Intermediate and expanded FMR1 alleles in an autistic Costa Rican population.
- Published in:
- Revista Mexicana de Neurociencia, 2022, v. 23, n. 2, p. 51, doi. 10.24875/RMN.21000044
- By:
- Publication type:
- Article
Works matching DE "FMR protein"
Results: 19
1
2
Pathological Effects of the FMR1 CGG-Repeat Polymorphism (5-55 Repeat Numbers): Systematic Review and Meta-Analysis.
- Published in:
- Tohoku Journal of Experimental Medicine, 2016, v. 239, n. 1, p. 57, doi. 10.1620/tjem.239.57
- By:
- Publication type:
- Article
3
Clinical and molecular implications of mosaicism in FMR1 full mutations.
- Published in:
- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00318
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- Publication type:
- Article
4
Low-normal FMR1 CGG repeat length: phenotypic association.
- Published in:
- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00309
- By:
- Publication type:
- Article
5
Recent advances in assays for the fragile X-related disorders.
- Published in:
- Human Genetics, 2017, v. 136, n. 10, p. 1313, doi. 10.1007/s00439-017-1840-5
- By:
- Publication type:
- Article
6
Screening for intermediate CGG alleles of FMR1 gene in male Iranian patients with Parkinsonism.
- Published in:
- Neurological Sciences, 2017, v. 38, n. 1, p. 123, doi. 10.1007/s10072-016-2723-6
- By:
- Publication type:
- Article
7
A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population.
- Published in:
- 2015
- By:
- Publication type:
- journal article
8
The effects of optimism, religion, and hope on mood and anxiety disorders in women with the FMR1 premutation.
- Published in:
- Journal of Intellectual Disability Research, 2017, v. 61, n. 10, p. 916, doi. 10.1111/jir.12409
- By:
- Publication type:
- Article
9
The Emergence of Effortful Control in Young Boys With Fragile X Syndrome.
- Published in:
- 2018
- By:
- Publication type:
- journal article
10
Correlation of normal-range FMR1 repeat length or genotypes and reproductive parameters.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2016, v. 33, n. 9, p. 1149, doi. 10.1007/s10815-016-0732-2
- By:
- Publication type:
- Article
11
Deletion of Fmr1 Alters Function and Synaptic Inputs in the Auditory Brainstem.
- Published in:
- PLoS ONE, 2015, v. 10, n. 2, p. 1, doi. 10.1371/journal.pone.0117266
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- Publication type:
- Article
12
Consistency of Network Modules in Resting-State fMRI Connectome Data.
- Published in:
- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0044428
- By:
- Publication type:
- Article
13
The Role of AGG Interruptions in the Transcription of FMR1 Premutation Alleles.
- Published in:
- PLoS ONE, 2011, v. 6, n. 7, p. 1, doi. 10.1371/journal.pone.0021728
- By:
- Publication type:
- Article
14
The impact of androgen metabolism and FMR1 genotypes on pregnancy potential in women with dehydroepiandrosterone (DHEA) supplementation.
- Published in:
- Human Reproduction, 2012, v. 27, n. 11, p. 3287, doi. 10.1093/humrep/des265
- By:
- Publication type:
- Article
15
Sub-synaptic, multiplexed analysis of proteins reveals Fragile X related protein 2 is mislocalized in Fmr1 KO synapses.
- Published in:
- eLife, 2016, p. 1, doi. 10.7554/eLife.20560
- By:
- Publication type:
- Article
16
Modeling Fragile X Syndrome Using Human Pluripotent Stem Cells.
- Published in:
- Genes, 2016, v. 7, n. 10, p. 77, doi. 10.3390/genes7100077
- By:
- Publication type:
- Article
17
CMP-N-acetylneuraminic acid synthetase interacts with fragile X related protein 1.
- Published in:
- Molecular Medicine Reports, 2016, v. 14, n. 2, p. 1501, doi. 10.3892/mmr.2016.5438
- By:
- Publication type:
- Article
18
Reversing Fragile X.
- Published in:
- JAMA: Journal of the American Medical Association, 2012, v. 307, n. 21, p. 2247, doi. 10.1001/jama.2012.5440
- By:
- Publication type:
- Article
19
FMR1 gene mutations cause neurodevelopmental-degenerative disorders: Importance of fragile X testing in Serbia.
- Published in:
- 2016
- By:
- Publication type:
- Editorial