Aberrant Expressions and Variant Screening of SEMA3D in Indonesian Hirschsprung Patients
出版年份 2020 全文链接
标题
Aberrant Expressions and Variant Screening of SEMA3D in Indonesian Hirschsprung Patients
作者
关键词
-
出版物
Frontiers in Pediatrics
Volume 8, Issue -, Pages -
出版商
Frontiers Media SA
发表日期
2020-03-11
DOI
10.3389/fped.2020.00060
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Aberrant expressions of miRNA-206 target, FN1, in multifactorial Hirschsprung disease
- (2019) Gunadi et al. Orphanet Journal of Rare Diseases
- Molecular Genetic Anatomy and Risk Profile of Hirschsprung’s Disease
- (2019) Joseph M. Tilghman et al. NEW ENGLAND JOURNAL OF MEDICINE
- Functional outcomes in Hirschsprung disease patients after transabdominal Soave and Duhamel procedures
- (2018) Amira Widyasari et al. BMC GASTROENTEROLOGY
- The impact of down-regulated SK3 expressions on Hirschsprung disease
- (2018) Gunadi et al. BMC Medical Genetics
- Histopathologic and immunohistochemical findings in congenital anorectal malformations
- (2018) Hui Xiao et al. MEDICINE
- Combined Genetic Effects of RET and NRG1 Susceptibility Variants on Multifactorial Hirschsprung Disease in Indonesia
- (2018) Gunadi et al. JOURNAL OF SURGICAL RESEARCH
- Testing the Ret and Sema3d genetic interaction in mouse enteric nervous system development
- (2017) Ashish Kapoor et al. HUMAN MOLECULAR GENETICS
- Epigenetics in ENS development and Hirschsprung disease
- (2016) A. Torroglosa et al. DEVELOPMENTAL BIOLOGY
- Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease
- (2016) Clara Sze-man Tang et al. HUMAN MOLECULAR GENETICS
- Altered neurotransmitter expression profile in the ganglionic bowel in Hirschsprung's disease
- (2016) David Coyle et al. JOURNAL OF PEDIATRIC SURGERY
- Decreased expression of NEDL2 in Hirschsprung's disease
- (2016) Anne Marie O'Donnell et al. JOURNAL OF PEDIATRIC SURGERY
- Expression of connexin 26 and connexin 43 is reduced in Hirschsprung's disease
- (2016) David Coyle et al. JOURNAL OF SURGICAL RESEARCH
- Analysis of protein-coding genetic variation in 60,706 humans
- (2016) Monkol Lek et al. NATURE
- Effects of SEMA3 polymorphisms in Hirschsprung disease patients
- (2016) Gunadi et al. PEDIATRIC SURGERY INTERNATIONAL
- Long-term results of transanal pull-through for Hirschsprung’s disease: a meta-analysis
- (2016) J. Zimmer et al. PEDIATRIC SURGERY INTERNATIONAL
- Functional Loss of Semaphorin 3C and/or Semaphorin 3D and Their Epistatic Interaction with Ret Are Critical to Hirschsprung Disease Liability
- (2015) Qian Jiang et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphisms
- (2015) Ashish Kapoor et al. HUMAN MOLECULAR GENETICS
- Effects ofMTHFRc.677C>T,F2c.20210G>A andF5Leiden Polymorphisms in Gastroschisis
- (2015) Akhmad Makhmudi et al. JOURNAL OF INVESTIGATIVE SURGERY
- Altered distribution of small-conductance calcium-activated potassium channel SK3 in Hirschsprung’s disease
- (2015) David Coyle et al. JOURNAL OF PEDIATRIC SURGERY
- Disruption of theSEMA3DGene in a Patient with Congenital Heart Defects
- (2014) Marta Sanchez-Castro et al. HUMAN MUTATION
- Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung disease
- (2014) Gunadi et al. JOURNAL OF PEDIATRIC SURGERY
- Methylation analysis of EDNRB in human colon tissues of Hirschsprung’s disease
- (2013) Weibing Tang et al. PEDIATRIC SURGERY INTERNATIONAL
- Mutational Spectrum of Semaphorin 3A and Semaphorin 3D Genes in Spanish Hirschsprung patients
- (2013) Berta Luzón-Toro et al. PLoS One
- Association of genetic polymorphisms in the RET-protooncogene and NRG1 with Hirschsprung disease in Thai patients
- (2012) Theerawut Phusantisampan et al. JOURNAL OF HUMAN GENETICS
- Aberrant high expression of NRG1 gene in Hirschsprung disease
- (2012) Weibing Tang et al. JOURNAL OF PEDIATRIC SURGERY
- Comprehensive Analysis of NRG1 Common and Rare Variants in Hirschsprung Patients
- (2012) Berta Luzón-Toro et al. PLoS One
- Differential Contributions of Rare and Common, Coding and Noncoding Ret Mutations to Multifactorial Hirschsprung Disease Liability
- (2010) Eileen Sproat Emison et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Islet1 selectively promotes peripheral axon outgrowth in Rohon-Beard primary sensory neurons
- (2010) Hideomi Tanaka et al. DEVELOPMENTAL DYNAMICS
- A map of human genome variation from population-scale sequencing
- (2010) Richard M. Durbin et al. NATURE
- Chromatin and DNA methylation dynamics during retinoic acid-induced RET gene transcriptional activation in neuroblastoma cells
- (2010) T. Angrisano et al. NUCLEIC ACIDS RESEARCH
- Two Novel Mutations in the ED1 Gene in Japanese Families With X-Linked Hypohidrotic Ectodermal Dysplasia
- (2009) Gunadi et al. PEDIATRIC RESEARCH
- Genome-wide association study identifiesNRG1as a susceptibility locus for Hirschsprung's disease
- (2009) Maria-Mercè Garcia-Barcelo et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started