Ding H, Lei W, Xiao S, Deng H, Yuan L, Xu L
Pediatr Surg Int. 2024; 40(1):38.
PMID: 38253735
DOI: 10.1007/s00383-023-05620-w.
Bhattarai C, Poudel P, Ghosh A, Kalthur S
AIMS Neurosci. 2022; 9(1):128-149.
PMID: 35434281
PMC: 8941195.
DOI: 10.3934/Neuroscience.2022008.
Li L, Ma J, He X, Zhou Y, Zhang Y, Chen Q
Biosci Rep. 2020; 41(6).
PMID: 33345266
PMC: 8217986.
DOI: 10.1042/BSR20193375.
Chatmethakul T, Phaltas R, Minzes G, Martinez J, Bhat R
J Pediatr Genet. 2019; 8(3):142-146.
PMID: 31406620
PMC: 6688876.
DOI: 10.1055/s-0038-1677551.
Anvesh G, Raju S, Prasad K, Sharma A, Surendra M
Indian J Nephrol. 2018; 28(3):226-228.
PMID: 29962674
PMC: 5998718.
DOI: 10.4103/ijn.IJN_55_17.
Endothelin signaling regulates mineralization and posttranscriptionally regulates SOST in TMOb cells via miR 126-3p.
Johnson M, Konicke K, Kristianto J, Gustavson A, Garbo R, Wang X
Physiol Rep. 2017; 5(4).
PMID: 28235973
PMC: 5328763.
DOI: 10.14814/phy2.13088.
Prospect of Human Pluripotent Stem Cell-Derived Neural Crest Stem Cells in Clinical Application.
Zhu Q, Lu Q, Gao R, Cao T
Stem Cells Int. 2017; 2016:7695836.
PMID: 28090209
PMC: 5206454.
DOI: 10.1155/2016/7695836.
Deriving human ENS lineages for cell therapy and drug discovery in Hirschsprung disease.
Fattahi F, Steinbeck J, Kriks S, Tchieu J, Zimmer B, Kishinevsky S
Nature. 2016; 531(7592):105-9.
PMID: 26863197
PMC: 4846424.
DOI: 10.1038/nature16951.
Chromosomal and related Mendelian syndromes associated with Hirschsprung's disease.
Moore S
Pediatr Surg Int. 2012; 28(11):1045-58.
PMID: 23001136
DOI: 10.1007/s00383-012-3175-6.
Genetic interactions and modifier genes in Hirschsprung's disease.
Wallace A, Anderson R
World J Gastroenterol. 2011; 17(45):4937-44.
PMID: 22174542
PMC: 3236992.
DOI: 10.3748/wjg.v17.i45.4937.
Genetic background impacts developmental potential of enteric neural crest-derived progenitors in the Sox10Dom model of Hirschsprung disease.
Walters L, Cantrell V, Weller K, Mosher J, Southard-Smith E
Hum Mol Genet. 2010; 19(22):4353-72.
PMID: 20739296
PMC: 2957318.
DOI: 10.1093/hmg/ddq357.
Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4.
Bondurand N, Dastot-Le Moal F, Stanchina L, Collot N, Baral V, Marlin S
Am J Hum Genet. 2007; 81(6):1169-85.
PMID: 17999358
PMC: 2276340.
DOI: 10.1086/522090.
[Molecular biology, basic research and diagnosis of Hirschsprung's disease].
Martucciello G, Luinetti O, Romano P, Magrini U
Pathologe. 2007; 28(2):119-24.
PMID: 17279407
DOI: 10.1007/s00292-007-0897-7.
Functional analysis of the endogenous retroviral promoter of the human endothelin B receptor gene.
Landry J, Mager D
J Virol. 2003; 77(13):7459-66.
PMID: 12805445
PMC: 164795.
DOI: 10.1128/jvi.77.13.7459-7466.2003.
Association study of PHOX2B as a candidate gene for Hirschsprung's disease.
Garcia-Barcelo M, Sham M, Lui V, Chen B, Ott J, Tam P
Gut. 2003; 52(4):563-7.
PMID: 12631670
PMC: 1773584.
DOI: 10.1136/gut.52.4.563.
A founding locus within the RET proto-oncogene may account for a large proportion of apparently sporadic Hirschsprung disease and a subset of cases of sporadic medullary thyroid carcinoma.
Borrego S, Wright F, Fernandez R, Williams N, Lopez-Alonso M, Davuluri R
Am J Hum Genet. 2002; 72(1):88-100.
PMID: 12474140
PMC: 420016.
DOI: 10.1086/345466.
Gdnf haploinsufficiency causes Hirschsprung-like intestinal obstruction and early-onset lethality in mice.
Shen L, Pichel J, Mayeli T, Sariola H, Lu B, Westphal H
Am J Hum Genet. 2002; 70(2):435-47.
PMID: 11774071
PMC: 384918.
DOI: 10.1086/338712.
Hirschsprung disease, associated syndromes, and genetics: a review.
Amiel J, Lyonnet S
J Med Genet. 2001; 38(11):729-39.
PMID: 11694544
PMC: 1734759.
DOI: 10.1136/jmg.38.11.729.
Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease.
Gath R, Goessling A, Keller K, Koletzko S, Coerdt W, Muntefering H
Gut. 2001; 48(5):671-5.
PMID: 11302967
PMC: 1728268.
DOI: 10.1136/gut.48.5.671.
Developmental disorders of the enteric nervous system.
Kapur R
Gut. 2000; 47 Suppl 4:iv81-3; discussion iv87.
PMID: 11076927
PMC: 1766802.
DOI: 10.1136/gut.47.suppl_4.iv81.
