Myelomeningocele genotype–phenotype correlation findings in cilia, HH, PCP, and WNT signaling pathways
出版年份 2021 全文链接
标题
Myelomeningocele genotype–phenotype correlation findings in cilia, HH, PCP, and WNT signaling pathways
作者
关键词
-
出版物
Birth Defects Research
Volume -, Issue -, Pages -
出版商
Wiley
发表日期
2021-01-20
DOI
10.1002/bdr2.1872
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。- A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly
- (2018) M. Ishida et al. CLINICAL GENETICS
- Vangl2 disruption alters the biomechanics of late spinal neurulation leading to spina bifida in mouse embryos
- (2018) Gabriel L. Galea et al. Disease Models & Mechanisms
- STRING v11: protein–protein association networks with increased coverage, supporting functional discovery in genome-wide experimental datasets
- (2018) Damian Szklarczyk et al. NUCLEIC ACIDS RESEARCH
- Genomic approaches to the assessment of human spina bifida risk
- (2017) M. Elizabeth Ross et al. Birth Defects Research
- Primary Cilia and Mammalian Hedgehog Signaling
- (2016) Fiona Bangs et al. Cold Spring Harbor Perspectives in Biology
- KEGG as a reference resource for gene and protein annotation
- (2015) Minoru Kanehisa et al. NUCLEIC ACIDS RESEARCH
- Spina bifida
- (2015) Andrew J. Copp et al. Nature Reviews Disease Primers
- Neural Tube Defects
- (2014) Nicholas D.E. Greene et al. Annual Review of Neuroscience
- Traffic jam in the primitive streak: The role of defective mesoderm migration in birth defects
- (2014) Nils J. Herion et al. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
- Genetic studies ofANKRD6as a molecular switch between Wnt signaling pathways in human neural tube defects
- (2014) Redouane Allache et al. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
- Roles for Hedgehog signaling in adult organ homeostasis and repair
- (2014) R. Petrova et al. DEVELOPMENT
- Shaping the nervous system: role of the core planar cell polarity genes
- (2013) Fadel Tissir et al. NATURE REVIEWS NEUROSCIENCE
- The MIntAct project—IntAct as a common curation platform for 11 molecular interaction databases
- (2013) Sandra Orchard et al. NUCLEIC ACIDS RESEARCH
- Detection of Copy Number Variants Reveals Association of Cilia Genes with Neural Tube Defects
- (2013) Xiaoli Chen et al. PLoS One
- A consideration of the evidence that genetic defects in planar cell polarity contribute to the etiology of human neural tube defects
- (2012) Diana M. Juriloff et al. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
- Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects
- (2012) Faith Pangilinan et al. BMC Medical Genetics
- Genetic Analysis of Disheveled 2 and Disheveled 3 in Human Neural Tube Defects
- (2012) Patrizia De Marco et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- InnateDB: systems biology of innate immunity and beyond—recent updates and continuing curation
- (2012) Karin Breuer et al. NUCLEIC ACIDS RESEARCH
- Spina bifida subtypes and sub-phenotypes by maternal race/ethnicity in the National Birth Defects Prevention Study
- (2011) A.J. Agopian et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Cilia in the nervous system: linking cilia function and neurodevelopmental disorders
- (2011) Ji E Lee et al. CURRENT OPINION IN NEUROLOGY
- Cilia in the CNS: The Quiet Organelle Claims Center Stage
- (2011) Angeliki Louvi et al. NEURON
- A Genetic Signature of Spina Bifida Risk from Pathway-Informed Comprehensive Gene-Variant Analysis
- (2011) Nicholas J. Marini et al. PLoS One
- An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure
- (2010) Muriel J. Harris et al. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
- Contribution of VANGL2 mutations to isolated neural tube defects
- (2010) Z Kibar et al. CLINICAL GENETICS
- Epidemiologic and genetic aspects of spina bifida and other neural tube defects
- (2010) Kit Sing Au et al. Developmental Disabilities Research Reviews
- A method and server for predicting damaging missense mutations
- (2010) Ivan A Adzhubei et al. NATURE METHODS
- VANGL2Mutations in Human Cranial Neural-Tube Defects
- (2010) Yun-Ping Lei et al. NEW ENGLAND JOURNAL OF MEDICINE
- Genetics of human neural tube defects
- (2009) N. D.E. Greene et al. HUMAN MOLECULAR GENETICS
- Novel mutations inVANGL1in neural tube defects
- (2009) Zoha Kibar et al. HUMAN MUTATION
- Genetics and development of neural tube defects
- (2009) Andrew J Copp et al. JOURNAL OF PATHOLOGY
- Detecting gene–gene interactions that underlie human diseases
- (2009) Heather J Cordell NATURE REVIEWS GENETICS
- SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies
- (2009) Zongli Xu et al. NUCLEIC ACIDS RESEARCH
- Analysis of genomic diversity in Mexican Mestizo populations to develop genomic medicine in Mexico
- (2009) I. Silva-Zolezzi et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Spina bifida before and after folic acid fortification in Canada
- (2008) Philippe De Wals et al. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
- C2cd3 is required for cilia formation and Hedgehog signaling in mouse
- (2008) A. N. Hoover et al. DEVELOPMENT
- Large-Scale Analysis of Association Between LRP5 and LRP6 Variants and Osteoporosis
- (2008) Joyce B. J. van Meurs JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Epistasis — the essential role of gene interactions in the structure and evolution of genetic systems
- (2008) Patrick C. Phillips NATURE REVIEWS GENETICS
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 MoreFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search