-
Full Article (HTML) (85) -
Full Article (PDF) (29) -
Send to Friends (0)
Citation of this article
Corresponding Author of This Article
Article-Type of This Article
Open-Access Policy of This Article
Times Cited Counts in Google of This Article
Number of Hits and Downloads for This Article
- Total Article Views (3698)
All Articles published online
|
Dec 7, 2011 (publication date) through Oct 18, 2021
Times Cited of This Article
Journal Information of This Article
Publication Name
World Journal of Gastroenterology
ISSN
1007-9327
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Wallace AS, Anderson RB. Genetic interactions and modifier genes in Hirschsprung's disease. World J Gastroenterol 2011; 17(45): 4937-4944 [PMID: 22174542 DOI: 10.3748/wjg.v17.i45.4937] |
|---|---|
| URL: | https://www.wjgnet.com/1007-9327/full/v17/i45/4937.htm |
| Number | Citing Articles |
| 1 |
Yuli Watanabe, Florence Broders-Bondon, Viviane Baral, Perrine Paul-Gilloteaux, Veronique Pingault, Sylvie Dufour, Nadege Bondurand. Sox10 and Itgb1 interaction in enteric neural crest cell migration. Developmental Biology 2013; 379(1): 92 doi: 10.1016/j.ydbio.2013.04.013
|
| 2 |
Qiyang Shen, Hua Zhang, Yang Su, Zechao Wen, Zhongxian Zhu, Guanglin Chen, Lei Peng, Chunxia Du, Hua Xie, Hongxing Li, Xiaofeng Lv, Changgui Lu, Yankai Xia, Weibing Tang. Identification of two novel PCDHA9 mutations associated with Hirschsprung's disease. Gene 2018; 658: 96 doi: 10.1016/j.gene.2018.02.054
|
| 3 |
Keisuke Sugimoto, Tomoki Miyazawa, Hitomi Nishi, Kohei Miyazaki, Takuji Enya, Mitsuru Okada, Tsukasa Takemura. Heterozygous p.S811F RET gene mutation associated with renal agenesis, oligomeganephronia and total colonic aganglionosis: a case report. BMC Nephrology 2016; 17(1) doi: 10.1186/s12882-016-0354-z
|
| 4 |
A. J. Barlow, J. Dixon, M. Dixon, P. A. Trainor. Tcof1 acts as a modifier of Pax3 during enteric nervous system development and in the pathogenesis of colonic aganglionosis. Human Molecular Genetics 2013; 22(6): 1206 doi: 10.1093/hmg/dds528
|
| 5 |
D. Henderson, J. Zimmer, H. Nakamura, Prem Puri. Hirschsprung’s disease in twins: a systematic review and meta-analysis. Pediatric Surgery International 2017; 33(8): 855 doi: 10.1007/s00383-017-4110-7
|
| 6 |
Jean-Marie Gasc, Maud Clemessy, Pierre Corvol, Hervé Kempf. A chicken model of pharmacologically-induced Hirschsprung disease reveals an unexpected role of glucocorticoids in enteric aganglionosis. Biology Open 2015; 4(5): 666 doi: 10.1242/bio.201410454
|
| 7 |
Toshiki Takenouchi, Hiroshi Yoshihashi, Yuri Sakaguchi, Tomoko Uehara, Masataka Honda, Takao Takahashi, Kenjiro Kosaki, Sahoko Miyama. Hirschsprung disease as a yet undescribed phenotype in a patient withARID1Bmutation. American Journal of Medical Genetics Part A 2016; 170(12): 3249 doi: 10.1002/ajmg.a.37861
|
| 8 |
Yang Su, Zechao Wen, Qiyang Shen, Hua Zhang, Lei Peng, Guanglin Chen, Zhongxian Zhu, Chunxia Du, Hua Xie, Hongxing Li, Yankai Xia, Weibing Tang. Long non-coding RNA LOC100507600 functions as a competitive endogenous RNA to regulate BMI1 expression by sponging miR128-1-3p in Hirschsprung's disease. Cell Cycle 2018; 17(4): 459 doi: 10.1080/15384101.2017.1403688
|
| 9 |
I. Zaitoun, C. S. Erickson, A. J. Barlow, T. R. Klein, A. F. Heneghan, J. F. Pierre, M. L. Epstein, A. Gosain. Altered neuronal density and neurotransmitter expression in the ganglionated region ofEdnrbnull mice: implications for Hirschsprung's disease. Neurogastroenterology & Motility 2013; 25(3): e233 doi: 10.1111/nmo.12083
|
| 10 |
Ellen Merrick Schill, Jonathan I. Lake, Olga A. Tusheva, Nandor Nagy, Saya K. Bery, Lynne Foster, Marina Avetisyan, Stephen L. Johnson, William F. Stenson, Allan M. Goldstein, Robert O. Heuckeroth. Ibuprofen slows migration and inhibits bowel colonization by enteric nervous system precursors in zebrafish, chick and mouse. Developmental Biology 2016; 409(2): 473 doi: 10.1016/j.ydbio.2015.09.023
|
| 11 |
Yuli Watanabe, Laure Stanchina, Laure Lecerf, Nadjet Gacem, Andrea Conidi, Viviane Baral, Veronique Pingault, Danny Huylebroeck, Nadege Bondurand. Differentiation of Mouse Enteric Nervous System Progenitor Cells Is Controlled by Endothelin 3 and Requires Regulation of Ednrb by SOX10 and ZEB2. Gastroenterology 2017; 152(5): 1139 doi: 10.1053/j.gastro.2016.12.034
|
| 12 |
Berta Luzón‐Toro, Leticia Villalba‐Benito, Ana Torroglosa, Raquel M. Fernández, Guillermo Antiñolo, Salud Borrego. What is new about the genetic background of Hirschsprung disease?. Clinical Genetics 2020; 97(1): 114 doi: 10.1111/cge.13615
|
| 13 |
Yunmin Li, Tatsuo Kido, Maria M. Garcia-Barcelo, Paul K. H. Tam, Z. Laura Tabatabai, Yun-Fai Chris Lau. SRY interference of normal regulation of the RET gene suggests a potential role of the Y-chromosome gene in sexual dimorphism in Hirschsprung disease. Human Molecular Genetics 2015; 24(3): 685 doi: 10.1093/hmg/ddu488
|
| 14 |
C. Tomuschat, P. Puri. RET gene is a major risk factor for Hirschsprung’s disease: a meta-analysis. Pediatric Surgery International 2015; 31(8): 701 doi: 10.1007/s00383-015-3731-y
|
| 15 |
Marta Lorente-Ros, Ane Miren Andrés, Alba Sánchez-Galán, Cinthia Amiñoso, Sixto García, Pablo Lapunzina, Jesús Solera-García. New mutations associated with Hirschsprung disease. Anales de Pediatría (English Edition) 2020; 93(4): 222 doi: 10.1016/j.anpede.2019.05.007
|
| 16 |
Raj P Kapur, Lusine Ambartsumyan, Caitlin Smith. Are We Underdiagnosing Hirschsprung Disease?. Pediatric and Developmental Pathology 2020; 23(1): 60 doi: 10.1177/1093526619889434
|
| 17 |
K-F Bergeron, DW Silversides, N Pilon. The developmental genetics of Hirschsprung's disease. Clinical Genetics 2013; 83(1): 15 doi: 10.1111/cge.12032
|
| 18 |
David R. Blair, Christopher S. Lyttle, Jonathan M. Mortensen, Charles F. Bearden, Anders Boeck Jensen, Hossein Khiabanian, Rachel Melamed, Raul Rabadan, Elmer V. Bernstam, Søren Brunak, Lars Juhl Jensen, Dan Nicolae, Nigam H. Shah, Robert L. Grossman, Nancy J. Cox, Kevin P. White, Andrey Rzhetsky. A Nondegenerate Code of Deleterious Variants in Mendelian Loci Contributes to Complex Disease Risk. Cell 2013; 155(1): 70 doi: 10.1016/j.cell.2013.08.030
|
| 19 |
Prem Puri, Florian Friedmacher. Rickham's Neonatal Surgery. 2018; : 809 doi: 10.1007/978-1-4471-4721-3_40
|
| 20 |
L. Lauriina Porokuokka, Heikki T. Virtanen, Jere Lindén, Yulia Sidorova, Tatiana Danilova, Maria Lindahl, Mart Saarma, Jaan-Olle Andressoo. Gfra1 Underexpression Causes Hirschsprung’s Disease and Associated Enterocolitis in Mice. Cellular and Molecular Gastroenterology and Hepatology 2019; 7(3): 655 doi: 10.1016/j.jcmgh.2018.12.007
|
| 21 |
Julia Ganz. Gut feelings: Studying enteric nervous system development, function, and disease in the zebrafish model system. Developmental Dynamics 2018; 247(2): 268 doi: 10.1002/dvdy.24597
|
| 22 |
|
| 23 |
Hilary Schenck Eidam, John Russell, Kaushik Raha, Michael DeMartino, Donghui Qin, Huiping Amy Guan, Zhiliu Zhang, Gong Zhen, Haiyu Yu, Chengde Wu, Yan Pan, Gerard Joberty, Nico Zinn, Sylvie Laquerre, Sharon Robinson, Angela White, Amanda Giddings, Ehsan Mohammadi, Beverly Greenwood-Van Meerveld, Allen Oliff, Sanjay Kumar, Mui Cheung. Discovery of a First-in-Class Gut-Restricted RET Kinase Inhibitor as a Clinical Candidate for the Treatment of IBS. ACS Medicinal Chemistry Letters 2018; 9(7): 623 doi: 10.1021/acsmedchemlett.8b00035
|
| 24 |
Florian Obermayr, Ryo Hotta, Hideki Enomoto, Heather M. Young. Development and developmental disorders of the enteric nervous system. Nature Reviews Gastroenterology & Hepatology 2013; 10(1): 43 doi: 10.1038/nrgastro.2012.234
|
| 25 |
Naho Fujiwara, Katsumi Miyahara, Nana Nakazawa-Tanaka, Chihiro Akazawa, Atsuyuki Yamataka. Increased expression of Semaphorin 3A in the endothelin receptor-B null mouse model of Hirschsprung disease. Journal of Pediatric Surgery 2018; 53(2): 326 doi: 10.1016/j.jpedsurg.2017.11.034
|
| 26 |
Juntao Ke, Ying Zhu, Xiaoping Miao. The advances of genetics research on Hirschsprung's disease. PEDIATRIC INVESTIGATION 2018; 2(3): 189 doi: 10.1002/ped4.12062
|
| 27 |
J. M. Darlow, M. G. Dobson, R. Darlay, C. M. Molony, M. Hunziker, A. J. Green, H. J. Cordell, P. Puri, D. E. Barton. A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development. Molecular Genetics & Genomic Medicine 2014; 2(1): 7 doi: 10.1002/mgg3.22
|
| 28 |
Jiarui Pu, Shaotao Tang, Qiangsong Tong, Guobin Wang, Haibo Jia, Qiong Jia, Kang Li, Dan Li, Dehua Yang, Jun Yang, Hang Li, Shuai Li, Hong Mei. Neuregulin 1 is involved in enteric nervous system development in zebrafish. Journal of Pediatric Surgery 2017; 52(7): 1182 doi: 10.1016/j.jpedsurg.2017.01.005
|
| 29 |
Wei-Bo Niu, Mei-Rong Bai, Huan-Lei Song, Yan-Jiao Lu, Wen-Jie Wu, Yi-Ming Gong, Xian-Xian Yu, Zhi-Liang Wei, Wen-Wen Yu, Bei-Lin Gu, Wei Cai, Xun Chu. Association of Variants in PLD1, 3p24.1, and 10q11.21 Regions With Hirschsprung’s Disease in Han Chinese Population. Frontiers in Genetics 2020; 11 doi: 10.3389/fgene.2020.00738
|
| 30 |
Yang Wang, Qian Jiang, Aravinda Chakravarti, Hao Cai, Ze Xu, Wenjie Wu, Beilin Gu, Long Li, Wei Cai. MicroRNA-4516-mediated regulation of MAPK10 relies on 3′ UTR cis-acting variants and contributes to the altered risk of Hirschsprung disease. Journal of Medical Genetics 2020; 57(9): 634 doi: 10.1136/jmedgenet-2019-106615
|
| 31 |
Maria M. Alves, Yunia Sribudiani, Rutger W.W. Brouwer, Jeanne Amiel, Guillermo Antiñolo, Salud Borrego, Isabella Ceccherini, Aravinda Chakravarti, Raquel M. Fernández, Maria-Mercè Garcia-Barcelo, Paola Griseri, Stanislas Lyonnet, Paul K. Tam, Wilfred F.J. van IJcken, Bart J.L. Eggen, Gerard J. te Meerman, Robert M.W. Hofstra. Contribution of rare and common variants determine complex diseases—Hirschsprung disease as a model. Developmental Biology 2013; 382(1): 320 doi: 10.1016/j.ydbio.2013.05.019
|
| 32 |
Heather M. Young, Lincon A. Stamp, Toshihiro Uesaka, Marlene M. Hao, Donald F. Newgreen, Hideki Enomoto. Physiology of the Gastrointestinal Tract. 2018; : 273 doi: 10.1016/B978-0-12-809954-4.00011-6
|
| 33 |
Jieping Huang, Ruihua Dang, Daisuke Torigoe, Anqi Li, Chuzhao Lei, Nobuya Sasaki, Jinxi Wang, Takashi Agui. Genetic variation in the GDNF promoter affects its expression and modifies the severity of Hirschsprung's disease (HSCR) in rats carrying Ednrbsl mutations. Gene 2016; 575(1): 144 doi: 10.1016/j.gene.2015.08.051
|
| 34 |
|
| 35 |
Naomi E. Butler Tjaden, Paul A. Trainor. The developmental etiology and pathogenesis of Hirschsprung disease. Translational Research 2013; 162(1): 1 doi: 10.1016/j.trsl.2013.03.001
|
| 36 |
P. N. Plowman, C. E. Plowman. Onco-ontogeny recapitulates phylogeny – a consideration. Oncogene 2021; 40(8): 1542 doi: 10.1038/s41388-020-01624-1
|
| 37 |
Allan M. Goldstein, Nikhil Thapar, Tennekoon Buddhika Karunaratne, Roberto De Giorgio. Clinical aspects of neurointestinal disease: Pathophysiology, diagnosis, and treatment. Developmental Biology 2016; 417(2): 217 doi: 10.1016/j.ydbio.2016.03.032
|
| 38 |
Tanja Mederer, Stefanie Schmitteckert, Julia Volz, Cristina Martínez, Ralph Röth, Thomas Thumberger, Volker Eckstein, Jutta Scheuerer, Cornelia Thöni, Felix Lasitschka, Leonie Carstensen, Patrick Günther, Stefan Holland-Cunz, Robert Hofstra, Erwin Brosens, Jill A. Rosenfeld, Christian P. Schaaf, Duco Schriemer, Isabella Ceccherini, Marta Rusmini, Joseph Tilghman, Berta Luzón-Toro, Ana Torroglosa, Salud Borrego, Clara Sze-man Tang, Mercè Garcia-Barceló, Paul Tam, Nagarajan Paramasivam, Melanie Bewerunge-Hudler, Carolina De La Torre, Norbert Gretz, Gudrun A. Rappold, Philipp Romero, Beate Niesler, Andrew S. McCallion. A complementary study approach unravels novel players in the pathoetiology of Hirschsprung disease. PLOS Genetics 2020; 16(11): e1009106 doi: 10.1371/journal.pgen.1009106
|
| 39 |
Donald F. Newgreen, Sylvie Dufour, Marthe J. Howard, Kerry A. Landman. Simple rules for a “simple” nervous system? Molecular and biomathematical approaches to enteric nervous system formation and malformation. Developmental Biology 2013; 382(1): 305 doi: 10.1016/j.ydbio.2013.06.029
|
| 40 |
Benjamin J. Binder, Kerry A. Landman, Donald F. Newgreen, Joshua V. Ross. Incomplete penetrance: The role of stochasticity in developmental cell colonization. Journal of Theoretical Biology 2015; 380: 309 doi: 10.1016/j.jtbi.2015.05.028
|
| 41 |
Marta Lorente-Ros, Ane Miren Andrés, Alba Sánchez-Galán, Cinthia Amiñoso, Sixto García, Pablo Lapunzina, Jesús Solera García. Nuevas mutaciones asociadas a la enfermedad de Hirschsprung. Anales de Pediatría 2020; 93(4): 222 doi: 10.1016/j.anpedi.2019.05.019
|
| 42 |
Maggie L. Westfal, Allan M. Goldstein. Diagnosing and Managing Hirschsprung Disease in the Newborn. NeoReviews 2018; 19(10): e577 doi: 10.1542/neo.19-10-e577
|
| 43 |
Yang Wang, Weihui Yan, Jun Wang, Ying Zhou, Jie Chen, Beilin Gu, Wei Cai.
Common genetic variants in
GAL
,
GAP
43
and
NRSN
1
and interaction networks confer susceptibility to Hirschsprung disease
. Journal of Cellular and Molecular Medicine 2018; 22(7): 3377 doi: 10.1111/jcmm.13612
|
| 44 |
Yu-Rong Liu, Fang Ba, Lan-Jie Cheng, Xu Li, Shi-Wei Zhang, Shu-Cheng Zhang. Efficacy of Sox10 Promoter Methylation in the Diagnosis of Intestinal Neuronal Dysplasia From the Peripheral Blood. Clinical and Translational Gastroenterology 2019; 10(12): e00093 doi: 10.14309/ctg.0000000000000093
|
| 45 |
M. Barrenschee, M. Böttner, I. Hellwig, J. Harde, J. H. Egberts, T. Becker, T. Wedel. Site-specific gene expression and localization of growth factor ligand receptors RET, GFRα1 and GFRα2 in human adult colon. Cell and Tissue Research 2013; 354(2): 371 doi: 10.1007/s00441-013-1690-y
|
| 46 |
Soo-Min Jung, Suhg Namgoong, Jeong-Meen Seo, Dae-Yeon Kim, Jung-Tak Oh, Hyun-Young Kim, Jeong-Hyun Kim. Potential association between TSGA13 variants and risk of total colonic aganglionosis in Hirschsprung disease. Gene 2019; 710: 240 doi: 10.1016/j.gene.2019.06.007
|