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Items: 1 to 20 of 120

1.

Hirschsprung disease: a developmental disorder of the enteric nervous system.

McKeown SJ, Stamp L, Hao MM, Young HM.

Wiley Interdiscip Rev Dev Biol. 2013 Jan-Feb;2(1):113-29. doi: 10.1002/wdev.57. Epub 2012 Apr 24. Review.

PMID:
23799632
2.

The developmental etiology and pathogenesis of Hirschsprung disease.

Butler Tjaden NE, Trainor PA.

Transl Res. 2013 Jul;162(1):1-15. doi: 10.1016/j.trsl.2013.03.001. Epub 2013 Mar 22. Review.

3.

Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease.

Salomon R, Attié T, Pelet A, Bidaud C, Eng C, Amiel J, Sarnacki S, Goulet O, Ricour C, Nihoul-Fékété C, Munnich A, Lyonnet S.

Nat Genet. 1996 Nov;14(3):345-7.

PMID:
8896569
4.

Diminished Ret expression compromises neuronal survival in the colon and causes intestinal aganglionosis in mice.

Uesaka T, Nagashimada M, Yonemura S, Enomoto H.

J Clin Invest. 2008 May;118(5):1890-8. doi: 10.1172/JCI34425.

5.

Hirschsprung Disease Overview.

Parisi MA.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
2002 Jul 12 [updated 2015 Oct 1].

6.

The developmental genetics of Hirschsprung's disease.

Bergeron KF, Silversides DW, Pilon N.

Clin Genet. 2013 Jan;83(1):15-22. doi: 10.1111/cge.12032. Epub 2012 Nov 7.

PMID:
23043324
7.

A chicken model of pharmacologically-induced Hirschsprung disease reveals an unexpected role of glucocorticoids in enteric aganglionosis.

Gasc JM, Clemessy M, Corvol P, Kempf H.

Biol Open. 2015 Apr 2;4(5):666-71. doi: 10.1242/bio.201410454.

8.

[Molecular genetics of Hirschsprung disease: a model of multigenic neurocristopathy].

Amiel J, Salomon R, Attié-Bitach T, Touraine R, Steffann J, Pelet A, Nihoul-Fékété C, Vekemans M, Munnich A, Lyonnet S.

J Soc Biol. 2000;194(3-4):125-8. Review. French.

PMID:
11324313
9.

Hirschsprung's disease as a model of complex genetic etiology.

Borrego S, Ruiz-Ferrer M, Fernández RM, Antiñolo G.

Histol Histopathol. 2013 Sep;28(9):1117-36. Epub 2013 Apr 19. Review.

PMID:
23605783
10.

Advances in molecular genetics of Hirschsprung's disease.

Pan ZW, Li JC.

Anat Rec (Hoboken). 2012 Oct;295(10):1628-38. doi: 10.1002/ar.22538. Epub 2012 Jul 19. Review.

11.

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.

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 Jun 28. pii: S0012-1606(16)30133-6. doi: 10.1016/j.ydbio.2016.06.042. [Epub ahead of print] Review.

PMID:
27370713
14.

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.

15.

Knockout mouse models of Hirschsprung's disease.

Zimmer J, Puri P.

Pediatr Surg Int. 2015 Sep;31(9):787-94. doi: 10.1007/s00383-015-3747-3. Epub 2015 Jul 3. Review.

PMID:
26137873
16.

Novel mutations at RET ligand genes preventing receptor activation are associated to Hirschsprung's disease.

Ruiz-Ferrer M, Torroglosa A, Luzón-Toro B, Fernández RM, Antiñolo G, Mulligan LM, Borrego S.

J Mol Med (Berl). 2011 May;89(5):471-80. doi: 10.1007/s00109-010-0714-2. Epub 2011 Jan 5.

PMID:
21206993
17.

Developmental determinants of the independence and complexity of the enteric nervous system.

Gershon MD.

Trends Neurosci. 2010 Oct;33(10):446-56. doi: 10.1016/j.tins.2010.06.002. Epub 2010 Jul 13. Review.

PMID:
20633936
18.

[From monogenic to polygenic: model of Hirschsprung disease].

Salomon R, Amiel J, Attié T, Pelet A, Munnich A, Lyonnet S.

Pathol Biol (Paris). 1998 Nov;46(9):705-7. Review. French.

PMID:
9885824
19.

Balancing on the crest - Evidence for disruption of the enteric ganglia via inappropriate lineage segregation and consequences for gastrointestinal function.

Musser MA, Michelle Southard-Smith E.

Dev Biol. 2013 Oct 1;382(1):356-64. doi: 10.1016/j.ydbio.2013.01.024. Epub 2013 Jan 31. Review.

20.

Genome-wide linkage identifies novel modifier loci of aganglionosis in the Sox10Dom model of Hirschsprung disease.

Owens SE, Broman KW, Wiltshire T, Elmore JB, Bradley KM, Smith JR, Southard-Smith EM.

Hum Mol Genet. 2005 Jun 1;14(11):1549-58. Epub 2005 Apr 20.

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