Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 41


Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease.

Yang D, Yang J, Li S, Jiang M, Cao G, Yang L, Zhang X, Zhou Y, Li K, Tang ST.

Sci Rep. 2017 Mar 3;7:43222. doi: 10.1038/srep43222.


Sip1 regulates the generation of the inner nuclear layer retinal cell lineages in mammals.

Menuchin-Lasowski Y, Oren-Giladi P, Xie Q, Ezra-Elia R, Ofri R, Peled-Hajaj S, Farhy C, Higashi Y, Van de Putte T, Kondoh H, Huylebroeck D, Cvekl A, Ashery-Padan R.

Development. 2016 Aug 1;143(15):2829-41. doi: 10.1242/dev.136101. Epub 2016 Jul 6.


Mouse models of Hirschsprung disease and other developmental disorders of the enteric nervous system: Old and new players.

Bondurand N, Southard-Smith EM.

Dev Biol. 2016 Sep 15;417(2):139-57. doi: 10.1016/j.ydbio.2016.06.042. Epub 2016 Jun 28. Review.


WNT/β-catenin signaling mediates human neural crest induction via a pre-neural border intermediate.

Leung AW, Murdoch B, Salem AF, Prasad MS, Gomez GA, García-Castro MI.

Development. 2016 Feb 1;143(3):398-410. doi: 10.1242/dev.130849.


A de novo triplication on 2q22.3 including the entire ZEB2 gene associated with global developmental delay, multiple congenital anomalies and behavioral abnormalities.

Yuan H, Zhang L, Chen M, Zhu J, Meng Z, Liang L.

Mol Cytogenet. 2015 Dec 23;8:99. doi: 10.1186/s13039-015-0206-8. eCollection 2015.


Regulation of C. elegans neuronal differentiation by the ZEB-family factor ZAG-1 and the NK-2 homeodomain factor CEH-28.

Ramakrishnan K, Okkema PG.

PLoS One. 2014 Dec 4;9(12):e113893. doi: 10.1371/journal.pone.0113893. eCollection 2014.


Sip1 mediates an E-cadherin-to-N-cadherin switch during cranial neural crest EMT.

Rogers CD, Saxena A, Bronner ME.

J Cell Biol. 2013 Dec 9;203(5):835-47. doi: 10.1083/jcb.201305050. Epub 2013 Dec 2.


Four amino acids within a tandem QxVx repeat in a predicted extended α-helix of the Smad-binding domain of Sip1 are necessary for binding to activated Smad proteins.

Conidi A, van den Berghe V, Leslie K, Stryjewska A, Xue H, Chen YG, Seuntjens E, Huylebroeck D.

PLoS One. 2013 Oct 11;8(10):e76733. doi: 10.1371/journal.pone.0076733. eCollection 2013.


Enteric nervous system development: migration, differentiation, and disease.

Lake JI, Heuckeroth RO.

Am J Physiol Gastrointest Liver Physiol. 2013 Jul 1;305(1):G1-24. doi: 10.1152/ajpgi.00452.2012. Epub 2013 May 2. Review.


Riding the crest of the wave: parallels between the neural crest and cancer in epithelial-to-mesenchymal transition and migration.

Powell DR, Blasky AJ, Britt SG, Artinger KB.

Wiley Interdiscip Rev Syst Biol Med. 2013 Jul-Aug;5(4):511-22. doi: 10.1002/wsbm.1224. Epub 2013 Apr 10. Review.


Aptamers and their potential to selectively target aspects of EGF, Wnt/β-catenin and TGFβ-smad family signaling.

Conidi A, van den Berghe V, Huylebroeck D.

Int J Mol Sci. 2013 Mar 26;14(4):6690-719. doi: 10.3390/ijms14046690. Review.


Mowat-Wilson syndrome: the first clinical and molecular report of an indonesian patient.

Mundhofir FE, Yntema HG, van der Burgt I, Hamel BC, Faradz SM, van Bon BW.

Case Rep Genet. 2012;2012:949507. doi: 10.1155/2012/949507. Epub 2012 Dec 1.


Building a brain in the gut: development of the enteric nervous system.

Goldstein AM, Hofstra RM, Burns AJ.

Clin Genet. 2013 Apr;83(4):307-16. doi: 10.1111/cge.12054. Epub 2012 Nov 27. Review.


Pleiotropic effects of the bone morphogenetic proteins on development of the enteric nervous system.

Chalazonitis A, Kessler JA.

Dev Neurobiol. 2012 Jun;72(6):843-56. doi: 10.1002/dneu.22002. Review.


Genetic interactions and modifier genes in Hirschsprung's disease.

Wallace AS, Anderson RB.

World J Gastroenterol. 2011 Dec 7;17(45):4937-44. doi: 10.3748/wjg.v17.i45.4937. Review.


Copy number variants in candidate genes are genetic modifiers of Hirschsprung disease.

Jiang Q, Ho YY, Hao L, Nichols Berrios C, Chakravarti A.

PLoS One. 2011;6(6):e21219. doi: 10.1371/journal.pone.0021219. Epub 2011 Jun 21.


Hepatocyte-derived Snail1 propagates liver fibrosis progression.

Rowe RG, Lin Y, Shimizu-Hirota R, Hanada S, Neilson EG, Greenson JK, Weiss SJ.

Mol Cell Biol. 2011 Jun;31(12):2392-403. doi: 10.1128/MCB.01218-10. Epub 2011 Apr 11.


Clinical utility gene card for: Mowat-Wilson syndrome.

Zollino M, Garavelli L, Rauch A.

Eur J Hum Genet. 2011 Aug;19(8). doi: 10.1038/ejhg.2011.12. Epub 2011 Feb 23. No abstract available.


Fine mapping of the NRG1 Hirschsprung's disease locus.

Tang CS, Tang WK, So MT, Miao XP, Leung BM, Yip BH, Leon TY, Ngan ES, Lui VC, Chen Y, Chan IH, Chung PH, Liu XL, Wu XZ, Wong KK, Sham PC, Cherny SS, Tam PK, Garcia-Barceló MM.

PLoS One. 2011 Jan 20;6(1):e16181. doi: 10.1371/journal.pone.0016181.


Bone morphogenetic proteins regulate enteric gliogenesis by modulating ErbB3 signaling.

Chalazonitis A, D'Autréaux F, Pham TD, Kessler JA, Gershon MD.

Dev Biol. 2011 Feb 1;350(1):64-79. doi: 10.1016/j.ydbio.2010.11.017. Epub 2010 Nov 19.

Supplemental Content

Support Center