Lack of Pur-alpha alters postnatal brain development and causes megalencephaly-Reference-Cited by-同舟云学术

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Lack of Pur-alpha alters postnatal brain development and causes megalencephaly

Published:2011-10-18 Issue:3 Volume:21 Page:473-484
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Hokkanen S.,Feldmann H. M.,Ding H.,Jung C. K. E.,Bojarski L.,Renner-Muller I.,Schuller U.,Kretzschmar H.,Wolf E.,Herms J.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/21/3/473/1674901/ddr476.pdf

Reference54 articles.

1. The HeLa Pur factor binds single-stranded DNA at a specific element conserved in gene flanking regions and origins of DNA replication.

2. Sequence of cDNA comprising the human pur gene and sequence-specific single-stranded-DNA-binding properties of the encoded protein.

3. SURVEY AND SUMMARY: Puralpha: a multifunctional single-stranded DNA- and RNA-binding protein

4. Role of Purα in targeting mRNA to sites of translation in hippocampal neuronal dendrites

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1. Genome-wide epigenetic signatures facilitated the variant classification of the PURA gene and uncovered the pathomechanism of PURA-related neurodevelopmental disorders;Genetics in Medicine;2024-08

2. PURA and GLUT1: Sweet partners for brain health;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2024-08

3. PURA syndrome-causing mutations impair PUR-domain integrity and affect P-body association;eLife;2024-04-24

4. PURA syndrome-causing mutations impair PUR-domain integrity and affect P-body association;eLife;2024-04-24

5. Case Report: Expanding the phenotypic spectrum of PURA syndrome in South America with the first presentation of concurrent vitiligo;Frontiers in Pediatrics;2024-03-28

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