| P50 | author | Wei Wu | Q87791000 |
| P2093 | author name string | Jie Zhang | |
| | Bo Li | |
| | Yankai Xia | |
| | Xinru Wang | |
| | Jiahao Sha | |
| | Zhigang Zhou | |
| | Junwei Tang | |
| | Weibing Tang | |
| | Weiwei Jiang | |
| | Xiaoqun Xu | |
| | Qiming Geng | |
| | Jingjing Qin | |
| P2860 | cites work | The neuregulin-I/ErbB signaling system in development and disease | Q24302487 |
| | The NRG1 gene is frequently silenced by methylation in breast cancers and is a strong candidate for the 8p tumour suppressor gene | Q24645371 |
| | Let-7 microRNA inhibits the proliferation of human glioblastoma cells | Q28287254 |
| | Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease | Q28943464 |
| | Chromatin modifications by methylation and ubiquitination: implications in the regulation of gene expression | Q29619380 |
| | Frequent long-range epigenetic silencing of protocadherin gene clusters on chromosome 5q31 in Wilms' tumor | Q30945124 |
| | Comparing the DNA hypermethylome with gene mutations in human colorectal cancer | Q33300134 |
| | Fine mapping of the NRG1 Hirschsprung's disease locus | Q33809286 |
| | DNA methylation changes in a human cell model of breast cancer progression | Q33857557 |
| | Developmentally regulated expression of Sox9 and microRNAs 124, 128 and 23 in neuroepithelial stem cells in the developing spinal cord. | Q34142875 |
| | The contribution of associated congenital anomalies in understanding Hirschsprung's disease | Q34565449 |
| | Hirschsprung disease, associated syndromes and genetics: a review | Q34584242 |
| | Hirschsprung's disease, one of the most difficult diagnoses in pediatric surgery: a review of the problems from clinical practice to the bench. | Q34780080 |
| | Genetic basis of Hirschsprung's disease. | Q34986444 |
| | Neuregulins: functions, forms, and signaling strategies | Q35089314 |
| | Epigenetics in male germ cells | Q36730959 |
| | DNA methylation in development and human disease | Q37110130 |
| | The role of epigenetics in aging and age-related diseases | Q37589034 |
| | Epigenetics: molecular mechanisms and implications for disease. | Q39917642 |
| | The transcription factor Sox10 is a key regulator of peripheral glial development. | Q40423560 |
| | X-chromosome inactivation in mammals | Q41689513 |
| | Epigenetics and microRNAs | Q46057707 |
| | Neural crest neuroblasts can colonise aganglionic and ganglionic gut in vivo. | Q50470223 |
| | Special basic science review | Q55918741 |
| | Mutations in the NRG1 gene are associated with Hirschsprung disease | Q57233951 |
| | Sox10 haploinsufficiency affects maintenance of progenitor cells in a mouse model of Hirschsprung disease | Q78477481 |
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1694-1698 | |
| P577 | publication date | 2012-09-01 | |
| P1433 | published in | Journal of Pediatric Surgery | Q15761821 |
| P1476 | title | Aberrant high expression of NRG1 gene in Hirschsprung disease | |
| P478 | volume | 47 | |