Candidate Genes Associated With Neurological Findings in a Patient With Trisomy 4p16.3 and Monosomy 5p15.2-Reference-Cited by-同舟云学术

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Candidate Genes Associated With Neurological Findings in a Patient With Trisomy 4p16.3 and Monosomy 5p15.2

Published:2020-06-17 Issue: Volume:11 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Corrêa Thiago,Poswar Fabiano,Feltes Bruno César,Riegel Mariluce

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

CNPq

Publisher

Frontiers Media SA

Subject

Genetics(clinical),Genetics,Molecular Medicine

Reference60 articles.

1. Telomerase reverse transcriptase protects against angiotensin ii-induced microvascular endothelial dysfunction;Ait-Aissa;Am. J. Physiol. Heart Circ. Physiol.,2018

2. TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function;Ba;Hum. Mol. Genet.,2016

3. A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects;Beck;Neurogenetics,2016

4. A pathogenic CtBP1 missense mutation causes altered cofactor binding and transcriptional activity;Beck;Neurogenetics,2019

5. Mutation of the α-tubulin Tuba1a leads to straighter microtubules and perturbs neuronal migration;Belvindrah;J. Cell Biol.,2017

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1. Meta-Analysis Identifies BDNF and Novel Common Genes Differently Altered in Cross-Species Models of Rett Syndrome;International Journal of Molecular Sciences;2022-09-22

2. Prenatal diagnosis of de novo isochromosome 4p with an unbalanced t(4;9) translocation in a fetus with congenital anomalies: A case report and literature review;Taiwanese Journal of Obstetrics and Gynecology;2022-01

3. Shared Neurodevelopmental Perturbations Can Lead to Intellectual Disability in Individuals with Distinct Rare Chromosome Duplications;Genes;2021-04-23

4. Network‐based analysis using chromosomal microdeletion syndromes as a model;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2021-03-22

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