Association Analysis of Variants of DSCAM and BACE2 With Hirschsprung Disease Susceptibility in Han Chinese and Functional Evaluation in Zebrafish

by Yan-Jiao Lu, Yan-Jiao Lu, Yan-Jiao Lu, Wen-Wen Yu, Wen-Wen Yu, Wen-Wen Yu, Meng-Meng Cui, Meng-Meng Cui, Meng-Meng Cui, Xian-Xian Yu, Xian-Xian Yu, Xian-Xian Yu, Huan-Lei Song, Huan-Lei Song, Huan-Lei Song, Mei-Rong Bai, Mei-Rong Bai, Mei-Rong Bai, Wen-Jie Wu, Wen-Jie Wu, Wen-Jie Wu, Bei-Lin Gu, Bei-Lin Gu, Bei-Lin Gu, Jun Wang, Jun Wang, Jun Wang, Wei Cai, Wei Cai, Wei Cai, Xun Chu, Xun Chu, Xun Chu
Published 2021-05-01

Correction: Genetic Background Strongly Modifies the Severity of Symptoms of Hirschsprung Disease, but Not Hearing Loss in Rats Carrying Ednrbsl Mutations

by Ruihua Dang, Daisuke Torigoe, Sari Suzuki, Yoshiaki Kikkawa, Kanako Moritoh, Nobuya Sasaki, Takashi Agui
Published 2011-01-01

Overexpression of DNMT3b target genes during Enteric Nervous System development contribute to the onset of Hirschsprung disease

by Leticia Villalba-Benito, Ana Torroglosa, Raquel María Fernández, Macarena Ruíz-Ferrer, María José Moya-Jiménez, Guillermo Antiñolo, Salud Borrego
Published 2017-07-01

Characterization of Intestinal Microbiomes of Hirschsprung's Disease Patients with or without Enterocolitis Using Illumina-MiSeq High-Throughput Sequencing.

by Yuqing Li, Valeriy Poroyko, Zhilong Yan, Liya Pan, Yi Feng, Peihua Zhao, Zhoulonglong Xie, Li Hong
Published 2016-01-01

miR-100 rs1834306 A>G Increases the Risk of Hirschsprung Disease in Southern Chinese Children

by Zhu Y, Lin A, Zheng Y, Xie X, He Q, Zhong W
Published 2020-08-01

QTL analysis identifies a modifier locus of aganglionosis in the rat model of Hirschsprung disease carrying Ednrb(sl) mutations.

by Ruihua Dang, Daisuke Torigoe, Nobuya Sasaki, Takashi Agui
Published 2011-01-01

Higher G allele frequency of RET C2307t>G polymorphism in female patients with Hirschsprung disease in Yogyakarta, Indonesia

by Ahmad Hamim Sadewa, Saryono Saryono, Rochadi Rochadi, Wiryatun Lestariana, Wayan T Artama
Published 2008-05-01

Genetic background strongly modifies the severity of symptoms of Hirschsprung disease, but not hearing loss in rats carrying Ednrb(sl) mutations.

by Ruihua Dang, Daisuke Torigoe, Sari Suzuki, Yoshiaki Kikkawa, Kanako Moritoh, Nobuya Sasaki, Takashi Agui
Published 2011-01-01

A Sox10-GFP mutant mouse model for the study of abnormal enteric nervous system development in Hirschsprung disease

by Zhang, Mei, 章梅
Published 2013

Novel MLPA procedure using self-designed probes allows comprehensive analysis for CNVs of the genes involved in Hirschsprung disease

by Antiñolo Guillermo, Fernández Raquel M, Núñez-Torres Rocio, Sánchez-Mejías Avencia, Borrego Salud
Published 2010-05-01

POSTOPERATIVE REHABILITATION OF CHILDREN WHO UNDERWENT A SURGERY ON THE COLON AND ANORECTAL AREA

by V. A. TARAKANOV, A. E. STROKOVSKY, V. M. STARCHENKO, V. M. NADGERIEV, A. N. LUNJAKA, E. G. KOLESNIKOV, O. A. TERESHCHENKO, V. Sh. VARDOSANIDZE
Published 2018-10-01

Goldberg-Shprintzen Syndrome & Cerebral Dysgenesis

by J Gordon Millichap
Published 1994-02-01

Demographic study and management of colonic atresia: Single-center experience with review of literature

by Hinglaj Saha, Dipak Ghosh, Tapanjyoti Ghosh, Shibshankar Burman, Kaushik Saha
Published 2018-01-01

General versus general anaesthesia combined with caudal block in laparoscopic-assisted Soave pull-through of Hirschsprung disease: a retrospective study

by Zhixiong Lin, Yifan Fang, Lei Yan, Yu Lin, Mingkun Liu, Bing Zhang, Yuanbing He, Yong Shen, Dianming Wu, Longxin Zhang
Published 2021-08-01

نتیجه‌ی رنگ‌آميزي ايمونوهیستوشيمي در تعیین اختلال عملکرد روده بعد از عمل در كودكان مبتلا به بيماري هيرشپرونگ...

by Mehradad Hoseinpour, Sayed Mahmoud Mostafavi, Mojdeh Beyraghdar
Published 2020-10-01

Abnormal migration of vagal neural crest cells in dominant megacolon mouse embryos.

Published 2006

Incidental per-operative findings of anterior sacral meningocele during pull-through operation for Hirschsprung disease: An extremely rare case

by Md Hadiuzzaman, Biswanath Das, Dipak Ghosh, Koushik Saha
Published 2017-01-01

Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.

by Belinda K Cornes, Clara S Tang, Thomas Y Y Leon, Kenneth J W S Hui, Man-Ting So, Xiaoping Miao, Stacey S Cherny, Pak C Sham, Paul K H Tam, Maria-Merce Garcia-Barcelo
Published 2010-01-01

RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family

by Elisangela P. S. Quedas, Viviane C. Longuini, Tomoko Sekiya, Flavia L. Coutinho, Sergio P. A. Toledo, Uenis Tannuri, Rodrigo A. Toledo
Published 2012-01-01

Identification of genetic loci affecting the severity of symptoms of Hirschsprung disease in rats...

by Jieping Huang, Ruihua Dang, Daisuke Torigoe, Chuzhao Lei, Xianyong Lan, Hong Chen, Nobuya Sasaki, Jinxi Wang, Takashi Agui
Published 2015-01-01