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Expression of Three Zebrafish Orthologs of Human FMR1-Related Genes and Their Phylogenetic Relationships

Development Genes and Evolution, 2004
The original publication can be found at www.springerlink.comThe human fragile X mental retardation syndrome is caused by expansions of a CGG repeat in the FMR1 gene. FXR1 and FXR2 are autosomal paralogs of FMR1.
Michael Lardelli, Robert Ian Richards
exaly   +2 more sources

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Fragile X Syndrome Caused by Maternal Somatic Mosaicism of FMR1 Gene: Case Report and Literature Review

Genes, 2022
Irene Gómez-Manjón, Carmen Palma Milla, Juan Francisco Quesada-Espinosa   +2 more
exaly  

Efficient Delivery of FMR1 Across the Blood Brain Barrier Using AAVphp Construct in Adult FMR1 KO Mice Suggests the Feasibility of Gene Therapy for Fragile X Syndrome

Genes, 2023
Milen Velinov, Chun-Ling Dai, Kathryn K Chadman   +2 more
exaly  

Quantitative Analysis of DNA Demethylation and Transcriptional Reactivation of the FMR1 Gene in Fragile X Cells Treated With 5-Azadeoxycytidine.

Nucleic Acids Research, 2002
Pietro Chiurazzi, Giovanni Neri, Maria Grazia Pomponi   +2 more
exaly  

Synergistic Effect of Histone Hyperacetylation and DNA Demethylation in the Reactivation of the FMR1 Gene

Human Molecular Genetics, 1999
Pietro Chiurazzi, Giovanni Neri, Maria Grazia Pomponi   +2 more
exaly  

Alternative Splicing of the FMR1 Gene in Human Fetal Brain Neurons

American Journal of Medical Genetics, Part A, 1996
Yan Shen, George Y. Wu
exaly  

Mosaicism for an FMR1 Gene Deletion in a Fragile X Female

American Journal of Medical Genetics, Part A, 2005
Hongxin Fan, Rosann A. Farber, Jessica K Booker   +2 more
exaly  

CGG Repeat in the FMR1 Gene: Size Matters

Clinical Genetics, 2011
B A Oostra
exaly  

Pharmacological Reactivation of the Silenced FMR1 Gene as a Targeted Therapeutic Approach for Fragile X Syndrome

Brain Sciences, 2019
Daman Kumari, Karen Usdin, Inbal Gazy
exaly