervous system development.

Stanchina L, Van de Putte T, Goossens M, Huylebroeck D, Bondurand N. Stanchina L, et al. Dev Biol. 2010 May 15;341(2):416-28. doi: 10.1016/j.ydbio.2010.02.036. Epub 2010 Mar 4. Dev Biol. 2010. PMID: 20206619 Free article.

5

Clinical and mutational spectrum of Mowat-Wilson syndrome.

Zweier C, Thiel CT, Dufke A, Crow YJ, Meinecke P, Suri M, Ala-Mello S, Beemer F, Bernasconi S, Bianchi P, Bier A, Devriendt K, Dimitrov B, Firth H, Gallagher RC, Garavelli L, Gillessen-Kaesbach G, Hudgins L, Kääriäinen H, Karstens S, Krantz I, Mannhardt A, Medne L, Mücke J, Kibaek M, Krogh LN, Peippo M, Rittinger O, Schulz S, Schelley SL, Temple IK, Dennis NR, Van der Knaap MS, Wheeler P, Yerushalmi B, Zenker M, Seidel H, Lachmeijer A, Prescott T, Kraus C, Lowry RB, Rauch A. Zweier C, et al. Eur J Med Genet. 2005 Apr-Jun;48(2):97-111. doi: 10.1016/j.ejmg.2005.01.003. Epub 2005 Feb 25. Eur J Med Genet. 2005. PMID: 16053902

6

Nonsense mutations of the ZFHX1B gene in two Japanese girls with Mowat-Wilson syndrome.

Sasongko TH, Sadewa AH, Gunadi, Lee MJ, Koterazawa K, Nishio H. Sasongko TH, et al. Kobe J Med Sci. 2007;53(4):157-62. Kobe J Med Sci. 2007. PMID: 17932455 Free article.

7

Intrahepatic biliary anomalies in a patient with Mowat-Wilson syndrome uncover a role for the zinc finger homeobox gene zfhx1b in vertebrate biliary development.

Cui S, Erlichman J, Russo P, Haber BA, Matthews RP. Cui S, et al. J Pediatr Gastroenterol Nutr. 2011 Mar;52(3):339-44. doi: 10.1097/MPG.0b013e3181ff2e5b. J Pediatr Gastroenterol Nutr. 2011. PMID: 21336163

8

Mowat-Wilson syndrome affecting 3 siblings.

Ohtsuka M, Oguni H, Ito Y, Nakayama T, Matsuo M, Osawa M, Saito K, Yamada Y, Wakamatsu N. Ohtsuka M, et al. J Child Neurol. 2008 Mar;23(3):274-8. doi: 10.1177/0883073807309231. Epub 2008 Jan 29. J Child Neurol. 2008. PMID: 18230842

9

Atypical Mowat-Wilson patient confirms the importance of the novel association between ZFHX1B/SIP1 and NuRD corepressor complex.

Verstappen G, van Grunsven LA, Michiels C, Van de Putte T, Souopgui J, Van Damme J, Bellefroid E, Vandekerckhove J, Huylebroeck D. Verstappen G, et al. Hum Mol Genet. 2008 Apr 15;17(8):1175-83. doi: 10.1093/hmg/ddn007. Epub 2008 Jan 8. Hum Mol Genet. 2008. PMID: 18182442 Free article.

10

Mowat-Wilson syndrome: an underdiagnosed syndrome?

Engenheiro E, Møller RS, Pinto M, Soares G, Nikanorova M, Carreira IM, Ullmann R, Tommerup N, Tümer Z. Engenheiro E, et al. Clin Genet. 2008 Jun;73(6):579-84. doi: 10.1111/j.1399-0004.2008.00997.x. Epub 2008 Apr 28. Clin Genet. 2008. PMID: 18445050

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