Literature DB >> 31693581

The search for genetic determinants of human neural tube defects.

Paul Wolujewicz1, M Elizabeth Ross.   

Abstract

PURPOSE OF REVIEW: An update is presented regarding neural tube defects (NTDs) including spina bifida and anencephaly, which are among the most common serious birth defects world-wide. Decades of research suggest that no single factor is responsible for neurulation failure, but rather NTDs arise from a complex interplay of disrupted gene regulatory networks, environmental influences and epigenetic regulation. A comprehensive understanding of these dynamics is critical to advance NTD research and prevention. RECENT
FINDINGS: Next-generation sequencing has ushered in a new era of genomic insight toward NTD pathophysiology, implicating novel gene associations with human NTD risk. Ongoing research is moving from a candidate gene approach toward genome-wide, systems-based investigations that are starting to uncover genetic and epigenetic complexities that underlie NTD manifestation.
SUMMARY: Neural tube closure is critical for the formation of the human brain and spinal cord. Broader, more all-inclusive perspectives are emerging to identify the genetic determinants of human NTDs.

Entities:  

Mesh:

Year:  2019        PMID: 31693581      PMCID: PMC6993899          DOI: 10.1097/MOP.0000000000000817

Source DB:  PubMed          Journal:  Curr Opin Pediatr        ISSN: 1040-8703            Impact factor:   2.856


  41 in total

1.  Loss of p53 Causes Stochastic Aberrant X-Chromosome Inactivation and Female-Specific Neural Tube Defects.

Authors:  Alex R D Delbridge; Andrew J Kueh; Francine Ke; Natasha M Zamudio; Farrah El-Saafin; Natasha Jansz; Gao-Yuan Wang; Megan Iminitoff; Tamara Beck; Sue Haupt; Yifang Hu; Rose E May; Lachlan Whitehead; Lin Tai; William Chiang; Marco J Herold; Ygal Haupt; Gordon K Smyth; Tim Thomas; Marnie E Blewitt; Andreas Strasser; Anne K Voss
Journal:  Cell Rep       Date:  2019-04-09       Impact factor: 9.423

Review 2.  Finding the genetic mechanisms of folate deficiency and neural tube defects-Leaving no stone unturned.

Authors:  Kit Sing Au; Tina O Findley; Hope Northrup
Journal:  Am J Med Genet A       Date:  2017-09-25       Impact factor: 2.802

Review 3.  Structural variation in the 3D genome.

Authors:  Malte Spielmann; Darío G Lupiáñez; Stefan Mundlos
Journal:  Nat Rev Genet       Date:  2018-07       Impact factor: 53.242

4.  De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus.

Authors:  Charuta Gavankar Furey; Jungmin Choi; Sheng Chih Jin; Xue Zeng; Andrew T Timberlake; Carol Nelson-Williams; M Shahid Mansuri; Qiongshi Lu; Daniel Duran; Shreyas Panchagnula; August Allocco; Jason K Karimy; Arjun Khanna; Jonathan R Gaillard; Tyrone DeSpenza; Prince Antwi; Erin Loring; William E Butler; Edward R Smith; Benjamin C Warf; Jennifer M Strahle; David D Limbrick; Phillip B Storm; Gregory Heuer; Eric M Jackson; Bermans J Iskandar; James M Johnston; Irina Tikhonova; Christopher Castaldi; Francesc López-Giráldez; Robert D Bjornson; James R Knight; Kaya Bilguvar; Shrikant Mane; Seth L Alper; Shozeb Haider; Bulent Guclu; Yasar Bayri; Yener Sahin; Michael L J Apuzzo; Charles C Duncan; Michael L DiLuna; Murat Günel; Richard P Lifton; Kristopher T Kahle
Journal:  Neuron       Date:  2018-07-05       Impact factor: 17.173

5.  Association between PKA gene polymorphism and NTDs in high risk Chinese population in Shanxi.

Authors:  Jian Wu; Xiaolin Lu; Zhen Wang; Shaofang Shangguan; Shaoyan Chang; Rui Li; Lihua Wu; Yihua Bao; Bo Niu; Li Wang; Ting Zhang
Journal:  Int J Clin Exp Pathol       Date:  2013-11-15

6.  The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia.

Authors:  Valerie K Jordan; Tyler F Beck; Andres Hernandez-Garcia; Peter N Kundert; Bum-Jun Kim; Shalini N Jhangiani; Tomasz Gambin; Molly Starkovich; Jaya Punetha; Ingrid S Paine; Jennifer E Posey; Alexander H Li; Donna Muzny; Chih-Wei Hsu; Amber J Lashua; Xin Sun; Caraciolo J Fernandes; Mary E Dickinson; Kevin P Lally; Richard A Gibbs; Eric Boerwinkle; James R Lupski; Daryl A Scott
Journal:  Hum Mol Genet       Date:  2018-06-15       Impact factor: 6.150

Review 7.  The relationship between sonic Hedgehog signaling, cilia, and neural tube defects.

Authors:  Jennifer N Murdoch; Andrew J Copp
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2010-08

8.  Threshold for neural tube defect risk by accumulated singleton loss-of-function variants.

Authors:  Zhongzhong Chen; Yunping Lei; Yufang Zheng; Vanessa Aguiar-Pulido; M Elizabeth Ross; Rui Peng; Li Jin; Ting Zhang; Richard H Finnell; Hongyan Wang
Journal:  Cell Res       Date:  2018-07-05       Impact factor: 25.617

9.  Elevated H3K79 homocysteinylation causes abnormal gene expression during neural development and subsequent neural tube defects.

Authors:  Qin Zhang; Baoling Bai; Xinyu Mei; Chunlei Wan; Haiyan Cao; Shan Wang; Min Zhang; Zhigang Wang; Jianxin Wu; Hongyan Wang; Junsheng Huo; Gangqiang Ding; Jianyuan Zhao; Qiu Xie; Li Wang; Zhiyong Qiu; Shiming Zhao; Ting Zhang
Journal:  Nat Commun       Date:  2018-08-24       Impact factor: 14.919

10.  TRIM4 is associated with neural tube defects based on genome-wide DNA methylation analysis.

Authors:  Henan Zhang; Yi Guo; Hui Gu; Xiaowei Wei; Wei Ma; Dan Liu; Kun Yu; Wenting Luo; Ling Ma; Yusi Liu; Jia Xue; Jieting Huang; Yanfu Wang; Shanshan Jia; Naixuan Dong; Hongyan Wang; Zhengwei Yuan
Journal:  Clin Epigenetics       Date:  2019-02-01       Impact factor: 6.551

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  4 in total

1.  Neural Tube Defects and Associated Factors among Neonates Admitted to the Neonatal Intensive Care Units in Hiwot Fana Specialized University Hospital, Harar, Ethiopia.

Authors:  Yunus Edris; Hanan Abdurahman; Assefa Desalew; Fitsum Weldegebreal
Journal:  Glob Pediatr Health       Date:  2020-11-13

2.  Somatic and de novo Germline Variants of MEDs in Human Neural Tube Defects.

Authors:  Tian Tian; Xuanye Cao; Yongyan Chen; Lei Jin; Zhiwen Li; Xiao Han; Ying Lin; Bogdan J Wlodarczyk; Richard H Finnell; Zhengwei Yuan; Linlin Wang; Aiguo Ren; Yunping Lei
Journal:  Front Cell Dev Biol       Date:  2021-03-04

3.  Systems biology analysis of human genomes points to key pathways conferring spina bifida risk.

Authors:  Vanessa Aguiar-Pulido; Paul Wolujewicz; Alexander Martinez-Fundichely; Eran Elhaik; Gaurav Thareja; Alice Abdel Aleem; Nader Chalhoub; Tawny Cuykendall; Jamel Al-Zamer; Yunping Lei; Haitham El-Bashir; James M Musser; Abdulla Al-Kaabi; Gary M Shaw; Ekta Khurana; Karsten Suhre; Christopher E Mason; Olivier Elemento; Richard H Finnell; M Elizabeth Ross
Journal:  Proc Natl Acad Sci U S A       Date:  2021-12-21       Impact factor: 11.205

Review 4.  The implications of exosomes in pregnancy: emerging as new diagnostic markers and therapeutics targets.

Authors:  Roya Mahdavi; Zahra Akbari Jonoush; Mehri Ghafourian; Mahvash Sadeghi; Nooshin Ghadiri; Maryam Farzaneh; Abdolah Mousavi Salehi
Journal:  Cell Commun Signal       Date:  2022-04-12       Impact factor: 5.712

  4 in total

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