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Items: 1 to 20 of 98

1.

Hirschsprung-like disease is exacerbated by reduced de novo GMP synthesis.

Lake JI, Tusheva OA, Graham BL, Heuckeroth RO.

J Clin Invest. 2013 Nov;123(11):4875-87.

3.

Vitamin A facilitates enteric nervous system precursor migration by reducing Pten accumulation.

Fu M, Sato Y, Lyons-Warren A, Zhang B, Kane MA, Napoli JL, Heuckeroth RO.

Development. 2010 Feb;137(4):631-40. doi: 10.1242/dev.040550.

4.

Ibuprofen slows migration and inhibits bowel colonization by enteric nervous system precursors in zebrafish, chick and mouse.

Schill EM, Lake JI, Tusheva OA, Nagy N, Bery SK, Foster L, Avetisyan M, Johnson SL, Stenson WF, Goldstein AM, Heuckeroth RO.

Dev Biol. 2016 Jan 15;409(2):473-88. doi: 10.1016/j.ydbio.2015.09.023. Epub 2015 Nov 14.

5.

Tcof1 acts as a modifier of Pax3 during enteric nervous system development and in the pathogenesis of colonic aganglionosis.

Barlow AJ, Dixon J, Dixon M, Trainor PA.

Hum Mol Genet. 2013 Mar 15;22(6):1206-17. doi: 10.1093/hmg/dds528. Epub 2013 Jan 2.

6.

Neural crest requires Impdh2 for development of the enteric nervous system, great vessels, and craniofacial skeleton.

Lake JI, Avetisyan M, Zimmermann AG, Heuckeroth RO.

Dev Biol. 2016 Jan 1;409(1):152-65. doi: 10.1016/j.ydbio.2015.11.004. Epub 2015 Nov 10.

7.

Genetic background impacts developmental potential of enteric neural crest-derived progenitors in the Sox10Dom model of Hirschsprung disease.

Walters LC, Cantrell VA, Weller KP, Mosher JT, Southard-Smith EM.

Hum Mol Genet. 2010 Nov 15;19(22):4353-72. doi: 10.1093/hmg/ddq357. Epub 2010 Aug 25.

8.

Identification of GLI Mutations in Patients With Hirschsprung Disease That Disrupt Enteric Nervous System Development in Mice.

Liu JA, Lai FP, Gui HS, Sham MH, Tam PK, Garcia-Barcelo MM, Hui CC, Ngan ES.

Gastroenterology. 2015 Dec;149(7):1837-1848.e5. doi: 10.1053/j.gastro.2015.07.060. Epub 2015 Aug 7.

PMID:
26261006
9.

Regulators of gene expression in Enteric Neural Crest Cells are putative Hirschsprung disease genes.

Schriemer D, Sribudiani Y, IJpma A, Natarajan D, MacKenzie KC, Metzger M, Binder E, Burns AJ, Thapar N, Hofstra RM, Eggen BJ.

Dev Biol. 2016 Aug 1;416(1):255-65. doi: 10.1016/j.ydbio.2016.06.004. Epub 2016 Jun 4.

PMID:
27266404
10.

Differential gene expression and functional analysis implicate novel mechanisms in enteric nervous system precursor migration and neuritogenesis.

Vohra BP, Tsuji K, Nagashimada M, Uesaka T, Wind D, Fu M, Armon J, Enomoto H, Heuckeroth RO.

Dev Biol. 2006 Oct 1;298(1):259-71. Epub 2006 Jun 27.

11.

A Novel Zebrafish ret Heterozygous Model of Hirschsprung Disease Identifies a Functional Role for mapk10 as a Modifier of Enteric Nervous System Phenotype Severity.

Heanue TA, Boesmans W, Bell DM, Kawakami K, Vanden Berghe P, Pachnis V.

PLoS Genet. 2016 Nov 30;12(11):e1006439. doi: 10.1371/journal.pgen.1006439. eCollection 2016 Nov.

12.

Sox10 and Itgb1 interaction in enteric neural crest cell migration.

Watanabe Y, Broders-Bondon F, Baral V, Paul-Gilloteaux P, Pingault V, Dufour S, Bondurand N.

Dev Biol. 2013 Jul 1;379(1):92-106. doi: 10.1016/j.ydbio.2013.04.013. Epub 2013 Apr 19.

13.

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.

PMID:
27370713
14.

Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes.

Gui H, Schriemer D, Cheng WW, Chauhan RK, Antiňolo G, Berrios C, Bleda M, Brooks AS, Brouwer RW, Burns AJ, Cherny SS, Dopazo J, Eggen BJ, Griseri P, Jalloh B, Le TL, Lui VC, Luzón-Toro B, Matera I, Ngan ES, Pelet A, Ruiz-Ferrer M, Sham PC, Shepherd IT, So MT, Sribudiani Y, Tang CS, van den Hout MC, van der Linde HC, van Ham TJ, van IJcken WF, Verheij JB, Amiel J, Borrego S, Ceccherini I, Chakravarti A, Lyonnet S, Tam PK, Garcia-Barceló MM, Hofstra RM.

Genome Biol. 2017 Mar 8;18(1):48. doi: 10.1186/s13059-017-1174-6.

15.

Depletion of the IKBKAP ortholog in zebrafish leads to hirschsprung disease-like phenotype.

Cheng WW, Tang CS, Gui HS, So MT, Lui VC, Tam PK, Garcia-Barcelo MM.

World J Gastroenterol. 2015 Feb 21;21(7):2040-6. doi: 10.3748/wjg.v21.i7.2040.

16.

Deriving human ENS lineages for cell therapy and drug discovery in Hirschsprung disease.

Fattahi F, Steinbeck JA, Kriks S, Tchieu J, Zimmer B, Kishinevsky S, Zeltner N, Mica Y, El-Nachef W, Zhao H, de Stanchina E, Gershon MD, Grikscheit TC, Chen S, Studer L.

Nature. 2016 Mar 3;531(7592):105-9. doi: 10.1038/nature16951. Epub 2016 Feb 10.

17.

Balancing neural crest cell intrinsic processes with those of the microenvironment in Tcof1 haploinsufficient mice enables complete enteric nervous system formation.

Barlow AJ, Dixon J, Dixon MJ, Trainor PA.

Hum Mol Genet. 2012 Apr 15;21(8):1782-93. doi: 10.1093/hmg/ddr611. Epub 2012 Jan 6.

18.

Expression of PROKR1 and PROKR2 in human enteric neural precursor cells and identification of sequence variants suggest a role in HSCR.

Ruiz-Ferrer M, Torroglosa A, Núñez-Torres R, de Agustín JC, Antiñolo G, Borrego S.

PLoS One. 2011;6(8):e23475. doi: 10.1371/journal.pone.0023475. Epub 2011 Aug 12.

19.

Hirschsprung's disease, Down syndrome, and missing heritability: too much collagen slows migration.

Heuckeroth RO.

J Clin Invest. 2015 Dec;125(12):4323-6. doi: 10.1172/JCI85003. Epub 2015 Nov 16.

20.

Expression profiling the developing mammalian enteric nervous system identifies marker and candidate Hirschsprung disease genes.

Heanue TA, Pachnis V.

Proc Natl Acad Sci U S A. 2006 May 2;103(18):6919-24. Epub 2006 Apr 21.

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