In Vitro Reactivation of the FMR1 Gene Involved in Fragile X Syndrome-Reference-Cited by-同舟云学术

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In Vitro Reactivation of the FMR1 Gene Involved in Fragile X Syndrome

Published:1998-01-01 Issue:1 Volume:7 Page:109-113
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Chiurazzi P.,Pomponi M. G.,Willemsen R.,Oostra B. A.,Neri G.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/7/1/109/1787628/7-1-109.pdf

Reference28 articles.

1. A fragile gene

2. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

3. Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

4. DNA methylation of the fragile X locus in somatic and germ cells during fetal development: Relevance to the fragile X syndrome and X inactivation

5. Methylation analysis of CGG sites in the CpG island of the human FMR1 gene

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1. Epigenetic insights into Fragile X Syndrome;Frontiers in Cell and Developmental Biology;2024-08-16

2. Toward understanding the role of genomic repeat elements in neurodegenerative diseases;Neural Regeneration Research;2024-04-16

3. Epigenetic causes of intellectual disability—the fragile X syndrome paradigm;Neuropsychiatric Disorders and Epigenetics;2024

4. Methylation across the central dogma in health and diseases: new therapeutic strategies;Signal Transduction and Targeted Therapy;2023-08-25

5. Antisense oligonucleotide rescue of CGG expansion–dependent FMR1 mis-splicing in fragile X syndrome restores FMRP;Proceedings of the National Academy of Sciences;2023-06-26

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